Open Access

What have we learned from brucellosis in the mouse model?

  • María-Jesús Grilló1,
  • José María Blasco2,
  • Jean Pierre Gorvel3, 4, 5,
  • Ignacio Moriyón6, 7 and
  • Edgardo Moreno8, 9Email author
Veterinary Research201243:29

DOI: 10.1186/1297-9716-43-29

Received: 13 July 2011

Accepted: 13 April 2012

Published: 13 April 2012

Abstract

Brucellosis is a zoonosis caused by Brucella species. Brucellosis research in natural hosts is often precluded by practical, economical and ethical reasons and mice are widely used. However, mice are not natural Brucella hosts and the course of murine brucellosis depends on bacterial strain virulence, dose and inoculation route as well as breed, genetic background, age, sex and physiological statu of mice. Therefore, meaningful experiments require a definition of these variables. Brucella spleen replication profiles are highly reproducible and course in four phases: i), onset or spleen colonization (first 48 h); ii), acute phase, from the third day to the time when bacteria reach maximal numbers; iii), chronic steady phase, where bacterial numbers plateaus; and iv), chronic declining phase, during which brucellae are eliminated. This pattern displays clear physiopathological signs and is sensitive to small virulence variations, making possible to assess attenuation when fully virulent bacteria are used as controls. Similarly, immunity studies using mice with known defects are possible. Mutations affecting INF-γ, TLR9, Myd88, Tγδ and TNF-β favor Brucella replication; whereas IL-1β, IL-18, TLR4, TLR5, TLR2, NOD1, NOD2, GM-CSF, IL/17r, Rip2, TRIF, NK or Nramp1 deficiencies have no noticeable effects. Splenomegaly development is also useful: it correlates with IFN-γ and IL-12 levels and with Brucella strain virulence. The genetic background is also important: Brucella-resistant mice (C57BL) yield lower splenic bacterial replication and less splenomegaly than susceptible breeds. When inoculum is increased, a saturating dose above which bacterial numbers per organ do not augment, is reached. Unlike many gram-negative bacteria, lethal doses are large (≥ 108 bacteria/mouse) and normally higher than the saturating dose. Persistence is a useful virulence/attenuation index and is used in vaccine (Residual Virulence) quality control. Vaccine candidates are also often tested in mice by determining splenic Brucella numbers after challenging with appropriate virulent brucellae doses at precise post-vaccination times. Since most live or killed Brucella vaccines provide some protection in mice, controls immunized with reference vaccines (S19 or Rev1) are critical. Finally, mice have been successfully used to evaluate brucellosis therapies. It is concluded that, when used properly, the mouse is a valuable brucellosis model.

Table of content

  1. 1

    Introduction

     
  2. 2
    Infection models
    1. 2.1

      The Brucella stains: replication patterns and related effects

       
    2. 2.2

      Route of the infection

       
    3. 2.3

      Infective dose

       
    4. 2.4
      The mouse
      1. 2.4.1

        Resistant and susceptible mouse strains

         
      2. 2.4.2

        Mutant and knockout mice

         
      3. 2.4.3

        Age and sex

         
      4. 2.4.4

        Transmission

         
       
     
  3. 3
    Physiopathology
    1. 3.1

      Onset of the infection

       
    2. 3.2
      Acute phase
      1. 3.2.1

        Acute phase in pregnant mice

         
       
    3. 3.3

      Chronic steady phase

       
    4. 3.4

      Chronic declining phase

       
     
  4. 4

    Vaccination

     
  5. 5

    Superinfection and antigen therapy

     
  6. 6

    Passive transfer and immunomodulation

     
  7. 7

    Antibiotic treatment

     
  8. 8

    Concluding remarks

     
  9. 9

    Endnotes

     
  10. 10

    Competing interests

     
  11. 11

    Authors’ contributions

     
  12. 12

    Acknowledgments

     
  13. 13

    References

     

1 Introduction

The genus Brucella comprises at least eight species named according to their preferred mammal hosts. Brucella melitensis Brucella abortus and Brucella suis are the most economically important species and they preferentially infect goats and sheep, bovines and swine, respectively [1]. Livestock is the source of human infections, and brucellosis is a severe disease that affects a considerable number of people in the world [1]. These bacteria cause long lasting chronic infections, mainly colonizing the reticuloendothelial system and reproductive organs [2, 3], replicating in the internal milieu of trophoblasts, macrophages and dendritic cells [4]. Although able to multiply in life-less media, Brucella organisms are better described as facultative extracellular intracellular parasites [5].

For many years the pathophysiology of brucellosis was investigated in humans and natural hosts [3, 69]. However, experimentation in ruminants, humans and primates has economical and ethical concerns or is precluded for practical reasons. Consequently, small laboratory animals are frequently employed as models in brucellosis research. One of the first experimental models was the chicken embryo [10]. Although this model was useful for evaluating the intracellular multiplication of Brucella, it does not differentiate virulent from attenuated strains. The rabbit has been used in protocols designed to study Brucella toxicity and hypersensitivity, mainly because of its susceptibility to bacterial endotoxins and toxins [11]. Due to practical reasons related to size, management and cost, the rabbit has never been widely used as a model in brucellosis, although it is used to produce antibodies against Brucella antigens [12]. Owing to their high susceptibility to Brucella infections and similarities in reproducing human pathology, the guinea pig was extensively used as an experimental animal [13]. These rodents reproduce the pulmonary, hepatic, spleen and genital lesions and the hypersensitivity reactions observed in humans, and match the different phases of the infection caused by Brucella in natural hosts, including abortion [1315]. Thus, the guinea pig is one of the best models and it is still used for some immunological and vaccine studies [16, 17]. However, when large numbers of animals are necessary, guinea pigs become impractical for the same reasons as rabbits. Other laboratory rodents such as rats, hamsters and gerbils have been used sporadically [13].

The mouse (Mus musculus) has been the most widely used brucellosis model. Mice were first used by Holth in 1911 for Brucella vaccine testing. Thereafter, mice were used for the etiological confirmation of samples from infected animals, to test virulence and for the evaluation of the pathological lesions (see [18, 19]). The results in mice are not immediately applicable and transferable to humans or to the target animal species. However, the uncovering of a significant phenotype in mice using an appropriate protocol gives useful information. With the arrival of inbred, mutant, knockout and transgenic mice and the understanding of their biology and immunology [20, 21], this rodent has become the standard model for brucellosis research.

In this work we have reviewed the models of infection by O-polysaccharide containing (smooth) Brucella species and strains in mice. Although we have focused on in vivo assays, we occasionally refer to ex vivo studies in cells when they are relevant for understanding the biology of smooth brucellae in mice. For reasons related to the extent of the document, we have avoided reviewing the infection models induced by the rough brucellae. For a better understanding on the biological behavior of the rough strains in mice, we suggest the work of González et al. [22].

2 Infection models

The outcome of the infection in mice depends on the virulence and dose of the Brucella strain, the route of inoculation, and on the breed, genetic background, age, sex and physiological status of the mice. Since most studies in mice are devoted to investigate virulence, pathogenicity, immunology and vaccine properties, it is critical to include control groups inoculated with appropriate reference Brucella strains [23, 24]. In the following sections, we discuss the importance of these factors.

2.1 The Brucella strains: replication patterns and related effects

The affinity of some Brucella species for a particular mammal host is well-known [1]. It is also notorious that B. melitensis and some biovars of B. suis infect humans more frequently and cause a more severe disease than B. abortus[1]; though, these infectivity and virulence patterns do not always reproduce in mice. For instance, in a comparative study it was found that the order of virulence in mice was B. melitensis H38 (biovar 1) > B. abortus 2308 (biovar 1) > B. suis 1330 (biovar 1) [25]. Moreover, there are differences in the pathological behavior among biovars and strains of some virulent species, and the virulence demonstrated for their target hosts does not necessarily parallels that observed in mice [25, 26]. The appraisal of these issues becomes more complicated when different Brucella strains are simultaneously inoculated for comparative purposes. In addition to the eight recognized Brucella species and several biotypes (and more in the “waiting list”), a large number of bacterial mutants and constructs have been developed and tested in the murine system. In general, three different categories of Brucella strains may be distinguished in relation to pathogenicity, ability to multiply and persist in mice: virulent, attenuated and avirulent.

Although most organs of the reticuloendothelial system may become infected (depending upon the bacterial dose), the spleen and liver are the most conspicuously infected organs in mice. In these organs, virulent smooth brucellae (e.g. B. abortus 2308 and 544, B. melitensis 16 M and H38, and B. suis 1330) show a very reproducible pattern that is clearly different from that of the attenuated vaccines and the non-virulent brucellae. In the initial phases, the numbers of CFU/organ are similar in the liver and in the spleen, but the number of CFU/g of organ is lower in liver (one to two logarithms). In subsequent phases, the CFU are consistently lower in the liver [27, 28] and virulent brucellae are completely cleared from this organ beyond 3–4 weeks post-infection (pi) [29]. This pattern is somewhat different from that observed in spleens (see Physiopathology). In splenectomized mice, the liver becomes rapidly colonized [15]. It seems therefore, that the higher Brucella colonization of the spleen during the chronic phases guards the liver from a profound inflammation [15]. Due to this, liver is seldom used for estimating the number of CFU, and the spleen is the preferred target organ to study Brucella infections in mice.

The enumeration of bacteria in spleen (expressed as the mean ± SD of individual Log10 CFU/spleen or Log10 CFU/g of spleen; Figure 1) provides highly reproducible replication profiles. The lapse of the different infection phases (Figure 1) may vary depending upon the inoculation protocol. Nevertheless, at the optimal dose of infection (see below) a consistent replication profile for the reference Brucella strains is maintained within a certain range [29]. In the understanding that infection with virulent Brucella (at standard doses, see below) is a continuous process and that delimitations are not clear cut, this replication profile can be divided into four different phases (Figure 1A): i) the onset of the infection, marked by colonization during the first 48 h pi; ii) the acute phase, extending from the 3rd day to the time when CFU reach their maximum, generally between weeks 2 and 3; iii) the chronic steady phase, that corresponds to the CFU plateau, commonly lasting 8–11 weeks; and iv) the chronic declining phase, at which there is a slow elimination of the bacteria that may last beyond 36 weeks. The span of these phases may vary depending upon the bacterial dose, route, mouse strain and age [30]. Generally, experiments in mice are not prolonged more than 3–4 months and, therefore, data on the Brucella persistence in these animals after this period are scarce. It has been documented that Brucella organisms may still be recovered from the spleen and lymph nodes of mice after 6 months of infection [25, 31], suggesting that virulent Brucella might remain in mice for life. Although some quantitative variations have been observed, the spleen replication patterns of virulent strains follow similar kinetics [24, 25]. Fully avirulent strains (e.g. B. abortus bvrS mutant; Figure 1A) are unable to multiply or persist, regardless of the dose. In contrast, attenuated strains (e.g. S19 and Rev1) can multiply at the levels of the virulent strains at the early phases (Figure 1A) but persist for shorter times, even when inoculated at large doses (e.g. 108 CFU/animal) [31]. The degree to which attenuated bacteria are able to persist is the basis of the recommended Residual Virulence quality control of anti-Brucella vaccines [16]. It is expressed as the Recovery Time 50 (RT50), i.e. the time (in weeks) at which the bacterium is eliminated from the spleens in half of vaccinated mice. Used in this way, the murine model has demonstrated its usefulness to detect batches of poor immunogenic reference vaccines [3234].
https://static-content.springer.com/image/art%3A10.1186%2F1297-9716-43-29/MediaObjects/13567_2011_Article_157_Fig1_HTML.jpg
Figure 1

Replication profiles of B. abortus in mice spleens. (A) Spleen replication curves of virulent (2308 strain), vaccine-attenuated (S19 strain) and non-virulent (bvrS mutant) B. abortus strains during 36 weeks after inoculation in CD-1 mice. The abscissas axis (time after infection) of the inserted panel is expressed in logarithmic scale, to allow a better understanding of the initial phases of infection. The different phases of the infection (I, onset of infection; II, acute phase; III, chronic steady phase; IV, chronic declining phase) are depicted by the discontinuous vertical lines. (B) Spleen replication curves of virulent B. abortus 2308 strain in susceptible BALB/c and resistant C57BL/10 mice (adapted from [35], with permission).

The course of Brucella infections induced by attenuated strains, such as vaccines S19 and Rev1, or non-virulent mutants, such as VirB or BvrS [36, 37], is radically shortened and modified (Figure 1A). Similarly, the replication profiles in knockout or mutant mice may vary according to the defect displayed by the corresponding mouse strain (Table 1). In the case of vaccine S19 (which shows a conspicuous Residual Virulence), the replication kinetics in the spleen follows a rapid increase that peaks between weeks 1 and 3, and then decreases steadily at approximately one logarithm per week [23, 24]. Nonetheless, this vaccine may still be recovered from spleens 8 to 12 weeks pi. The replication profile of vaccine Rev1 shows some differences with respect to that of S19. In general, Rev1 does not display the rapid increase demonstrated by S19, declines more slowly, and is still present after 8 to 12 weeks [33]. As stated above, non-virulent strains do not multiply or increase in the initial phases of the infection, and then decline very fast (Figure 1A) being eliminated from the spleen and the liver between the 2nd and 7th week [37, 38].
Table 1

Replication and persistence of smooth virulent Brucella in mutant and knockout mice strains

Test mouse strain

Phenotypic defect

Reference mouse strain

Brucella spleen CFU increase and persistence relative to mouse reference straina

References

Early before 14 days

Late after 15 days

CBA/H

Inbred no specific defect

BALB/c

[39]

CBA/H

Inbred no specific defect

C57BL/10

[39]

CBA/NJ

Inbred no specific defect

BALB/c

[40]

DBA2

Inbred no specific defect

C57BL/6

[41, 42]

CD-1

Outbreed Swiss mice

BALB/c

[40]

BALB/c

Inbred no specific defect

C3H/HeN

[40]

BALB/c

Inbred no specific defect

C57BL/6

[39]

BALB/c

Inbred no specific defect

C57BL/10

[39]

BALB/c

Inbred no specific defect

C.CB (Nramp1r)

[43]

C57BL/10

Inbred no specific defect

B10Br

[39]

C57BL/6 (TLR9)

CpG motifs recognition

C57BL/6

[44, 45]

BALB/c (TLR9)

CpG motifs recognition

BALB/c

[46]

BALB/c (TLR4)

LPS detection

BALB/c

[46]

BALB/c (TLR4)

LPS detection

BALB/c

[44]

C3H/HeJ (TLR4)

LPS detection

C3H/HePas

[47]

C3H/HeJ (TLR4)

LPS detection

C3H/HeAu

[48]

C3H/HeJ (TLR4)

LPS detection

C3H/Heb

[41, 42]

C3H/HeJ (TLR4)

LPS detection

C3H/HeN

[40, 49]

C3H/HeJ (TLR4)

LPS detection

BALB/c

[40]

C57BL/6 (TLR4)

LPS detection

C57BL/6

[50]

C57BL/6 (TLR2)

Lipoproteins detection and peptidoglycan detection

C57BL/6

[47, 50]

BALB/c (TLR2)

Lipoproteins detection and peptidoglycan detection

BALB/c

[46]

BALB/c (TLR2)

Lipoproteins detection and peptidoglycan detection

BALB/c

[44]

C57BL/6 (TLR2/4)

LPS and lipoproteins detection

C57BL/6

[50]

BALB/c (TLR2/4)

LPS and lipoproteins detection

BALB/c

[44]

C57BL/6 (NOD1)

muramyl peptides

meso-diaminopimelic acid

C57BL/6

ND

[51]

C57BL/6 (NOD2)

muramyl dipeptides

C57BL/6

ND

[51]

C57BL/6 (Myd88)

Low proinflammatory response

C57BL/6

[44, 45, 50]

C57BL/6 (TRIF)

Low proinflammatory response

C57BL/6

[44]

C57BL/6 (TRIF)

Low proinflammatory response

129 Sv/Ev

ND

[44]

C57BL/10 (IRAK-4)

Low proinflammatory response

C57BL/6

[52]

C57BL/6 (Rip2)

NOD adaptor protein

C57BL/6

ND

[51]

C57BL/6 (gp91 phox )

Low respiratory burst in phagocytes

C57BL/6

[53]

C57BL/6 (iNOS)

Low respiratory burst in phagocyte

C57BL/6

[44]

C57BL/6 (iNOS)

Low respiratory burst in phagocytes

C57BL/6

[53]

C57BL/6 (IL-12p40)

Early differentiation of Th1 cells

C57BL/6

[53]

DBA/2j xC57BL/6 (iNOS/IL-12p40)

Early differentiation of Th1 cells and low respiratory burst

DBA/2j xC57BL/6

[53]

DBA/2 J (ICSBP)

Deficient in IL-12p40 and

low respiratory burst

C57BL/6

[53]

C57BL/6 xDBA/2 J (iNOS/ICSBP)

Deficient in IL-12p40 and

low respiratory burst

C57BL/6 xDBA/2 J

[53]

C57BL/6 (IRF-2)

Deficient in NK cells and dysregulation of IL-12p40

C57BL/6

[53]

C57BL/6 (igh6)

Affects B cells

C57BL/6

↔/↓

[54]

C57BL/6 (igh6)

Affects B cells

C57BL/6

[55]

BALB/c (jh)

Affects B cells

BALB/c

[55]

C57BL/6 (rag-1)

Affects B and T cells

C57BL/6

[54]

C57BL/6 (Cd4)

Affects CD4 T cells

C57BL/6

[54]

C57BL/6 (Aβ)

Affects CD4 T cells

C57BL/6

[56]

C57BL/6 (Aβ)

Affects CD4 T cells

C57BL/6

[55]

C57BL/6 (Pfp)

Affects Restriction of Tc mediated killing

C57BL/6

[57]

C57BL/6 (β2m)

Affects CD8 T cells

C57BL/6

[56]

C57BL/6 (β2m)

Affects CD8 T cells

C57BL/6

[54]

C57BL/6 (β2m)

Affects CD8 T cells

C57BL/6

[57]

C57BL/6 (β2m)

Affects CD8 T cells

C57BL/6

[55]

C57BL/6 (IL12/β2m)

Affects CD8 T cells and

early differentiation of Th1 cells

C57BL/6

[58]

C57BL/6 (nu/nu)

Lack thymus derived T cells

C57BL/6

[59]

BALB/c (ifng)

Absence of IFN-γ

BALB/c

↑ Dead

[57]

C57BL/6 (ifng)

Absence of IFN-γ production

C57BL/6

[44, 54, 58]

C57BL/6 (ifng)

Absence of IFN-γ production

C57BL/6

↑ Dead

[57]

C57BL/6 (ifng)

Absence of IFN-γ production

C57BL/6

[55]

C57BL/6 (ifng)

Absence of IFN-γ production

C57BL/6

ND

[60]

C57BL/6 (IRF-1)

CD8 T and NK cells dysregulation of IL-12p40 low respiratory burst

C57BL/6

↑ Dead

[53]

BALB/c (infar1)

More susceptible to viral Infections. Affects NK

BALB/c

[61]

C57BL/6 (INFαβR)

More susceptible to viral Infections. Affects NK

129 Sv/Ev

ND

[62]

C57BL/6 (TCRδ)

Absence of Tγδ cells

C57BL/6

[60]

C57BL/6 (GM-CSF)

Higher lung infection Defective alveolar macrophages

C57BL/6

[60]

C57BL/6 (IL-17Rα)

Defective in PMN recruitment and PMN activity

C57BL/6

ND

[60]

C57BL/6 (IL-1β)

Low proinflammatory response

C57BL/6

[50]

C57BL/6 (IL-18)

Early activation of NK and Th1 cells

C57BL/6

[50]

C57BL/6 (IL-1βx IL-18)

Low proinflammatory response and recruitment of NK and Th1 cells

C57BL/6

[50]

C57BL/10 (TNF-α)

Low proinflammatory response

C57BL/10

ND

[63]

Brucella susceptibility order: CBA/H>CBA/NJ=CD-1=BALB/c=C3H/HeN=C3H/HeJ>C57BL/10=C57BL/6≥B10Br.

a (↑) Significantly higher numbers of CFU in spleen than in controls; (↓) significantly lower numbers of CFU in spleen than in controls; (↔) no significant number of CFU in spleen in relation to the controls; ND, not done.

Simultaneously with bacterial replication, there is swelling of the spleen (Figure 2) and liver as well as draining through lymphatics from the site of the infection (see Physiopathology). The enlargement of the spleen is characterized by a weight peak (e.g. ≥ 400 mg) evident from weeks 3 to 16 (Figure 2A). This enlargement is a consequence of inflammation [25] and it depends on the Brucella dose and virulence [64], as well as on the immune status and genetic background of the mice [50, 53, 6567] (see Physiopathology). For example, B. melitensis H38 induces an intense splenic enlargement that generally surpasses that induced by other strains such as B. melitensis 16 M, B. suis 1330 or B. abortus 544. Attenuated S19 vaccine induces a characteristic peak of splenomegaly that occurs close to 2 weeks after inoculation and that, depending on the dose, may exceed that of B. abortus 2308 or 544. However, while in S19 infected mice the weight of the spleen rapidly decreases, the spleen of mice inoculated with virulent Brucella keeps increasing up to the end of the chronic steady phase (Figure 1B). Finally, killed Brucella or non-virulent strains (e.g. B. abortus BvrR/BvrS or VirB mutants) barely cause an increase in spleen size, even when injected in very large quantities (e.g. > 5 × 107/mouse) [68]. This corresponds to a general phenomenon linked to the rapid removal and killing of non-virulent strains by professional phagocytes.
https://static-content.springer.com/image/art%3A10.1186%2F1297-9716-43-29/MediaObjects/13567_2011_Article_157_Fig2_HTML.jpg
Figure 2

Spleen inflammation in mice infected with B. abortus . (A) Evolution of the average of spleen weights (as an indicator of inflammation) of CD-1 mice infected with virulent (2308 strain), vaccine-attenuated (S19 strain) and non-virulent (bvrS mutant) B. abortus strains during 25 weeks after inoculation. The abscissas axis (time after infection) of the inserted panel is expressed in logarithmic scale to allow a better understanding of spleen inflammation at the initial phases of infection. (B) Comparison of spleen size (left) and histological transversal sections stained with hematoxylin-eosine of normal spleen (upper panel) and B. abortus 2308 infected spleen, after 8 weeks pi (lower panel). Notice that the proportion between white pulp/red pulp in the normal spleen is close to 1/1, while in the infected spleen is close to 1/4. The histological section of normal mouse is from Dr Frank Voelker, Flagship Biosciences, with permission of Steve Pots Charting A New Course in Tissue Analysis [69].

Quality control of the Brucella strains is of paramount importance. In addition to its tendency to dissociate into rough forms [1, 70], smooth brucellae are prone to become attenuated upon storage at 4°C, after subculturing, or in old or prolonged cultures without showing appreciable biochemical or bacteriological modifications [32]. In vitro passages should be reduced to a minimum, and the original strain kept for comparison. To rule out attenuation as much as possible, it is recommended that the Brucella strain be expanded only once, and then frozen at −80°C or in liquid nitrogen until used. When expanded, these frozen stocks should maintain the expected parameters of the strain and pass at least one additional test in macrophages: non-opsonized smooth virulent brucellae multiply in non-activated macrophages (e.g. RAW 264.7, J774, human monocytes or bone marrow derived) and show a characteristic replication curve [66]. This profile often shows a 0.5 to 1.5 logarithm drop during the first 12 to 15 h, and then steadily levels up and increases 1 to 2 logs after 24 to 48 h. If the Brucella strain keeps a steady state after the critical period of 12 h (as it is the case of B. abortus S19) or drops quickly (like the avirulent VirB or BvrS-BvrR mutants), it is either attenuated or non-virulent. Alternatively, the macrophages may have been activated (e.g. endotoxin in the culture media), increasing their bactericidal abilities [66]. Once the Brucella strain has passed this test, the stored aliquots of the same stock shall be expanded and assayed in mice. Indeed, it may happen that some strains showing the adequate profile in macrophages fail to display a virulent profile in mice and are thus attenuated. This is the case of some mutants that, nevertheless, pass the multiplication test in macrophages [22, 71]. One alternative procedure when hesitating about the quality of a Brucella strain of known virulence is to inoculate the bacterium into mice and then recover the organisms from the spleen after 2 to 3 weeks [37, 72]. Once selection of the virulent phenotype has been ensured, the isolate has to be handled as described above, since some Brucella rough variants may arise in the spleens of infected mice [73].

Attenuated and non-virulent Brucella mutants present a particularly difficult problem because stocks of these strains in different laboratories frequently come from serial passages in vitro. This problem is exemplified by the differences in Residual Virulence found for various lots of vaccines [16, 32, 33]. A drawback of vaccine Rev1 is its tendency to dissociate from smooth to rough organisms. This event has a profound negative effect on the immunogenicity and Residual Virulence and efficacy, since rough bacteria are highly attenuated [32, 33]. The simultaneous presence of large and small colonies (evidenced only after 4 days culture) is a common change observed in S19 vaccines stocks that may be related to virulence differences in mice [33]. Similarly, when making mutants by genetic manipulation, a number of passages (frequently in the presence of antibiotics) is necessary, and these steps bias the selection in favor of bacteria that grow preferentially in vitro and that may introduce further attenuation not associated with the specific genetic defect studied. Therefore, it is always recommended to balance these studies with the use of complemented mutant strains, even if this method does not necessarily restore the levels of the original in vivo behavior [37].

The above-described Brucella replication profiles can be expressed either as log10 CFU/organ or as log10 CFU/g of organ. However, in some cases the CFU/organ may give statistical significant differences, whereas the normalized CFU/g of organ values may erase this statistical significance. Expressing the CFU/gram, while correcting for individual variations due to inflammatory responses, eliminates information on the absolute bacterial numbers recovered, and then the CFU values are lower. It is thus better to express the CFU per organ. One concern about the latter method is that it assumes that all mice have closely similar spleen weights. If deemed necessary because there are large differences in spleen weights, it is possible to include the individual spleen weights and CFU/organ in two “dot” graphics. In most cases, however, the overall significance does not change.

2.2 Route of the infection

Mice are commonly infected intraperitoneally (i.p.) or intravenously (i.v.) with doses ranging from 104 to 107 CFU/mouse in a volume of 0.2 to 0.05 mL. Both routes infect 100 % of the mice and induce similar levels of infection. However, the i.p. route is preferred: it is technically simpler, admits larger volumes and, therefore, it is less prone to inoculation errors. The i.p. route results in higher bacterial counts and faster colonization of the spleen than other organs [39, 65, 74]. On the other hand, the i.v. route (commonly in the tail vein) promotes a slightly faster and higher bacterial colonization of the liver in relation to the spleen during the first 10 days, an event that is reversed during the following 2 weeks and then maintained throughout the infection period, up to 120 days or more [29]. Smooth brucellae are quickly phagocytized by leukocytes following i.v. inoculation. The same phenomenon is observed after i.p. infection but with 1 to 3 h delay [14], suggesting that the bacteria promptly reach the blood via the thoracic duct and probably through the peritoneal capillary system as well. No matter if inoculated i.p. or i.v., bacteria are distributed throughout the reticuloendothelial system and placenta within the 1st week, and depending on the dose, they can also be isolated in testes, joints and salivary glands [25, 75, 76]. The central nervous system of the adult normal mouse does not seem to be colonized when using these routes, even at high doses [76]. Although strict experimentation concerning the presence of the bacterium in the meninges has not been performed, the behavior of infected mice does not suggest brain infection. It is striking that in contrast to what has been reported in humans, dolphins and the fetuses of ungulates [7779], there are no reports on neurobrucellosis in other juvenile or adult natural Brucella hosts, such as bovine, caprine or ovine. However, since domestic animals are most often culled upon evidence of the disease, this is an aspect that has not been studied in all its dimensions. Neurobrucellosis is quite an interesting syndrome because the hematoencephalic barrier imposes several unique conditions to the invading pathogen.

The subcutaneous (s.c.) inoculation, either in the back zone or in the footpad of mice results in lower levels of infection than the i.p. or i.v. routes [26, 74, 80, 81]. This effect may be due to local recruitment of bacteria at the site of inoculation. The s.c. route in the back zone is recommended for quality control of vaccines [16]. Inoculation of Brucella suspensions (e.g. 105 to 106 CFU/mouse in 0.05 mL) into the footpad causes local inflammation; enhanced by the relatively large volume deposited in a small area that induces tissue destruction and the subsequent phagocytosis by resident leukocytes. After footpad injection a spreading of the Brucella infection takes place through the lymphatics, favoring the localization of the bacterium in the popliteal lymph node [75, 8284]. At about 1 h pi, brucellae are already detected in blood, spleen and liver, reaching a transient plateau in these organs 6 h later [83, 84]. Then, they can extend to other organs [74]. The s.c. infection in the back zone (e.g. 105–109 CFU/mouse) follows a similar course as the footpad inoculation [74]. The s.c. inoculation of B. abortus or B. melitensis rarely induces pus. Nevertheless, depending on the bacterial dose and the volume injected, a local granuloma formed by mononuclear cells and neutrophils appears in the inoculation site after several days. Vaccine Rev1 can induce encapsulated local transient abscesses when inoculated by the s.c. route. However, this only happens at very high doses (≥ 108 CFU) and abscesses are of benign nature being resolved in a few days/weeks [22], in parallel with what it is observed in sheep inoculated by s.c. route with the same strain [85].

The respiratory route of infection (through aerosols or intranasal) has been considered by some authors as the most natural route, and a source of laboratory accidents and of potential bio-terrorism attacks [86, 87]. Leaving aside the inherent risks of this procedure, a precise assessment of the CFU inoculated is more inexact than when using other routes. The aerosol method requires estimating the bacterial inocula within a respiratory chamber by sacrificing a group of mice immediately after exposure to the aerosol [86, 87]. Moreover, simultaneous infection trough conjunctival, nasal and oral mucosae cannot be excluded during aerosol exposure, with the ensuing problems in interpretation. The intranasal route of infection displays similar problems because mice are very good at sneezing, generating local aerosols. In any case, these routes of inoculation induce an immediate infection of the lungs, which is then distributed by blood to the reticuloendothelial system [8688]. Early in lung infections, Brucella is present and replicates in alveolar macrophages. Then, bacteria are disseminated to the lung-draining mediastinal lymph nodes where they replicate in both migratory dendritic cells and migratory alveolar macrophages. These last phagocytic cells seem to be critical regulators of the early innate immune response within the lungs [4].

The oral route by gavage has been used in mice attempting to reproduce human or experimental goat [89] infection after ingestion of contaminated dairy products with Brucella[9092]. However, the gastrointestinal route is inefficacious to infect humans [7, 93] and mice [91] with Brucella. In addition to the challenges posed by the local microbiota, epithelial layers and specific local immune responses, the gastric acid pH and bile salts negatively affect bacteria that, like brucellae, hardly or not at all grow at pH below 5 and have outer membranes that are not barriers to hydrophobic substances [94]. The difficulties in infecting mice by this route may also be related to the robust local resistance associated with the presence of specialized Paneth cells in the intestinal tract. These cells are rich in bactericidal substances that, together with the strong acidic conditions, contribute to the gastrointestinal barrier in mice [21]. Moreover, there are some technical difficulties intrinsic to this route, and infection trough the oral mucosa and the “digestive” or “intestinal” infection are very different issues [3]. To achieve infection through gavage inoculation, very large numbers of Brucella (≥ 1010 CFU/mouse) have to be placed in the oro-esophageal cavity typically in 0.1 to 0.25 mL. Under these conditions, the plastic tubing or ball needles used in gavage are prone to deposit bacteria into the upper esophagus and in the oral cavity. Consequently, infections via both oral and throat mucous membranes are exceedingly difficult to rule out. Even with those large doses, only a low proportion of bacteria (1–2 %) translocate through gut cells, and are distributed in the reticuloendothelial organs. After 8 h, the bacteria may be recovered from the ileum, cecum and colon and to a lesser extent from the spleen, liver, mesenteric lymph nodes and Peyer´s patches. As expected, whereas in the intestine the numbers of bacteria decrease over time, the numbers in the spleen, liver and lymph nodes steadily increase during the first 2 weeks, indicating the high affinity of Brucella for the reticuloendothelial system. A proportion of mice do not show bacteria in the main target organs [91, 92], consistent with the idea that Brucella infection through the gastrointestinal route is unfavorable. As an alternative to gavage, large numbers of Brucella have been injected into intestinal loops, favoring the internalization of significant bacterial numbers by ileal Peyer´s patches dendritic cells [95]. This procedure induces little inflammatory response.

2.3 Infective dose

A myriad of bacterial doses have been used in experimental murine brucellosis. Indeed, it is essential to determine the dose retrospectively by plating aliquots of the inoculum [33, 68]. To know how many live bacteria have been inoculated is critical because, whereas live brucellae predominantly induce a Th1 response [66], dead brucellae have a tendency to induce T-independent responses [96]. This precaution is even more relevant when different Brucella strains are compared.

Brucella hardly induces mortality in mice and, therefore, it is not commonly used as a criterion of virulence. Singer-Brooks [19] performed a comprehensive study on the effects of Brucella dose in mice. She observed that a larger proportion of mice succumbed after i.p. injections of massive doses of virulent smooth Brucella (> 4 × 108 CFU/mouse), displaying obvious clinical signs. On the contrary, doses lower than 107 CFU/mouse did not induce death or relevant clinical symptoms. Nevertheless, these non-lethal doses induced necrotic areas in the liver and spleen enlargement within the first 3 weeks pi. Perusal of the literature shows that these observations have been repeatedly confirmed.

The optimal dose of Brucella infection is defined as the lower number of bacteria that infects the spleen of all mice (between 20–23 grams) at consistent significant levels [97]. This optimal dose varies depending on the bacterial strain and route of infection as well as on the genetic background and physiological status of the mice. The optimal dose has been determined only for classical brucellae [25, 35, 75, 81] as well as for some bacterial constructs [22, 98]. When inoculated at low doses (< 103 CFU/mouse), Brucella induces inconsistent infections in mice, generating wide standard deviations in CFU that complicate statistical interpretations. Doses lower than 103 CFU/mouse do not produce gross anatomical changes, despite the fact that some mice show bacteria in several organs and tissues during the first weeks [19]. In contrast, very high Brucella inocula (> 107 CFU/mouse) cause saturation of the spleen, to the point that the number of CFU per organ does not increase with respect to the optimal dose. Although these large doses induce a noticeable enlargement of the target organs (e.g. spleen and liver), distribution of Brucella in the reticuloendothelial system barely changes [29]; however, other organs may be also invaded [76]. If the mouse survives, the reduction of Brucella numbers follows its course albeit with a more protracted elimination time. B. abortus 2308 at i.p. doses between 5 × 108 and 109 CFU/mouse kill almost 50 % of the mice after 48 h, and 100 % before 1 week [48]. At these large doses, clinical symptoms such tachypnea, lethargy, piloerection, dehydration, and prostration were observed as early as 8 h pi. Since larger doses of killed Brucella are non-lethal, these symptoms relate to the massive organ invasion by live bacteria [48]. High numbers of attenuated Brucella (e.g. > 5 × 108 CFU), such as S19 or Rev1, seldom kill mice, although they may induce some clinical symptoms [22].

A relevant effect observed when inoculating large Brucella doses (e.g. > 5 × 107 CFU/mouse) is that blood and cytokine profiles approach those induced by endotoxic bacteria like Salmonella[48]. This is an indication that Brucella neither induces an obvious inhibitory action on immune cells nor hampers the synthesis of proinflammatory cytokines at the onset of the infection, and that there is a threshold over which some molecules carrying pathogen-associated molecular patterns may be available to innate immunity receptors.

2.4 The mouse

Mice are highly resistant to brucellosis because they are only killed by very large doses of virulent Brucella[19, 48]. However, mice seem more sensitive to brucellosis than rats, hamsters and rabbits [13, 99]. Mice infected with doses of virulent Brucella (e.g. B. abortus 2308) lower than 107 CFU/mouse, hardly show any changes in behavior, or cachexia or wasting syndromes, all signs induced by endotoxic bacteria [19, 48]. Nevertheless, and depending on the mouse strain, Brucella can cause long lasting infections that may extend throughout the lifespan, accompanied by characteristic pathological signs.

2.4.1 Resistant and susceptible mouse strains

All mouse breeds tested are susceptible to Brucella[49, 100], suggesting the inexistence of specific resistance murine genes to brucellosis. However, some breeds seem more resistant than others (Figure 1b and Table 1). The best examples are the “susceptible” DBA2, C3H/He and BALB/c strains and the “relatively resistant” C57BL/10 and C57BL/6 derived strains [35, 39, 41, 42, 101]. The difference between these mouse strains is not related to blood clearance rates or to the number of bacteria reaching the spleen at the onset of the infection, which seem similar. Moreover, the resistance displayed by C57BL mice is not due to a stronger microbicidal activity of macrophages or to any other early innate immunity effector [102]. Rather, this resistance is manifested as different levels of splenic colonization one week after inoculation as well as dissimilar Th1 responses [103]. The spleen and liver CFU during the plateau phase (1 to 10 weeks pi) are commonly about ten-fold lower in the resistant C57BL strains (Figure 1B). In addition, the C57BL mice show less splenomegaly. The central difference between resistant and susceptible mouse strains seems to be the inability of the latter to maintain the production of IFN-γ after the acute phase, a phenomenon that extends throughout the chronic steady phase up to at least the 6th week p.i. [65, 103]. As expected, this phenomenon is redundant to other events, such as the recruitment and activation of immune cells [66, 103]. A conspicuous difference between the BALB/c and C57BL/6 strains is the lymphocyte/granulocyte proportion in blood, which is close to 80/15 % in the former and to 90/9 % in the latter [20], a phenotype that may be related to Brucella clearance due to the regulatory action that neutrophils can display over macrophages [4].

B. melitensis replicates similarly in macrophages obtained from BALB/c and C57BL mice. Moreover, both strains of mice share the “sensitive” form (Nramp1 s ) of the Nramp1 r (natural resistance-associated macrophage protein) allele, which codes for a membrane phospho-glycoprotein implicated in the early activation of macrophages [43]. Unexpectedly, during the 1st week after infection, the spleen and liver of “sensitive” BALB/c contain less B. melitensis CFU per organ than mice (e.g. C.CB) harboring the resistant r1 r allele form (Table 1). However, the spleen and liver weights in the Nramp1 r mice are larger than in the Nramp1 s mice, suggesting a more profound inflammation. It is noteworthy that expressing the results as CFU/gram of organ reduces the difference between these two strains. The absence of significant role of Nramp1 s allele in brucellosis is striking, since this gene is implicated in the resistance/susceptibility to other intracellular bacteria [104].

In spite of the quantitative differences, the Brucella replication profiles in the sensitive and resistant mouse strains follow a more or less parallel path [35, 39]. This means that the slope of the replication curves is very similar in both strains (Figure 1B). Consequently, any Brucella strain displaying a more negatively pronounced slope must be considered attenuated, no matter whether the bacterium was tested in the resistant or in the sensitive mouse strain [22, 37]. This parallelism between mouse strains is also maintained when testing attenuated brucellae [35, 39]. Therefore, the differences in Brucella replication between the sensitive and resistant mouse strains should be interpreted in quantitative terms rather than in multiplication kinetics.

2.4.2 Mutant and knockout mice

Mice with defects or mutations influencing the innate or/and adaptive immune responses may show significant changes when infected with Brucella (Table 1). For instance, athymic nude mice do not clear Brucella after the acute phase [27, 59], a time when cell mediated immune response has fully developed in immunocompetent mice [103]. During this period, nude mice develop granuloma in the liver and persistent infections of the biliary tract. In spite of this, the infection is not lethal (at least in 3 months), possibly because of immune compensatory phenomena existing in these mice [59]. In fact, nude mice seem to perform better in eliminating Brucella during the onset and early acute phases of infection. This suggests that the enhanced innate immune response displayed by these mutant mice [27, 59] is able to partially control the infection, at least during this period. Moreover, nude mice are capable to develop a robust T-independent response against Brucella smooth lipopolysaccharide (LPS) [105]. Since antibodies against LPS are protective in murine brucellosis (Table 2), their generation in nude mice may well exert some protection at later times.
Table 2

Effect on bacterial counts in mouse spleen (CFU) after passive transfer of antibodies, cells or cytokines at different phases of smooth virulent Brucella infection

Treatment

Administration of treatment in relation to the time of infection

Main effect in infected mice

Brucella CFU in the spleena

References

Acute before 14 days

Chronic after 15 days

Rabbit anti-Brucella

2 h, 16 h before or 2 h after

Immune serum from Brucella infected mice directed against a variety of different antigens

[106]

Murine anti-Brucella

2 h, 16 h before or 2 h after

Immune serum from Brucella infected mice directed against a variety of different antigens

[84, 98, 107]

Anti-LPS

16 h before

Immune murine sera against Brucella LPS

[84]

Anti-O:9

16 h before

Immune murine sera against Yersinia enterocolitica O:9. It protects mice but to a lesser extent than anti-Brucella

[84]

Anti-peptido-glycan

16 h before

Polyclonal immune sera against peptidoglycan protein complex, probably contaminated with LPS

[84]

Mabs anti-O- chain LPS

4 h before

Several antibody isotypes reacting against A, M and C epitopes of the B. abortus O chain of LPS

[35, 108110]

Mabs anti-Omps

24 h before

Against Omps of molecular weight 10, 16.5, 19, 25–27, 31–34, 36–38 and 89

[109]

Mab-anti-Omp16

24 h before

It induces lower protection than anti- O chain antibodies; IgG2a isotype

ND

[109]

Mab-anti-Omp25

24 h before

It induces lower protection than anti-O chain antibodies; IgG2a isotype

ND

[109]

Mab-anti-Omp2b

4 h before

Reacts against B. abortus Omp2b, which generally is not accessible in smooth bacteria

ND

[35]

Mab-anti-Omp31

24 h before

It induces lower protection than anti-O chain LPS antibodies; IgG2a isotype

ND

[109]

Spleen cells

Same day as infection

Protection was efficiently transferred to naive mice using spleen cells from mice infected 5 or 12 weeks earlier

ND

[111]

Immune Tcells

2 h after infection

It gave similar protection than CD8+ or CD4+ cells passively transferred. Immune cells from six week infected mice. Before 4 week there is no protection.

ND

[98, 112]

Immune CD4+T cells

2 h after infection

It gave similar protection than CD8+ cells passively transferred. Immune cells from six week infected mice. Before 4 week there is no protection

ND

[107]

Immune CD8+T cells

2 h after infection

It gave similar protection than CD4+ cells passively transferred. Immune cells from six week infected mice. Before 4 week there is no protection

ND

[107]

Serum anti-Brucella and T cells

2 h after infection

Enhanced protection over administration of just T cells or Abs alone

ND

[107]

Immune T cell+anti- INF-γ

Anti- INF-γ 1day before T cells with challenge

It gave similar protection than passively transferred T cells

ND

[112]

Bovine Mø

1 day before infection

Transferred to NK1.1 cell-depleted Rag-1−/− mice

ND

[60]

Bovine Mø+γδT cells

1 day before infection

Transferred to NK1.1 cell-depleted Rag-1−/− mice

ND

[60]

Bovine Mø+CD4 T cells

1 day before infection

Transferred to NK1.1 cell-depleted Rag-1−/− mice

ND

[60]

INF-γ

1 day before and 2 and 4 day after

It Induces splenomegaly. Mice show enhanced peritoneal and splenic macrophage bactericidal activity

ND

[113]

IL-12

With the infection and every 3 days after

The levels of INF-γ increase during the third week of infection

[114]

IL-1α

4 h before

CSF-1 increases in serum during the first 12 h. Colony forming cells increase in the spleen, mainly Mø and PMNs. Thirty days after treatment, the effect is terminated.

[28]

Transfer factor

At the sametime

No effect in immune enhancement or antibody response

ND

[115]

Indomethacin

Daily s. c. for 7 days

Decrease of the cyclooxygenase activity by 80 to 90 % in spleen. Reduction of PGE2

ND

[113]

Poly A:U

2 h before and 2, 4, and 6 days after

Activation of NK cell activity

ND

[116]

Poly A:U

At the sametime

Polyadenylic acid-polyuridylic acid (poly A: U) is a non-toxic adjuvant that potentiates both humoral and cell-mediated immune responses

[27, 117]

Cyclosporine

Daily for 4 weeks

It induces low inflammatory response in spleen and liver. No significant changes in spleen macrophage population

ND

[107]

Corticosteroids

24 h before

It has a broad anti-inflammatory effects

[3]

Anti-Ia

24 h before

It depletes mostly B cells and some T cell subpopulation with “suppressor” activity

ND

[111]

Anti-CD8+ T cells

5 days before and 3 per week

Depletion of CD8+ cells. DTH response was unaffected after treatment. Treatment abolished the IgG antibody response without affecting bacterial numbers.

ND

[111]

Anti-CD8+ T cells

1 day before and every 4 days after

Depletion of CD8+ cells, significant increase of Møs in spleen. No significant effect in the number of CD4+, NK or γδ T cells

ND

[118]

Anti-CD8+

1 day before and every 3 days after

Depletion of CD8+ lymphocytes involved in cell mediated cytotoxicity of infected cells

ND

[119]

Anti-CD8+

2 days before and 1,4,7 10 days after

Depletion of CD8+ lymphocytes involved in cell mediated cytotoxicity of infected cells

ND

[56]

Anti-CD4+

2 days before and 1,4,7 10 days after

Influences the Th1 profile mainly INF-γ. It induces basal levels of IL2 and IL4

ND

[56]

Anti-CD4+

 

Reduces granulomatous inflammation, which seems to be mediated mainly by CD4+ T cells

ND

[119]

Anti-CD25+ T cells

3 days before

Depletion of CD4+ regulatory T cells. Increase levels of INF-γ in spleen cells

ND

[120]

Anti-NK1.1cells

24 h before

Depletion of NK cells and activity

ND

[116]

Anti-asialo-GM1

24 h before and 3 day after

Depletion of NK cells and activity

ND

[116]

Anti-PMN-RB6

24 h before and3, 6, 9 days after

It depletes neutrophils and a small population of Møs. It does not affect the course of brucellosis. In some cases CFU decrease in numbers after 9 days of treatment

↔/↓

ND

[48],unpublished results]

Anti-IL-10

1 day before and 4 days after

The levels of INF-γ increase during the first week of infection

ND

[121]

Anti-IL-10

1 day before and 4 days after

Augments the production of INF-γ in spleen cells of both, sensitive and resistant mouse strains

ND

[122]

Anti-IL-12

4 h before, or 2 days after, or 7 days after

Decrease in spleen weight and spleen inflammation in relation to infected non-treated mice. There is granuloma reduction and low levels of INF-γ

[123, 124]

Anti-IL-4

24 h before and 4 days after

Removal of IL-4 It depresses the Th2 Ab response and indirectly may favor the Th1 response

ND

[122]

Anti-INF-γ

1 day before infection

Reduces splenomegaly

ND

[112]

Anti-INF-γ

1 day before and every 5 days after

No significant effect was observed even after administration with IL-12

ND

[114]

Anti-INF-γ

1 day before and 4 days after

It removes secreted INF-γ and depressed Th1 response

ND

[121]

Anti-INF-γ

24 h before and 4 days after

It removes secreted INF-γ and depressed Th1 response

ND

[122]

Anti-TNF-α

1 day before and every 4 days after

No significant effect in the number of PMNs, CD4, CD8, NK, γδ T cells or Møs is observed

ND

[118]

Anti-TNF-α

4 h before, or 2 days after, or 7 days after

Decrease in spleen weight and spleen inflammation with respect to the infected non-treated mice. INF-γ is detected at normal levels

[60, 63, 124]

Anti-TCRγδ

The same day and 3 days after

Removes Tγδ cells if innate immunity. Depletion has similar effect in IL/17Rα KO, INF-γ KO and GM-CSF KO mice

ND

[60]

a (↑) Significantly higher numbers of CFU in spleen than in controls; (↓) significantly lower numbers of CFU in spleen than in controls; (↔) No significant number of CFU in spleen in relation to the controls; ND, not done.

Virulent or attenuated Brucella extensively replicate in mice deficient in INF-γ production, a cytokine required to develop an adequate Th1 immune response (Table 1). When infected, the INF-γ deficient mice show significant clinical signs, such as cachexia and a severe splenomegaly, with macrophages accounting for more than 75 % of the spleen cells; these mice eventually die [118]. Similarly, Brucella replicates extensively in knockout mice defective in IFN-γ regulatory factor (IRF)-1 or in mice displaying mutations in the IFN consensus sequence binding protein (ICSBP), which are transcriptional elements regulated by INF-γ [53]. Analogous to what has been observed in the INF-γ deficient mice, Brucella (e.g. > 5 × 105 CFU/mouse) are lethal for IRF-1 mutant mice. In these animals, not the spleen but the liver is the main target organ [53]. Furthermore, whereas the liver shows significant hepatitis and granuloma formation, the spleen yields CFU numbers similar to those obtained in the parental immunocompetent mice. Brucella also replicates better at later times in mice defective in regulatory cytokine IL-12 (Table 1), involved in maturation of T cells and necessary for the development of Th1 immune responses [53].

Mutations in genes coding for IL-1β, IL-18, TLR5, TLR2, NOD1, NOD2, GM-CSF, IL/17r, Rip2, TRIF or type-1 INFr, all key factors of innate immune response, have little or no effect on Brucella spleen replication (Table 1). However, mutations disturbing TLR9, Myd88, IRAK-4, Tγδ cells, or in the generation of TNF-α, influence the clearance and favor Brucella replication (Table 1). There is some controversy on the role of TLR4 in murine brucellosis. While two studies [44, 47] detected a slightly higher susceptibility in TLR4 knockout mice, others have found that the absence of TLR4 does not influence Brucella replication (Table 1). Brucella LPS signals through TLR4 but very inefficiently [50, 125] and the reported susceptibility associated with TLR4 is not as large as that observed for other Gram-negatives [48]. Mutations in the iNOS and gp91 phox , which affect several innate immunity pathways, are not lethal and favor the replication of Brucella, mainly at later times (Table 1). Hybrids harboring double mutations in some of these genes (e.g. iNOS/ICSBP) display profound deficiencies that favor Brucella replication (Table 1).

Defects in the adaptive immune response generate divergent phenotypes (Table 1). For instance, mutations such as rag1, which hampers the maturation of some populations of B and T cells, do not have significant influence in Brucella replication. In the case of the igh6 mutation that impedes the development of B lymphocytes, there are contradictory reports: while some authors detect a decrease of Brucella CFU in the spleens of igh6 mutant mice after the 1st week [55], others do not notice significant changes at early times, and barely some decrease at later times [54]. On the contrary, disruption of β2m or perforin (pfp) genes (that impact on the development and function of cytotoxic CD8+ T cells) seems to favor Brucella replication. However, there are reports indicating that the β2m mutation either does not have any influence [55] or supports the elimination of Brucella later in the infection [54]. Nonetheless, rag1 and igh6 knockouts have problems in eliminating extracellular non-virulent Brucella VirB mutants [126], suggesting that these genes may play some role [54].

Knockout mice showing other immune defects do not yield clear-cut results (Table 1). For example, mice with defects in IRF-2 (a transcriptional factor regulated by INF-γ), Cd4 (with a defect in the CD4+ T subset), or Aβ (MHC-II deficient) seem to eliminate Brucella more efficiently than the parental strains. However, some authors do not report changes in spleen CFU in Aβ deficient mice [55]. IRF-2 knockout mice also have a conspicuous defect in NK cells, but these cells do not play a relevant role against Brucella infection [53]. The absence of CD4+/CD25+ regulatory T cells (involved in the down regulation of T cells) in Cd4 and Aβ mutant mice may balance the response towards Th1, thus favoring the elimination of Brucella[54].

From experiments in mutant and knockout mice a few general conclusions may be drawn. For instance, several factors of the innate immune system that in other bacterial infections play an essential role, seem to be of minor importance (e.g. iNOS, type-1 INFr, and gp91 phox ) or irrelevant (e.g. IL-1β, IL-18, TLR4, TLR5, TLR2, NOD1, NOD2, GM-CSF, IL/17r, Rip2, TRIF, NK or Nramp1 s ) in murine brucellosis. It is also clear that Th1 response via INF-γ is crucial for controlling Brucella replication and that any event that negatively influence the generation of this cytokine (e.g. ifng, IRF-1, IL-12KO) severely compromise the overall adaptive immune response against brucellosis. Finally, the absence of some cell populations of the immune system (e.g. igh6, IRF-2, Cd4 and Aβ) seems to favor the elimination of Brucella, a fact that suggests that some regulatory phenomena are induced during infection. All these events are in agreement with the evolutionary stealthy strategy that Brucella has followed to hide from and modulate the immune system [4, 48, 125].

2.4.3 Age and sex

In the only study published on the influence of age [30], it was reported that a B. abortus 2308 dose of 4 × 108 CFU/mouse was similarly non-lethal for 2 and 18 month old DBA/2 mice, and that a ten-fold higher dose killed all animals in both age groups. Although such clear-cut differences between these two very high doses of a virulent strain are striking (see Infective Dose, above), these results may indicate that age does not significantly influences the susceptibility to lethality by B. abortus. However, whereas the bacterial counts in the spleen remained relatively high and stable for at least 8 weeks in the young adult mice, the numbers decreased in the spleen of older mice after the 5th week. In the same work, it was reported that the anti-Brucella immune responses in older mice were less-Th1 specific and showed higher levels of IL-17, and the authors suggested alternative pathways for combating brucellosis in aged mice.

With the exception of the Brucella "resistance" character of C57BL mice, which seem to be partially dominant with polygenic control in females [41, 42], no comparative studies have been performed between sexes. The placenta becomes infected in pregnant female mice and the testes constitute a site of Brucella colonization in the case of males [74, 76, 127, 128], two facts that are reminiscent of the events in domestic ungulates and humans with brucellosis [129, 130].

2.4.4 Transmission

Brucella horizontal and vertical transmissions are common in natural hosts [131] but rare in mice and humans [132, 133]. Although the mammary glands of nursing dams are colonized with Brucella, less than one percent of the mouse pups become infected [132, 133]. Similarly, Brucella colonizes salivary glands, kidneys and testes, but venereal transmission or contagion rarely occurs [25, 76]. This is striking since rats (closely related to mice) shed the bacteria in the urine and they are prone to transmit Brucella by the venereal route [134].

Transmission of virulent B. abortus 544 from the mother to the fetus was demonstrated in mice [25, 133], with profuse infection of placentas [127]. Although mice seem to be quite resistant to abortion, this event can be induced at specific time periods. Attenuated B. abortus S19 is also transmitted to the fetus, but it seldom induces abortion [135]. These two events are somewhat reminiscent of what happens in the natural host [136].

3 Physiopathology

The inoculation of virulent brucellae induces clinical and physiopathological responses in mice that differ from those caused by attenuated or non-virulent Brucella strains [53]. These responses are less severe in Brucella vaccinated or immunostimulated mice and more conspicuous in pregnant or immunodeficient mice (Table 1). In the following paragraphs, the main events taking place during different infection phases are described (Figure 1A).

3.1 Onset of the infection

Optimal doses (e.g. 104 to 5 × 106 CFU/mouse) of virulent brucellae by the i.p. or i.v. routes barely induce physiopathological symptoms at early stages of infection. The absence of obvious clinical signs correlates with: i) normal blood cell and platelet counts; ii) the lack of a recruitment of proinflammatory cells at the site of infection; iii) the presence of minimal levels of serum IL-1β, TNF-α, IL-10 and IL-6; iv) very low amounts of MCP-1 and RANTES chemokines [48, 137]; and, v) the absence of synthesis and degradation of fibrinogen and coagulopathies [48]. IL-10 is not detected in serum and its corresponding transcript only appears after 3 days of infection [126]. Although IL-10 may be extracted from murine spleen cells after 1 day of infection [138], the levels of this cytokine are far lower than those induced by other bacteria [139, 140]. This suggests that the regulatory role of IL-10 is minor or irrelevant at early times of Brucella infection. At these early times, INF-γ and IL-12, are barely detected in serum or cell extracts and these cytokines become evident only during the next infection phase [63, 135, 137, 138, 141]. However, the low levels of INF-γ and IL-12 are not unique to early Brucella infections, since they are also observed at the onset of murine salmonellosis [142]. Although transcripts of CXCL1 and MIP-2 chemokines, and IL-6 can be detected in spleen cells one day after infection [65], their levels are significantly lower than those induced by other bacteria. Anti-Brucella antibodies and IL-4 are not detected in serum or in spleen cells at the onset of the infection [138, 143]. In summary, the proinflammatory response to virulent brucellae is very low and it may have some significance only when compared with that induced by non-virulent strains such as VirB or BvrS [37, 126].

A few hours after infection, Brucella is detected inside phagocytic cells in the blood, spleen, liver and bone marrow of mice [14, 15, 76]. In the liver, bacteria are detected in sinusoids and within Kupffer´s cells as early as 3 h after i.p. inoculation. During the first 6 h, neutrophils gather around macrophage Kupffer´s cells; thereafter, the number of bacteria decreases and seems to disappear due to engulfment by liver phagocytic resident cells, which become engorged with intracellular brucellae [14, 15]. During the early phase of infection, spleen macrophage, neutrophil and colony forming cell numbers are not significantly different from those of non-infected mice [28, 43].

At the onset of infection, a normal distribution of spleen cells is observed with some minor congestion and presence of T cells, preferentially located in the periarteriolar lymphatic sheaths and within the red pulp. Concomitantly, B lymphocytes are mostly present in the corresponding B-cell zones, marginal zones and red pulp, while granulocytes and macrophages are scattered in the red pulp and marginal zones. Activated phagocytes expressing iNOS are not observed at these early times of infection [65]. Treatment of mice with the immune enhancer poly A:U 1 h before infection does not affect the number of CFU/spleen during the first 24 h. Nevertheless, it promotes the elimination of the bacteria after 48 h. This is an indication that an early activation of the innate immune system is detrimental for Brucella multiplication and that, when professional phagocytes are properly activated in vitro or in vivo, they are capable of eliminating the invading Brucella[48, 117].

3.2 Acute phase

This phase (from the 3rd day to the 2nd-3rd week) is marked by the rapid increase of bacterial numbers in the target organs, a significant inflammation of the spleen and lymph nodes and the appearance of the first pathological lesions in the liver. In addition, there is a development of type IV delayed type hypersensitivity (DTH), corresponding with the beginning of the Th1 response [65, 144]. Brucella can be readily isolated from blood and many organs. However, as time passes by, it becomes more difficult to find the bacteria in blood. Organ cell infiltration becomes significant at the end of this phase, with augmented frequencies of phagocytic cells [14, 15, 43, 65]. During the acute phase the non-gravid uterus, lungs, heart, kidneys, brain and gastrointestinal tract do not show conspicuous pathological signs [145].

The liver is the first organ to show significant histopathological changes. Mild perivascular mononuclear infiltrates are observed after the 3rd or 4th day of infection with virulent Brucella, because of the localization of bacteria inside Kupffer´s cells. Thereafter, granulomas become conspicuous, reaching their maximum intensity after the 1st week of infection (Figure 3). Granulomas are composed by clusters of macrophages and dendritic cells [146], generally known as epithelioid cells and histiocytes, several of which demonstrate ingested material as well as Brucella antigens (Figure 3). The presence of plasma cells and lymphocytes becomes evident, but very little or negligible granulocyte infiltration is present in the liver in this phase. At this stage, liver pathologies induced by the virulent B. abortus 2308 and the attenuated S19 strain are not significantly different. Mice infected with non-virulent Brucella BvrS/BvrR or VirB mutants do not generate significant pathological responses in the liver or the spleen at any stage of the infection [126], and Grilló, Blasco and Moreno, unpublished results]. However, some immunodeficient mice, like the IRF-1 mutants, develop more and larger liver granulomas during the acute phase when infected with virulent or attenuated B. abortus[53].
https://static-content.springer.com/image/art%3A10.1186%2F1297-9716-43-29/MediaObjects/13567_2011_Article_157_Fig3_HTML.jpg
Figure 3

Liver pathology and intracellular detection of Brucella antigens in macrophages of BALB/c mouse after 10 days of infection with virulent B. abortus 2308. (A) Liver granulomas (pointed by white arrows). (B) Large and smaller liver granulomas (white arrows) with giant cells (black arrow and insert). (C) Mononuclear infiltrate formed mainly by macrophages and histiocytes (white arrow). (D-E) immunoperoxidase detection of Brucella LPS antigen in matching histological sections of the corresponding upper A, B and C panels. Hematoxylin-eosin stain (A-C) and hematoxylin counterstain (D-F).

During the 1st week of infection with virulent Brucella, the spleen sizes increases (Figure 2A), showing a mild lymphoid depletion in the splenic nodules, moderate macrophage infiltration, few neutrophils and a mild extramedullary hematopoiesis in the red pulp [64]. In spite of this, the overall number of macrophages and neutrophils remains practically unaltered [43]. As expected, higher doses of smooth brucellae (e. g. > 107 CFU/mouse) induce larger inflammation [19, 145]. During the 1st week of the acute phase, the numbers of macrophages, neutrophils, CD4+, and CD8+ T cells remain grossly within the limits of uninfected spleens (Figure 4) [57, 65, 118]. After 10 days of infection, the spleen size increases as the number of CFU augment and the degree of lymphocyte depletion, macrophage infiltration and extramedullary hematopoiesis displaying mitotic cells is prominent. Some macrophages may have intracellular Brucella antigens.
https://static-content.springer.com/image/art%3A10.1186%2F1297-9716-43-29/MediaObjects/13567_2011_Article_157_Fig4_HTML.jpg
Figure 4

Spleen cell population profiles and histopathology after infection of BALB/c mice with B. abortus 2308. (A) Spleen cell populations. The total number of CD4 T cells, CD8 T cells, neutrophils (PMN) and macrophages (Mø) per spleen was determined by multiplying the percentage of positive cells obtained by differential microscopy observation after cytospin centrifugation and fluorescent flow cytometry analysis by the total leukocyte count. Standard deviation at all points is lower than 10 % of the respective value (adapted from [57]). (B) Spleen histopathology and detection of Brucella antigens in the spleen. (a) Normal spleen (arrow points to the central artery). (b-f) Histological sections of spleen nodules during the acute phase of infection with virulent B. abortus 2308 (b) Spleen nodule with a clearer area infiltrated by macrophages (arrow points to the central artery). (c) Macrophage and histiocytes (arrow) infiltrating the spleen nodule. (d) Active extramedullary hematopoiesis (white arrow and insert) with granulomas (black arrow) in some areas of the spleen. (e) Immunoperoxidase detection of Brucella LPS antigen around the central artery of a spleen nodule. (f) Immunoperoxidase detection of Brucella LPS antigen within macrophages (arrow).

At the end of the acute phase, the number of macrophages and neutrophils in the spleen increases slightly (Figure 4A) [43]. While the B-cell areas remain populated and the CD4+ and CD8+ T lymphocytes have decreased in the splenic nodules, the T-cell zones have been displaced by macrophages [112]. The overall number of B cells and CD4+ and CD8+ T cells in the spleen is slightly higher than in spleens of uninfected mice [57, 64, 112, 118]. Nevertheless, the confined depletion of lymphocytes seems to be relative to the spleen swelling, rather than to a true decrease in cell content [147].

During the acute phase there are just a few but significant differences between the spleen cell profiles induced by the virulent B. abortus 2308 in comparison to that generated by the attenuated vaccine S19. One week after inoculation, S19 produces a relatively more severe local lymphoid depletion than strain 2308 [64]. This corresponds to a slightly larger spleen size in S19 infected mice (Figure 2A), which also displays more intense neutrophil infiltration [64]. However, the most significant differences in the pathological signs induced by virulent and attenuated vaccine strains are evidenced at the end of the acute phase and in the next phase. Non-virulent brucellae (e.g. BvrR/BvrS) fail to induce significant spleen changes and hardly any signs of inflammation.

After the 1st week of the acute phase, significant amounts of INF-γ, IL-12, IL-6 and RANTES are present in sera of susceptible mice (Figure 5) [114, 135, 137, 141, 148, 149]. After the 2nd week, these cytokines steadily decrease approaching basal levels by the 6th week, already in the next infection phase (Figure 5A). The endogenous IL-12 extracted from spleen cells of infected mice seems to parallel the kinetics in sera, although at lower levels [138, 148]. Similarly, endogenous INF-γ (and its transcript) attains maximum levels during the first 2 weeks of the acute phase and is still detected (albeit at significant lower levels) after 8 weeks, in contrast to endogenous IL-12 [65, 138]. The difference between serum and endogenous INF-γ suggests that it may still remain as a reservoir pool inside cells of susceptible mice, but not released into circulation at later times. In contrast to what happens in the susceptible BALB/c mice, the resistant C57BL/10 strain does not display INF-γ in serum during the acute phase [114]. Moreover, the INF-γ kinetics profile depends on the Brucella virulence. For example, INF-γ levels decrease faster after inoculation with attenuated S19 than after infection with virulent B. abortus[65, 141].
https://static-content.springer.com/image/art%3A10.1186%2F1297-9716-43-29/MediaObjects/13567_2011_Article_157_Fig5_HTML.jpg
Figure 5

Cytokine and antibody serum profiles of B. abortus 2308 infected mice. (A) Serum cytokine levels in BALB/c mice after infection with virulent B. abortus (INF-γ, TNF-α, RANTES) or attenuated vaccine S19 (IL-6, IL-12) stains (adapted from [135, 137, 148, 149]). (B) Antibody response of virulent B. abortus 2308 infected CD-1 mice (adapted from [138]). Notice that in “A” the absolute units are different for each cytokine, according to the indication (e.g. while TNF-α, INF-γ, RANTES are measured in pg/mL, IL-12 are in pg/mL/5 and IL-6, in Units/mL). For clarity, the SD were not included.

Cultured spleen cells from infected mice are able to generate cytokines after ex vivo challenge with Brucella antigens. In this ex vivo protocol the kinetics of IFN-γ parallels those of GM-CSF and IL-10 production, displaying an early rise by the 3rd or 4th day after infection, reaching peak levels between days six and ten, and then declining sharply [65, 150, 151]. Regardless of whether the assays are performed in sensitive or resistant mouse strains, both IL-12 and IFN-γ are produced ex vivo during secondary stimulation of cultured spleen and CD4+ T cells with Brucella antigens during the 1st week of infection [92, 114, 122]. However, by the 3rd week of infection, at the beginning of the next phase, there is a decrease in IL-12 receptor-2 expression in spleen cells of the susceptible BALB/c mice, corresponding to their inability to produce IFN-γ at later times [114, 122]. In this mouse strain the IFN-γ levels remain low until the end of the next phase, close to week 10 pi. Then, the spleen cells can be specifically restimulated with Brucella antigens to generate this cytokine [65].

During the acute phase, the production of IL-18 (which works synergistically with IL-12 to induce the generation of INF-γ) is depressed in spleen cells of B. abortus infected mice [144]. Therefore, once the infection has been established, the limited secretion of IL-18 does not affect the endogenous production of IFN-γ. Simultaneously, small amounts of endogenous IL-10 (and its transcript) reach their maximum during the 1st week of the acute phase, disappearing from the splenocytes during the 2nd week pi [138]. It may be that the endogenous synthesis of IL-10 could, after all, influence the production of IFN-γ and the premature development of the Th1 response.

Although anti-Brucella antibody producing cells are present in the spleen early after infection, relevant levels of anti-Brucella immunoglobulins are detected only after the 2nd week pi (Figure 5B), with relatively higher levels of IgG3 [30, 65, 67, 138]. DTH to Brucella antigens becomes evident during the acute phase [153], reaching its maximum at 9 days pi (Figure 6). The second event (Figure 6, red line) observed after the 2nd week may correspond to a mixture of type III and IV hypersensitivity reactions. However, macrophages display their maximum unspecific killing activity at 18 days pi, at the end of the acute phase and persist for 4 weeks, albeit, at lower levels. This phenomenon is known as the Mackaness effect [153], described as “an immune response specifically induced but non-specifically expressed”. In addition, cultured spleen cells from Brucella infected mice do not proliferate in response to challenge with killed Brucella or soluble antigens (Figure 7) [152]. This suggests the presence of regulatory phenomena at this stage [4]. Only negligible amounts of TNF-α (Figure 5A), IL-4 and MCP-1 are present in the sera of Brucella infected mice in the acute phase and thereafter [38, 63, 135, 137, 138]. IL-2 and IL-4 are barely detected in spleen cells from infected mice stimulated with Brucella antigens during the acute phase [92, 122, 151]. The quality of Brucella antigens profoundly influences the outcome of the immune response. Cultured spleen cells from mice infected with live Brucella display a Th1 response marked by INF-γ and IL-12 production. However, spleen cells from mice immunized with soluble Brucella antigens generate preferentially a Th2-like response, with IL-4 and IL-2 production by CD4+ T cells [151]. In addition, there is a higher frequency of precursor IFN-γ-producing CD4+ T cells and a lower frequency of precursor IL-4-producing CD4+ T cells in B. abortus infected mice than in mice immunized with Brucella soluble antigens [151].
https://static-content.springer.com/image/art%3A10.1186%2F1297-9716-43-29/MediaObjects/13567_2011_Article_157_Fig6_HTML.jpg
Figure 6

DTH in B. abortus S19 infected mice after footpad injection of Brucella protein extracts. Note the biphasic response between the acute and chronic steady phases. The blue line in the graphic is compatible with type IV hypersensitivity, while the red line is compatible with a mix reaction of type IV and type III hypersensitivity (adapted from [153], with permission).

https://static-content.springer.com/image/art%3A10.1186%2F1297-9716-43-29/MediaObjects/13567_2011_Article_157_Fig7_HTML.jpg
Figure 7

Spleen cell proliferation ( 3 H-thymidine incorporation) in response to killed B. abortus 2308 in BALB/c mice infected with B. abortus virulent 2308 or vaccine-attenuated S19 strains, during 20 weeks [adapted from [[152]] with permission]. Notice the delay in response of spleen cells from 2308 infected mice in relation to those infected with the attenuated strain S19.

3.2.1 Acute phase in pregnant mice

Pregnant mice offer a special environment for Brucella replication [145]. Murine brucellosis during pregnancy has been explored mainly throughout the acute phase, because the mouse gestation time has an average of 19 days. B. abortus (i.p. 104 CFU/mouse) induces higher “abortion” rate (death pups on day 18.5, before natural delivery) when administrated on day 4.5 of pregnancy than when injected at later times of the gestation [135, 137, 154]. The degree of colonization and placental damage depends on the doses and the pregnancy period. After the 7th day of pregnancy, doses lower than 2 × 105 CFU/mouse seldom induce miscarriages or fetal deaths, independently of the infection route. This is an indication of the mouse resistance against Brucella-induced abortion [74, 127, 132, 133]. However, in close parallelism to the events in natural hosts, placentas are more intensively colonized when mice are challenged during mid pregnancy (days 7–11) than when inoculated during early (e.g. day 3) or late (e.g. day 15) pregnancy [135, 137, 154]. Placental colonization and abortion are not always linked. In some experiments, virulent B. abortus 2308 colonizes the placenta without inducing abortions, although it may cause fetal deaths [145]. When mice are infected at day 9 of gestation, the invaded placentas have lost weight, look edematous and frequently harbor pale and shrunken autolyzed fetuses 9 days later (day 18 of pregnancy) [145]. Strikingly, mice born alive from infected dams do not demonstrate gross macroscopic or microscopic alterations [145], and no differences in bacterial loads between the live and aborted fetus are detected [135]. All these observations suggest the existence of refractory “placental windows” to Brucella infection. Attenuated (e.g. S19) and non-virulent Brucella (e.g. VirB mutants) seldom induce abortions, although S19 may cause restricted placental infections [38, 137].

Brucella replicates within giant trophoblasts located in the deciduas basalis, 3 days after infection of mice in the 12th day of pregnancy (Figure 8) [135]. Two days later, most bacteria are already found within giant trophoblasts, and necrotic foci become evident within the spongiotrophoblastic zone. Inflammatory cells are mainly found along the regressing layer of the endometrium overlying the implanted chorionic vesicle, or free within the newly formed uterine lumen [135]. The occurrence of neutrophils is likely the result of tissue destruction in necrotic areas. Indeed, when bacteria are solely located within giant trophoblasts with no cell destruction, neutrophilic inflammatory response is not observed. This confirms the absence of granulocyte recruitment by Brucella organisms at the site of infection [48]. A multifocal necrosis of the spongiotrophoblastic zone of the placenta coalescing in several zones is produced, 7 to 9 days after infection (corresponding to 16 to 18 days of gestation) [135]. In this region, which extends from Reichert’s membrane at the periphery of the disk to the interior, extracellular bacterial colonies are present together with a few giant trophoblasts remaining infected. Throughout the necrotic regions, there is massive bacterial colonization and phagocytosis of Brucella. In some placentas, thrombosis of the uterine vessels in the junctional zone resulted in infarction of the labyrinth zone. All these lesions resemble those observed in the placentas of Brucella infected natural hosts [89].
https://static-content.springer.com/image/art%3A10.1186%2F1297-9716-43-29/MediaObjects/13567_2011_Article_157_Fig8_HTML.jpg
Figure 8

Brucella invasion of mouse placenta. (A) Model of a mouse placenta with trophoblast giant cells (in ocher) infected with Brucella (in red). (B) Immunochemical detection of intracellular Brucella inside giant trophoblasts (arrows) of ICR mice infected with virulent B. abortus 544, at 15 days of gestation; Meyer's hematoxylin stain. (C) Indicate the magnified image from panel (B) (adapted from [135], with permission).

Abortion in mice seems linked to INF-γ increase, RANTES production and to low expression of heme oxygenase-1 in the giant trophoblasts [135, 137, 154]. Neutralization of INF-γ and RANTES inhibits abortion in mice inoculated with Brucella at day 4.5 of gestation. Moreover, down-regulation of heme oxygenase-1 expression in giant trophoblasts is enhanced by IFN-γ treatment. TNF-α or MCP-1 are not involved in Brucella induced abortion in mice. Non-virulent Brucella VirB mutants do not lower the amounts of heme oxygenase-1 in murine giant trophoblasts and barely induce production of INF-γ, RANTES.

3.3 Chronic steady phase

The chronic steady phase (from the 3rd to the 8th–11th week) is noticeable by high levels of infection, describing a plateau with a maximum and sustained number of CFU in the target organs (Figure 1A). During this phase, bacteremic episodes are transient and the chances to isolate Brucella form blood are scarce. The liver granulomas increase in size, mainly because of the merging of disperse smaller granulomas developed in the acute phase [59]. At this stage, macrophages contain Brucella antigens, indicating bacterial destruction within phagocytes [59]. Some macrophages fuse and become polykaryons and multinucleated giant cells within the well demarcated liver granulomas. Commonly, these giant cells are located in the granuloma centers and contain from 5 to 20 nuclei (known as Langhans cells). The bone marrow of infected mice also shows granulomas but the lungs, heart, kidneys or gastrointestinal tract do not show significant pathological lesions [88, 145]. The appearance of granulomas and giant cells in the liver seems to correspond to an innate phenomenon not mediated by T cells. Indeed, granulomas and giant cells equally occur in normal and athymic nude mice [59]. The number and size of liver granulomas are larger in mice infected with virulent B. abortus than with attenuated S19. Moreover, mice infected with S19 seldom display giant cells. Unless deeply immunosuppressed, mice infected with non-virulent Brucella do not enter into this phase; therefore, granulomas are rarely present.

After the 2nd week of infection and parallel to spleen swelling (Figure 2B), granulomas and giant cells increase in this organ, until the middle of the chronic steady phase (5th to 6th week) (Figure 4B). Thereafter, there is a slow decrease in the size and number of granulomas. This becomes evident at the end of the chronic steady phase (Figure 9) [64]. During the 3rd week pi, the apparent depletion of lymphocytes in the white pulp reaches its maximum. Then, after the 4th week, there is a gradual increase in lymphoid hyperplasia and extramedullary hematopoiesis with several mitotic figures and multifocal accumulation of macrophages that surround and sometimes cover the periarteriolar lymphoid sheaths (Figure 4B). In spite of the apparent lymphocyte local depletion, the total number of CD4+ and CD8+ cells increases moderately (two and one fold, respectively) about the 3rd week of infection (Figure 4A) [57, 118]. Along with this, infiltrating macrophages and neutrophils increase to relatively large proportions (seven and eight fold, respectively) (Figure 4). This increase is proportional to the swelling and infiltration of blood and phagocytic cells in the spleen. However, there is some controversy regarding the suggested lymphocyte depletion in the spleen of infected mice [65]. Morphometric and histopathologic analysis of spleens of B. abortus infected mice do not reveal significant decrease in lymphocytes in the white pulp [147]. This indicates that the apparent depletion of lymphocytes is a local phenomenon related to the inflammation and influx of blood, rather than an absolute decrease of these cells.
https://static-content.springer.com/image/art%3A10.1186%2F1297-9716-43-29/MediaObjects/13567_2011_Article_157_Fig9_HTML.jpg
Figure 9

Spleen inflammation after infection of BALB/c mice with attenuated B. abortus S19 vaccine strain or virulent B. abortus 2308 (A) Generation of granulomas in the spleen (adapted from [[64]], with permission). (B) Histological sections stained with hematoxylin-eosine of spleens of CD-1 mice infected with B. abortus S19 after 6 weeks and with B. abortus 2308 after 8 weeks. As shown in Figure 2a, the spleen of S19 inoculated mice after 6 weeks of infection is considerably smaller than those infected with 2308. The proportion of the white pulp has been reestablished and the number of macrophages and neutrophils in the periphery of the central arteries of the nodules has considerably diminished in the spleens of S19 infected mice in relation to those infected with virulent 2308 strain, which is hyperemic and infiltrated with inflammatory cells.

At the end of the steady chronic phase, the splenomegaly has already decreased (Figure 1A) and splenocytes come close to normal numbers and distribution [57, 64]. Parallel to the reduction of macrophage infiltration and B cells repopulation of the germinal centers, the CD4+ and CD8+ T lymphocytes recolonize the periarteriolar lymphatic regions [65]. By this time, colocalizing Brucella antigen and iNOS-positive activated macrophages are observed in periarteriolar lymphatic sheaths [65]. At these later times, Brucella antigens confined in macrophages are still present in the spleen [152]. However, there is no significant change in MHC-I or MHC-II expression on the surface of spleen macrophages [118].

After the 4th week, the differences between spleens of mice infected with virulent or attenuated B. abortus S19 become evident [2]. The number of spleen granulomas in mice infected with virulent B. abortus is significantly higher (Figure 9), displaying extensive hyperplasia of the periarteriolar tissue. In addition, extramedullary hematopoiesis, neutrophil and macrophage infiltration are significantly higher in mice infected with virulent Brucella. Following the decline of S19, a decrease in splenic granulomas, neutrophil infiltration and extramedullary hematopoiesis is observed. However, the number of macrophages remains high and lymphoid hyperplasia is evident (Figure 9). The emergence of large germinal centers in the spleen with reduction of macrophage accumulations does not occur before 6 to 10 weeks pi with S19, and after 10 weeks pi with the virulent strains. The presence of antigen in macrophages persists longer in mice infected with virulent B. abortus than in those inoculated with S19 [152].

In addition, spleen cells of mice infected with S19 readily proliferate at 6 weeks pi while the splenocytes of mice inoculated with virulent B. abortus multiply later (Figure 7) [17, 152]. This phenomenon (linked to the virulence of Brucella strains and to the severity of the infection) is consistent with the observed pathological changes of the spleen and suggests some inhibitory action related to the presence of regulatory CD4 + CD25+ T cells [4, 120]. This is also in agreement with the tendency of spleen lymphocytes from mice repeatedly immunized with Brucella antigens to produce less INF-γ when stimulated in culture with the cognate antigen [155]. It is worth noting that cultures of spleen cells proliferate in response to Brucella antigens 2 weeks earlier when mice are infected with the attenuated rough B. abortus RB51 than when infected with S19 [152]. This event seems to be related to the lesser spleen inflammation and faster elimination of the rough strain in relation to smooth bacteria. It seems, therefore, that in murine brucellosis the immune regulatory events are linked to the overall bacterial virulence, rather than to specific bacterial mutations.

infected BALB/c mice produce substantial amounts of serum IFN-γ during the acute phase but much less during the chronic steady phase (Figure 5A). On the contrary, in the resistant C57BL/10 serum IFN-γ is just detected in significant amounts at latter phases (50–75 days), corresponding to bacterial clearance in this strain of mice [114]. The lack of measurable IFN-γ in the serum of infected mice does not necessarily mean that cells are not producing this cytokine in response to Brucella infection (in order to detect IFN-γ in serum, relatively large amounts of this cytokine need to be produced) [114]. Nevertheless, in clear contrast to the C57BL resistant mouse strain, the levels of IFN-γ produced ex vivo by BALB/c spleen cells are about two fold higher during the 1st week of the acute phase. Then, a hiatus in IFN-γ production is observed in the sensitive but not in the resistant mice at the beginning of the chronic steady phase [118]. In the middle of the chronic steady phase, the amount of IFN-γ secreted by stimulated splenocytes of BALB/c is reestablished and parallels those of the resistant mice [118]. This difference does not relate to a lower ability of BALB/c to generate IFN-γ because in vitro stimulation of naïve splenocytes later in time generates comparable quantities of this cytokine in both murine strains [118]. Rather, it seems connected to a reduced expression of the IL-12 receptor in BALB/c mice. Since responsiveness to IL-12 is linked to INF-γ production, a temporal suspension of the Th1 response seems to occur in BALB/c at the beginning of the chronic steady phase [114, 118]. It is important to note that IFN-γ production appears to be mainly promoted by CD4+ rather than by CD8+ lymphocytes [65, 149].

Serum IL-6 peaks at the end of the acute phase and remains relatively high until the first 2 weeks of the chronic steady phase [149]. Moreover, upon stimulation with killed Brucella, spleen cells from infected mice still produce significant amounts of IL-6 in the middle of the chronic steady phase [149]. Similarly to the production of IFN-γ, the generation of IL-6 seems to be mainly promoted by CD4+ lymphocytes [17, 65, 149]. However, while the ex vivo generation of INF-γ only responds to the cognate antigen, the ex vivo generation of IL-6 can also be induced by heterologous antigens such as killed Listeria[149]. This is reminiscent of the Mackaness effect, in which the maximum activity against live Listeria is expressed by the Brucella infected mice at the beginning of the chronic steady state, mainly through activated macrophages directly stimulated by CD4+ cells [119, 153]. IL-10, GM-CSF, and IL-4 are barely secreted during most of the chronic steady phase by spleen cells of Brucella infected mice challenged ex vivo with cognate antigens [17, 65, 122, 138]. In addition, CD4+ cells stimulated ex vivo with Brucella antigens produce close to twenty times less IL-2 than the same cells stimulated with concanavalin A [17]. At the end of this phase, splenocytes may be re-stimulated to produce INF-γ, IL-10, GM-CSF and IL-2 [65]. The significance of this is unclear. Increase of spleen regulatory T cells may be directly involved in the suppression of effector T lymphocytes devoted to cytokine release and to the control of the infection [4, 120].

Th1 immunity is also denoted by the distribution of different antibody isotypes against Brucella LPS during the chronic steady phase (Figure 5B). While no endogenous production of IL-4 is detected at any time during infection, there is a predominance of IgG3 and IgG2a, with a minimum response of IgG1 at the end of the acute phase and up to the 14th week pi [138]. In addition to the anti-LPS specific response, a polyclonal IgG3 and IgG2a production dependent upon the endogenous IFN-γ has also been observed in B. abortus infected mice [143] as well as in mice immunized with killed Brucella[156]. Moreover, the IgG3, IgG2a, IgG2b, IgG1 isotype profiles generated against purified Brucella LPS are also generated in both euthymic and athymic mice [157]. This suggests that INF-γ influences the IgG isotope synthesis in mice by Th1-dependent mechanisms and also by T-independent responses.

One striking phenomenon is the second wave in the increase of foot-pad thickness observed between the 3rd and 8th week (Figure 6). Although this second wave has been related to type IV delayed hypersensitivity reaction [153], it corresponds most likely to a mixed reaction with intervention of type III hypersensitivity. Indeed, the increasing levels of antibodies and antigen after the 2nd week of infection (Figure 5B) are in agreement with the occurrence of a type III reaction.

3.4 Chronic declining phase

Despite being longest (more than 250 days), the chronic declining phase has been the least studied one [31]. Although there is a declining in DTH [119] and most blood cytokines decrease or become undetectable, the memory response seems fully consolidated because this phase is characterized by a bacterial declining in the target organs and the progressive disappearance of splenomegaly and pathological lesions in liver and spleen [59]. The reduced number of liver granulomas [65] parallels the decrease of IFN-γ. The spleen diminishes in size but it seldom reaches a normal dimension, even at the latest times of infection (Figure 2A), possibly because of the persistence of small numbers of Brucella in several organs, mainly in lymph nodes. Nevertheless, Brucella is rarely isolated from the blood. Spleen cells maintain their ability to be restimulated by Brucella antigens at least for 5 months after infection (Figure 6B) [152], demonstrating long lasting immunological memory against brucellosis [36]. Moreover, antigen stimulated spleen cells produce GM-CSF, IFN-γ and some IL-10, but not IL-4, 6 to 12 months pi [65]. The secretion of INF-γ at these later times is related to CD4+ T cells, since functional blockade of CD4+ T cells by the addition of CD4 + −specific antibody abrogates the cytokine response [65]. The antibody levels stay high throughout the infection period (Figure 10). The sequelae observed in chronic brucellosis in humans and cetaceans [77, 129] have not been reported in mice.
https://static-content.springer.com/image/art%3A10.1186%2F1297-9716-43-29/MediaObjects/13567_2011_Article_157_Fig10_HTML.jpg
Figure 10

Antibiotic treatment and antibody response of B. melitensis 16 M infected mice. Blue, pink and white circles represent log10 CFU/spleen in the left ordinates axis of the figure. White and black squares represent ELISA values at the right ordinates axis of the figure. Notice that the antibody titers in mice treated with antibiotics remain high over the 34 week period of the assay, in spite of the disappearance of Brucella CFU from the spleen. Some of the animals treated only with doxycycline may still harbor bacteria after 34 week period (adapted from [158, 159], with permission).

4 Vaccination

The availability of successful live Brucella vaccines for over 75 years (since the discovery of S19) is outstanding [6] because such early developments are exceptions rather than a rule in the field of attenuated vaccines. In spite of their success, the available anti-Brucella vaccines are not perfect [22] and their use is restricted to bovines, goats and sheep [16]. There is an increasing interest in developing vaccines for humans and animals other than those domestic ruminants, including wildlife, none of which are covered by the available vaccines [87, 128].

Routine testing of Brucella vaccines in the natural hosts is precluded due to economical and practical difficulties. Therefore, the mouse model has been extensively used [16, 22, 33, 36, 68]. There is, however, substantial anarchy in the protocols used. The literature is plenty of experiments in which the protective efficacy is assessed by comparing the levels of infection of vaccinated and non-vaccinated mice as the only control. By this criterion alone, practically all live strains (no matter whether they are partially or fully attenuated) or even killed Brucella provide significant levels of protection [22, 29, 35, 36, 68, 160]. Moreover, immunization with Brucella LPS, outer membrane proteins, bacterial extracts or even with phylogenetically related bacteria (e.g. Ochrobactrum) may reduce infection with respect to unvaccinated mice [161165]. The fact that both cell mediated immunity and antibodies protect mice against brucellosis [107, 166] may explain in part why a broad collection of immunogens have such a protective action. A second factor to consider is the Mackaness effect: an “unspecific” activation of the immune system that can protect against Brucella challenge within certain periods [153]. Other facts are the particularities of the immune system and short life span of mice, as well as the experimental time intervals used.

The protective efficacy greatly depends on the Brucella virulence and challenge dose. Thus, a considerable number of studies has been dedicated to standardize the mouse model for vaccine testing [23, 24, 32, 75, 97, 167, 168]. As a result, a standardized protocol for controlling the quality of B. abortus S19 and B. melitensis Rev 1 vaccines has been accepted by the World Organization for Animal Health (OIE) [16]. The premise of this model is the fact that these efficient smooth vaccines retain a significant degree of persistence in the host that renders them highly immunogenic and protective [23, 24, 75]. Since a direct relationship between attenuation and protective efficacy cannot be unambiguously established, this model requires the simultaneous determination of two parameters [3234, 167, 168]. The first parameter is the Residual Virulence expressed as RT50 (see above). The second parameter is the Immunogenicity, defined with respect to the ability of the vaccinated mice to control the number of bacteria in the spleen after a standardized challenge [32] (see below). This pa-rameter has to be analyzed at precise intervals after vaccination and is expressed as the mean CFU number of the challenge strain in the spleens. These two parameters do not stand alone, and each vaccine candidate or new vaccine batch should be compared with standard Rev1 or S19 reference strains of known origin and performance. In the case of Rev1 and S19, doses of 108 CFU/mouse injected by s.c. route are used to define the RT50. The same statistical approach may be applied to determine the RT50 of other Brucella strains, no matter whether they are virulent, attenuated or non-virulent. However, for non-virulent brucellae, like the VirB or BvrS/BvrR mutants that persist just for a short period, the intervals for spleen culture have to be shortened (e.g. every 3 days) [37]. On the contrary, for assessing the RT50 of virulent strains like B. melitensis H38, B. melitensis 16 M, B. abortus 544, B. abortus 2308, and B. suis 1330, the inoculum should be much lower (e.g. 104 CFU/mouse). This is so because the virulent Brucella strains inoculated at larger doses (e.g. > 105/mouse) persist longer than 30 weeks in the spleen and the RT50 calculation becomes unpractical [31]. The recommended mice are outbred CD-1 or inbred BALB/c females, with body weights ranging between 20–23 grams. Although these mouse strains seem equally susceptible to Brucella, the optimal challenge dose for immunogenicity assessment may vary according to the age of the animals, whose body weights relate to their particular growth rates (8–10 weeks of age for BALB/c strain and 4–6 weeks for CD-1.

The original OIE protocol was expensive and cumbersome. The graphical statistical procedures initially proposed for determining the RT50 values had some mathematical complexity and other unpractical inconveniencies that limited its use [33]. For a friendlier statistical tool that facilitates the RT50 (details see Table 3). Two criteria must be met for an adequate RT50 estimation: i) four time points must be analyzed for presence of bacteria in the spleens; and ii) these time points should be such that the first and the last yield an accumulated percentage of cured mice ≤ 16 % and ≥ 84 %, respectively. Statistical comparisons should be performed exclusively between RT50 values obtained with the same protocol and, ideally, in the same experiment. Alternatively, an indirect or relative estimation of the Residual Virulence of a given strain could be obtained assessing the splenic growth curves described above. In this case, at least one of the reference Rev1 or S19 strains has to be included in the study [22].
Table 3

Problems when performing experiments with Brucella in the mouse model and general recommendations

Experimental variables

Problems

Recommendations

Mouse breed

- Different susceptibility to Brucella infections. - Heterogeneity of infection.

- Eight to ten weeks old (20 g) female BALB/c.- For BALB/c, n = 5 gives homogeneous spleen counts. For outbred breeds (e.g. CD1) the number per group should be increased (n ≥ 6) and the body weight factor taken into account (see Vaccination). For the recommended weight at the Mouse Phenome Database [169].

Target organ

- Inconsistent infection in some organs.

- Count CFU in spleens (consistently colonized in infected animals; longer persistence than in liver or other organs) after determining the individual organ weight.

Brucella wild-type challenging strain and virulence controls

- Attenuation by inappropriate storage and/or handling. - Species, biovar and reference strain differences.

- Use only reference strains (B. abortus 2308 or 544, B. melitensis 16 M or H38, B. ovis PA, B. suis 1330). Aliquots should be maintained in cryoprotective solution at–80°C (or below), or freeze-dried at 4°C.- Stocks seeded on agar plates and then cultured only once on new plates to obtain final inoculi.- Plates checked for contaminants and freed from condensation or syneresis water.- Make sure that reference strains reproduce typical virulence patterns (see The Brucella strains: replication patterns and related effects)

Attenuated Brucella strains and virulence control

- Over-attenuation by inappropriate storage and/or handling. - Inappropriate infectious dose. - Lack of appropriate controls. - Competing events in superinfection protocols

- See above for storage and inoculum preparation.- Typical multiplication (acute phase) and persistence (chronic phase) patterns in spleens should be assessed.- Use adequate virulent controls (see above, Wild-type strains). In genetic manipulation experiments, consider appropriateness of complemented strains and controls for unrelated attenuation cause by in vitro manipulations.- Avoid using protocols in which mixtures of virulent and attenuated Brucella strains are used as an attempt to determine the relative virulence of the former in relation to the latter bacteria.

Brucella infectious dose and route

- Not optimized for the purpose of the experiment. - Dose not adequate to the route. - Animal handling during inoculation.Intrinsic problems in some routes.

- Use PBS pH 6.85 for preparing the inoculum.- In a preliminary dose–response assay, determine the optimal dose/route (see Route of the infection) for each Brucella species, biovar and reference strain (e.g. B. abortus 2308 vs. 544 or B. melitensis 16 M vs. H38) and also for each mouse breed. For outbred mice, doses must also be adapted to the body weight/age (Physiopathology).- The intraperitoneal route is recommended for most purposes. To avoid intra-intestinal inoculation, displace the intestines and inoculate in the lateral of the abdomen (not in the linea alba). Intravenous inoculation in tail is exceedingly difficult and poses repeatability problems, particularly in small breeds. Oral and aerosol routes are not recommended (see Route of the infection).

Vaccination/attenuated strains dose

- Inappropriate dose and route. - Absence of controls

- For classical smooth vaccines, follow the OIE protocol (1 × 105 CFU/subcutaneously).- To evaluate B. melitensis and B. abortus vaccines, always include Rev1 or S19 reference strain controls, respectively.

Time intervals for virulence studies

Not meaningful.

- For screening, analyze two times corresponding to the multiplication phase and the persistence (e.g. 2 and 8 weeks post-infection). For definite results, test four times (e.g. 2, 4, 6, and 8 weeks post-infection).

Assessment of vaccine efficacy

- Challenge strain. - Time intervals. - Differentiation of vaccine and challenge strains.

- Use fully virulent reference strains and a control reference vaccine strain (see above).- Challenge 4 weeks after vaccination (see Vaccination).- Whenever possible, the challenge strain should carry identifiable marker(s).

CFU determination

- Limit of detection not optimized. - Expression of results (CFU/organ vs. CFU/weight)

- Homogenize the organ in 1:9 (weight:volume) PBS and plate 100 μL by triplicate of each dilution (limit of detection of this method = 3.3 CFU/mL of dilution, corresponding to less than 5 CFU/spleen)- Express the results as log CFU/organ and report spleen weights separately (inflammation varies depending on the Brucella strain and among mouse strains).

Evaluation of immune response

- Presence of antigens and bacteria when performing ex vivo experiments. - Lack of correlation between transcripts and protein immune mediators - Lack of sensitivity- Lack of specificity - Inappropriate plotting of data

- Procure APC from non-infected mice to avoid dragging antigen or bacteria. Whenever possible perform direct assays (e.g. flow cytometry, microscopy, cell protein extraction, and serum detection).- Contrast the results obtained with indirect methods with those generated by direct methods.- Use times of maximum expression of cell types or immune mediators.- Consider the “Mackaness effect”.- Include a saturating control that could reveal the real magnitude of the response. Whenever possible, avoid expressing data in relative numbers or “fold responses” and procure the inclusion of absolute values.

Assessment of depletion of cells and immune factors

- Inefficient depletion

- Check antibody concentration, reactivity, dose and time intervals of administration. Consider that depletion seldom last more than 8 days due to neutralization by generation of anti-antibodies

Statistical analysis

- Inappropriate normalization and statistical tests - Outlier values

- Transform logarithmically the individual number of CFU/spleen, calculate the mean Log10 CFU/spleen, and compare means by the Fisher’s Protected Least Significant Differences test (PLSD), using a maximum of 4 groups per comparison (including reference or wild-type strain and, for protection studies, both the reference vaccine and placebo control groups). The RT50 calculations should be performed in the freely available statistical program at [170]. - If controls do not give expected values, the assay should be discarded (do not remove outliers).

For Immunogenicity assessment, mice are injected s.c. with the reference vaccine at doses of 105 CFU/mouse. Thirty days after vaccination, mice are challenged by the i.p. route with the standard challenge dose (2 × 105 CFU) of CO2-dependent B. abortus 544. Two weeks later, the CFU of the challenge strain are counted in the spleens using differential growth conditions for identifying vaccine and challenge coloniesa. Under these conditions, immunogenicity is expressed as the mean ± SD of log10 (X/log10X), where X is the number of CFU in each individual spleen. The mean log10 (X/log10X) obtained in the testing vaccine group should be compared with that obtained in the vaccinated and unvaccinated control groups, preferentially by ANOVA followed by the Fisher's Protected Least Significant Differences tests.

Since protection against Brucella infection (at least in the mouse model) is genus-specific and not species-specific [75, 168], B. abortus 544 has been recommended as the standard challenge strain, even when B. melitensis Rev1 is used as vaccine. In spite of this, and whenever possible, a homologous challenge strain should be used. Accordingly, species-specific reference virulent strains such as B. melitensis H38 or 16 M for anti-B. melitensis vaccines, B. abortus 544 or 2308 for anti-B. abortus vaccines and B. suis 1330 for anti-B. suis vaccines have been used as a challenge in some works [22, 72, 75, 81].

In all cases, the vaccine must also be easily distinguishable from the challenge strain. Live vaccines may survive longer than the time of challenge, and even become reactivated [23]. As consequence, they may be present when the number of CFU of the challenge strain in the spleen is estimated. To distinguish the vaccine and the challenge strains on the culture plates, markers like erythritol sensitivity (e.g. S19), CO2 dependence (e.g. B. abortus 544), antibiotic resistance (e.g. B. melitensis Rev1) or antibiotic sensitivity (e. g. B. abortus 2308 nalidixic acid sensitive) have been used [22, 75, 87, 171, 172]. As an alternative, the vaccination-challenge interval can be extended to ensure the complete elimination of the vaccine from the spleen [23, 24]. Following this method, challenge with B. abortus 2308 or B. melitensis H38 in BALB/c mice generally render more reproducible results than those obtained with B. abortus 544 or B. melitensis 16 M [22, 35, 68, 172]. One reason for this is that the two former strains give a broader range of values between controls inoculated with the placebo or the reference vaccine. The replication of the challenge strain in mice vaccinated with a reference vaccine (S19 or Rev1) is lower than in unvaccinated mice during the first 2 weeks and, therefore, the CFU/spleen reach very different values [23, 24]. After the 4th week, the CFU values in vaccinated and unvaccinated mice decrease in parallel usually maintaining a difference of two to three logarithms. Thus, vaccine efficacy is generally analyzed 2 weeks after challenge, when the differences between the reference-vaccinated and unvaccinated controls are already at a maximum, and longer times do not offer a better discrimination span with respect to protection.

Different statistical procedures for evaluating vaccine efficacy are used. The Fisher's Protected Least Significant Differences or the Bonferroni's tests (depending on the number of groups compared) usually give statistically weighted (i.e. equilibrium between alpha and beta errors) results. In this, both reference-vaccinated and unvaccinated controls act respectively as upper and lower reference limits of protection in the ANOVA test. As indicated above, the level of protection is expressed as log10(X/log10X) in the reference method. Reportedly, this transformation allows better data normalization than log10X when this value is below 1.58 [173] but in the authors’ experience it is not necessary in most casesb.

It is necessary to emphasize that new vaccine candidates as well as stocks or batches of commercial S19 and Rev1 should be contrasted with well-standardized Brucella reference strains applying always the appropriate statistical methods to measure both virulence and efficacy [33]. Variations in S19 virulence (Figure 11) and Rev1 efficacy [32] among different stocks have been detected using this methodology.
https://static-content.springer.com/image/art%3A10.1186%2F1297-9716-43-29/MediaObjects/13567_2011_Article_157_Fig11_HTML.jpg
Figure 11

Splenic growth curves of BALB/c mice infected with several B. abortus S19 vaccine strains, from different sources. Mice were intraperitoneally inoculated with 105 CFU/mouse of the corresponding strain and the number of bacteria estimated in the spleens at different times pi (adapted from [34], with permission).

5 Superinfection and antigen therapy

One common practice in some countries has been the revaccination or vaccination of infected animals [174]. Since abortion tends to stop or decrease after mass vaccination with smooth vaccines, it has been hypothesized that vaccination of infected animals may have some therapeutic effect. In addition, vaccinated animals cohabiting with infected flocks may be naturally challenged and become infected with Brucella field strains [175]. Moreover, “antigen therapy” has been used to treat human brucellosis and claimed to be effective in improving the clinical status of brucellosis infected patients [3, 9, 176]. However, these practices are of dubious value and most of them have been abandoned because of the undesirable side effects. In this regard, the mouse model has revealed significant flaws in the claims made on the usefulness of these practices in human medicine.

Treatments with either live brucellae or subcellular bacterial antigens during the acute or chronic phases do not modify the course of Brucella infections in mice [29, 81, 83]. This resembles what happens in the natural hosts [175]. It seems that, whereas the immune response has reached a “saturating level” in the acute and steady chronic phases (related to an extensive Brucella reticuloendothelial system colonization), the declining chronic phase resembles an immunosuppression state, an event also observed in chronic brucellosis [4, 177]. This last phenomenon may be associated to a progressive decrease of macrophage activation [153, 177] as well as to immune regulatory mechanisms [4, 65].

The evolution of brucellosis after superinfection as a treatment in mice is related to the virulence of the strains involved. Macrophage reactivation has been reported after inoculating Brucella antigens in B. abortus S19 infected animals [178]. Similarly, B. abortus S19 reinoculation in previously S19 infected mice results in a regression of the primary infection [153]. Nevertheless, this apparent therapeutic effect is questionable. Indeed, a transient reactivation of the attenuated Brucella strains may occur. In S19 vaccinated mice, the vaccine strain may become reactivated and increase in numbers after inoculation with virulent Brucella, brucellin or LPS [23]. This suggests that S19 does not “saturate” the reticuloendothelial system as it is the case of virulent strains. Moreover, mice infected with attenuated brucellae are less resistant to challenge with virulent strains than animals already infected with virulent Brucella[179]. These competing events are not trivial, mainly in protocols in which mixtures of virulent and attenuated Brucella strains have been used as an attempt to determine the relative virulence of the former in relation to the latter bacteria [91].

6 Passive transfer and immunomodulation

Passive transfer of antibodies and cells, and treatment with cytokines and immune enhancers are widely used methods to investigate the immune responses during murine brucellosis (Table 2). These procedures may be divided into five groups: i) passive transfer of antibodies; ii) passive transfer of immune cells; iii) treatment with cytokines or immunomodulators; iv) antibody depletion of cytokines; and v) antibody depletion of immune cells.

Passive transfer of homologous or heterologous polyclonal antisera from infected or immunized animals (syngenic, allogenic or xenogenic) protects mice against Brucella challenge [84, 98, 106, 107]. Using monoclonal antibodies (Mabs), it has been established that the most relevant targets are epitopes of N-formylperosamine sugars of the O chain of the LPS and NH polysaccharides [1] as well as some Omps like Omp31, Omp25 and Omp16 (Table 2). No correlation between the protection mediated by passive antibody transfer and the immunoglobulin isotype has been recorded. Strikingly, the efficient clearance of Brucella observed in the spleens of B cell deficient mice (Table 1) is not reversed or improved by passive administration of immune serum [55]. This suggests that the control of Brucella infection is also dependent on some B cell effectors not necessarily related to the presence of antibodies.

Passive transfer of immune splenocytes or purified populations of CD4+ and CD8+ T cells obtained after 4 weeks of infection [98, 112] protect mice against brucellosis (Table 2). As expected, a higher protection is achieved when both immune sera and cells are transferred simultaneously [107]. Similarly, passive transfer of xenogenic macrophages together with autologous Tγδ cells protects mice against Brucella replication; however, passive transfer of xonogenic macrophages alone or macrophages with autologous unprimed T cells do not (Table 2). In addition, the administration of cytokines generated during the Th1 response (e.g. INF-γ and IL-12) or the injection of immunostimulants (e.g. poly-A:U or indomethacin), promote the elimination of Brucella in mice. Indomethacin (used to stop suppressive actions mediated by the secretion of cyclooxygenase-dependent prostaglandins) does not prevent the decline in Brucella-induced INF-γ production [113]. Similarly, IL-1α (involved in the early activation of macrophages and recruitment of cells) induces protection during the acute and chronic phases of brucellosis when administered before infection [28]. In contrast, general immunossupresive agents such as corticosteroids, enhance Brucella proliferation and avoid inflammation in the target organs [3].

Depletion of immune cells has revealed significant but controversial results (Table 2). For example, antibody mediated depletion of B and NK cells barely influences the outcome of Brucella infection. In contrast, removal of CD8+ favors the invasion and increase of Brucella numbers in the spleen of mice. Noticeably, antibody mediated depletion of PMNs, CD4+ or CD25+ T cells favors the elimination of Brucella from the target organs in mice, suggesting some regulatory events. Indeed, these cells may exert some suppressive regulatory action on macrophages and dendritic cells, and perhaps on T-cytotoxic lymphocytes [4], all cells that constitute primary defenses against brucellosis.

Antibody mediated depletion of INF-γ, IL-12 and TNF-α promotes Brucella replication in mice. In contrast, depletion of regulatory IL-10 or IL-4 favors Brucella elimination (Table 2). This last event may be the result of balancing the immune response towards Th1, and therefore, favoring the efficient elimination of brucellae by cell mediated immunity. Depletion of CD8+ T cells results in a significant increase in Brucella numbers, which is associated to macrophage increase in the spleen. As expected, depletion of Tγδ cells, participating in innate immunity also favors Brucella replication. The role of TNF-α may depend upon the presence of INF-γ early in the infection, since when TNF-α is neutralized in INF-γ deficient mice there is an increase of macrophages, NK cells and neutrophils in the spleens [57]. These effects are in keeping with the preferential Th1 immune response during brucellosis, as well as with the participation of TNF-α in activating phagocytic cells, mainly during the acute and early chronic phases.

7 Antibiotic treatment

The mouse model has been successfully used to evaluate antibiotic doses, delivery, and efficacy, as well as for studying the course of brucellosis and antibody response during and after antibiotic treatments [159, 180, 181]. As in the human disease, murine brucellosis is better treated by a combination of doxycycline and aminoglycosides (streptomycin or gentamicin), or rifampicin [159, 182, 183]. While doxycycline also exerts its killing action inside cells, the second group preferentially acts extracellularly. Rifampicin is capable of reducing the Brucella loads in the spleen of mice, since it can penetrate inside leukocyte vacuoles. Consequently, it has better intracellular activity than aminoglycosides [158, 183]. The effectiveness of rifampicin or gentamicin combined with doxycycline against streptomycin-resistant B. melitensis Rev1 has been demonstrated both in humans and mice [184, 185]. However, treatments with a combination of gentamicin-doxycycline seem to be the most efficient against this vaccine strain.

The combination of doxycycline (50 mg/kg body weight/12 h for 45 days, orally), and streptomycin (i.p., 10–20 mg/kg body weight/l2 h, for 14 days) is the most efficient treatment against brucellosis in mice. This regime, which is very similar to that given to humans, does not cause relapses in mice, as far as 7 months after antibiotic treatment [159]. Accordingly, 13 days after treatment, the bacterial loads in the spleen are reduced more than three logarithms with respect to untreated mice, and bacteria are not detected in the spleen after 47 days of treatment (Figure 10). This combined regime is superior to single treatments. Indeed, regimes using only doxycycline do not completely eliminate the bacteria and may cause relapses after the 30th week of infection (Figure 10). Efforts to find substitutes for doxycycline and alternative tetracyclines for brucellosis treatment have failed. Despite the good brucellicidal action in vitro, experiments in mice using fluoroquinolones (moxifloxacin, gatifloxacin, ciprofloxacin and levofloxacin) or macrolides (erythromycin, dirithromycin or azithromycin), have been unsuccessful [180, 181, 186188].

Various protocols to evaluate intracellular delivery of antibiotics inside the Brucella replication vacuole have been tested in mice. Gentamicin containing microspheres, obtained by spray drying, reduced significantly the splenic infection in mice after i.p. or i.v. administration [188]. However, some mice died of pulmonary embolism due to aggregation of the particles. Attempts to solve this were done by including gentamicin within polymeric nanoparticles made out of D,L-lactide-coglycolide [189]. In this model, gentamicin-containing microspheres administrated i.v. reduced but not eliminated the burden of B. melitensis infection. Interestingly, the microsphere body distribution was similar to that followed by Brucella organisms, being spleen and liver the main target organs. An alternative approach to improve antibiotic treatment has been the inclusion of streptomycin and doxycycline into macromolecular nanoplexes [190]. Intravenous administration of two doses reduced the number of B. melitensis 16 M in spleens and livers of mice, and seemed more effective than free drugs. Pharmacokinetics of these nanoparticles containing antibiotics has not been studied.

Decline of antibody titers against LPS and proteins after antibiotic treatment in human patients frequently corresponds with successful elimination of the Brucella[182]. In contrast, titers of antibodies against Brucella LPS have a tendency to remain elevated in treated mice (Figure 10). This is evident with high challenge doses (e.g. >106B. melitensis CFU/mouse) and with antibiotic regimes (e.g. doxycycline or doxycycline-streptomycin) given orally after the 3rd week of infection [159]. The difference between mice and humans may be due to the shorter life span of the former and/or the ability of anti-LPS antibodies to protect mice against brucellosis (Table 2). However, when treatment starts during the 1st week of infection and the challenge dose is lower (<104B. melitensis CFU/mouse), the antibody response against Brucella cytoplasmic proteins decreases to undetectable levels in mice [191]. This parallels the low or lack of anti-protein responses in human patients receiving early antibiotic treatment [192].

8 Concluding remarks

There are several differences and similarities between experimental brucellosis in mice and the disease in the natural hosts and in humans. For instance, mice are quite resistant to Brucella infection but, in contrast to natural hosts, do not seem to shed Brucella significantly and the infection seems to be contained. Therefore, horizontal transmission does not seem important in experimental murine brucellosis. In non-treated human patients or in dolphins, brucellosis may become chronic, causing cardiopathies, extensive bone lesions and neurobrucellosis, as well as other severe pathologies [9, 77, 129]. Strikingly, all these syndromes are seldom recorded in infected mice when using current protocols and adequate bacterial doses (e.g. large doses may saturate the organs and overcome the immune response). In mice, the liver is the shock organ and the inflammatory immune response in the spleen protects the liver from massive Brucella invasion [14, 15]. Similarly, humans also display splenomegaly and during chronic brucellosis the liver becomes one of the sites for Brucella replication [3, 9]. In contrast, prominent liver granuloma formation and large splenomegaly have seldom been reported in ruminants [130]. While active spleen hematopoiesis is a conspicuous feature in murine brucellosis, it is a very rare event in humans and ruminants [21]. A common feature of murine, human and domestic animal brucellosis is the absence of endotoxic symptoms at the onset of the infection, a phenomenon related to the stealthy strategy of Brucella[4, 48].

As in other mammals, the mouse giant mononuclear placental trophoblasts are also target cells for Brucella. The invasion of placenta occurs at specific periods in experimentally infected mice and natural hosts but with different clinical consequences. In fact, Brucella infections occurring later in pregnancy (i.e. after the last one-third of pregnancy) or close to delivery, induce less abortions in both natural hosts and mice [135]. However, there are fundamental differences between placental infections in mice and in natural hosts. Mice are quite resistant to Brucella induced abortion and abortion is linked to a particular immune response within a narrow window of the gestation period in which the placenta is effectively colonized by the invading Brucella[135]. In contrast, in bovines and small ruminants, abortion generally occurs during the last one-third of pregnancy, irrespectively of whether they were infected months or years before [8, 130, 193]. This difference between mice and ruminants may be related not only to the nature of trophoblastic cells but also to placental structure [194]. For instance, in ungulates there is no transplacentary transfer of antibodies while in rodents there is a significant transmission of antibodies from the mother to the fetus. This is relevant since the antibody response in mice against Brucella could protect the fetuses. Regarding the reproductive organs of male mice, Brucella colonize the testes very early after experimental infection [76] with invasion of the epididymis [128], a phenomenon that resembles brucellosis in human, bovine, ovine and caprine males.

The understanding of immune mechanisms during brucellosis has been a significant contribution of the mouse model. The furtive strategy of Brucella to overcome the innate immunity at the onset of the infection, the role of INF-γ and the Th1 responses in controlling brucellosis during the rise of adaptive immunity, have been partially elucidated using the mouse model [4, 48, 66, 103, 125]. There are, however, significant discrepancies in both innate and adaptive immunity mechanisms between mice, humans and ruminants [20, 21, 195, 196]. For instance, mouse macrophages seem to be more bactericidal and less permissive than human macrophages [66, 197]. The mouse resistance to Brucella may be also related to a higher proportion of lymphocytes in relation to other cells such a neutrophils. The murine C'2 and C'3 complement activities are quite low, and the serum contains a potent inhibitor of lytic activity precluding this function in mice. The properties of immunoglobulin isotypes are also different in mice, bovines and humans. Other significant variations are the absence of defensins in mouse leukocytes, different subsets of TLR, inducible NO synthase, the NK inhibitory receptor families Ly49 and KIR, FcR, the B cell (BLNK, Btk, and λ5), T cell (ZAP70 and common γ-chain) signaling pathway components, Thy-1, γδT cells, cytokines and cytokine receptors, Th1/Th2 differentiation, costimulatory molecule expression and function, antigen-presenting function of endothelial cells, chemokines and chemokine receptor expression and the absence of granulysin in murine Tc lymphocytes [21].

It is intriguing that various acquired or innate immune deficiencies do not seem to alter the outcome of Brucella infection in mice (Tables 1 and 2). For instance, neutrophil depletion and B cells immune deficiency seem to favor the elimination of Brucella from the spleens of the corresponding treated or knockout mice more readily than what it happens in the wild type. This suggests that complex immune regulatory and compensatory events may take place during Brucella infection in mice [4]. It has been proposed that the augmented bacterial clearance in B-cell deficient mutant mice corresponds to an increase in IFN-γ-producing T cells and a reduction in IL-10-producing cells [55]. Similarly, in B cell deficient jh knockout mice, bacterial clearance seems also to be dependent on IFN-γ production but inversely related to the levels of TGF-β at early stages of infection.

Some confusion results from the different methods used to evaluate the immune responses in mice. The most reliable are the classical methods that consist in: i) determining the DTH, the amount of antibodies and cytokines in sera by immunochemical assays; and ii) the number and type of cells in blood and organ by microscopy or cytometry. In spite of their relative low sensitivity, these methods are specific and render consistent results. The interpretation of the immune response by ex vivo indirect assays, in which cell proliferation or cytokines are measured in cell cultures exposed to antigens, is not straightforward, particularly when cytokines are indirectly determined by detecting transcripts. Among other sources of variation, the immune cells harbor Brucella antigens and frequently live bacteria depending upon the time at which cells are taken from the infected mice (e.g. 7 to 60 days). This fact is rarely mentioned or taken into consideration in experimental works. Similarly, the estimated transcripts seldom parallel the quantitative measurement of proteins [195]. Therefore, it is recommended to contrast the results obtained by indirect procedures with those generated by direct methods.

A significant number of reports present replication and persistence patterns of reference or type Brucella strain that do not reproduce those established in mice. Generally, this means that the Brucella type strain used has become attenuated, and this is important source of misunderstanding, mainly in pathogenicity and virulence studies. Other source of confusion corresponds to the manner in which data are expressed or presented. It is common to notice published information schematically plotted to display “significant” conspicuous values (e. g. bars or peaks) without including a full virulent positive control administered at the optimal dose that could reveal the real magnitude of the response. Taking into account that ordinate axis can represent different scales the risk is that the plotted values may appear significant, when no adequate saturating control (inducing the maximum response) is included. Similarly, in other type of experiments, it is necessary to contrast the results obtained with Brucella with those of unrelated infections, mitogens or immunostimulants (e.g. Listeria, Salmonella, concanavaline A or LPS) that generate well known saturating responses.

Few live vaccines are able to confer adequate protection in domestic ruminants, and subcellular vaccines or killed bacterins are not protective enough in the natural hosts. This is in clear contrast with many experimental results in mice. Nevertheless, under well-standardized conditions the mouse model is a useful tool for screening vaccines, even though one vaccine that performs efficiently in mice may not work in the natural host. The opposite, however, has not been reported: vaccines that protect poorly in mice are useless in the natural hosts [85, 198, 199]. In any case, for vaccine evaluation it is always necessary to use controls vaccinated with the reference vaccine strains and to apply the correct statistical tests. A summary of the general problems and recommendations when performing experiments with Brucella in the mouse model is presented in Table 3.

Mus musculus seems to be the second most abundant and disperse mammalian species in the world, after Homo sapiens. This rodent diverged from ungulates and primates about 90 million years ago [200], probably at the time when Brucella speciation occurred in various animal hosts [201]. Although for many decades Brucella organisms have been isolated in some species of Muroidea, [202, 203], M. musculus has not been found to be a reservoir of Brucella. This is remarkable, taken into consideration that “house mice” have shared habitat and food with humans and domestic animals for millennia, mainly after the domestication of crops and ruminants [204]. Thus, whereas it is clear that M. musculus constitutes a valuable non-natural host for brucellosis studies, the advantages and limitations of the model should be properly understood within the right experimental context.

9 Endnotes

aFor example, for B. abortus 544 and S19 differentiation, incubate under a CO2 atmosphere (where both strains grow) and under normal atmosphere (where only S19 grows) and subtract the values obtained for the same spleen dilution.

bFor a practical example, see (Additional file 1: Table S1).

Declarations

12 Acknowledgments

We thank Montserrat Barberán (University of Zaragoza, Spain) and Rocío González-Barrientos (MAG, Costa Rica) for supplying the histopathological spleen figures. This work was performed under agreement contract 2010020113, subscribed by UNA from Costa Rica and, CSIC, CITA, and UN from Spain. This work was funded by grants FIDA-2009 UNA, FS-CONARE UNA/UCR, NeTropica 8, and MICIT/CONICIT, CSIC-CRUSA (2010CR0005) from Costa Rica; and CICYT-MICINN (AGL2010-20247, AGL2008-04514-C03-00 and AGL2011-30453-C04-00) projects from Spain and grant ANR2010BLAN1308 Brutir., form France. This work was done as part of the UCR/DAAD Humboldt Fellow award 2012 to EM.

Authors’ Affiliations

(1)
Instituto de Agrobiotecnología, CSIC-UPNA-Gobierno de Navarra
(2)
Centro de Investigación y Tecnología Agroalimentaria (CITA) de Aragón
(3)
Centre d'Immunologie de Marseille-Luminy, Aix Marseille Université, Faculté de Sciences de Luminy
(4)
Institut National de la Santé et de la Recherche Médicale U631
(5)
Centre National de la Recherche Scientifique UMR6102
(6)
Departamento de Microbiología y Parasitología, Universidad de Navarra
(7)
Instituto de Salud Tropical, Universidad de Navarra
(8)
Programa de Investigación en Enfermedades Tropicales, Escuela de Medicina Veterinaria, Universidad Nacional
(9)
Instituto Clodomiro Picado, Facultad de Microbiología, Universidad de Costa Rica

References

  1. Moreno E, Moriyón I: The genus Brucella. The Prokaryotes, Volume 5. Part 1, section 31. Edited by: Dworkin M, Falkow S, Rosenberg E, Schleifer KH, Stackebrant E. 2006, Springer, Ne York, 315-456.
  2. Enright FM: The pathogenesis and pathobiology of Brucella infection in domestic animals. Animal Brucellosis. Edited by: Nielsen KH, Duncan JR. 1990, CRC Press, Boca Raton, 301-320.
  3. Spink WW: The Nature of Brucellosis. 1956, The University of Minnesota Press, Minnesota
  4. Martirosyan A, Moreno E, Gorvel JP: An evolutionary strategy for a stealthy intracellular Brucella pathogen. Immunol Rev. 2011, 240: 211-234. 10.1111/j.1600-065X.2010.00982.x.PubMedView Article
  5. Moreno E, Moriyón I: Brucella melitensis: a nasty bug with hidden credentials for virulence. Proc Nat Acad Sci USA. 2002, 99: 1-3. 10.1073/pnas.022622699.PubMed CentralPubMedView Article
  6. Cotton WE, Buck JM, Smith HE: Efficacy and safety of abortion vaccines prepared from Brucella abortus strains of different degrees of virulence. J Agricul Res. 1933, 46: 291-314.
  7. Morales-Otero P: Experimental infection of Brucella abortus in man: Preliminary report, Puerto Rico. J Pub Health Trop Med. 1929, 5: 144-157.
  8. Plommet M: Studies of experimental brucellosis in cows in France. Bovine Brucellosis. Edited by: Crawford RM, Hidalgo RJ. 1977, Texas A&M University Press, College Station, Texas, 116-1134.
  9. Ruiz-Castañeda M: Brucelosis. 1986, Ediciones Científicas, Prensa Médica Mexicana, S A, Copilco-Universidad, México, DF, 3
  10. Buddingh GJ, Womack FC: Observations on the infections of chick embryos with Bacterium tularense, Brucella and Pasteurella pestis. J Exp Med. 1941, 74: 213-222. 10.1084/jem.74.3.213.PubMed CentralPubMedView Article
  11. Díaz R, Oyeledun A: Studies of some biological activities of Brucella endotoxin in normal and infected animals and the role of the hypersensitivity factor. Ann Sclavo. 1977, 19: 117-130.PubMed
  12. Alton GG, Jones LM, Angus RD, Verger JM: Techniques for the brucellosis laboratory. 1988, Institut National de la Recherche Agronomique (INRA), Paris
  13. García-Carrillo C: Laboratory animal models for brucellosis studies. Animal Brucellosis. Edited by: Nielsen K, Duncan JR. 1990, CRC Press, Boca Raton, FL, 423-442.
  14. Braude AI: Studies in the pathology and pathogenesis of experimental brucellosis II The formation of the hepatic granuloma and its evolution. J Infect Dis. 1951, 89: 87-102. 10.1093/infdis/89.1.87.PubMedView Article
  15. Braude AI, Spink WW: Studies in the pathology and pathogenesis of experimental brucellosis III Investigations pertaining to the function of the spleen. J Infect Dis. 1951, 89: 272-297. 10.1093/infdis/89.3.272.PubMedView Article
  16. Office International des Épizooties Bovine brucellosis: Manual of Diagnostic Tests and Vaccines for Terrestrial Animals. Volume 2. 2008, Paris
  17. Oliveira SC, Harms JS, Banai M, Splitter GA: Recombinant Brucella abortus proteins that induce proliferation and gamma-interferon secretion by CD4+ T cells from Brucella-vaccinated mice and delayed-type hypersensitivity in sensitized guinea pigs. Cell Immunol. 1996, 172: 262-268. 10.1006/cimm.1996.0241.PubMedView Article
  18. Feldman WH, Olson C: The pathogenecity of Brucella abortus for white mice. J Infect Dis. 1935, 57: 212-222. 10.1093/infdis/57.2.212.View Article
  19. Singer-Brooks CH: Brucella infection in white mice. J Infect Dis. 1937, 60: 265-275. 10.1093/infdis/60.3.265.View Article
  20. Green EL: Biology of the Laboratory Mouse. 1966, Dover publication Inc, New York, 2
  21. Mestas J, Hughes CC: Of mice and not men:differences between mouse and human immunology. J Immunol. 2004, 172: 2731-2738.PubMedView Article
  22. González D, Grilló MJ, De Miguel MJ, Ali T, Arce-Gorvel V, Delrue RM, Conde-Alvarez R, Muñoz P, López-Goñi I, Iriarte M, Marín CM, Weintraub A, Widmalm G, Zygmunt M, Letesson JJ, Gorvel JP, Blasco JM, Moriyón I: Brucellosis vaccines: assessment of Brucella melitensis lipopolysaccharide rough mutants defective in core and O-polysaccharide synthesis and export. PLoS One. 2008, 3: e2760-10.1371/journal.pone.0002760.PubMed CentralPubMedView Article
  23. Plommet M, Plommet AM: Reactivation of a residual Brucella abortus 19 vaccine infection in mice by a virulent challenge or by injection of brucellin or of Brucella lipopolysaccharide. Ann Rech Vet. 1988, 19: 245-251.PubMed
  24. Plommet M, Plommet AM: Virulence of Brucella: bacterial growth and decline in mice. Ann Rech Vet. 1988, 19: 65-67.PubMed
  25. Bosseray N, Plommet M, De Rycke J: Evolution de l'infection de la souris par Brucella abortus, Brucella melitensis et Brucella suis vers l'état chronique et la guérison. Ann Rech Vet. 1982, 13: 153-161. in FrenchPubMed
  26. Pardon P: Development of spleenic infection in the mouse following intravenous inoculation of various species of Brucella in smooth (S) or rough (R) phases. C R Acad Sci Hebd Seances Acad Sci D. 1975, 281: 81-84.PubMed
  27. Cheers C, Cone RE: Effect of polyadenine: polyuridine on brucellosis in conventional and congenitally athymic mice. J Immunol. 1974, 112: 1535-1539.PubMed
  28. Zhan YF, Stanley ER, Cheers C: Prophylaxis or treatment of experimental brucellosis with interleukin-1. Infect Immun. 1991, 59: 1790-1794.PubMed CentralPubMed
  29. Pardon P, Marly J: Resistance of Brucella abortus infected mice to intravenous or intraperitoneal Brucella reinfection. Ann Immunol Inst Pasteur. 1976, 127C: 57-70.
  30. High KP, Prasad R, Marion CR, Schurig GG, Boyle SM, Sriranganathan N: Outcome and immune responses after Brucella abortus infection in young adult and aged mice. Biogerontology. 2007, 8: 583-593. 10.1007/s10522-007-9106-6.PubMedView Article
  31. Sangari FJ, Grilló MJ: Jiménez De Bagüés MP, González-Carreró MI, García-Lobo JM, Blasco JM, Agüero J: The defect in the metabolism of erythritol of the Brucella abortus B19 vaccine strain is unrelated with its attenuated virulence in mice. Vaccine. 1988, 16: 1640-1645.View Article
  32. Bosseray N: Brucella melitensis Rev 1 living attenuated vaccine: stability of markers, residual virulence and immunogenicity in mice. Biologicals. 1991, 19: 355-363. 10.1016/S1045-1056(05)80025-9.PubMedView Article
  33. Grilló MJ, Bosseray N, Blasco JM: In vitro markers and biological activity in mice of seed lot strains and commercial Brucella melitensis Rev1 and Brucella abortus B19 vaccines. Biologicals. 2000, 28: 119-127. 10.1006/biol.2000.0249.PubMedView Article
  34. Mukherjee F, Jain J, Grilló MJ, Blasco JM, Nair M: Evaluation of Brucella abortus S19 vaccine strains by bacteriological tests, molecular analysis of ery loci and virulence in BALB/c mice. Biologicals. 2005, 33: 153-160. 10.1016/j.biologicals.2005.04.003.PubMedView Article
  35. Montaraz JA, Winter AJ: Comparison of living and nonliving vaccines for Brucella abortus in BALB/c mice. Infect Immun. 1986, 53: 245-251.PubMed CentralPubMed
  36. Kahl-McDonagh MM, Ficht TA: Evaluation of protection afforded by Brucella abortus and Brucella melitensis unmarked deletion mutants exhibiting different rates of clearance in BALB/c mice. Infect Immun. 2006, 74: 4048-4057. 10.1128/IAI.01787-05.PubMed CentralPubMedView Article
  37. Manterola L, Guzmán-Verri C, Chaves-Olarte E, Barquero-Calvo E, de Miguel MJ, Moriyón I, Grilló MJ, López-Goñi I, Moreno E: BvrR/BvrS-controlled outer membrane proteins Omp3a and Omp3b are not essential for Brucella abortus virulence. Infect Immun. 2007, 75: 4867-4874. 10.1128/IAI.00439-07.PubMed CentralPubMedView Article
  38. Kim S, Kurokawa D, Watanabe K, Makino S, Shirahata T, Watarai M: Brucella abortus nicotinamidase (PncA) contributes to its intracellular replication and infectivity in mice. FEMS Microbiol Lett. 2004, 234: 289-295. 10.1111/j.1574-6968.2004.tb09546.x.PubMedView Article
  39. Ho M, Cheers C: Resistance and susceptibility of mice to bacterial infection IV Genetic and cellular basis of resistance to chronic infection with Brucella abortus. J Infect Dis. 1982, 146: 381-387. 10.1093/infdis/146.3.381.PubMedView Article
  40. Pugh GW, Zehr ES, Meador VP, Phillips M, McDonald TJ, Deyoe BL: Immunologic, histopathologic, and bacteriologic responses of five strains of mice to Brucella abortus strain 2308. Am J Vet Res. 1989, 50: 323-328.PubMed
  41. Cannat A, Serre A: Genetic factors involved in murine resistance to experimental brucellosis. Dev Biol Stand. 1984, 56: 307-313.PubMed
  42. Cannat A, Serre A: Genetic factors involved in murine susceptibility to experimental brucellosis. Ann Immunol. 1981, 132D: 15-24.
  43. Guilloteau LA, Dornand J, Gross A, Olivier M, Cortade F, Vern YL, Kerboeuf D: Nramp1 is not a major determinant in the control of Brucella melitensis infection in mice. Infect Immun. 2003, 71: 621-628. 10.1128/IAI.71.2.621-628.2003.PubMed CentralPubMedView Article
  44. Copin R, De Baetselier P, Carlier Y, Letesson JJ, Muraille E: MyD88-dependent activation of B220-CD11b + LY-6 C + dendritic cells during Brucella melitensis infection. J Immunol. 2007, 178: 5182-5191.PubMedView Article
  45. Macedo GC, Magnani DM, Carvalho NB, Bruna-Romero O, Gazzinelli RT, Oliveira SC: Central role of MyD88-dependent dendritic cell maturation and proinflammatory cytokine production to control Brucella abortus infection. J Immunol. 2008, 180: 1080-1087.PubMedView Article
  46. Surendran N, Hiltbold EM, Heid B, Akira S, Standiford TJ, Sriranganathan N, Boyle SM, Zimmerman KL, Makris MR, Witonsky SG: Role of TLRs in Brucella mediated murine DC activation in vitro and clearance of pulmonary infection in vivo. Vaccine. 2012, 30: 1502-1512. 10.1016/j.vaccine.2011.12.036.PubMedView Article
  47. Campos MA, Rosinha GM, Almeida IC, Salgueiro XS, Jarvis BW, Splitter GA, Qureshi N, Bruna-Romero O, Gazzinelli RT, Oliveira SC: Role of Toll-like receptor 4 in induction of cell-mediated immunity and resistance to Brucella abortus infection in mice. Infect Immun. 2004, 72: 176-186. 10.1128/IAI.72.1.176-186.2004.PubMed CentralPubMedView Article
  48. Barquero-Calvo E, Chaves-Olarte E, Weiss DS, Guzmán-Verri C, Chacón-Díaz C, Rucavado A, Moriyón I, Moreno E: Brucella abortus uses a stealthy strategy to avoid activation of the innate immune system during the onset of infection. PLoS One. 2007, 2: e631-10.1371/journal.pone.0000631.PubMed CentralPubMedView Article
  49. Phillips M, Pugh GW, Deyoe BL: Duration of strain 2308 infection and immunogenicity of Brucella abortus lipopolysaccharide in five strains of mice. Am J Vet Res. 1989, 50: 318-322. 50PubMed
  50. Weiss DS, Takeda K, Akira S, Zychlinsky A, Moreno E: MyD88, but not toll-like receptors 4 and 2, is required for efficient clearance of Brucella abortus. Infect Immun. 2005, 73: 5137-5143. 10.1128/IAI.73.8.5137-5143.2005.PubMed CentralPubMedView Article
  51. Oliveira FS, Carvalho NB, Zamboni DS, Oliveira SC: Nucleotide-binding oligomerization domain-1 and −2 play no role in controlling Brucella abortus infection in mice. Clin Dev Immunol. 2012, 2012: 861426-PubMed CentralPubMed
  52. Oliveira FS, Carvalho NB, Brandão AP, Gomes MT, de Almeida LA, Oliveira SC: Interleukin-1 receptor-associated kinase 4 is essential for initial host control of Brucella abortus infection. Infect Immun. 2011, 79: 4688-4695. 10.1128/IAI.05289-11.PubMed CentralPubMedView Article
  53. Ko J, Gendron-Fitzpatrick A, Ficht TA, Splitter GA: Virulence criteria for Brucella abortus strains as determined by interferon regulatory factor 1-deficient mice. Infect Immun. 2002, 70: 7004-7012. 10.1128/IAI.70.12.7004-7012.2002.PubMed CentralPubMedView Article
  54. Rolán HG, Tsolis RM: Mice lacking components of adaptive immunity show increased Brucella abortus virB mutant colonization. Infect Immun. 2007, 75: 2965-2973. 10.1128/IAI.01896-06.PubMed CentralPubMedView Article
  55. Goenka R, Parent MA, Elzer PH, Baldwin CL: B cell-deficient mice display markedly enhanced resistance to the intracellular bacterium Brucella abortus. J Infect Dis. 2011, 203: 1136-1146. 10.1093/infdis/jiq171.PubMedView Article
  56. Oliveira SC: A Splitter G: CD8+ type 1 CD44hi CD45 RBlo T lymphocytes control intracellular Brucella abortus infection as demonstrated in major histocompatibility complex class I- and class II-deficient mice. Eur J Immunol. 1995, 25: 2551-2557. 10.1002/eji.1830250922.PubMedView Article
  57. Murphy EA, Sathiyaseelan J, Parent MA, Zou B, Baldwin CL: Interferon-gamma is crucial for surviving a Brucella abortus infection in both resistant C57BL/6 and susceptible BALB/c mice. Immunology. 2001, 103: 511-518. 10.1046/j.1365-2567.2001.01258.x.PubMed CentralPubMedView Article
  58. Brandão AP, Oliveira FS, Carvalho NB, Vieira LQ, Azevedo V, Macedo GC, Oliveira SC: Host susceptibility to Brucella abortus infection is more pronounced in IFN-γ knockout than IL-12/β2-microglobulin double-deficient mice. Clin Dev Immunol. 2012, 2012: 589494-PubMed CentralPubMedView Article
  59. Cheville NF, Kunkle RA, Jensen AE, Palmer MV: Persistence of Brucella abortus in the livers of T cell-deficient nude mice. Lab Invest. 1995, 73: 96-102.PubMed
  60. Skyberg JA, Thornburg T, Rollins M, Huarte E, Jutila MA, Pascual DW: Murine and bovine γδ T cells enhance innate immunity against Brucella abortus infections. PLoS One. 2011, 6: e21978-10.1371/journal.pone.0021978.PubMed CentralPubMedView Article
  61. Roux CM, Rolán HG, Santos RL, Beremand PD, Thomas TL, Adams LG, Tsolis RM: Brucella requires a functional Type IV secretion system to elicit innate immune responses in mice. Cell Microbiol. 2007, 9: 1851-1869. 10.1111/j.1462-5822.2007.00922.x.PubMedView Article
  62. de Almeida LA, Carvalho NB, Oliveira FS, Lacerda TL, Vasconcelos AC, Nogueira L, Bafica A, Silva AM, Oliveira SC: MyD88 and STING signaling pathways are required for IRF3-mediated IFN-β induction in response to Brucella abortus infection. PLoS One. 2011, 6: e23135-10.1371/journal.pone.0023135.PubMed CentralPubMedView Article
  63. Zhan Y, Cheers C: Control of IL-12 and IFN-gamma production in response to live or dead bacteria by TNF and other factors. J Immunol. 1998, 161: 1447-1453.PubMed
  64. Enright FM, Araya LN, Elzer PH, Rowe GE, Winter AJ: Comparative histopathology in BALB/c mice infected with virulent and attenuated strains of Brucella abortus. Vet Immunol Immunopathol. 1990, 26: 171-182. 10.1016/0165-2427(90)90065-Z.PubMedView Article
  65. Hort GM, Weisenburger J, Borsdorf B, Peters C, Banai M, Hahn H, Jacob J, Mielke ME: Delayed type hypersensitivity-associated disruption of splenic periarteriolar lymphatic sheaths coincides with temporary loss of IFN-gamma production and impaired eradication of bacteria in Brucella abortus-infected mice. Microbes Infect. 2003, 5: 95-106. 10.1016/S1286-4579(02)00076-X.PubMedView Article
  66. Baldwin CL, Goenka R: Host immune responses to the intracellular bacteria Brucella: does the bacteria instruct the host to facilitate chronic infection?. Crit Rev Immunol. 2006, 26: 407-442. 10.1615/CritRevImmunol.v26.i5.30.PubMedView Article
  67. Stevens MG, Olsen SC, Pugh GW, Brees D: Comparison of immune responses and resistance to brucellosis in mice vaccinated with Brucella abortus 19 or RB51. Infect Immun. 1995, 63: 264-270.PubMed CentralPubMed
  68. Grilló MJ, Manterola L, de Miguel MJ, Muñoz PM, Blasco JM, Moriyón I, López-Goñi I: Increases of efficacy as vaccine against Brucella abortus infection in mice by simultaneous inoculation with avirulent smooth bvrS/bvrR and rough wbkA mutants. Vaccine. 2006, 24: 2910-2916. 10.1016/j.vaccine.2005.12.038.PubMedView Article
  69. Charting A New Course in Tissue Analysis http://​www.​flagshipbio.​com/​uncategorized/​the-spleen-the-whole-spleen-and-nothing-but-the-spleen/​
  70. Mancilla M, López-Goñi I, Moriyón I, Zárraga AM: Genomic island 2 is an unstable genetic element contributing to Brucella lipopolysaccharide spontaneous smooth-to-rough dissociation. J Bacteriol. 2010, 192: 6346-6351. 10.1128/JB.00838-10.PubMed CentralPubMedView Article
  71. Yang X, Thornburg T, Walters N, Pascual DW: DeltaznuADeltapurE Brucella abortus 2308 mutant as a live vaccine candidate. Vaccine. 2010, 28: 1069-1074. 10.1016/j.vaccine.2009.10.113.PubMedView Article
  72. Winter AJ, Schurig GG, Boyle SM, Sriranganathan N, Bevins JS, Enright FM, Elzer PH, Kopec JD: Protection of BALB/c mice against homologous and heterologous species of Brucella by rough strain vaccines derived from Brucella melitensis and Brucella suis biovar 4. Am J Vet Res. 1996, 57: 677-683.PubMed
  73. Turse JE, Pei J, Ficht TA: Lipopolysaccharide-deficient Brucella variants arise spontaneously during infection. Front Microbiol. 2011, 2: 54-PubMed CentralPubMedView Article
  74. Bosseray N: Colonization of mouse placentas by Brucella abortus inoculated during pregnancy. Br J Exp Pathol. 1980, 61: 361-368.PubMed CentralPubMed
  75. Bosseray N, Plommet M: Brucella suis S2, Brucella melitensis Rev 1 and Brucella abortus S19 living vaccines: residual virulence and immunity induced against three Brucella species challenge strains in mice. Vaccine. 1990, 8: 462-468. 10.1016/0264-410X(90)90247-J.PubMedView Article
  76. Rajashekara G, Glover DA, Krepps M, Splitter GA: Temporal analysis of pathogenic events in virulent and avirulent Brucella melitensis infections. Cell Microbiol. 2005, 7: 1459-1473. 10.1111/j.1462-5822.2005.00570.x.PubMedView Article
  77. González-Barrientos R, Morales JA, Hernández-Mora G, Barquero-Calvo E, Guzmán-Verri C, Chaves-Olarte E, Moreno E: Pathology of striped dolphins (Stenella coeruleoalba) infected with Brucella ceti. J Comp Pathol. 2010, 142: 347-352. 10.1016/j.jcpa.2009.10.017.PubMedView Article
  78. Hong CB, Donahue JM, Giles RC, Poonacha KB, Tuttle PA, Cheville NF: Brucella abortus-associated meningitis in aborted bovine fetuses. Vet Pathol. 1991, 28: 492-496. 10.1177/030098589102800605.PubMedView Article
  79. Shakir RA, Al-Din AS, Araj GF, Lulu AR, Mousa AR, Saadah MA: Clinical categories of neurobrucellosis a report on 19 cases. Brain. 1987, 110: 213-223. 10.1093/brain/110.1.213.PubMedView Article
  80. Chen TH, Elberg SS: Immunization against Brucella infections: immune response of mice, guinea pigs, and Cynomolgus philipinensis to live and killed Brucella melitensis strain Rev I administered by various methods. J Infect Dis. 1970, 122: 489-500. 10.1093/infdis/122.6.489.PubMedView Article
  81. Jiménez-de-Bagüés MP, Marín CM, Barberán M, Blasco JM: Evaluation of vaccines and of antigen therapy in a mouse model for Brucella ovis. Vaccine. 1993, 11: 61-66. 10.1016/0264-410X(93)90340-4.PubMedView Article
  82. Pardon P: Resistance against a subcutaneous Brucella challenge of mice immunized with living or dead Brucella or by transfer of immune serum. Ann Immunol Inst Pasteur. 1977, 128C: 1025-1037.
  83. Plommet M, Plommet AM, Bosseray N: L’evolution de la brucellose chronique de la souris n’est pas améliorée par I’administration d’un antigène vaccinal. Ann Rech Vet. 1982, 13: 127-132.PubMed
  84. Plommet M, Plommet AM: Immune serum-mediated effects on brucellosis evolution in mice Infect Immun. Infect Immun. 1983, 41: 97-105.PubMed CentralPubMed
  85. Barrio MB, Grilló MJ, Muñoz PM, Jacques I, González D, de Miguel MJ, Marín CM, Barberán M, Letesson JJ, Gorvel JP, Moriyón I, Blasco JM, Zygmunt MS: Rough mutants defective in core and O-polysaccharide synthesis and export induce antibodies reacting in an indirect ELISA with smooth lipopolysaccharide and are less effective than Rev1 vaccine against Brucella melitensis infection of sheep. Vaccine. 2009, 27: 1741-1749. 10.1016/j.vaccine.2009.01.025.PubMedView Article
  86. Kahl-McDonagh MM, Arenas-Gamboa AM, Ficht TA: Aerosol infection of BALB/c mice with Brucella melitensis and Brucella abortus and protective efficacy against aerosol challenge. Infect Immun. 2007, 75: 4923-4932. 10.1128/IAI.00451-07.PubMed CentralPubMedView Article
  87. Smither SJ, Perkins SD, Davies C, Stagg AJ, Nelson M, Atkins HS: Development and characterization of mouse models of infection with aerosolized Brucella melitensis and Brucella suis. Clin Vaccine Immunol. 2009, 16: 779-783. 10.1128/CVI.00029-09.PubMed CentralPubMedView Article
  88. Mense MG, Van De Verg LL, Bhattacharjee AK, Garrett JL, Hart JA, Lindler LE, Hadfield TL, Hoover DL: Bacteriologic and histologic features in mice after intranasal inoculation of Brucella melitensis. Am J Vet Res. 2001, 62: 398-405. 10.2460/ajvr.2001.62.398.PubMedView Article
  89. Anderson TD, Meador VP, Cheville NF: Pathogenesis of placentitis in the goat inoculated with Brucella abortus I Gross and histologic lesions. Vet Pathol. 1986, 23: 219-226.PubMed
  90. Delpino MV, Marchesini MI, Estein SM, Comerci DJ, Cassataro J, Fossati CA, Baldi PC: A bile salt hydrolase of Brucella abortus contributes to the establishment of a successful infection through the oral route in mice. Infect Immun. 2007, 75: 299-305. 10.1128/IAI.00952-06.PubMed CentralPubMedView Article
  91. Paixão TA, Roux CM, den Hartigh AB, Sankaran-Walters S, Dandekar S, Santos RL, Tsolis RM: Establishment of systemic Brucella melitensis infection through the digestive tract requires urease, the type IV secretion system, and lipopolysaccharide O antigen. Infect Immun. 2009, 77: 4197-4208. 10.1128/IAI.00417-09.PubMed CentralPubMedView Article
  92. Pasquali P, Rosanna A, Pistoia C, Petrucci P, Ciuchini F: Brucella abortus RB51 induces protection in mice orally infected with the virulent strain B abortus 2308. Infect Immun. 2003, 71: 2326-2330. 10.1128/IAI.71.5.2326-2330.2003.PubMed CentralPubMedView Article
  93. Morales-Otero P: Brucella abortus in Puerto Rico. J Pub Health Trop Med. 1930, 6: 3-22.
  94. Gorvel JP, Moreno E, Moriyón I: Is Brucella an enteric pathogen?. Nat Rev Microbiol. 2009, 7: 250-PubMedView Article
  95. Salcedo SP, Marchesini MI, Lelouard H, Fugier E, Jolly G, Balor S, Muller A, Lapaque N, Demaria O, Alexopoulou L, Comerci DJ, Ugalde RA, Pierre P, Gorvel JP: Brucella control of dendritic cell maturation is dependent on the TIR-containing protein Btp1. PLoS Pathog. 2008, 4: e21-10.1371/journal.ppat.0040021.PubMed CentralPubMedView Article
  96. Tanay A, Strober S: T cell regulation of the thymus-independent antibody response to trinitrophenylated-Brucella abortus (TNP-BA). J Immunol. 1985, 134: 3669-3674.PubMed
  97. Plommet M, Bosseray N: Proposed general method of controlling the activity of Brucella vaccines. Dev Biol Stand. 1984, 56: 247-255.PubMed
  98. Jiménez-de-Bagüés MP, Elzer PH, Jones SM, Blasco JM, Enright FM, Schurig GG, Winter AJ: Vaccination with Brucella abortus rough mutant RB51 protects BALB/c mice against virulent strains of Brucella abortus, Brucella melitensis, and Brucella ovis. Infect Immun. 1994, 62: 4990-4996.PubMed CentralPubMed
  99. Thorpe BD, Sidwell RW, Lundgren DL: Experimental studies with four species of Brucella in selected wildlife, laboratory, and domestic animals Am. J Trop Med Hyg. 1967, 16: 665-674.
  100. Cheers C, Ho M: Resistance and susceptibility of mice to bacterial infection. IV. Functional specificity in natural resistance to facultative intacellular bacteria. J Reticuloendothel Soc. 1983, 34: 299-309.PubMed
  101. Baldwin CL, Parent M: Fundamentals of host immune response against Brucella abortus: what the mouse model has revealed about control of infection. Vet Microbiol. 2002, 90: 367-382. 10.1016/S0378-1135(02)00222-5.PubMedView Article
  102. Sathiyaseelan J, Jiang X, Baldwin CL: Growth of Brucella abortus in macrophages from resistant and susceptible mouse strains. Clin Exp Immunol. 2000, 121: 289-294. 10.1046/j.1365-2249.2000.01295.x.PubMed CentralPubMedView Article
  103. Baldwin CL, Goenka R: Host cellular immune responses against Brucella spp evaluated using the mouse model. Brucella: Molecular and Cellular Biology. Edited by: López-Goñi I, Moriyón I. 2004, Horizon Scientific Press, United Kindom, 287-312.
  104. Vidal S, Tremblay ML, Govoni G, Gauthier S, Sebastiani G, Malo D, Skamene E, Olivier M, Jothy S, Gros P: The Ity/Lsh/Bcglocus: natural resistance to infection with intracellular parasites is abrogated by disruption of the Nramp1 gene. J Exp Med. 1995, 182: 655-666. 10.1084/jem.182.3.655.PubMedView Article
  105. Moreno E, Kurtz RS, Berman DT: Induction of immune and adjuvant immunoglobulin G responses in mice by Brucella lipopolysaccharide. Infect Immun. 1984, 46: 74-80.PubMed CentralPubMed
  106. Sulitzeanu D, Jones L, Stableforth AW: Protective action of monospecific anti-Brucella sera in mice. Nature. 1955, 175: 1040-1041. 10.1038/1751040a0.PubMedView Article
  107. Araya LN, Elzer PH, Rowe GE, Enright FM, Winter AJ: Temporal development of protective cell-mediated and humoral immunity in BALB/c mice infected with Brucella abortus. J Immunol. 1989, 143: 3330-3337.PubMed
  108. Limet JN, Bosseray N, Garin-Bastuji B, Dubray G, Plommet M: Humoral immunity in mice mediated by monoclonal antibodies against the A and M antigens of Brucella. J Med Microbiol. 1989, 30: 37-43. 10.1099/00222615-30-1-37.PubMedView Article
  109. Cloeckaert A, Jacques I, Bosseray N, Limet JN, Bowden R, Dubray G, Plommet M: Protection conferred on mice by monoclonal antibodies directed against outer-membrane-protein antigens of Brucella. J Med Microbiol. 1991, 34: 175-180. 10.1099/00222615-34-3-175.PubMedView Article
  110. Cloeckaert A, Jacques I, de Wergifosse P, Dubray G, Limet JN: Protection against Brucella melitensis or Brucella abortus in mice with immunoglobulin G (IgG), IgA, and IgM monoclonal antibodies specific for a common epitope shared by the Brucella A and M smooth lipopolysaccharides. Infect Immun. 1992, 60: 312-315.PubMed CentralPubMed
  111. Pavlov H, Hogarth M, McKenzie IF, Cheers C: In vivo and in vitro effects of monoclonal antibody to Ly antigens on immunity to infection. Cell Immunol. 1982, 71: 127-138. 10.1016/0008-8749(82)90502-0.PubMedView Article
  112. Zhan Y: Cheers C Endogenous gamma interferon mediates resistance to Brucella abortus infection. Infect Immun. 1993, 61: 4899-4901.PubMed CentralPubMed
  113. Stevens MG, Pugh GW: Tabatabai LB: Effects of gamma interferon and indomethacin in preventing Brucella abortus infections in mice. Infect Immun. 1992, 60: 4407-4409.PubMed CentralPubMed
  114. Sathiyaseelan J, Goenka R, Parent M, Benson RM, Murphy EA, Fernandes DM, Foulkes AS, Baldwin CL: Treatment of Brucella-susceptible mice with IL-12 increases primary and secondary immunity. Cell Immunol. 2006, 243: 1-9. 10.1016/j.cellimm.2006.10.003.PubMedView Article
  115. Stevens MG, G Pugh W: Effect of Brucella abortus transfer factor in preventing murine brucellosis. FEMS Immunol Med Microbiol. 1995, 11: 279-284. 10.1111/j.1574-695X.1995.tb00157.x.PubMedView Article
  116. Fernandes DM, Benson R, Baldwin CL: Lack of a role for natural killer cells in early control of Brucella abortus 2308 infections in mice. Infect Immun. 1995, 63: 4029-4033.PubMed CentralPubMed
  117. Madraso ED, Cheers C: Polyadenylic acid-polyuridylic acid (poly A:U) and experimental murine brucellosis I Effect of single and double-stranded polynucleotides on Brucella abortus in vivo and in vitro. Immunology. 1978, 35: 69-76.PubMed CentralPubMed
  118. Murphy EA, Parent M, Sathiyaseelan J, Jiang X, Baldwin CL: Immune control of Brucella abortus 2308 infections in BALB/c mice. FEMS Immunol Med Microbiol. 2001, 32: 85-88. 10.1111/j.1574-695X.2001.tb00536.x.PubMedView Article
  119. Mielke ME: T cell subsets in granulomatous inflammation and immunity to L monocytogenes and B abortus. Behring Inst Mitt. 1991, 88: 99-111.PubMed
  120. Pasquali P, Thornton AM, Vendetti S, Pistoia C, Petrucci P, Tarantino M, Pesciaroli M, Ruggeri F, Battistoni A, Shevach EM: CD4 + CD25+ T regulatory cells limit effector T cells and favor the progression of brucellosis in BALB/c mice. J Clin Microbiol. 2010, 48: 3806-3809. 10.1128/JCM.00721-10.PubMed CentralPubMedView Article
  121. Fernandes DM, Baldwin CL: Interleukin-10 downregulates protective immunity to Brucella abortus. Infect Immun. 1995, 63: 1130-1133.PubMed CentralPubMed
  122. Fernandes DM, Jiangn X, Jung JH, Baldwin CL: Comparison of T cell cytokines in resistant and susceptible mice infected with virulent Brucella abortus strain 2308 FEMS. Immunol Med Microbiol. 1996, 16: 193-203. 10.1111/j.1574-695X.1996.tb00136.x.View Article
  123. Zhan Y, Cheers C: Endogenous interleukin-12 is involved in resistance to Brucella abortus infection. Infect Immun. 1995, 63: 1387-1390.PubMed CentralPubMed
  124. Zhan Y, Liu Z, Cheers C: Tumor necrosis factor alpha and interleukin-12 contribute to resistance to the intracellular bacterium Brucella abortus by different mechanisms. Infect Immun. 1996, 64: 2782-2786.PubMed CentralPubMed
  125. Barquero-Calvo E, Conde-Alvarez R, Chacón-Díaz C, Quesada-Lobo L, Martirosyan A, Guzmán-Verri C, Iriarte M, Mancek-Keber M, Jerala R, Gorvel JP, Moriyón I, Moreno E, Chaves-Olarte E: The differential interaction of Brucella and Ochrobactrum with innate immunity reveals traits related to the evolution of stealthy pathogens. Plos One. 2009, 4: e5893-10.1371/journal.pone.0005893.PubMed CentralPubMedView Article
  126. Rolán HG, Xavier MN, Santos RL, Tsolis RM: Natural antibody contributes to host defense against an attenuated Brucella abortus virB mutant. Infect Immun. 2009, 77: 3004-3013. 10.1128/IAI.01114-08.PubMed CentralPubMedView Article
  127. Bosseray N: Kinetics of placental colonization of mice inoculated intravenously with Brucella abortus at day 15 of pregnancy. Br J Exp Pathol. 1983, 64: 612-616.PubMed CentralPubMed
  128. Izadjoo MJ, Mense MG, Bhattacharjee AK, Hadfield TL, Crawford RM, Hoover DL: A study on the use of male animal models for developing a live vaccine for brucellosis. Transbound Emerg Dis. 2008, 55: 145-151. 10.1111/j.1865-1682.2008.01019.x.PubMedView Article
  129. Bosilkovski M, Krteva L, Dimzova M, Kondova I: Brucellosis in 418 patients from the Balkan Peninsula: exposure-related differences in clinical manifestations, laboratory test results, and therapy outcome. Int J Infect Dis. 2007, 11: 342-347. 10.1016/j.ijid.2006.10.002.PubMedView Article
  130. Carvalho-Neta AV, Mol P, Xavier MN, Paixão A, Lage AP, Santos RL: Pathogenesis of bovine brucellosis. Vet J. 2010, 184: 146-155. 10.1016/j.tvjl.2009.04.010.PubMedView Article
  131. Philippon A, Renoux G, Plommet M: Brucellose bovine experimentale 3 Excretion vaginale de Brucella abortus. Ann Rech Vet. 1970, 1: 215-224.PubMed
  132. Bosseray N: Mother to young transmission of Brucella abortus infection in mouse model. Ann Rech Vet. 1982, 13: 341-349.PubMed
  133. Bosseray N, Plommet M: Serum- and cell-mediated immune protection of mouse placenta and fetus against a Brucella abortus challenge: expression of barrier effect of placenta. Placenta. 1988, 9: 65-79. 10.1016/0143-4004(88)90074-4.PubMedView Article
  134. Baek BK, Lee BO, Hur J, Rahman MS, Lee SI, Kakoma I: Evaluation of the Sprague–Dawley rat as a model for vertical transmission of Brucella abortus. Can J Vet Res. 2005, 69: 305-308.PubMed CentralPubMed
  135. Kim S, Lee DS, Watanabe K, Furuoka H, Suzuki H, Watarai M: Interferon-gamma promotes abortion due to Brucella infection in pregnant mice. BMC Microbiol. 2005, 5: 22-10.1186/1471-2180-5-22.PubMed CentralPubMedView Article
  136. Fensterbank R: Some aspects of experimental bovine brucellosis. Ann Rech Vet. 1987, 18: 421-428.PubMed
  137. Watanabe K, Iwai N, Tachibana M, Furuoka H, Suzuki H, Watarai M: Regulated upon activation normal T-cell expressed and secreted (RANTES) contributes to abortion caused by Brucella abortus infection in pregnant mice. J Vet Med Sci. 2008, 70: 681-686. 10.1292/jvms.70.681.PubMedView Article
  138. Fernández-Lago L, Monte M, Chordi A: Endogenous gamma interferon and interleukin-10 in Brucella abortus 2308 infection in mice. FEMS Immunol Med Microbiol. 1996, 15: 109-114.PubMedView Article
  139. Chen M, Chen J, Liao W, Zhu S, Yu J, Leung WK, Hu P, Sung JJ: Immunization with attenuated Salmonella typhimurium producing catalase in protection against gastric. Helicobacter. 2003, 8: 613-625. 10.1111/j.1523-5378.2003.00182.x.PubMedView Article
  140. Pouliot K, Pan N, Wang S, Lu S, Lien E, Goguen JD: Evaluation of the role of LcrV-Toll-like receptor 2-mediated immunomodulation in the virulence of Yersinia pestis. Infect Immun. 2007, 75: 3571-3580. 10.1128/IAI.01644-06.PubMed CentralPubMedView Article
  141. Cha SB, Rayamajhi N, Kang ML, Lee WJ, Shin MK, Yoo HS: Comparative study of gamma interferon production in mice immunized with outer membrane proteins and whole bacteria of Brucella abortus. Jpn J Infect Dis. 2010, 63: 49-51.PubMed
  142. Koebernick H, Grode L, David JR, Rohde W, Rolph MS, Mittrücker HW, Kaufmann SH: Macrophage migration inhibitory factor (MIF) plays a pivotal role in immunity against Salmonella typhimurium. Proc Natl Acad Sci U SA. 2002, 99: 13681-13686. 10.1073/pnas.212488699.View Article
  143. Elzer PH, Jacobson RH, Nielsen KH, Douglas JT, Winter AJ: BALB/c mice infected with Brucella abortus express protrected polyclonal responses of both IgG2a and IgG3 isotypes. Immunol Lett. 1994, 42: 145-150. 10.1016/0165-2478(94)90078-7.PubMedView Article
  144. Fernández-Lago L, Orduña A, Vizcaíno N: Reduced interleukin-18 secretion in Brucella abortus 2308-infected murine peritoneal macrophages and in spleen cells obtained from B abortus 2308- infected mice. J Med Microbiol. 2005, 54: 527-531. 10.1099/jmm.0.45936-0.PubMedView Article
  145. Tobias L, Cordes DO, Schurig GG: Placental pathology of the pregnant mouse inoculated with Brucella abortus strain 2308. Vet Pathol. 1993, 30: 119-129. 10.1177/030098589303000204.PubMedView Article
  146. Yoneyama H, Ichida T: Recruitment of dendritic cells to pathological niches in inflamed liver. Med Mol Morphol. 2005, 38: 136-141. 10.1007/s00795-005-0289-0.PubMedView Article
  147. Palmer V, Cheville F, Tatum M: Morphometric and histopathologic analysis of lymphoid depletion in murine spleens following infection with Brucella abortus strains 2308 or RB51 or an htrA deletion mutant. Vet Pathol. 1996, 33: 282-289. 10.1177/030098589603300304.PubMedView Article
  148. Fernández-Lago L, Rodríguez-Tarazona E, Vizcaíno N: Differential secretion of interleukin-12 (IL-12) subunits and heterodimeric IL-12p70 protein by CD-1 mice and murine macrophages in response to intracellular infection by Brucella abortus. J Med Microbiol. 1999, 48: 1065-1073. 10.1099/00222615-48-12-1065.PubMedView Article
  149. Saunders BM, Liu Z, Zhan Y, Cheers C: Interleukin-6 production during chronic experimental infection Immunol. Cell Biol. 1993, 71: 275-280.
  150. Pasquali P, Adone R, Gasbarre LC, Pistoia C, Ciuchini F: Mouse cytokine profiles associated with Brucella abortus RB51 vaccination or B. abortus 2308 infection. Infect Immun. 2001, 69: 6541-6544. 10.1128/IAI.69.10.6541-6544.2001.PubMed CentralPubMedView Article
  151. Zhan Y, Kelso A, Cheers C: Differential activation of Brucella-reactive CD4+ T cells by Brucella infection or immunization with antigenic extracts. Infect Immun. 1995, 63: 969-975.PubMed CentralPubMed
  152. Stevens MG, Olsen SC, Pugh GW: Lymphocyte proliferation in response to Brucella abortus 2308 or RB51 antigens in mice infected with strain 2308, RB51, or 19. Infect Immun. 1994, 62: 4659-4663.PubMed CentralPubMed
  153. Mackaness GB: The immunological basis of acquired cellular resistance. J Exp Med. 1964, 120: 105-120. 10.1084/jem.120.1.105.PubMed CentralPubMedView Article
  154. Tachibana M, Watanabe K, Yamasaki Y, Suzuki H, Watarai M: Expression of heme oxygenase-1 is associated with abortion caused by Brucella abortus infection in pregnant mice. Microb Pathog. 2008, 45: 105-109. 10.1016/j.micpath.2008.04.002.PubMedView Article
  155. Oñate A, Andrews E, Beltran A, Eller G, Schurig G, Folch H: Frequent exposure of mice to crude Brucella abortus proteins down-regulates immune response. J Vet Med B Infect Dis Vet Public Health. 2000, 47: 677-682. 10.1046/j.1439-0450.2000.00402.x.PubMedView Article
  156. Finkelman FD, Katona IM, Mosmann TR, Coffman RL: IFN-gamma regulates the isotypes of Ig secreted during in vivo humoral immune responses. J Immunol. 1988, 140: 1022-1027.PubMed
  157. Kurtz S, Berman DT: Influence of endotoxin-protein in immunoglobulin G isotype responses of mice to Brucella abortus lipopolysaccharide. Infect Immun. 1986, 54: 728-734.PubMed CentralPubMed
  158. Felek S, Demirdag K, Kalkan A, Akbulut A: Therapeutic effects of rifampin and erythromycin in experimental murine brucellosis. Clin Microbiol Infect. 2000, 6: 111-114. 10.1046/j.1469-0691.2000.00016-4.x.PubMedView Article
  159. Domingo S, Díaz R, Gamazo C: Antibiotic treatment induces an increase of the specific antibody levels in Brucella melitensis infected mice. FEMS Immunol Med Microbiol. 1995, 12: 91-95. 10.1111/j.1574-695X.1995.tb00180.x.PubMedView Article
  160. Magnani DM, Harms JS, Durward MA, Splitter GA: Nondividing but metabolically active gamma-irradiated Brucella melitensis is protective against virulent B melitensis challenge in mice. Infect Immun. 2009, 77: 5181-5189. 10.1128/IAI.00231-09.PubMed CentralPubMedView Article
  161. Bhattacharjee AK, Izadjoo MJ, Zollinger WD, Nikolich MP, Hoover DL: Comparison of protective efficacy of subcutaneous versus intranasal immunization of mice with a Brucella melitensis lipopolysaccharide subunit vaccine. Infect Immun. 2006, 74: 5820-5825. 10.1128/IAI.00331-06.PubMed CentralPubMedView Article
  162. Da Costa Martins R, Irache JM, Blasco JM, Muñoz MP, Marín CM, Jesús Grilló M, Jesús De Miguel M, Barberán M, Gamazo C: Evaluation of particulate acellular vaccines against Brucella ovis infection in rams. Vaccine. 2010, 28: 3038-3046. 10.1016/j.vaccine.2009.10.073.PubMedView Article
  163. Delpino MV, Estein SM, Fossati CA, Baldi PC: Partial protection against Brucella infection in mice by immunization with nonpathogenic alphaproteobacteria. Clin Vaccine Immunol. 2007, 14: 1296-1301. 10.1128/CVI.00459-06.PubMed CentralPubMedView Article
  164. Kaushik P, Singh DK, Kumar SV, Tiwari AK, Shukla G, Dayal S, Chaudhuri P: Protection of mice against Brucella abortus 544 challenge by vaccination with recombinant OMP28 adjuvanted with CpG oligonucleotides. Vet Res Commun. 2010, 34: 119-132. 10.1007/s11259-009-9337-x.PubMedView Article
  165. Pugh GW: Tabatabai LB, Bricker BJ, Mayfield JE, Phillips M, Zehr ES, Belzer CA: Immunogenicity of Brucella-extracted and recombinant protein vaccines in CD-1 and BALB/c mice. Am J Vet Res. 1990, 51: 1413-1420.PubMed
  166. Araya LN, Winter AJ: Comparative protection of mice against virulent and attenuated strains of Brucella abortus by passive transfer of immune T cells or serum. Infect Immun. 1990, 58: 254-256.PubMed CentralPubMed
  167. Bosseray N: Control methods and thresholds of acceptability for anti-Brucella vaccines. Dev Biol Stand. 1992, 79: 121-128.PubMed
  168. Bosseray N, Plommet AM, Plommet M: Theoretical, practical and statistical basis for a general control method of activity for anti-Brucella vaccines. Dev Biol Stand. 1984, 56: 257-270.PubMed
  169. The Mouse Phenome Database http://​phenome.​jax.​org/​
  170. REV-2: Calculation of the RT 50 for vaccines http://​www.​afssa.​fr/​interne/​rev2.​html
  171. Arenas-Gamboa AM, Ficht TA, Kahl-McDonagh MM, Gomez G, Rice-Ficht AC: The Brucella abortus S19ΔvjbR live vaccine candidate is safer than S19 and confers protection against wild-type challenge in BALB/c mice when delivered in a sustained-release vehicle. Infect Immun. 2009, 77: 877-884. 10.1128/IAI.01017-08.PubMed CentralPubMedView Article
  172. Cloeckaert A, Jacques I, Grilló MJ, Marín CM, Grayon M, Blasco JM, Verger JM: Development and evaluation as vaccines in mice of Brucella melitensis Rev1 single and double deletion mutants of the bp26 and omp31 genes coding for antigens of diagnostic significance in ovine brucellosis. Vaccine. 2004, 22: 2827-2835. 10.1016/j.vaccine.2004.01.001.PubMedView Article
  173. Bosseray N, Plommet M: Transformation normalisant la distribution du nombre de Brucella dans la rate de souris inoculées par voie intrapéritonéale. J Biol Stand. 1976, 4: 341-351. 10.1016/S0092-1157(76)80019-4. in FrenchPubMedView Article
  174. Vargas-O FJ: Brucellosis in Venezuela. Vet Microbiol. 2002, 90: 39-44. 10.1016/S0378-1135(02)00243-2.PubMedView Article
  175. Herrera-López E, Suárez-Güemes F, Hernández-Andrade L, Córdova-López D, Díaz-Aparicio E: Epidemiological study of Brucellosis in cattle, immunized with Brucella abortus RB51 vaccine in endemic zones. Vaccine. 2010, 5 (Suppl): F59-F63.View Article
  176. Bertrand A: Expressions cliniques et biologiques de la Brucellose humaine. Place actuelle de l'immunotherapie. Bull Soc SciVét Méd Comp. 1981, 83: 53-57. in French
  177. Cheers C, Pagram F: Macrophage activation during experimental murine brucellosis: a basis for chronic infection. Infect Immun. 1979, 23: 197-205.PubMed CentralPubMed
  178. Halliburton BL, Hinsdill RD: Recall of acquired cellular resistance in mice by antigens from killed Brucella. Infect Immun. 1972, 5: 42-47.PubMed CentralPubMed
  179. Stoenner HG: The behavior of Brucella neotomae and Brucella suis in reciprocal superinfection experiments in mice and guinea pigs. Am J Vet Res. 1963, 24: 376-380.PubMed
  180. Atkins HS, Spencer S, Brew SD, Jenner DC, Russell P, MacMillan AP, Eley SM, Simpson AJ: Efficacy of ciprofloxacin versus doxycycline as prophylaxis against experimental murine Brucella melitensis infection. Int J Antimicrob Agents. 2009, 34: 474-476. 10.1016/j.ijantimicag.2009.04.006.PubMedView Article
  181. Atkins HS, Spencer S, Brew SD, Laws TR, Thirlwall RE, MacMillan AP, Brooks TJ, Simpson AJ: Efficacy of moxifloxacin or gatifloxacin as prophylaxis against experimental murine Brucella melitensis infection. Int J Antimicrob Agents. 2009, 34: 471-473. 10.1016/j.ijantimicag.2009.06.018.PubMedView Article
  182. Ariza J, Bosilkovski M, Cascio A, Colmenero JD, Corbel MJ, Falagas ME, Memish ZA, Roushan MR, Rubinstein E, Sipsas NV, Solera J, Young EJ, Pappas G: International Society of Chemotherapy; Institute of Continuing Medical Education of Ioannina: Perspectives for the treatment of brucellosis in the 21st century: the Ioannina recommendations. PLoS Med. 2007, 4: e317-10.1371/journal.pmed.0040317.PubMed CentralPubMedView Article
  183. Solberg CO, Halstensen A, Digranes A, Hellum KB: Penetration of antibiotics into human leukocytes and dermal suction blisters. Rev Infect Dis. 1983, 3: S468-S473.View Article
  184. Blasco JM, Díaz R: Brucella melitensis Rev1 vaccine as a cause of human brucellosis. Lancet. 1993, 342: 805-PubMedView Article
  185. Grilló MJ, De Miguel MJ, Muñoz PM, Marín CM, Ariza J, Blasco JM: Efficacy of several antibiotic combinations against Brucella melitensis Rev1 experimental infection in BALB/c mice. J Antimicrob Chemother. 2006, 58: 622-626. 10.1093/jac/dkl289.PubMedView Article
  186. Arda B, Tunçel M, Yaimazhan T, Gökengin D, Gürel O: Efficacy of oral levofloxacin and dirithromycin alone and in combination with rifampicin in the treatment of experimental murine Brucella abortus. Int J Antimicrob Agents. 2004, 23: 204-207. 10.1016/j.ijantimicag.2003.07.005.PubMedView Article
  187. Doming S, Gamazo C: Inadequate azithromycin activity against Brucella melitensis in mice with acute or chronic infections. J Chemother. 1996, 8: 55-58.View Article
  188. Prior S, Gander B, Irache JM, Gamazo C: Gentamicin-loaded microspheres for treatment of experimental Brucella abortus infection in mice. J Antimicrob Chemother. 2005, 55: 1032-1036. 10.1093/jac/dki144.PubMedView Article
  189. Lecaroz MC, Blanco-Prieto MJ, Campanero MA, Salman H, Gamazo C: Poly(D, L-lactide-coglycolide) particles containing gentamicin:pharmacokinetics and pharmacodynamics in Brucella melitensis-infected mice. Antimicrob Agents Chemother. 2007, 51: 1185-1190. 10.1128/AAC.00809-06.PubMed CentralPubMedView Article
  190. Seleem MN, Jain N, Pothayee N, Ranjan A, Riffle JS, Sriranganathan N: Targeting Brucella melitensis with polymeric nanoparticles containing streptomycin and doxycycline. FEMS Microbiol Lett. 2009, 294: 24-31. 10.1111/j.1574-6968.2009.01530.x.PubMedView Article
  191. Bowden RA, Racaro GC, Baldi PC: Effect of early antibiotic treatment on the antibody response to cytoplasmic proteins of Brucella melitensis in mice. Clin Diag Lab Immunol. 1999, 16: 440-443.
  192. Baldi PC, Miguel SE, Fossati CA, Wallach JC: Serological follow-up of human brucellosis by measuring IgG antibodies directed to S-LPS and cytoplasmic proteins of Brucella. Clin Infect Dis. 1996, 22: 446-455. 10.1093/clinids/22.3.446.PubMedView Article
  193. Bardenstein S, Banai M: Brucella species synchronize their life cycle to the gestation cycle of their ruminant hosts. The Challenge of Highly Pathogenic Microorganisms. Edited by: Baruch Velan B, Shafferman A, Ordentlich A. 2010, Springer Verlag, New York, 135-146.View Article
  194. Watson ED, Cross JC: Development of structures and transport functions in the mouse placenta. Physiology (Bethesda). 2005, 20: 180-193. 10.1152/physiol.00001.2005.View Article
  195. Huang SS, Fraenkel E: Integrating proteomic, transcriptional, and interactome data reveals hidden components of signaling and regulatory networks. Sci Signal. 2009, 2: ra40-10.1126/scisignal.2000350.PubMed CentralPubMed
  196. Tizard IR: Veterinary Immunology. 2008, Saunders Elsevier, Philadelphia, 8
  197. Jubier-Maurin V, Loisel S, Liautard JP, Köhler S: The intramacrophagic environment of Brucella spp and their replicative niche. Brucella: Molecular and Cellular Biology. Edited by: López-Goñi I, Moriyón I. 2004, Horizon Scientific Press, United Kindom, 313-340.
  198. Moriyón I, Grilló MJ, Monreal D, González D, Marín C, López-Goñi I, Mainar-Jaime RC, Moreno E, Blasco JM: Rough vaccines in animal brucellosis: structural and genetic basis and present status. Vet Res. 2004, 35: 1-38. 10.1051/vetres:2003037.PubMedView Article
  199. Verger JM, Grayon M, Zundel E, Lechopier P, Olivier-Bernardin V: Comparison of the efficacy of Brucella suis strain 2 and Brucella melitensis Rev. 1 live vaccines against a Brucella melitensis experimental infection in pregnant ewes. Vaccine. 1995, 13: 191-196. 10.1016/0264-410X(95)93135-V.PubMedView Article
  200. Murphy WJ, Pringle TH, Crider TA, Springer MS, Miller W: Using genomic data to unravel the root of the placental mammal phylogeny. Genome Res. 2007, 17: 413-421. 10.1101/gr.5918807.PubMed CentralPubMedView Article
  201. Moreno E: Brucella evolution. Prevention of Brucellosis in Mediterranean Countries. Edited by: Plommet M. 1992, International Center for Advanced Mediterranean Agronomic Studies, Pudoc Scientific Publishers, Wageningen, 198-218.
  202. Meyer ME: Evolution and taxonomy of the genus Brucella: brucellosis of rodents. Theriogenology. 1976, 6: 263-273. 10.1016/0093-691X(76)90019-4.View Article
  203. Scholz HC, Hubalek Z, Sedlácek I, Vergnaud G, Tomaso H, Al Dahouk S, Melzer F, Kämpfer P, Neubauer H, Cloeckaert A, Maquart M, Zygmunt MS, Whatmore AM, Falsen E, Bahn P, Göllner C, Pfeffer M, Huber B, Busse HJ, Nöckler K: Brucella microti sp nov, isolated from the common vole Microtus arvalis. Int J Syst Evol Microbiol. 2008, 58: 375-382. 10.1099/ijs.0.65356-0.PubMedView Article
  204. Boursot P, Auffray JC, Britton-Davidian J, Bonhomme F: The evolution of house mice. Ann Rev Ecol Syst. 1993, 24: 119-152. 10.1146/annurev.es.24.110193.001003.View Article

Copyright

© Grillo et al.; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License(http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.