- Research Article
- Open Access
Salmonella enterica serovar Choleraesuis vector delivering SaoA antigen confers protection against Streptococcus suis serotypes 2 and 7 in mice and pigs
© The Author(s) 2017
- Received: 26 May 2017
- Accepted: 28 November 2017
- Published: 21 December 2017
Streptococcus suis is one of the major pathogens that cause economic losses in the swine industry worldwide. However, current bacterins only provide limited prophylactic protection in the field. An ideal vaccine against S. suis should protect pigs against the clinical diseases caused by multiple serotypes, or at least protect against the dominant serotype in a given geographic region. A new recombinant Salmonella enterica serotype Choleraesuis vaccine vector, rSC0011, that is based on the regulated delayed attenuation system and regulated delayed antigen synthesis system, was developed recently. In this study, an improved recombinant attenuated Salmonella Choleraesuis vector, rSC0016, was developed by incorporating a sopB mutation to ensure adequate safety and maximal immunogenicity. In the spleens of mice, rSC0016 colonized less than rSC0011. rSC0016 and rSC0011 colonized similarly in Peyer’s patches of mice. The recombinant vaccine rSC0016(pS-SaoA) induced stronger cellular, humoral, and mucosal immune responses in mice and swine against SaoA, a conserved surface protein that is present in many S. suis serotypes, than did rSC0011(pS-SaoA) without sopB or rSC0018(pS-SaoA), which is an avirulent, chemically attenuated vaccine strain. rSC0016(pS-SaoA) provided 100% protection against S. suis serotype 2 in mice and pigs, and full cross-protection against SS7 in pigs. This new vaccine vector provides a foundation for the development of a universal vaccine against multiple serotypes of S. suis in pigs.
Streptococcus suis (S. suis) strains are classified into 35 serotypes based on the capsular polysaccharide antigens. Globally, the predominant S. suis serotype isolated from clinical cases of the disease in pigs is serotype 2, followed by serotypes 9, 3, 1/2, and 7, together with 15.5% nontypable strains . To date, only vaccination with S. suis bacterins is performed to prevent S. suis infection in swine. Although several studies have demonstrated homologous protection , the procedure usually has a high rate of failure because the antigenicity of the vaccine is damaged by heat and formalin processing, which leads to the production of antibodies that are not associated with protection and/or are cross-reactive [3, 4]. Current vaccine research for S. suis focuses on subunit vaccine based on conserved proteins among different serotypes to protect pigs against clinical diseases caused by various S. suis serotypes, or protect against the dominant serotype in a given geographic region. However, the cost of many vaccines made from conserved proteins in veterinary medicine and swine medicine is relatively high compared to traditional bacterins.
To date, at least 24 subunit vaccine candidates have been identified [5–22]. Most of them were tested in mouse models [5, 8, 11, 12, 15, 17–22], and only a few were evaluated in pigs [5, 7, 9, 10, 12, 14, 16, 19, 23, 24]. The results showed that the protection conferred in swine is usually lower than that conferred in mice [10, 23]. Therefore, it is necessary to evaluate the candidate antigen in the target animal, pig. Moreover, the capacities to induce cross-protection were evaluated for a few antigens. Of these antigens, the surface-anchored protein (Sao) is a membrane-anchored bacterial protein reacting with 28 of 33 S. suis serotypes and 25 of 26 serotype 2 isolates, suggesting that it is a highly conserved protein in S. suis . The effectiveness of Sao as a vaccine candidate depends upon the adjuvant used. Sao formulated with Emulsigen-Plus® provided no protection against S. suis serotype 2 (SS2) because the induced antibodies lacked opsonizing activity against SS2 , whereas Sao formulated with the Quil-A adjuvant partially protected pigs against aerosol challenge with SS2 because it induced opsonizing antibodies . So far, Sao is the only protein that has been shown to induce cross-protection against serotype 1 and 7 strains in mice and pigs . These results indicate that the efficacy of the protection induced by Sao as a subunit vaccine candidate may depend on the choice of appropriate vector or adjuvant.
Streptococcus suis is an encapsulated microorganism. Host protection against infection by S. suis is primarily mediated by opsonophagocytosis, which is mainly associated with a Th1-type immune response . Salmonella has excellent adjuvant attributes and induces high mucosal, cellular and humoral responses . However, live attenuated Salmonella, traditionally generated by deletion of its virulence genes, can lack a balance between the loss of its disease-causing ability and the ability to persist and induce immune responses , and is therefore not an ideal vaccine vector. In addition, constitutive high-level antigen synthesis causes a metabolic burden to the vaccine vector strain that can reduce the vaccine strain’s ability to interact with host lymphoid tissues, resulting in a compromised immune response . To solve these problems, the regulated delayed attenuation system was developed to make a strain displaying features of wild-type virulent strains of Salmonella at the time of immunization to enable strains to effectively colonize lymphoid tissues and then exhibit a regulated delayed attenuation in vivo to preclude inducing disease symptoms . The regulated delayed antigen synthesis system could regulate antigen gene expression and permit high levels of antigen synthesis only after the vaccine strain reaches its target tissues . The regulated delayed attenuation strategy includes a smooth-to-rough phenotypic change in lipopolysaccharides (LPS) with the presence or absence of mannose , and the replacement of the promoters of some virulence genes (fur, crp, and phoPQ) with a tightly regulated araC PBAD cassette so that the expression of these genes is dependent on arabinose supplement during in vitro growth . Following the colonization of the lymphoid tissues, these virulence-associated proteins cease to be synthesized because no mannose or arabinose is present in vivo . Therefore, attenuation manifests gradually in vivo, precluding the induction of disease symptoms and inducing the desired antigen-specific immune responses . Furthermore, an araC PBAD cassette was used to regulate the expression of chromosomal lacI repressor gene, which binds to Ptrc on an expression plasmid and blocks antigen synthesis in the presence of arabinose in vitro. Once Salmonella reaches arabinose-free, host immunocompetent sites, the concentration of LacI decreases with each cell division, allowing upregulation of antigen synthesis and induction of desired antigen-specific immune responses .
In a previous study, a recombinant attenuated Salmonella enterica serotype Choleraesuis (Salmonella Choleraesuis) vaccine strain rSC0011 with the regulated delayed strategy in the wild-type Salmonella Choleraesuis C78-3 background was constructed . Strain rSC0011, carrying 6-phosphogluconate dehydrogenase (6-PGD) gene of SS2, conferred 100% protection against an SS2 challenge in mice , but less than 50% protection in pigs (unpublished data). To increase the efficacy of our vaccine strain, a sopB mutation was introduced into rSC0011 vector to generate a new recombinant attenuated Salmonella Choleraesuis strain rSC0016 based on the previous report that the sopB mutation could improve the immunogenicity of Salmonella vaccine vector in mice . The heterologous antigen gene, saoA from S. suis, was cloned into the Asd+ expression plasmid pYA3493, generating plasmid pS-SaoA, which was used to transform the vector strain rSC0016, generating the candidate vaccine rSC0016 (pS-SaoA). The virulence and immune attributes of rSC0016 (pS-SaoA) in mice and piglets, and its cross-protection against SS2 and SS7 in piglets were evaluated. Our results showed that the improved recombinant attenuated Salmonella Choleraesuis, which combines the regulated delayed strategy and the sopB deletion, is more immunogenic than the parent strain rSC0011. It induces cross-protection against multiple serotypes of S. suis when delivering the heterologous protective antigen Sao. This could be a candidate for a universal vaccine against S. suis.
All animal experiments were approved by the Jiangsu Administrative Committee for Laboratory Animals (permission number SYXK-SU-2007-0005) and complied with the Jiangsu Laboratory Animal Welfare and Ethics guidelines of the Jiangsu Administrative Committee of Laboratory Animals.
Strains, plasmids and culture conditions
Strains and plasmids
Strain or plasmid
Relevant characteristics or genotype
Source or references
E. coli strains
F− pT hsdSB(rB− mB− al dcm (DE3)
thi-1 thr-1 leuB6 fhuA21 lacY1 glnV44 asdA4 recA1 RP4 2-Tc::Mu pir; Km r
Dr Curtiss gift
Wild type, virulent, CVCC79103
Salmonella Choleraesuis vaccine strain attenuated by chemical mutation, CVCC79500
ΔPcrp527::TT araC PBAD crp Δpmi-2426 ΔrelA199::araC PBAD lacI TT
ΔPcrp527::TT araC PBAD crp Δpmi-2426 ΔrelA199::araC PBAD lacI TT ΔasdA33
Streptococcus suis serotype 2
Wild-type, virulent, CVCC3928
Streptococcus suis serotype 7
Wild-type isolated in field
Plasmid Asd + ; pBR ori, β-lactamase signal sequence-based periplasmic secretion plasmid
expression vector, T7 promoter; Kmr
oriT oriV sacB CmR
suicide vector for ΔsopB1686
suicide vector for ΔasdA33
expression vector for purification of Hig-tag SaoA, T7 promoter, Km+
pYA3493 with SaoA
Construction and characterization of Salmonella Choleraesuis mutant strains
To detect the effect of sopB deletion, the fluid secretion in rabbit ileal loops after inoculation with wild-type strain C78-3, rSC0017 (Salmonella Choleraesuis C78-3 with sopB mutation), vaccine strains rSC0018(pS-SaoA), rSC0011(pS-SaoA), and rSC0016(pS-SaoA) were compared as previously described . Briefly, 38-week-old New Zealand White rabbits were fasted overnight and anesthetized with isoflurane by an endotracheal tube. The ileum was exposed and ligated into several loops of 5–6 cm long with 1 cm spacers. 1 mL of indicated strains, containing around 1 × 109 colony-forming units (CFU), were injected into separate loops. LB medium was injected into one of the loops as a control. The abdominal musculature was closed using 3–0 chromic gut sutures and the skin closed with 3–0 ethilon sutures. Rabbits were maintained in a thermal blanket at 37 °C. After 8 h, the rabbits were euthanized with an overdose of sodium pentobarbital. The abdomen was reopened and the fluid within the ligated loops was collected and measured. The loops were fixed in 10% formalin and subjected to histopathological examination.
All mutations were verified by PCR using corresponding primers. The ΔPcrp527::TT araC PBAD crp deletion-insertion mutation was confirmed by growing on MacConkey maltose agar with or without 0.2% arabinose . LPS profiles were examined by silver staining in 12% sodium dodecyl sulfate–polyacrylamide gel for Δpmi mutation . LacI production for ΔrelA::araC PBAD lacI TT mutation was confirmed by Western blot . The ΔasdA mutation was confirmed by growth with or without DAP in LB media .
Construction and analysis of the plasmid stability of the attenuated Salmonella Choleraesuis vector with plasmids pYA3493 and pS-SaoA
Primers for S. suis saoA gene were designed according to GenBank accession no. GI:8151617 (saoA-F:ATGGATCCCAACCTGATGGGGGAC; saoA-R: GCGTCGACCATTGCTTCCTTAGAG) to amplify N-terminal (121–1593 bp) of saoA gene . The DNA of saoA either from SS2 or SS7 was amplified by PCR, purified by AxyPrep TM PCR Cleanup kit (Axygen, Union, CA, USA), and cloned into the expression vector pET28a to generate plasmid pET28a-SaoA according to the manufacturer’s instructions (Novagen, Darmstadt, Germany). The identity of the insert in pET28a was verified by DNA sequence analysis. Following digestion of plasmids pET28a-SaoA and pYA3493 with BamHI and SalI, the saoA from SS2 was cloned into pYA3493 to generate pS-SaoA. pS-SaoA and empty vector pYA3493 were transformed into the live attenuated Salmonella Choleraesuis (Figure 1B).
To evaluate the production of SaoA in live attenuated Salmonella Choleraesuis, sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) was performed as described . Strains harboring plasmid pS-SaoA or control vector pYA3493 were grown in LB medium with indicating supplements (0.2% arabinose and mannose) at 37 °C with aeration. When the culture reached an OD600 of 0.8, Isopropyl-d-thiogalactopyranoside (IPTG) was added to the culture, and the culture continued to grow for 3 h. The bacteria numbers were normalized by OD600. 1 mL of culture was collected for Western blot analysis using anti-SaoA antiserum as previously described . Briefly, total protein samples were separated on a 10% (wt/vol) SDS-PAGE gel and transferred onto nitrocellulose membranes. Phosphate buffered saline (PBS) with 5% fat-free milk powder and 0.05% Tween 20 (PBS-T) was used for blocking. The membrane was incubated with an appropriate anti-rabbit polyclonal antibody (1:10 000, anti-SaoA) or anti-GroEL (Sigma, St. Louis, MO, USA) for 1 h at room temperature, washed three times with PBS-T, and then horseradish peroxidase-conjugated goat anti-rabbit immunoglobulin G was used as the secondary antibody (Sigma). The membrane was developed with a chemiluminescent substrate using the kit ECL Plus Western Blotting System (GE Healthcare, Chalfont St Giles, UK) according to manufacturer’s instructions. Densitometry was quantified using Image J software (Image J2) .
To examine the stability of plasmids pS-SaoA and pYA3493 in Salmonella Choleraesuis vector, the strains containing pS-SaoA or pYA3493 were cultured with the daily passage of 1:1000 dilutions for 5 consecutive days (about 50 generations) in LB medium with DAP, arabinose, and mannose. At the 50th generation, Asd+ plasmids pS-SaoA and pYA3493 were tested by endonuclease digestion. The mutations of the live attenuated Salmonella Choleraesuis vector were confirmed by PCR. SaoA production was evaluated by Western blot.
Preparation the SaoA protein of SS2 or SS7, antiserum to the SaoA protein of SS2, and Salmonella outer membrane proteins (SOMPs) of Salmonella Choleraesuis
Escherichia coli strain BL21 carrying pET28a-SaoA was used for the synthesis of the His-tagged SaoA fusion protein (Table 1). Cells were grown to mid-log phase (OD600 of 0.6) in LB medium with kanamycin at 37 °C and induced with 1 mM IPTG for 3 h. The His-tagged SaoA protein was purified by using a CelLytic B Plus kit (Sigma) and a His-Select nickel affinity gel (Sigma) according to manufacturer’s instructions. To create rabbit antibodies to SaoA, two female New Zealand White rabbits (8 weeks old) were injected subcutaneously with an emulsion consisting of a 1:1 ratio of 400 μg of the His-tagged SaoA protein to complete Freund adjuvant (Sigma). Two weeks after the primary injection, the immunization was repeated but with incomplete Freund adjuvant (Sigma) instead of complete adjuvant. Three weeks after the second immunization, the rabbits were boosted with 200 μg of the His-tagged SaoA protein without adjuvant. Two weeks after the third immunization, the rabbits were bled to obtain anti-SaoA rabbit antiserum .
Salmonella outer membrane proteins (SOMPs) were prepared from wild-type Salmonella Choleraesuis C78-3. Briefly, total envelope pellets were suspended in 4 mL of 20 mM Tris–HCl (pH 8.6) containing 1% Sarkosyl and incubated for 30 min on ice. The outer membrane fraction was obtained as a pellet after centrifugation at 132 000 × g at 4 °C for 1 h. The pellet was re-suspended in 4 mL of 20 mM Tris–HCl buffer (pH 8.6) and stored at −20 °C.
Distribution of Salmonella bacteria in BALB/c mice
Colonization assay for mutant strain was carried out as described . 140 7-week-old female BALB/c mice were divided into seven groups with 20 mice per group. Groups of mice were orally inoculated with 20 μL buffered saline with gelatin (BSG) containing 1 × 109 CFU of Salmonella strains. Liver, spleen, and Peyer’s patches of mice were collected on days 3, 7, 14, and 21 post-infection. Tissues were weighed and homogenized in a final volume of 1 mL BSG . Serial dilutions were plated onto MacConkey agar plates containing 1% lactose, with or without 0.2% arabinose and 0.2% mannose, to determine the number of viable bacteria. Plates were incubated at 37 °C for at least 18 h. The residual 900 mL of homogenized tissues were inoculated into 5 mL Tetrathionate Broth (Difco) for Salmonella enrichment when no colonies were observed on the plates. Samples that were negative by direct plating and positive by enrichment were recorded as 10 CFU/g. Samples that were negative by both direct plating and enrichment were recorded as 0 CFU/g . The assay was performed twice, and the data were pooled.
Immunization of mice and piglets
Immunization of mice
Salmonella Choleraesuis vector strains harboring plasmids pS-SaoA or pYA3493 (empty vector) were grown in LB broth with 0.2% arabinose and 0.2% mannose overnight at 37 °C as standing cultures that were diluted 1:100 in the same medium. The culture was grown with aeration (180 rpm) at 37 °C to an OD600 of 0.85–0.9. Bacteria were collected by centrifugation at room temperature and re-suspended in BSG. 15 7-week-old BALB/c female mice were inoculated orally with 20 μL BSG containing 1 ± 0.3 × 109 CFU of Salmonella Choleraesuis vectors with pS-SaoA or plasmid pYA3493 or 20 μL BSG control. Mice were boosted with the same dose of the same strain 3 weeks later. About 100 μL of whole blood was obtained by mandibular vein puncture 3 weeks after primary inoculation and 2 weeks after boosting. Serum was removed from the whole-blood samples and stored at −20 °C. Vaginal-wash samples in mice were collected at the indicated time and stored at −20 °C as described [33, 34]. Ten mice from each group were challenged with SS2, and five mice were used for cytokine detection. This experiment was performed twice, with each group (15 mice) receiving approximately the same dose of vaccine. The results from both experiments were similar and the data were pooled for analysis.
Immunization of piglets
The preparation of the inoculum of Salmonella Choleraesuis vector strains harboring plasmids pS-SaoA or pYA3493 was performed as described in a previous section. Seventy-five 3-week-old castrated piglets were purchased from a commercial pig farm in Jiangsu Province, China. To select the pigs with negative antibody titers against SS2, SS7, and Salmonella Choleraesuis, blood was obtained from pigs by cranial vena cava and incubated at 37 °C for 60 min. The resulting clot was pelleted by centrifugation. Serum was removed from the whole-blood sample and stored at −20 °C. Serum IgG responses to SS2 SaoA, SS7 SaoA, and Salmonella Choleraesuis outer membrane proteins (OMPs) were measured by enzyme-linked immunosorbent assay (ELISA) (see below) [33, 44, 45]. The IgG titer that was less than cut-off value was considered as seronegative. These piglets were randomly assigned to five groups with 15 piglets/group, named rSC0016(pS-SaoA) group, rSC0016(pYA3493) group, rSC0018(pS-SaoA) group, rSC0018(pYA3493) group, and BSG group. Piglets were inoculated orally with 10 mL 1 ± 0.3 × 109 CFU of Salmonella Choleraesuis vector strains carrying either the SaoA expression plasmid pS-SaoA or empty plasmid pYA3493 or BSG control. Piglets were boosted with the same dose of the same strain 3 weeks later. Serum and nasal swabs were collected at 3, and 5 weeks after first immunization [10, 16]. In each group, five piglets were challenged with SS2 and five with SS7 at 2 weeks after a boost. Five piglets were used to detect cytokine levels in the blood and spleen at different time points (0.5, 3, 5, and 7 days after boost). This experiment was performed twice with each group receiving approximately the same dose of vaccine. The results from both experiments were similar and the data were pooled for analysis.
Serum IgG responses to SaoA, to OMPs of Salmonella Choleraesuis in mice and pigs, and vaginal wash IgA antibody to SaoA in mice and nasal cavity wash IgA in pigs against SaoA were measured by ELISA. The initial dilutions of serum or vaginal/nasal wash from an individual animal were 1:50 or 1:10, respectively. Briefly, 100 µL solutions containing either 1 μg/well of Salmonella OMPs or of SaoA in sodium carbonate-bicarbonate coating buffer (pH 9.6) was used to coat Nunc-Immuno MaxiSop 96-well plates (Corning, NY, USA). The plates were then incubated overnight at 4 °C. The next day, the plates were washed 3 times with PBST (PBS with 0.1% Tween 20) and then blocked with a PBST containing 2% BSA solution for 2 h at room temperature. A 100 μL volume of serially diluted sample was added in triplicate to individual wells, and the plates were incubated for 1 h at room temperature. After washing wells with PBST, goat anti-mouse or goat anti-pig IgG-horseradish peroxidase (HRP) detection antibody (Sigma, St. Louis, MO, USA) diluted 1:5000 in PBST was added to the wells and the plate was incubated at room temperature for 60 min with gentle rocking. Plates were developed with 1-Step TM Ultra TMB-ELISA (Thermo Fisher Scientific, Waltham, MA, USA) and quenched with 3N H2SO4. Absorbance was recorded at 450 nm using an automated ELISA plate reader (model EL311SX; Biotek, Winooski, VT). Absorbance readings 2.1 times higher than the baseline values of preimmune sera (negative control: about 0.045–0.052) were considered positive [33, 44–46].
Sera were collected from mice or piglets on 0.5, 3, and 5 days. In addition, spleen tissues were removed at 7 days after boost immunization. Spleens were homogenized in a final volume of 1 mL (mouse tissues) or 5 mL (pig tissues) BSG at a ratio of weight: volume of 1:9. The supernatants were stored at −70 °C. Cytokines in sera and spleen of mice or pigs were analyzed by sandwich ELISA using commercial kits (Abcam, Cambridge, UK, except pig-specific IL4 ELISA kit, which was purchased from Thermo Fisher Scientific) according to manufacturer’s protocols.
Analysis of the cross-reactivity between SS2 and SS7 in pigs
Since the saoA gene was from SS2, the cross-reactivity of sera from pigs immunized with rSC0018(pS-SaoA) or rSC0016(pS-SaoA) was checked against total cell lysates from SS2 or SS7, respectively. Total S. suis proteins (SS2 or SS7 strain) were extracted from bacterial culture and 10 μg of proteins were separated by 12% SDS-PAGE gel electrophoresis and transferred to nitrocellulose membrane. The membrane was incubated with immunized pig serum (1:100 dilution) for 1 h at room temperature and subsequently washed three times with 0.05% w/v Tween-20 in TBS for 5 min. Anti-pig IgG conjugated to horseradish peroxidase (1:5000 dilution, Sigma) was used as secondary antibodies. The membrane was developed with a chemiluminescent substrate using the kit ECL Plus Western Blotting System (GE Healthcare) according to manufacturer’s instructions.
Challenge experiment with SS2 in mice or SS2 and SS7 in pigs
Ten mice were challenged with 3 × 108 CFU of SS2 intraperitoneally (i.p.) at 2 weeks after the booster. The 50% lethal dose (LD50) of SS2 in BALB/c mice was 1.2 × 107 CFU. Challenged mice were monitored daily for 15 days .
Five pigs in each group were challenged with SS2 by intravenous injection (i.v.) with 5.0 × 108 CFU (LD50 of SS2 in pigs was 5.6 × 107 CFU). The clinical symptoms and survival of pigs were monitored for 14 days. When needed, the brain of pigs was fixed in 10% formalin buffer (pH 7.2). Thin sections (5 mm) of tissue were stained with hematoxylin/eosin and examined by light microscopy to detect histological changes caused by SS2. Another five pigs in each group were challenged by i.v. with 1.0 × 1010 CFU of SS7. The rectal temperatures of pigs challenged with SS7 were measured at 0, 1, 2, 3, 4, 5, 6, and 7 days post-inoculation .
Data were presented as the geometric means and standard deviations for all assays. The Mann–Whitney U test (GraphPad Software, Inc., San Diego, CA) was used to evaluate the persistence of strains in vivo and antibody levels of mice. The Kaplan–Meier method (SPSS software) was applied to obtain the survival fractions following i.p. challenges of immunized mice and i.v. challenges of immunized pigs. A P value of 0.05 was considered statistically significant.
Construction of sopB deletion in Salmonella Choleraesuis vaccine vectors
Previous reports have shown that the inactivation of sopB in Salmonella Typhimurium improves humoral and cellular immunity in the host [35, 48]. To improve the safety and increase the immunogenicity of Salmonella Choleraesuis vector, a sopB mutation was introduced into wild-type Salmonella Choleraesuis C78-3 to generate strain rSC0017 (Figure 1A) or into Salmonella Choleraesuis rSC0013 to generate strain rSC0016 (Table 1). Strain rSC0016 has the mutations for the regulated delayed attenuation system and the regulated delayed antigen synthesis system, characterized by ΔPcrp::TT araC PBAD crp, Δpmi, and ΔrelA::araC PBAD lacI TT , in addition to the sopB mutation. It also has a ΔasdA mutation for the balanced-lethal system to facilitate its use as a vector.
Phenotypic characterization of live attenuated Salmonella Choleraesuis vaccine vector with sopB mutation
SopB plays a role in water efflux, fluid secretion, and subsequent diarrhea associated with Salmonella infection . In this study, the vaccine strains rSC0018(pS-SaoA), rSC0011(pS-SaoA), rSC0016(pS-SaoA), the strain rSC0017 with a sopB deletion mutation, the parental wild-type strain C78-3, and a LB control were injected into six parts of the ileal loop in rabbits to detect the effect of the sopB deletion in Salmonella Choleraesuis. Hematoxylin–eosin staining of ileal loop sections revealed populations of neutrophilic cells in the ileum loops infected by the wild-type strain C78-3, but not in those infected by rSC0017, rSC0018(pS-SaoA), rSC0011(pS-SaoA), or rSC0016(pS-SaoA). These loops were similar to the loops injected by LB (Figure 1C). The fluid accumulation in the ileal loops injected with the wild-type parental strain C78-3 was significantly higher than those injected with rSC0017, rSC0018(pS-SaoA), rSC0011(pS-SaoA), rSC0016(pS-SaoA) and LB (Figure 1D). Particularly, the inflammatory exudate in the ileal loops injected with rSC0016(pS-SaoA) containing sopB mutation was significantly reduced compared to that injected with rSC0011(pS-SaoA) without the sopB mutation. In addition, the fluid accumulation in the ileal loops injected with rSC0018(pS-SaoA) was significantly more than that in those injected with rSC0011(pS-SaoA) and rSC0016(pS-SaoA), even higher than that of rSC0017 (Figure 1D). Little fluid was detected in the loops injected with LB control, which was significantly less than those injected with C78-3, rSC0017, SC0018(pS-SaoA), rSC0011(pS-SaoA), and rSC0016(pS-SaoA) (Figure 1D).
Plasmids pYA3493 and pS-SaoA are stable in attenuated Salmonella Choleraesuis rSC0016 strain
A single colony of rSC0018, rSC0016 and rSC0011 either with pS-SaoA or pYA3493 was grown in LB with 0.2% mannose, 0.2% arabinose, and 50 µg/mL DAP for 50 generations . All the colonies that were examined using PCR or endonuclease digestion contained either plasmid pS-SaoA or plasmid pYA3493, indicating that pS-SaoA and pYA3493 are equally stable in the vaccine strains (data not shown). These colonies can produce the expected SaoA protein (data not shown).
Distribution of Salmonella Choleraesuis rSC0016 vector in BALB/c mice
Salmonella Choleraesuis vaccine vector with sopB mutation induces higher antibody responses in mice
Salmonella Choleraesuis vaccine vector with sopB mutation induces higher interferon γ (IFN-γ), interleukin 4 (IL-4), and interleukin 17A (IL-17A) responses in mice
Higher IFN-γ, IL-4, and IL-17A levels were produced in the sera and spleens of mice immunized with rSC0016 or rSC0011 carrying either the empty vector pYA3493 or the SaoA-expressing plasmid pS-SaoA than in those with rSC0018 (Figures 5A–C; # P < 0.05, ## P < 0.01). rSC0011 with pYA3493 or pS-SaoA induced similar levels of IL-4 to those of rSC0018 with pYA3493 or pS-SaoA (Figure 5B). Higher levels of IFN-γ, IL-4, and IL-17A were observed in the sera and spleens of mice immunized with rSC0016(pS-SaoA) compared to those in mice immunized with rSC0011(pS-SaoA) (Figures 5A–C; # P < 0.05, ## P < 0.01). Alternatively, the level of IL-17A in the spleens of mice immunized with rSC0016(pS-SaoA) was similar to rSC0011(pS-SaoA) (Figure 5C). The levels of IFN-γ, IL-4, and IL-17A that were induced by rSC0016(pYA3493) were significantly higher than those induced by rSC0011(pYA3493) in the sera at 3, and 5 days after the booster, as well as in the spleen (Figures 5A–C; # P < 0.05, ## P < 0.01). These results indicate that the vector rSC0016 with the ΔsopB mutation induced enhanced responses more than the rSC0011 strain did .
Salmonella Choleraesuis vaccine vector with sopB mutation confers protection against SS2 in mice
Vaccine strains carrying plasmid pS-SaoA confer protection against i.p. challenge with SS2 in BALB/c mice
Percentage of survival (Number of mice Survival/Total)a
ΔPcrp527::TT araC PBAD crp Δpmi-2426 ΔrelA199::araC PBAD lacI TT ΔsopB1686 ΔasdA33
ΔPcrp527::TT araC PBAD crp Δpmi-2426 ΔrelA199::araC PBAD lacI TT ΔsopB1686 ΔasdA33
ΔPcrp527::TT araC PBAD crp Δpmi-2426 ΔrelA199::araC PBAD lacI TT ΔasdA33
ΔPcrp527::TT araC PBAD crp Δpmi-2426 ΔrelA199::araC PBAD lacI TT ΔasdA33
Salmonella Choleraesuis vaccine vector with sopB mutation induces higher antibody responses in piglets
Salmonella Choleraesuis vaccine vector with sopB mutation induces higher levels of IFN-γ, IL-4, and IL-17A in piglets
Salmonella Choleraesuis vaccine vector with sopB mutation confers protection against SS2 in piglets
Salmonella Choleraesuis vaccine vector with sopB mutation confers cross-protection against SS7 in piglets
Sao is a highly conserved protein in S. suis . The protection against SS7, one of the main S. suis serotypes in China, conferred by rSC0016(pS-SaoA) was evaluated in piglets. SS7 is not lethal in pigs and only led to a fever in pigs after intravenous challenge. The cross-reactivity of the sera from pigs immunized with Salmonella Choleraesuis vector rSC0016, carrying SS2 SaoA protein, against SS7 SaoA protein was tested by Western blot. The results showed that the sera from the pigs vaccinated with rSC0016 or rSC0018, carrying SS2 SaoA protein, could recognize the SS7 SaoA protein as well as the SS2 SaoA protein (Figure 8C).
At days 1–4 after challenge with SS7, the swine immunized with rSC0016(pYA3493), rSC0018(pYA3493), rSC0018(pS-SaoA), or BSG showed severe fever (Figure 8D), drowsiness, and asthma. All these symptoms disappeared 6 days after challenge. In contrast, the swine immunized with rSC0016(pS-SaoA) showed no symptoms during the 7-day observation period.
Recently, an innovative Salmonella Choleraesuis live attenuated vaccine vector rSC0011 with the mutations for regulated delayed attenuation (Δpmi-2426 deletion mutation, ΔPcrp527::TT araC PBAD crp deletion-insertion mutation) [29, 33], and regulated delayed antigen synthesis (ΔrelA::araC PBAD lacI TT deletion-insertion mutation) was developed [29, 57]. This vaccine vector, delivering a conserved protein of S. suis, only conferred protection against a low-dose challenge of SS2 in mice , but not a high-dose challenge of SS2 (Table 2). Therefore, it was necessary to improve the immunogenicity of the strain, rSC0011. The SopB protein of Salmonella Typhimurium plays an immunosuppressive role , and its inactivation improves humoral and cellular immune responses of the host [35, 48]. In this study, a sopB deletion mutation was introduced into our Salmonella Choleraesuis vector with the regulated delayed attenuation system to generate the new strain rSC0016. This new strain displayed the expected phenotypes of reduced fluid secretion and inflammation in rabbit ileal loop test, indicating that the ΔsopB deletion in Salmonella Choleraesuis had the same effect as it had in other Salmonella serotypes [52, 58]. Strain rSC0016 showed a similar distribution to that of strain rSC0011 in Peyer’s patches of mice, confirming that the sopB mutation did not affect the gut colonization of the strain [48, 52]. However, the bacterial load of rSC0016 in the spleen was significantly lower than that of rSC0011. This result indicates that strain rSC0016 is more attenuated than rSC0011 in deep lymphoid tissue.
Our results demonstrated that strain rSC0016, with the ΔsopB mutation, induces higher levels of IgA, IgG, IFN-γ, IL-4 γ and IL-17A in mice than the other strains tested. These results may relate to the immunosuppressive function of sopB. In addition, it might also be related to the higher antigen loads of rSC0016 in the tissues than those of rSC0018. When Salmonella enters the cell, 10–20% of the bacteria remain in the cytosol, whereas the majority of the internalized bacteria remain within a modified phagosome, the Salmonella-containing vacuole [59, 60]. The cytosolic bacteria replicate faster than the vacuolar bacteria and are invasion-primed and -competent . A small but significant amount of the cytosolic bacteria can leave epithelial cells, facilitating a rapid secondary infection and inducing both enteric and systemic infections . The sopB deletion mutant does not affect the intracellular replication of the bacterium but does induce the early death of these cells, increases lysis, and promotes the transmission of the bacteria . The premature death of epithelial cells exposes the strain to the immune system at a great efficiency, which may contribute to the increased immune responses triggered by rSC0016 compared to rSC0011.
The Salmonella Choleraesuis C500 vaccine induces mucosal IgA and IFN-γ responses during its protection of pigs , whereas our strain rSC0016 induced greater IgA, IgG, IFN-γ, IL4, and IL17A responses compared to strain rSC0018, which was derived from C500. IL-17A induces and mediates proinflammatory responses and the expression of many other cytokine genes. The higher levels of IL-17A detected in the sera (34–50 fold) of swine immunized with rSC0016 compared to those with rSC0018 may help the swine clear the infecting pathogen and confer greater protective immunity. The detailed mechanism underlying high IL-17A levels induced by rSC0016 in pig warrants further study.
The immune responses induced by strains rSC0016 and rSC0018 in both mice and weaned piglets were compared. In mice, the antibody titers of IgG and IgA against Sao of S. suis and IgG against the OMPs of Salmonella Choleraesuis induced by rSC0016 were significantly higher than those induced by rSC0011. Both were higher than those induced by rSC0018, indicating that the immune responses induced by the combination of the regulated delayed strategy and the sopB mutation were superior to those induced by the regulated delayed strategy alone or with chemically attenuated rSC0018. The trends in the immune responses of weaned piglets were similar to those of mice. It is noteworthy that the mucosal IgA responses induced by rSC0016 were significantly higher than those induced by rSC0011 in mice, and were significantly higher than those induced by rSC0018 in mice or in piglets after immunization. Our orally delivered Salmonella vaccine vectors induced strong mucosal and humoral responses against the Sao antigen (Figures 4 and 6). IgA could prevent the adhesion of pathogens to mucosal cells and improve the protection efficiency of vaccine strains. However, current challenge models (i.p. in mice and i.v. in pig) did not address this. Current challenge models focused on the effectiveness of our candidate vaccine against septicemia, since both i.p. and i.v. challenge could induce severe sepsis or even death. If a vaccine candidate could protect the animal from more severe septicemia, it will reduce more severe consequence, even the host is infected with S. suis. Since Sao is not a major virulence factor , IgG response is important for the opsonophagocytic killing of S. suis . The role of IgA in the protection against S. suis needs to be studied.
Globally, the predominant S. suis serotypes isolated from clinical cases of the disease in pigs are serotypes 2, 9, 3, 1/2, and 7 . Preventing the diseases caused by S. suis in swine with a universal vaccine is a long-sought goal. The Sao protein is highly conserved in S. suis . However, cross-protection against serotypes 1 and 7, in addition to SS2, have only been reported in mice [19, 64]. Whether the Sao protein delivered by Salmonella Choleraesuis could be a universal vaccine for swine against other S. suis serotypes is not known. Our results showed that the sera from the pigs vaccinated with rSC0016 or rSC0018 carrying SS2 SaoA protein recognized the SS7 SaoA protein, which shared 95.2% amino acid homology with SS2 SaoA (data not show). Piglets immunized with rSC0016(pS-SaoA) had normal body temperatures after challenge with SS7, whereas pigs immunized with either rSC0018(pS-SaoA), a control strain carrying the empty vector, or BSG experienced fever 1–4 days after challenge. This indicates that SaoA delivered by the innovative Salmonella Choleraesuis vector, which combines the regulated delayed strategy and the sopB mutation, provides cross-protection against SS7.
In conclusion, the new recombinant attenuated Salmonella Choleraesuis vector, which combines the regulated delayed strategy and the sopB mutation, displays a balance between adequate attenuation and safety, and induces improved immune responses. The new recombinant attenuated Salmonella Choleraesuis strain, synthesizing the SaoA protein, provided full protection against SS2 in mice and pigs. SS7 is not lethal and only leads to fever in pigs by intravenous injection without displaying other clinical signs. Vaccinated pigs did not develop fever after challenge with SS7, indicating that our vaccine is cross-protective against SS7 in swine. In the future, the protection afforded by the new recombinant attenuated Salmonella Choleraesuis vector against other serotypes of S. suis, such as serotypes 9, 3, and 1/2 will be evaluated in pigs. The data reported in this study laid the foundation for the development of a universal vaccine against S. suis.
The authors declare that they have no competing interests.
YAL, ZYJ, XBW, SFW and HYS: conceived and designed the experiments. YAL, ZYJ, XBW: performed the experiments. YAL, SFW, and HYS: wrote the paper. All authors read and approved the final manuscript.
This work was supported by the National Natural Science Foundation of China (31672516, 31172300), supported by the Grant No. BE2016343 from Jiangsu province, and the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD). We thank Dr Curtiss for kindly providing χ7213, pRE112, pYA3493, and the antibody of LacI. We also thank Matthew Bellefleur for help in editorial advice.
Ethics approval and consent to participate
Veterinarians took the samples for analysis purposes and/or to check the health status of the mice and pigs population. Both actions do not require ethical approval or were permitted for animal experimentation according to the Jiangsu Administrative Committee for Laboratory Animals (permission number SYXK-SU-2007-0005) and complied with the Jiangsu Laboratory Animal Welfare and Ethics guidelines of the Jiangsu Administrative Committee of Laboratory Animals.
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- Goyette-Desjardins G, Auger JP, Xu J, Segura M, Gottschalk M (2014) Streptococcus suis, an important pig pathogen and emerging zoonotic agent-an update on the worldwide distribution based on serotyping and sequence typing. Emerg Microbes Infect 3:e45View ArticlePubMedPubMed CentralGoogle Scholar
- Kerdsin A, Hatrongjit R, Gottschalk M, Takeuchi D, Hamada S, Akeda Y, Oishi K (2017) Emergence of Streptococcus suis serotype 9 infection in humans. J Microbiol Immunol Infect 50:545–546View ArticlePubMedGoogle Scholar
- Segura M, Zheng H, de Greeff A, Gao GF, Grenier D, Jiang Y, Lu C, Maskell D, Oishi K, Okura M, Osawa R, Schultsz C, Schwerk C, Sekizaki T, Smith H, Srimanote P, Takamatsu D, Tang J, Tenenbaum T, Tharavichitkul P, Hoa NT, Valentin-Weigand P, Wells JM, Wertheim H, Zhu B, Xu J, Gottschalk M (2014) Latest developments on Streptococcus suis: an emerging zoonotic pathogen: part 2. Future Microbiol 9:587–591View ArticlePubMedGoogle Scholar
- Segura M, Zheng H, de Greeff A, Gao GF, Grenier D, Jiang Y, Lu C, Maskell D, Oishi K, Okura M, Osawa R, Schultsz C, Schwerk C, Sekizaki T, Smith H, Srimanote P, Takamatsu D, Tang J, Tenenbaum T, Tharavichitkul P, Hoa NT, Valentin-Weigand P, Wells JM, Wertheim H, Zhu B, Gottschalk M, Xu J (2014) Latest developments on Streptococcus suis: an emerging zoonotic pathogen: part 1. Future Microbiol 9:441–444View ArticlePubMedGoogle Scholar
- Wisselink HJ, Vecht U, Stockhofe-Zurwieden N, Smith HE (2001) Protection of pigs against challenge with virulent Streptococcus suis serotype 2 strains by a muramidase-released protein and extracellular factor vaccine. Vet Rec 148:473–477View ArticlePubMedGoogle Scholar
- Quessy S, Dubreuil JD, Caya M, Letourneau R, Higgins R (1994) Comparison of pig, rabbit and mouse IgG response to Streptococcus suis serotype 2 proteins and active immunization of mice against the infection. Can J Vet Res 58:220–223PubMedPubMed CentralGoogle Scholar
- Zhang A, Chen B, Li R, Mu X, Han L, Zhou H, Chen H, Meilin J (2009) Identification of a surface protective antigen, HP0197 of Streptococcus suis serotype 2. Vaccine 27:5209–5213View ArticlePubMedGoogle Scholar
- Li W, Hu X, Liu L, Chen H, Zhou R (2011) Induction of protective immune response against Streptococcus suis serotype 2 infection by the surface antigen HP0245. FEMS Microbiol Lett 316:115–122View ArticlePubMedGoogle Scholar
- Okwumabua O, Chinnapapakkagari S (2005) Identification of the gene encoding a 38-kilodalton immunogenic and protective antigen of Streptococcus suis. Clin Diagn Lab Immunol 12:484–490PubMedPubMed CentralGoogle Scholar
- Tan C, Liu M, Liu J, Yuan F, Fu S, Liu Y, Jin M, Bei W, Chen H (2009) Vaccination with Streptococcus suis serotype 2 recombinant 6PGD protein provides protection against S. suis infection in swine. FEMS Microbiol Lett 296:78–83View ArticlePubMedGoogle Scholar
- Chen B, Zhang A, Li R, Mu X, He H, Chen H, Jin M (2010) Evaluation of the protective efficacy of a newly identified immunogenic protein, HP0272, of Streptococcus suis. FEMS Microbiol Lett 307:12–18View ArticlePubMedGoogle Scholar
- Seele J, Hillermann LM, Beineke A, Seitz M, von Pawel-Rammingen U, Valentin-Weigand P, Baums CG (2015) The immunoglobulin M-degrading enzyme of Streptococcus suis, Ide Ssuis, is a highly protective antigen against serotype 2. Vaccine 33:2207–2212View ArticlePubMedGoogle Scholar
- Tan C, Fu S, Liu M, Jin M, Liu J, Bei W, Chen H (2008) Cloning, expression and characterization of a cell wall surface protein, 6-phosphogluconate-dehydrogenase, of Streptococcus suis serotype 2. Vet Microbiol 130:363–370View ArticlePubMedGoogle Scholar
- Jacobs AA, van den Berg AJ, Loeffen PL (1996) Protection of experimentally infected pigs by suilysin, the thiol-activated haemolysin of Streptococcus suis. Vet Rec 139:225–228View ArticlePubMedGoogle Scholar
- Liu L, Cheng G, Wang C, Pan X, Cong Y, Pan Q, Wang J, Zheng F, Hu F, Tang J (2009) Identification and experimental verification of protective antigens against Streptococcus suis serotype 2 based on genome sequence analysis. Curr Microbiol 58:11–17View ArticlePubMedGoogle Scholar
- Li Y, Martinez G, Gottschalk M, Lacouture S, Willson P, Dubreuil JD, Jacques M, Harel J (2006) Identification of a surface protein of Streptococcus suis and evaluation of its immunogenic and protective capacity in pigs. Infect Immun 74:305–312View ArticlePubMedPubMed CentralGoogle Scholar
- Garibaldi M, Rodriguez-Ortega MJ, Mandanici F, Cardaci A, Midiri A, Papasergi S, Gambadoro O, Cavallari V, Teti G, Beninati C (2010) Immunoprotective activities of a Streptococcus suis pilus subunit in murine models of infection. Vaccine 28:3609–3616View ArticlePubMedGoogle Scholar
- Mandanici F, Gomez-Gascon L, Garibaldi M, Olaya-Abril A, Luque I, Tarradas C, Mancuso G, Papasergi S, Barcena JA, Teti G, Beninati C, Rodriguez-Ortega MJ (2010) A surface protein of Streptococcus suis serotype 2 identified by proteomics protects mice against infection. J Proteom 73:2365–2369View ArticleGoogle Scholar
- Hsueh KJ, Lee JW, Hou SM, Chen HS, Chang TC, Chu CY (2014) Evaluation on a Streptococcus suis vaccine using recombinant sao-l protein manufactured by bioreactors as the antigen in pigs. Transbound Emerg Dis 61:e35–e43View ArticlePubMedGoogle Scholar
- Feng Y, Pan X, Sun W, Wang C, Zhang H, Li X, Ma Y, Shao Z, Ge J, Zheng F, Gao GF, Tang J (2009) Streptococcus suis enolase functions as a protective antigen displayed on the bacterial cell surface. J Infect Dis 200:1583–1592View ArticlePubMedGoogle Scholar
- Gomez-Gascon L, Cardoso-Toset F, Amarilla PS, Tarradas C, Carrasco L, Olaya-Abril A, Jimenez-Munguia I, Rodriguez-Ortega MJ, Luque I (2014) A new recombinant SsnA protein combined with aluminum hydroxide protects mouse against Streptococcus suis. Vaccine 32:6992–6999View ArticlePubMedGoogle Scholar
- Huang K, Yuan Z, Li J, Zhang Q, Xu Z, Yan S, Zhang A, Jin M (2015) Identification and characterisation a surface-associated arginine peptidase in Streptococcus suis serotype 2. Microbiol Res 170:168–176View ArticlePubMedGoogle Scholar
- Li J, Xia J, Tan C, Zhou Y, Wang Y, Zheng C, Chen H, Bei W (2011) Evaluation of the immunogenicity and the protective efficacy of a novel identified immunogenic protein, SsPepO, of Streptococcus suis serotype 2. Vaccine 29:6514–6519View ArticlePubMedGoogle Scholar
- Li Y, Gottschalk M, Esgleas M, Lacouture S, Dubreuil JD, Willson P, Harel J (2007) Immunization with recombinant Sao protein confers protection against Streptococcus suis infection. Clin Vaccine Immunol 14:937–943View ArticlePubMedPubMed CentralGoogle Scholar
- Chabot-Roy G, Willson P, Segura M, Lacouture S, Gottschalk M (2006) Phagocytosis and killing of Streptococcus suis by porcine neutrophils. Microb Pathog 41:21–32View ArticlePubMedGoogle Scholar
- Park SM, Ko HJ, Shim DH, Yang JY, Park YH, Curtiss R 3rd, Kweon MN (2008) MyD88 signaling is not essential for induction of antigen-specific B cell responses but is indispensable for protection against Streptococcus pneumoniae infection following oral vaccination with attenuated Salmonella expressing PspA antigen. J Immunol 181:6447–6455Google Scholar
- Curtiss R 3rd (2002) Bacterial infectious disease control by vaccine development. J Clin Invest 110:1061–1066Google Scholar
- Galen JE, Levine MM (2001) Can a ‘flawless’ live vector vaccine strain be engineered? Trends Microbiol 9:372–376View ArticlePubMedGoogle Scholar
- Curtiss R 3rd, Wanda S-Y, Gunn BM, Zhang X, Tinge SA, Ananthnarayan V, Mo H, Wang S, Kong W (2009) Salmonella enterica serovar Typhimurium strains with regulated delayed attenuation in vivo. Infect Immun 77:1071–1082Google Scholar
- Wang S, Li Y, Scarpellini G, Kong W, Shi H, Baek CH, Gunn B, Wanda SY, Roland KL, Zhang X, Senechal-Willis P, Curtiss R 3rd (2010) Salmonella vaccine vectors displaying delayed antigen synthesis in vivo to enhance immunogenicity. Infect Immun 78:3969–3980Google Scholar
- Collins LV, Attridge S, Hackett J (1991) Mutations at rfc or pmi attenuate Salmonella typhimurium virulence for mice. Infect Immun 59:1079–1085PubMedPubMed CentralGoogle Scholar
- Katzman RL, Lisowska E, Jeanloz RW (1970) Invertebrate connective tissue. Isolation of d-arabinose from sponge acidic polysaccharide. Biochem J 119:17–19View ArticlePubMedPubMed CentralGoogle Scholar
- Shi H, Santander J, Brenneman KE, Wanda SY, Wang S, Senechal P, Sun W, Roland KL, Curtiss R 3rd (2010) Live recombinant Salmonella Typhi vaccines constructed to investigate the role of rpoS in eliciting immunity to a heterologous antigen. PLoS One 5:e11142Google Scholar
- Ji Z, Shang J, Li Y, Wang S, Shi H (2015) Live attenuated Salmonella enterica serovar Choleraesuis vaccine vector displaying regulated delayed attenuation and regulated delayed antigen synthesis to confer protection against Streptococcus suis in mice. Vaccine 33:4858–4867View ArticlePubMedGoogle Scholar
- Li Y, Wang S, Xin W, Scarpellini G, Shi Z, Gunn B, Roland KL, Curtiss R 3rd (2008) A sopB deletion mutation enhances the immunogenicity and protective efficacy of a heterologous antigen delivered by live attenuated Salmonella enterica vaccines. Infect Immun 76:5238–5246Google Scholar
- Zhao Z, Xue Y, Wu B, Tang X, Hu R, Xu Y, Guo A, Chen H (2008) Subcutaneous vaccination with attenuated Salmonella enterica serovar Choleraesuis C500 expressing recombinant filamentous hemagglutinin and pertactin antigens protects mice against fatal infections with both S. enterica serovar Choleraesuis and Bordetella bronchiseptica. Infection Immun 76:2157–2163View ArticleGoogle Scholar
- Li Q, Hu Y, Xu L, Xie X, Tao M, Jiao X (2014) Complete genome sequence of Salmonella enterica serovar Choleraesuis vaccine strain C500 attenuated by chemical mutation. Genome Announc 2:e01022–e01024PubMedPubMed CentralGoogle Scholar
- Bertani G (1951) Studies on lysogenesis. I. The mode of phage liberation by lysogenic Escherichia coli. J Bacteriol 62:293–300PubMedPubMed CentralGoogle Scholar
- Curtiss R 3rd (1965) Chromosomal aberrations associated with mutations to bacteriophage resistance in Escherichia Coli. J Bacteriol 89:28–40Google Scholar
- Briles DE, King JD, Gray MA, McDaniel LS, Swiatlo E, Benton KA (1996) PspA, a protection-eliciting pneumococcal protein: immunogenicity of isolated native PspA in mice. Vaccine 14:858–867View ArticlePubMedGoogle Scholar
- Gunn BM, Wanda SY, Burshell D, Wang C, Curtiss R 3rd (2010) Construction of recombinant attenuated Salmonella enterica serovar Typhimurium vaccine vector strains for safety in newborn and infant mice. Clin Vaccine Immunol 17:354–362Google Scholar
- Shi J (2009) Study on triple genetic engineering vaccine of Salmonella enterica serovar Choleraesuis swine Streptococcus. Master Thesis, Hua Zhong Agriculture University, ChinaGoogle Scholar
- Schindelin J, Rueden CT, Hiner MC, Eliceiri KW (2015) The ImageJ ecosystem: an open platform for biomedical image analysis. Mol Reprod Dev 82:518–529View ArticlePubMedPubMed CentralGoogle Scholar
- Xin W, Wanda S-Y, Li Y, Wang S, Mo H, Curtiss R 3rd (2008) Analysis of type II secretion of recombinant pneumococcal PspA and PspC in a Salmonella enterica Serovar Typhimurium vaccine with regulated delayed antigen synthesis. Infect Immun 76:3241–3254Google Scholar
- Fusco WG, Afonina G, Nepluev I, Cholon DM, Choudhary N, Routh PA, Almond GW, Orndorff PE, Staats H, Hobbs MM, Leduc I, Elkins C (2010) Immunization with the Haemophilus ducreyi hemoglobin receptor HgbA with adjuvant monophosphoryl lipid A protects swine from a homologous but not a heterologous challenge. Infect Immun 78:3763–3772View ArticlePubMedPubMed CentralGoogle Scholar
- Kang HY, Srinivasan J, Curtiss R 3rd (2002) Immune responses to recombinant pneumococcal PspA antigen delivered by live attenuated Salmonella enterica serovar typhimurium vaccine. Infect Immun 70:1739–1749Google Scholar
- Klaasen HLBM, Segers RPAM (2012) Vaccine for protection against Streptococcus suis bacteria of various serotypes. Patent EP2411047A1, 1 Feb 2012Google Scholar
- Link C, Ebensen T, Standner L, Dejosez M, Reinhard E, Rharbaoui F, Guzman CA (2006) An SopB-mediated immune escape mechanism of Salmonella enterica can be subverted to optimize the performance of live attenuated vaccine carrier strains. Microbes Infect 8:2262–2269View ArticlePubMedGoogle Scholar
- Galyov EE, Wood MW, Rosqvist R, Mullan PB, Watson PR, Hedges S, Wallis TS (1997) A secreted effector protein of Salmonella dublin is translocated into eukaryotic cells and mediates inflammation and fluid secretion in infected ileal mucosa. Mol Microbiol 25:903–912View ArticlePubMedGoogle Scholar
- Nakayama KKSM, Curtiss R 3rd (1988) Construction of an ASD + expression-cloning vector: stable maintenance and high level expression of cloned genes in a Salmonella vaccine strain. Nat Biotech 6:693–697Google Scholar
- Zhang S, Santos RL, Tsolis RM, Stender S, Hardt WD, Baumler AJ, Adams LG (2002) The Salmonella enterica serotype typhimurium effector proteins SipA, SopA, SopB, SopD, and SopE2 act in concert to induce diarrhea in calves. Infect Immun 70:3843–3855View ArticlePubMedPubMed CentralGoogle Scholar
- Reis BP, Zhang S, Tsolis RM, Baumler AJ, Adams LG, Santos RL (2003) The attenuated sopB mutant of Salmonella enterica serovar Typhimurium has the same tissue distribution and host chemokine response as the wild type in bovine Peyer’s patches. Vet Microbiol 97:269–277View ArticlePubMedGoogle Scholar
- Aarvak TCM, Miossec P, Natvig JB (1999) IL-17 is produced by some proinflammatory Th1/Th0 cells but not by Th2 cells. J Immunol 162:1246–1251PubMedGoogle Scholar
- Sassu EL, Ladinig A, Talker SC, Stadler M, Knecht C, Stein H, Frombling J, Richter B, Spergser J, Ehling-Schulz M, Graage R, Hennig-Pauka I, Gerner W (2017) Frequency of Th17 cells correlates with the presence of lung lesions in pigs chronically infected with Actinobacillus pleuropneumoniae. Vet Res 48:4View ArticlePubMedPubMed CentralGoogle Scholar
- Stepanova H, Mensikova M, Chlebova K, Faldyna M (2012) CD4 + and gdTCR + T lymphocytes are sources of interleukin-17 in swine. Cytokine 58:152–157View ArticlePubMedGoogle Scholar
- Teunissen MB, Koomen CW, de Waal Malefyt R, Wierenga EA, Bos JD (1998) Interleukin-17 and interferon-gamma synergize in the enhancement of proinflammatory cytokine production by human keratinocytes. J Invest Dermatol 111:645–649View ArticlePubMedGoogle Scholar
- Shi H, Wang S, Curtiss R 3rd (2013) Evaluation of regulated delayed attenuation strategies for Salmonella enterica serovar Typhi vaccine vectors in neonatal and infant mice. Clin Vaccine Immunol 20:931–944Google Scholar
- Norris FA, Wilson MP, Wallis TS, Galyov EE, Majerus PW (1998) SopB, a protein required for virulence of Salmonella dublin, is an inositol phosphate phosphatase. Proc Natl Acad Sci U S A 95:14057–14059Google Scholar
- Finn CE, Chong A, Cooper KG, Starr T, Steele-Mortimer O (2017) A second wave of Salmonella T3SS1 activity prolongs the lifespan of infected epithelial cells. PLoS Pathog 13:e1006354View ArticlePubMedPubMed CentralGoogle Scholar
- Knodler LA, Vallance BA, Celli J, Winfree S, Hansen B, Montero M, Steele-Mortimer O (2010) Dissemination of invasive Salmonella via bacterial-induced extrusion of mucosal epithelia. Proc Natl Acad Sci U S A 107:17733–17738View ArticlePubMedPubMed CentralGoogle Scholar
- Zhu L, Zhao X, Yin Q, Liu X, Chen X, Huang C, Suo X (2017) Mucosal IgA and IFN-g+ CD8 T cell immunity are important in the efficacy of live Salmonella enteria serovar Choleraesuis vaccines. Sci Rep 7:46408View ArticlePubMedPubMed CentralGoogle Scholar
- Roy D, Fittipaldi N, Dumesnil A, Lacouture S, Gottschalk M (2014) The protective protein Sao (surface antigen one) is not a critical virulence factor for Streptococcus suis serotype 2. Microb Pathog 67–68:31–35View ArticlePubMedGoogle Scholar
- Segura M (2015) Streptococcus suis vaccines: candidate antigens and progress. Expert Rev Vaccines 14:1587–1608View ArticlePubMedGoogle Scholar
- Zhang A, Chen B, Mu X, Li R, Zheng P, Zhao Y, Chen H, Jin M (2009) Identification and characterization of a novel protective antigen, Enolase of Streptococcus suis serotype 2. Vaccine 27:1348–1353View ArticlePubMedGoogle Scholar
- Kang K (2008) Chinese veterinary strains directory. China agricultural science and technology press, BeijingGoogle Scholar