Skip to main content
  • Research article
  • Open access
  • Published:

Endogenous transplacental transmission of Neospora caninum during successive pregnancies across three generations of naturally infected sheep


Endogenous transplacental transmission, which occurs during pregnancy as the result of reactivation of a latent infection in the dam, is the main mechanism of propagation of Neospora caninum within cattle herds. However, the importance of this propagation mechanism has not yet been evaluated in relation to ovine neosporosis. In this study, involving three generations of ewes naturally infected by N. caninum, we demonstrated that endogenous transplacental transmission may also be highly efficient in the ovine host since transmission of infection occurred in 96.6% of gestations and the congenital infection rate ranged between 66.7 and 93%. Nevertheless, parasite burdens decreased gradually in consecutive generations. Reactivation of latent infections had a strong impact on the pregnancy outcome, with high mortality rates recorded in the offspring of the two first generations of ewes (21.4–46.1%). Histological examination of the brain revealed that all aborted foetuses had characteristic lesions of neosporosis (necrotic glial foci) and a few parasite cysts, whereas most stillborn and newborn lambs that died shortly after birth had non-specific lesions (mild glial foci without necrosis) and parasite cysts were more frequent. Microsatellite analysis revealed scarce genetic variability in the N. caninum population, in accordance with a scenario in which infections were of a single origin and were exclusively maintained by clonal propagation through endogenous transplacental transmission.


Neospora caninum is a protozoan parasite (Apicomplexa: Sarcocystidae) with a facultative heteroxenous life cycle involving mainly ruminants and other ungulates as intermediate hosts and canids as definitive hosts. Infection of ruminants can occur postnatally, via ingestion of food and water contaminated with oocysts shed by a canid (horizontal transmission), or it can take place in utero by transplacental passage of tachyzoites (vertical transmission) from the dam to the foetus during gestation. Two types of transplacental infection have been described: (i) exogenous transplacental infection, which occurs when the dam becomes infected during pregnancy; and (ii) endogenous transplacental infection, which occurs after reactivation of a pre-existing chronic infection in the dam [1]. The infection is usually asymptomatic in dams, but can have devastating effects on their foetuses [2, 3].

Clinical neosporosis causing abortions and perinatal deaths has been recorded in all species of domestic ruminants. It is particularly prevalent and widely distributed in cattle, in which it is considered one of the main causes of reproductive failure [4,5,6], so that the pathological, immunological and epidemiological aspects of bovine neosporosis as well as its impact on livestock production have been studied in detail [2, 7,8,9,10,11,12,13,14,15]. By contrast, many aspects of infection in small ruminants remain largely unknown [16]. However, recent findings suggest that ovine neosporosis may be a more important cause of reproductive disorders than generally believed, at least in some geographical areas [17,18,19,20,21]. In a previous study, we demonstrated that N. caninum infection was the cause of the dramatic reduction in the reproductive performance of a sheep flock during two consecutive years [20]. The fact that no horizontal infections were detected on this farm led us to believe that endogenous transplacental transmission, until now considered irrelevant in sheep, merited reappraisal. We therefore designed a 3-year study in which the absence of horizontal infection was guaranteed, enabling us to demonstrate that endogenous transplacental transmission of N. caninum can take place in naturally infected sheep and may play a significant role in maintaining the infection in sheep flocks. Here, we provide information about the changes in the infection rate acquired by this route as well as its impact on the outcome of pregnancies in three generations of sheep. Genotyping of the N. caninum population implicated in abortion and perinatal deaths caused by this infection mechanism was also carried out.

Materials and methods

Animals: selection and management

Three consecutive generations of ewes were studied during a period of 3 years. Initially, a group of 28 Berrichon × Romanov ewes aged between 3 and 7 years was selected from a commercial flock in which N. caninum infection caused low fertility and a high rate of perinatal mortality [20]. These animals, categorized as the “Original population” (G0), were chosen for the following reasons: (1) all had chronic neosporosis confirmed by detection of specific antibodies in their sera and of parasite DNA in the brains of the offspring from their two last pregnancies, and (2) they were demonstrated to be seronegative to the main infectious agents causing abortion in sheep (Toxoplasma gondii, Brucella melitensis, Coxiella burnetii, Chlamydia abortus, Border disease virus and Schmallenberg virus). These 28 ewes were dewormed with albendazole (Albendex, SP Veterinaria, S.A., Tarragona, Spain) before being moved to the experimental farm facilities owned by the CIAM (Centro de Investigaciones Agrarias de Mabegondo), where they were mated. All resulting female lambs congenitally infected with N. caninum (i.e. with specific precolostral antibodies) were selected as “First generation” (G1) lambs. Similarly, congenitally infected female lambs produced by G1 constituted the “Second generation” (G2) (Figure 1). Throughout the study, the sheep were maintained in isolation in the CIAM facilities, so that exogenous infection by N. caninum was precluded. Notwithstanding, four Galician breed ewes (3 years old) from the CIAM’s Neospora-free flock were housed in the same facilities to act as a sentinel group for exogenous infection. All ewes and rams used for breeding were tested annually for antibodies to the aforementioned abortifacient agents.

Figure 1
figure 1

Outline of the reproductive management and outcome of gestations for the three generations of ewes under study throughout three consecutive years (2014–2016). The “Original population” (G0), which included 24 ewes from a commercial flock with chronical neosporosis, lambed three times. The “First generation” (G1) of ewes (n = 14), comprising the congenitally infected lambs born to G0 in 2014, lambed twice. The “Second generation” (G2) of ewes (n = 6 ), comprising the congenitally infected lambs born to G1 in 2015, lambed once.

Reproductive management of the sheep was as follows. During each year of the study, all ewes were oestrus-synchronized and then exposed for 7 days to Galician breed rams from the CIAM flock proven to be free of N. caninum infection. Pregnancy was diagnosed by transabdominal ultrasonography on day 45 post-mating (counting from the first day of exposure to ram). Sheep that did not become pregnant were excluded from the study, while pregnant ewes were subjected to close surveillance to record all abortions (nonviable foetuses expulsed before 140 days post-mating) and full-term births (lambs delivered from 140 days post-mating). Regarding the mortality of full-term lambs, we differentiated between stillborn lambs (prenatal death confirmed by hydrostatic pulmonary docimasy) and newborn lambs that died within 2 weeks of birth. All surviving lambs remained with their dams until weaning at age 3 months, at which time all except ewe lambs selected for further breeding were first sedated with xylazine (Rompun®, Bayer, Mannhein, Germany) and then euthanized with embutramide and mebezonio iodide (T61®; Intervet, Salamanca, Spain). Ewes older than 8 years were culled after their lambs were weaned (Figure 1).

Ewes were fed on concentrate (16% crude protein) and alfalfa hay. Different amounts of concentrate were supplied daily at the different physiological stages of the ewes, as follows: 400 g per ewe, from weaning to 30 days before mating; 750 g per ewe from day 29 pre-mating to day 100 post-mating; and 1000 g per ewe from day 101 post-mating to weaning. Alfalfa hay was supplied ad libitum. Ewes were vaccinated every year against clostridial diseases, in the last third of gestation (90 days post-mating).

Sample collection

In each of the 3 years of the study, blood samples were collected from ewes (at mating and lambing), rams (at mating) and lambs (before first suckling). Serum samples from adult sheep were analysed fresh, while samples from lambs were stored at −20 °C until analysis. All dead offspring (aborted foetuses, stillborn lambs and lambs that died within 2 weeks of birth) were necropsied under sterile conditions to obtain samples of thoracic exudate, abomasal fluid, liver, lung, spleen, heart, kidney, semitendinosus muscle and brain. A portion of each sample was analysed fresh for microbiological isolation, and the other portion was stored frozen at −20 °C and/or fixed in 10% buffered formalin. In the lambs sacrificed after weaning, samples of semitendinosus muscle and brain were conserved frozen at −20 °C.

Analysis for diagnosis of abortifacient agents (other than Neospora)

Different tests were carried out in order to rule out the presence of the infectious agents that most commonly cause abortion in sheep. Serum samples obtained from ewes and rams were screened for the presence of specific antibodies against Border disease virus, Schmallenberg virus, C. burnetii, C. abortus and T. gondii. For the four first infections, specific antibodies were determined using ELISA tests (IDEXX BVDV p80 Ab Test, IDEXX Schmallenberg Ab Test, IDEXX Q Fever Ab Test and IDEXX Chlamydiosis Total Ab Test; IDEXX Laboratories, Barcelona, Spain). Antibodies against T. gondii were determined by a latex agglutination test (Mast Toxoreagent test, Mast Group Ltd, Bootle, UK). All tests were performed following the manufacturer’s instructions.

Samples obtained during necropsy of dead lambs were analysed by different techniques [22, 23]. For the isolation and growth of B. melitensis, Salmonella abortusovis and Listeria monocytogenes, fresh samples of liver, lung, spleen and abomasal fluid were cultured in appropriate media. For diagnosis of C. abortus, impression smears from liver and abomasal fluid stained using the Ziehl–Neelsen technique were examined by microscopy. When positive results were obtained, the abomasal fluid was analysed by immune-chromatography (Clear View Chlamydia MF test, Inverness Medical, NJ, USA) for detection of bacterial antigen. Diagnosis of C. burnetii was based on the detection of microbial DNA in liver samples by quantitative PCR (LSI VetMAX Coxiella burnetii Real Time PCR kit; Life Technologies, Thermo Fisher Scientific, Delaware, USA). For detection of Border disease virus, spleen samples were analysed by quantitative reverse transcription PCR (BehiBVD/BD-VK, Vacunek S.L., Bizkaia, Spain). For diagnosis of Leptospira spp. and T. gondii, two in-house PCRs were applied to samples of kidney and brain, respectively [24, 25]. Formalin fixed samples from foetal viscera were also processed for conventional histological evaluation.

Detection of specific IgG antibodies to N. caninum

For determining IgG antibody levels against N. caninum in ewes and rams, we used an in-house ELISA previously validated in adult sheep [20]. Briefly, the assay was carried out as follows: (1) microtitre plates were coated with 0.25 μg/well of soluble extract of tachyzoites of strain NC-1; (2) duplicate serum samples (100 μL) diluted 1:100 in phosphate buffer saline (PBS; pH = 7.4) with 0.2% Tween 20 (PBS-T) and 1% dry skimmed milk (PBS-TM) were added to the plates, which were then incubated (2 h at 37 °C); (3) plates were incubated with peroxidase conjugated anti-ovine monoclonal IgG (Sigma-Aldrich, Madrid, Spain) diluted 1:20 000 in PBS-TM (100 μL/well); (4) substrate (OPD, Sigma-Aldrich, Madrid, Spain) was added, and the optical density (OD) of the mixtures was read at 492 nm. The plates were always washed with PBS-T and all incubations were carried out at 37 °C. The same positive and negative control sera were included in each plate. The results were expressed as OD. The cut-off value for this ELISA is 0.25 (calculated from analysis of serum samples taken from 100 sheep chosen at random from neosporosis-free flocks) [20]. For lambs, the antibody response was assessed using an immunofluorescent antibody test (IFAT). Briefly, glass slides were prepared by fixing tachyzoites (105/well) of strain NC-1 as previously described [26]. Precolostral sera or thoracic exudates were tested at a 1:8 dilution in PBS. The conjugate (monoclonal anti-sheep IgG labelled with fluorescein isothiocyanate, Sigma-Aldrich, Madrid, Spain) was diluted 1:500 in PBS with 0.05% Evans blue. The slides were examined under a fluorescence microscope with B-2A filters (450–520 nm). Only samples with unbroken peripheral fluorescence were considered positive.

Detection and quantification of N. caninum DNA in ovine tissues

Parasite DNA was detected in samples of brain and semitendinosus muscle from foetuses and lambs. For extraction of the genomic DNA, tissue samples (20–50 mg) were treated using the commercial Realpure Genomic DNA extraction kit (Durviz S.L., Valencia, Spain) following the manufacturer’s recommendations. After adjusting the concentration of DNA to 60 ng/μL, all samples were analysed in duplicate using a nested-ITS1 PCR adapted to a single tube, as previously described [15]. Samples that tested positive by nested-ITS1 PCR were analysed by real-time quantitative PCR in order to quantify the parasite loads. This analysis included two amplification reactions, carried out in separate wells: (1) amplification of the N. caninum Nc-5 sequence [27] with a specifically designed primer pair [28] for parasite quantification, and (2) amplification of the ovine ß-actin gene with the previously described primer pair [29], to quantify host DNA. In both cases, the reaction mixture (total volume = 20 µL) contained Power SYBR PCR Master Mix (Thermo Fisher Scientific, Warrington, UK), the corresponding primers (20 pmol of each primer for amplification of Nc-5 sequence or 18 pmol of each primer for amplification of ß-actin gene) and 60 ng of DNA template. The amplifications were performed, under previously described conditions [28], in a Bio-Rad Multicolor Real Time PCR Detection System (Bio-Rad Laboratories, Inc., CA, USA). The number of parasites and the weight (mg) of host tissue in the samples were calculated by interpolation of Ct values from two standard curves: (1) one curve equivalent to 104–10−2 tachyzoites with tenfold serial dilutions in a solution of ovine genomic DNA (12 ng/µL); and (2) a curve of 80–2.5 ng with two-fold serial dilutions of genomic DNA for ovine DNA quantifications. The standard curve for N. caninum had an average slope of −3.40 and a detection limit of 10−1 tachyzoites. The standard curve for ß-actin had an average slope of −3.36. The correlation coefficient for both curves was 0.99. Parasite burden was expressed as tachyzoites/mg of tissue. When the concentration of tachyzoites was not quantifiable (i.e. when it was below the detection limit of the real-time PCR), a minimum parasite burden of 10−2 tachyzoites was arbitrarily assigned.

N. caninum genotyping

DNA samples obtained from N. caninum PCR-positive brains were used for genotyping by multilocus microsatellite analysis. Specifically, MS4, MS5, MS6A, MS6B, MS7, MS8, MS10, MS12 and MS21 markers were amplified using specific primers and nested-PCR conditions, as previously described [14]. For all microsatellites, the size of the PCR products was determined in a 48-capillary 3730 DNA Analyser (Applied Biosystems, Foster City, CA, USA) with GeneScan-500 (LIZ) size standards (Applied Biosystems) at the Unidad Genómica del Parque Científico de Madrid. The results were analysed with GeneMapper1 software, v3.5. For confirmation of allele identification, microsatellite alleles MS4, MS5, MS6A, MS7, MS10 and MS21 from representative samples were also sequenced using a Big Dye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems) and a 3730 DNA Analyser (Applied Biosystems). The sequencing was conducted at the Unidad Genómica del Parque Cientifico de Madrid. Sequences were analysed using BioEdit Sequence Alignment Editor v.7.0.1 software (Copyright 1997–2004 Tom Hall, Ibis Therapeutics, Carlsbad, CA, USA). Allele assignment was performed as previously described [13].

Histology and immunohistochemistry

Buffered formalin fixed tissue samples of aborted foetuses and dead lambs were processed for conventional histological analysis. Tissue samples were dehydrated, embedded in paraffin, cut into 4 µm-thick sections, and finally stained with haematoxylin and eosin (HE). Immunohistochemical detection of N. caninum antigen was carried out, according to a previously described protocol [30], on brain and semitendinosus muscle. Tissue sections were first treated with a commercial trypsin solution (Abcam, Cambridge, UK), for 15 min at 37 °C, to enhance labelling, and they were then incubated overnight with an in-house rabbit polyclonal antiserum against N. caninum tachyzoites [31], diluted 1:3000. A polymer-based detection system (EnVision + system Labelled Polymer-HRP anti-rabbit; Dako, Glostrup, Denmark) was applied for 30 min at room temperature, and the reaction was developed with 3, 3′-diaminobenzidine tetrahydrochloride (DAB Peroxidase Substrate Kit; Vector Laboratories, CA, USA). The sections were counterstained with Mayer’s haematoxylin. The technique was assessed by using appropriate controls (i.e. tissue sections containing cysts of N. caninum, T. gondii or Sarcocystis spp. and negative controls). According to the histological features, lesions were categorized as (a) non-specific, when mild glial foci without necrosis and/or diffuse congestion were observed (Figure 2A), or (b) characteristic of protozoan encephalitis when necrotic foci surrounded by microglial and mononuclear cell infiltration were observed (Figure 2B). The presence of protozoan tissue cysts in the brain was noted, when they were observed in HE stained slides (Figure 2C) or during immunohistochemical labelling (Figure 2D).

Figure 2
figure 2

Microscopic lesions in brain of lambs naturally infected with N. caninum. A Focus of gliosis (arrowhead) at the cerebral cortex. HE. 4×. B Diffuse congestion, mainly seen at the white matter of the corona radiata and a focus of necrosis with peripheral gliosis. HE. 4×. C Tissue cyst of N. caninum containing structures compatible with bradyzoites. Note the thick membrane of the cyst. HE. 40×. D Positive labelling of N. caninum tissue cyst. IHC. 40×. All pictures come from lamb offspring of G0 ewes.

Statistical analysis

Pearson’s Chi square and Fisher’s exact tests were used for data involving dichotomous variables, namely transplacental passage of the parasite, establishment of the infection (presence of parasite DNA), development of antibody response in lambs and offspring mortality. The Kruskal–Wallis and Mann–Whitney tests were used to compare parasite burdens. Differences were considered significantly different at p < 0.05. All statistical analyses were performed using SPSS v. 24.0 (Chicago, IL, USA).


Efficacy of endogenous transplacental transmission of N. caninum in naturally infected sheep

The efficacy of endogenous transplacental transmission was assessed in 97 gestations, which produced 174 lambs (see Figure 1). The results for each sheep generation throughout the study period are shown in Table 1. In all 3 generations, antibody levels at mating were high (mean values between 1.598 ± 0.424 and 2.094 ± 0.318) and they increased at lambing or abortion (mean values between 1.866 ± 0.372 and 2.480 ± 0.267); these increases were statistically significant (p < 0.05) in G0 and G1, but not in G2. At both sampling times, ewes of the latter generation also had lower (p < 0.05) antibody levels than those of the two previous generations. Transplacental passage of N. caninum (presence of specific antibodies and/or parasite DNA in at least one lamb in the litter) was detected in most gestations (84/87). The N. caninum infection status of the lambs produced from gestations with transplacental transmission is shown in the right half of Table 1. Establishment of the infection (presence of parasite DNA) was significantly higher (p < 0.05) in the offspring of G0 (93% infected lambs) than in offspring of G1 and G2 (73% and 66.7% infected lambs, respectively). Parasite burdens were also lower in offspring of G2 (median = 2 tachyzoites/mg) than in the offspring of G0 (median = 19 tachyzoites/mg) and G1 (median = 32 tachyzoites/mg), although the differences were not statistically significant.

Table 1 Specific antibody levels and efficacy of endogenous transplacental transmission in ewes with chronic neosporosis

When offspring results were broken down by lambing year (Table 2), we observed that the percentage of lambs congenitally infected by N. caninum decreased progressively during successive gestations (from 98 to 81.8% and from 77.8 to 68.4% in G0 and G1, respectively), so that the prevalence of infection in the offspring of G0 ewes was significantly lower (p < 0.05) in their third year of parturition (2016). Parasite burdens followed a similar trend, as lambs born to G0 ewes had a significantly higher concentration of tachyzoites (p < 0.05) in 2014 than in 2015 and 2016. This pattern was also observed, although it was not statistically significant, in the offspring of G1, with the lambs born in the first parturition having more parasites than those born in the second lambing (median values of 50 and 18 tachyzoites/mg in 2015 and 2016 respectively). Analysis of precolostral antibodies showed that most infected lambs were able to generate an immune response to N. caninum. In fact, only 3 lambs were positive for DNA (2 born to G0 in 2014 and 1 born to G1 in 2015) with negative serology (Table 2). In ewes in the control group, the serology was always negative and neither precolostral antibodies nor parasite DNA were detected in their offspring.

Table 2 N. caninum infection in the offspring of each generation of ewes (G0, G1 and G2)

Neospora caninum genotypes were determined by multilocus microsatellite analysis in PCR-positive brain samples from ewes (n = 5) and newly delivered lambs (abortions, stillborn lambs and lambs that died shortly after birth; n = 61). Complete or partial genotypes were obtained for a total of 51 (77.3%) samples (Table 3). Most samples from both ewes and lambs shared a predominant genotype (shown at the bottom of the table). More specifically, this genotype was identified in 19 of the 25 (76%) samples in which complete genotype was determined. Moreover, the remaining 6 genotypes only varied slightly from the predominant genotype, as they differed in only 1 or 2 repeat units in only 1 and/or 2 of the MS4, MS5, MS6A, MS10 and MS21 loci. On the other hand, most sibling lambs had the same genotype, and when they did not (see offspring of G0–3, G0–11 and G0–12 ewes), the genotype variant differed by only one microsatellite and it was only observed in one of the siblings. Only the offspring of G0–17 differed from this pattern as their genotypes, although incomplete, were different from the predominant one in a least two microsatellites. Nevertheless, we could not determine whether all siblings shared the same genotype variant. All of these allelic variations were confirmed by double microsatellite analysis and DNA sequencing, by the Sanger’s method. Mixed infections by different genotypes were not detected in any of the ewes or lambs.

Table 3 N. caninum multilocus microsatellite genotypes identified in brain samples from ewes and lambs

Impact of reactivation of latent N. caninum infections on pregnancy outcome

In most pregnant ewes in this study, a reactivation of the latent N. caninum infection occurred with the subsequent transplacental passage of the parasite. Notwithstanding, most of these gestations came to full term, as only 6 out of 84 (7.1%) failed, with 9 foetuses aborted between days 87 and 130 after mating (ewes of G0; Table 4). Nevertheless, many G0 ewes gave birth to stillborn or weak lambs, which had to be helped with first suckling and perished within 2 weeks of birth. The mortality rate among the offspring was therefore very high in the three lambings of G0 ewes (44.4–50%). In G1 and G2 ewes, there were no abortions and only one lamb was born dead. However, G1 ewes delivered a high proportion of weak lambs that died within 2 weeks of birth, so that mortality rate of the offspring remained high (21.4%–46.1%), with no significant differences relative to G0. All infected offspring of G2 survived until weaning; however, the number of lambs in this group was very small, so that statistical analysis of the data was not possible. The four ewes in the control group had a total of 12 gestations over the 3 years study period, giving birth to 22 lambs, 21 of which lived until weaning (data not shown).

Table 4 Infected offspring

Histological lesions, either non-specific or characteristic for protozoan encephalitis, were observed in 77.5% of aborted foetuses, stillborn lambs or lambs that died shortly after birth. The proportions of infected lambs with non-specific or characteristic lesions in the brain (see Figure 2) are shown in Table 5. Characteristic lesions were present in all aborted foetuses (100%), but were scarce in stillborn and dead newborn lambs (14% and 8%, respectively), which mainly presented non-specific lesions (found in 66% and 47%, respectively). Many dead newborn lambs did not have any lesions (45%). Identification of tissue cysts in the slides was more frequent in stillborn and dead newborn lambs (62% and 69% respectively) than in aborted foetuses (18%). Apart from lesions in the brain, there were no other histopathological lesions in the other organs examined. Histopathological examination of semitendinosus muscle did not show evident lesions, even though this is a usual site of establishment of N. caninum, as demonstrated by detection of both DNA and antigen of the parasite by respectively PCR and immunohistochemistry. Finally, all ewes and lambs from the control group tested negative for any other abortifacient agents analysed. In the dead lamb from this group, no histological changes were observed and the parasite was not detected by immunohistochemistry.

Table 5 Percentage of infected lambs presenting brain lesions and/or parasite cysts


This is the first study to demonstrate that naturally occurring neosporosis is efficiently transmitted in successive gestations across generations of sheep through the endogenous transplacental route. Previous research in naturally infected sheep has not shed light on this aspect owing to several limitations such as the duration of the studies (only one gestation) and the impossibility of completely ruling out the horizontal transmission route [17, 21, 32]. Furthermore, the scant research carried out with experimentally infected sheep has yield discrepant findings regarding the importance of the endogenous transplacental transmission of N. caninum in this host species. Thus, both a high proportion (75%) [33] and a low proportion (13.9%) [34] of lambs have been reported to be infected by this route. These discrepancies may have been caused by infection with different N. caninum isolates (NC1 or NC-Liverpool), the dose of inoculum used (1 × 107 or 1.7 × 105 tachyzoites) or the route of administration (subcutaneous or intravenous), among other factors. Moreover, the study conditions are also unlikely to reflect what occurs in the field.

Endogenous transplacental transmission is the main mechanism responsible for perpetuation of neosporosis in cattle herds because of two different factors. On one hand, the transmission is highly efficient, so that most chronically infected cows give birth to infected calves. On the other hand, neosporosis rarely causes abortion or clinical signs in offspring, so that the infected female calves are often reared for breeding and continue to transmit the infection during future pregnancies [4, 5, 35]. Both of these aspects have been addressed in this study in order to assess the importance of this route in the transmission of natural ovine neosporosis. The rates of congenital infection (referred to as percentage of lambs with N. caninum DNA) recorded in the three generations of sheep (66.7–93%) are within the range of those reported in cattle with naturally occurring neosporosis (40.7–100%) [2, 5, 36], demonstrating that endogenous transplacental transmission may be also highly efficient in the ovine host. Consequently, neosporosis can remain for long periods of time in flocks, even in the absence of exposure to N. caninum oocysts. Notwithstanding, we also demonstrated that the transmission efficiency decreases gradually over gestations in the same animal but also over generations, as also observed in bovine neosporosis [11, 37] and that it has been attributed to the capacity of cows to develop a certain degree of immunity which would reduce parasite transmission. Most of the data on neosporosis transmission in naturally infected cattle have been obtained by comparison of seroprevalence in dams and their progeny. Nevertheless, detection of antibodies may not reflect the actual status and/or the evolution of the infection. In this respect, our study enabled us to confirm a significant reduction in parasite burdens of the lambs delivered by the third generation dams.

Microsatellite analysis enabled genetic characterization of the N. caninum population causing abortions and perinatal deaths in this study. As expected, scarce genetic variability in the circulating parasite population was observed, in accordance with a scenario in which infections had a single origin and were maintained exclusively by clonal propagation through endogenous transplacental transmission. In this respect, the predominant genotype and the variant in the MS5 locus identified in this study are the same as those previously found in the original herd from which the experimental sheep (G0) were obtained [20]. Allele variations in the less frequent genotypes would occur from the predominant genotype through the successive addition or subtraction of one or two repeat units. This allelic variation resembles the mutation pattern previously associated with these markers on the basis of the stepwise mutation model [14]. The stability of these microsatellites was therefore established in vitro, so that the observed variations could be attributed to spontaneous shifts during the transmission and spread of N. caninum in vivo.

During assessment of the reproductive performance of the sheep, we observed that chronic latent neosporosis did not impair fertility, as in all three generations of ewes, the pregnancy rates (percentage of pregnant ewes relative to those exposed to the ram) remained within the range of those recorded in the Neospora-free flocks in this region (80–86%). These observations are consistent with those reported for naturally infected cows [38, 39]. By contrast, the spontaneous reactivation of the infection during gestation had a dramatic impact on the conceptus viability, and high rates of perinatal mortality were registered over two generations. Although reactivation and transplacental transmission of the infection also occurred during gestations in the third generation of ewes (G2), the congenitally infected lambs lived until weaning. The absence of deleterious effects in these lambs was probably due to the fact that they harboured very low parasite burdens (median = 2 tachyzoites/mg of tissue). However, this could not be definitely demonstrated, because of the small number of animals in this group. Nevertheless, it has been demonstrated in sheep experimentally infected with N. caninum at mid gestation that the severity of the lesions caused in placenta and/or foetus as well as the course of the clinical disease are closely related to the parasite burden [40]. Judging by the evolution of parasite burdens, our study demonstrates that N. caninum infection may be gradually cleared over successive gestations and generations. It is tempting to hypothesize that such clearance is related to the gradual development of an effective immune response by the sheep that could help to limit the transmission of the parasite and progression of the infection. As no similar studies regarding endogenous transplacental transmission in natural ovine neosporosis have been conducted, we do not know whether the clinical course described in this work constitutes a specific pattern for the ovine host. Notwithstanding, the results of the present study clearly differ from those reported for natural bovine neosporosis, where the recrudescence of infection does not disturb gestation and most of their calves are born healthy, although congenitally infected, with survival rates of 83–100% [7, 41]. The absence of clinical signs in bovine natural persistent neosporosis has been associated with the fact that spontaneous recrudescence of N. caninum and the subsequent infection of the calves occur in the second half of gestation (between 20 and 33 weeks) [7, 11]. In the present study, congenital infections also occurred in the second half of gestation as inferred from the fact that most of the lambs (142/145) had specific precolostral antibodies, which are not produced at an earlier gestational age. Indeed, it has been demonstrated that the adequate functional and structural development of lymphoid tissues is reached by around 75 days of gestation [42,43,44]. Nevertheless, as previously mentioned, most of the lambs in our study were stillborn or died shortly after birth. These clinical findings are consistent with those recorded in ewes experimentally infected with N. caninum tachyzoites injected during mid (90 days) and late gestation (120 days) [40, 45], thereby suggesting that the effects of neosporosis are more damaging to sheep than to cattle, even though transplacental passage of the parasite occurs when the foetal lambs have already developed immunocompetency.

Neospora caninum infection in lambs was characterized by the presence of low numbers of parasites, frequently at their cyst stage and mainly located in the brain and striated muscle, apparently confirming that both tissues are key sites for long-term persistence of N. caninum. In this respect, T. gondii has been demonstrated to sense some environmental factors in brain and muscle that induce the conversion of proliferative tachyzoites to quiescent encysted bradyzoites that avoided the host immune response and persisted within the long-lived post-mitotic cells present in both tissues [46, 47]. Histological analysis revealed that aborted foetuses had a high proportion of characteristic lesions of protozoan encephalitis (i.e. necrotic glial foci) and some tissue cysts, while the stillborn lambs and lambs that died shortly after birth presented milder lesions, but more parasite cysts. This suggests that the infection was better controlled, to a certain extent, in stillborn and newborn lambs than in aborted foetuses. In the former, the larger number of tissue cysts and milder lesions are consistent with an immunologically controlled infection, so that host immune response would be less aggressive, thereby allowing the parasite to reach a quiescent stage. In aborted foetuses, a more aggressive immune response would have developed and may have been effective in avoiding the formation of tissue cyst while also causing more severe lesions that may somehow compromise the survival of the foetus. Consequently, perinatal deaths in this study would not be directly affected by growth and multiplication of the parasite in the foetal tissues. Analysis of the placentas would probably provide further useful information about this aspect of the disease; however, unfortunately the placentas recovered after natural lambing presented severe autolysis and could not be analysed. Damage caused by the multiplication of N. caninum and/or the in situ maternal immune response might disturb the functioning of the placenta, i.e. its capacity to deliver sufficient nutrients and oxygen to the growing foetus. Restriction of foetal growth during late stages of gestation may give rise to weakened lambs that do not resist birth stress or die shortly after being born. In this regard, placental deficiency is also known to impair neurological development of the lambs, so that they are born behaviourally slow and show poor homeothermy, which finally endangers their lives [48,49,50]. Only one death among the offspring of the control sheep was recorded, thereby ruling out other potential causes of perinatal mortality such as nutritional deficiencies and/or unsuitable management practices during pre-breeding period and gestation. However, it was not possible to determine whether the clinical pattern of infection was related to the breed.

In conclusion, our study findings demonstrate that endogenous transplacental transmission may be an important mechanism whereby naturally occurring ovine neosporosis can be widely disseminated among the offspring of various consecutive generations, thus perpetuating infection within the flocks. Notwithstanding, further evaluation of the influence of other factors, such as sheep breed and the N. caninum isolate, is required.


  1. Trees AJ, Williams DJ (2005) Endogenous and exogenous transplacental infection in Neospora caninum and Toxoplasma gondii. Trends Parasitol 21:558–561

    Article  Google Scholar 

  2. Mazuz ML, Fish L, Reznikov D, Wolkomirsky R, Leibovitz B, Savitzky I, Golenser J, Shkap V (2014) Neosporosis in naturally infected pregnant dairy cattle. Vet Parasitol 205:85–91

    Article  Google Scholar 

  3. Wilson DJ, Orsel K, Waddington J, Rajeev M, Sweeny AR, Joseph T, Grigg ME, Raverty SA (2016) Neospora caninum is the leading cause of bovine fetal loss in British Columbia, Canada. Vet Parasitol 218:46–51

    Article  Google Scholar 

  4. Dubey JP, Buxton D, Wouda W (2006) Pathogenesis of bovine neosporosis. J Comput Pathol 134:267–289

    Article  CAS  Google Scholar 

  5. Dubey JP, Schares G, Ortega-Mora LM (2007) Epidemiology and control of neosporosis and Neospora caninum. Clin Microbiol Rev 20:323–367

    Article  CAS  Google Scholar 

  6. Pessoa GA, Martini AP, Trentin JM, Dalcin VC, Leonardi CE, Vogel FS, de Sá Filho MF, Rubin MI, Silva CA (2016) Impact of spontaneous Neospora caninum infection on pregnancy loss and subsequent pregnancy in grazing lactating dairy cows. Theriogenology 85:519–527

    Article  Google Scholar 

  7. Guy CS, Williams DJL, Kelly DF, McGarry JW, Guy F, Björkman C, Smith RF, Trees AJ (2001) Neospora caninum in persistently infected, pregnant cows: spontaneous transplacental infection is associated with an acute increase in maternal antibody. Vet Rec 149:443–449

    Article  CAS  Google Scholar 

  8. Rosbottom A, Guy CS, Gibney EH, Smith RF, Valarcher JF, Taylor G, Williams DJ (2007) Peripheral immune responses in pregnant cattle following Neospora caninum infection. Parasite Immunol 29:219–228

    Article  CAS  Google Scholar 

  9. Rosbottom A, Gibney EH, Guy CS, Kipar A, Smith RF, Kaiser P, Trees AJ, Williams DJ (2008) Upregulation of cytokines is detected in the placentas of cattle infected with Neospora caninum and is more marked early in gestation when fetal death is observed. Infect Immun 76:2352–2361

    Article  CAS  Google Scholar 

  10. Rosbottom A, Gibney H, Kaiser P, Hartley C, Smith RF, Robinson R, Kipar A, Williams DJ (2011) Up regulation of the maternal immune response in the placenta of cattle naturally infected with Neospora caninum. PLoS One 6:e15799

    Article  CAS  Google Scholar 

  11. Dijkstra T, Barkema HW, Eysker M, Beiboer ML, Wouda W (2003) Evaluation of a single serological screening of dairy herds for Neospora caninum antibodies. Vet Parasitol 110:161–169

    Article  Google Scholar 

  12. González-Warleta M, Castro-Hermida JA, Carro-Corral C, Cortizo-Mella J, Mezo M (2008) Epidemiology of neosporosis in dairy cattle in Galicia (NW Spain). Parasitol Res 102:243–249

    Article  Google Scholar 

  13. González-Warleta M, Castro-Hermida JA, Carro-Corral C, Mezo M (2011) Anti-Neospora caninum antibodies in milk in relation to production losses in dairy cattle. Prev Vet Med 101:58–64

    Article  Google Scholar 

  14. Regidor-Cerrillo J, Díez-Fuertes F, García-Culebras A, Moore DP, González-Warleta M, Cuevas C, Schares G, Katzer F, Pedraza-Díaz S, Mezo M, Ortega-Mora LM (2013) Genetic diversity and geographic population structure of bovine Neospora caninum determined by microsatellite genotyping analysis. PLoS One 8:e72678

    Article  CAS  Google Scholar 

  15. Regidor-Cerrillo J, Arranz-Solís D, Benavides J, Gómez-Bautista M, Castro-Hermida JA, Mezo M, Pérez V, Ortega-Mora LM, González-Warleta M (2014) Neospora caninum infection during early pregnancy in cattle: how the isolate influences infection dynamics, clinical outcome and peripheral and local immune responses. Vet Res 45:10

    Article  Google Scholar 

  16. Dubey JP, Schares G (2011) Neosporosis in animals—the last five years. Vet Parasitol 180:90–108

    Article  CAS  Google Scholar 

  17. West DM, Pomroy WE, Collett MG, Hill FI, Ridler AL, Kenyon PR, Morris ST, Pattison RS (2006) A possible role for Neospora caninum in ovine abortion in New Zealand. Small Ruminant Res 62:135–138

    Article  Google Scholar 

  18. Bishop S, King J, Windsor P, Reichel MP, Ellis J, Slapeta J (2010) The first report of ovine cerebral neosporosis and evaluation of Neospora caninum prevalence in sheep in New South Wales. Vet Parasitol 170:137–142

    Article  Google Scholar 

  19. Moreno B, Collantes-Fernándes E, Villa A, Navarro A, Regidor-Cerrillo J, Ortega-Mora LM (2012) Occurrence of Neospora caninum and Toxoplasma gondii infections in ovine and caprine abortions. Vet Parasitol 187:312–318

    Article  CAS  Google Scholar 

  20. González-Warleta M, Castro-Hermida JA, Regidor-Cerrillo J, Benavides J, Álvarez-García G, Fuertes M, Ortega-Mora LM, Mezo M (2014) Neospora caninum infection as a cause of reproductive failure in a sheep flock. Vet Res 45:88

    PubMed  PubMed Central  Google Scholar 

  21. Filho PCGA, Oliveira JMB, Andrade MR, Silva JG, Kim PCP, Almeida JC, Porto WJN, Mota RA (2017) Incidence and vertical transmission rate of Neospora caninum in sheep. Comput Immunol Microbiol Infect Dis 52:19–22

    Article  Google Scholar 

  22. Ortega-Mora LM, Gottsein B, Conraths FJ, Buxton D (2007) Protozoal abortion in farm ruminants: guidelines for diagnosis and control. CAB International, Wallingford

    Google Scholar 

  23. OIE (2016) Manual of diagnostic tests and vaccines for terrestrial animals. World Organisation for Animal Health, Paris

    Google Scholar 

  24. Hurtado A, Aduriz G, Moreno B, Barandika J, García-Pérez AL (2001) Single tube nested PCR for the detection of Toxoplasma gondii in fetal tissues from naturally aborted ewes. Vet Parasitol 102:17–27

    Article  CAS  Google Scholar 

  25. Hernández-Rodríguez P, Díaz CA, Dalmau EA, Quintero GM (2011) A comparison between polymerase chain reaction (PCR) and traditional techniques for the diagnosis of leptospirosis in bovines. J Microbiol Methods 84:1–7

    Article  Google Scholar 

  26. Schares G, Peters M, Wurm R, Bärwald A, Conraths FJ (1998) The efficiency of vertical transmission of Neospora caninum in dairy cattle analysed by serological techniques. Vet Parasitol 80:87–98

    Article  CAS  Google Scholar 

  27. Kaufmann H, Yamage M, Roditi I, Dobbelaere D, Dubey JP, Holmdahl OJM, Trees A, Gottstein B (1996) Discrimination of Neospora caninum from Toxoplasma gondii and other apicomplexan parasites by hybridization and PCR. Mol Cell Prob 10:289–297

    Article  CAS  Google Scholar 

  28. Collantes-Fernández E, Zaballos A, Álvarez-García G, Ortega-Mora LM (2002) Quantitative detection of Neospora caninum in bovine aborted fetuses and experimentally infected mice by real-time PCR. J Clin Microbiol 40:1194–1198

    Article  Google Scholar 

  29. Gutiérrez J, O’Donovan J, Proctor A, Brady C, Marques PX, Worrall S, Nally JE, McElroy M, Bassett H, Fagan J, Maley S, Buxton D, Sammin D, Markey BK (2012) Application of quantitative real-time polymerase chain reaction for the diagnosis of toxoplasmosis and enzootic abortion of ewes. J Vet Diagn Invest 24:846–854

    Article  Google Scholar 

  30. Benavides J, Katzer F, Maley SW, Bartley PM, Cantón G, Pararea-Albadalejo J, Purslow CA, Pang Y, Rocchi MS, Chianini F, Buxton D, Innes EA (2012) High rate of transplacental infection and transmission of Neospora caninum following experimental challenge of cattle at day 210 of gestation. Vet Res 43:83

    Article  Google Scholar 

  31. Álvarez-García G, Collantes-Fernández E, Costas E, Rebordosa X, Ortega-Mora LM (2003) Influence of age and purpose for testing on the cut-off selection of serological methods in bovine neosporosis. Vet Res 34:341–352

    Article  Google Scholar 

  32. Hässig M, Sager H, Reitt K, Ziegler D, Strabel D, Gottstein B (2003) Neospora caninum in sheep: a herd case report. Vet Parasitol 117:213–220

    Article  Google Scholar 

  33. Jolley WR, McAllister MM, McGuire AM, Wills RA (1999) Repetitive abortion in Neospora-infected ewes. Vet Parasitol 82:251–257

    Article  CAS  Google Scholar 

  34. Buxton D, Wright S, Maley SW, Rae AG, Lundén A, Innes EA (2001) Immunity to experimental neosporosis in pregnant sheep. Parasite Immunol 23:85–91

    Article  CAS  Google Scholar 

  35. Williams DJ, Hartley CS, Björkman C, Trees AJ (2009) Endogenous and exogenous transplacental transmission of Neospora caninum—how the route of transmission impacts on epidemiology and control of disease. Parasitology 136:1895–1900

    Article  CAS  Google Scholar 

  36. Dijkstra T, Lam TJ, Bartels CJ, Eysker M, Wouda W (2008) Natural postnatal Neospora caninum infection in cattle can persist and lead to endogenous transplacental infection. Vet Parasitol 152:220–225

    Article  Google Scholar 

  37. Romero JJ, Perez P, Dolz G, Frankena K (2002) Factors associated with Neospora caninum serostatus in cattle of 20 specialised Costa Rican dairy herds. Prev Vet Med 53:263–273

    Article  CAS  Google Scholar 

  38. López-Gatius F, Santolaria P, Almería S (2005) Neospora caninum infection does not affect the fertility of dairy cows in herds with high incidence of Neospora-associated abortions. J Vet Med B Infect Dis Vet Public Health 52:51–53

    Article  Google Scholar 

  39. Santolaria P, López-Gatius F, Yániz J, García-Ispierto I, Nogareda C, Bech-Sàbat G, Serrano B, Almeria S (2009) Early postabortion recovery of Neospora-infected lactating dairy cows. Theriogenology 72:798–802

    Article  CAS  Google Scholar 

  40. Arranz-Solís D, Benavides J, Regidor-Cerrillo J, Fuertes M, Ferre I, Ferreras Mdel C, Collantes-Fernández E, Hemphill A, Pérez V, Ortega-Mora LM (2015) Influence of the gestational stage on the clinical course, lesional development and parasite distribution in experimental ovine neosporosis. Vet Res 46:19

    Article  Google Scholar 

  41. Piergili Fioretti PD, Pasquali P, Diaferia M, Mangili V, Rosignoli L (2003) Neospora caninum infection and congenital transmission: serological and parasitological study of cows up to the fourth gestation. J Vet Med B Infect Dis Vet Public Health 50:399–404

    Article  CAS  Google Scholar 

  42. Press CM, Hein WR, Landsverk T (1993) Ontogeny of leucocyte populations in the spleen of fetal lambs with emphasis on the early prominence of B cells. Immunology 80:598–604

    CAS  PubMed  PubMed Central  Google Scholar 

  43. Alitheen N, McClure S, McCullagh P (2007) Detection and quantification of IgM(+) lymphocytes in fetal lamb spleen, liver and lymph nodes by flow cytometry. Immunol Cell Biol 85:391–393

    Article  CAS  Google Scholar 

  44. Nalubamba KS, Gossner AG, Dalziel RG, Hopkins J (2008) Differential expression of pattern recognition receptors during the development of foetal sheep. Dev Comp Immunol 32:869–874

    Article  CAS  Google Scholar 

  45. McAllister MM, McGuire AM, Jolley WR, Lindsay DS, Trees AJ, Stobart RH (1996) Experimental neosporosis in pregnant ewes and their offspring. Vet Pathol 33:647–655

    Article  CAS  Google Scholar 

  46. Schlüter D, Däubener W, Schares G, Groß U, Pleyer U, Lüder C (2014) Animals are key to human toxoplasmosis. Int J Med Microbiol 304:917–929

    Article  Google Scholar 

  47. Wohlfert EA, Blader IJ, Wilson EH (2017) Brains and brawn: toxoplasma infections of the central nervous system and skeletal muscle. Trends Parasitol 33:519–531

    Article  Google Scholar 

  48. Dwyer CM, Calvert SK, Farish M, Donbavand J, Pickup HE (2005) Breed, litter and parity effects on placental weight and placentome number, and consequences for the neonatal behaviour of the lamb. Theriogenology 63:1092–1110

    Article  CAS  Google Scholar 

  49. Ocak S, Emsen E, Köycegiz F, Kutluca M, Onder H (2009) Comparison of placental traits and their relation to litter size and parity weight in sheep. J Anim Sci 87:3196–3201

    Article  CAS  Google Scholar 

  50. Ocak S, Ogun S, Onder H (2013) Relationship between placental traits and maternal intrinsic factors in sheep. Anim Reprod Sci 139:31–37

    Article  CAS  Google Scholar 

Download references

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

MGW, JACH, CC and MM conceived the study and participated in its design, performed the experiment, carried out sampling, necropsies, serological assays and PCR analysis, interpreted results and drafted the manuscript. VP and DGE carried out histopathological and immunohistochemical assays and helped in discussion of results. JRC and LMOM carried out molecular analysis and helped in discussion of results. All authors read and approved the final manuscript.


The authors gratefully acknowledge excellent technical assistance provided by Carmen Carro and Xabier Cortizo (CIAM).

Ethics approval and consent to participate

This study was carried out in strict accordance with the guidelines of the European Directive 2010/63/EU and the Spanish Law (RD53/2013) on Care and Use of Laboratory Animals. The protocol was approved by the Ethics Committee of the Consellería do Medio Rural of the Xunta de Galicia (Spain).


The present study was supported by the Ministerio de Ciencia, Innovación y Universidades of Spain (INIA project RTA2014-00013).

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Marta González-Warleta.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

González-Warleta, M., Castro-Hermida, J.A., Calvo, C. et al. Endogenous transplacental transmission of Neospora caninum during successive pregnancies across three generations of naturally infected sheep. Vet Res 49, 106 (2018).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: