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Revista Brasileira de Parasitologia Veterinária

Print version ISSN 0103-846XOn-line version ISSN 1984-2961

Rev. Bras. Parasitol. Vet. vol.24 no.3 Jaboticabal July/Sept. 2015

http://dx.doi.org/10.1590/S1984-29612015057 

Original Article

Brazilian donkeys (Equus asinus) have a low exposure to Neospora spp.

Asininos (Equus asinus) brasileiros têm uma baixa exposição à Neospora spp.

Cynthia Maria Morais de Queiroz Galvão 1  

Mariana Marrega Rezende-Gondim 1  

Ana Carla Rodrigues Chaves 1  

Gereon Schares 2  

Jorge Raimundo Lins Ribas 3  

Luís Fernando Pita Gondim 1   *  

1Departamento de Anatomia, Patologia e Clínicas, Escola de Medicina Veterinária e Zootecnia, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil

2Friedrich-Loeffler-Institut - FLI, Federal Research Institute for Animal Health, Institute of Epidemiology, Südufer, Greifswald-Insel Riems, Germany

3Agência Estadual de Defesa Agropecuária da Bahia - ADAB, Salvador, BA, Brasil

ABSTRACT

Donkeys (Equus asinus) are closely related to horses and are known to be infected by several equine pathogens. Neospora caninum and Neospora hughesi are protozoan parasites that infect horses, but they were not confirmed in donkeys up to this date. The aim of this study was to evaluate the exposure of donkeys (Equus asinus) to Neospora spp. using tachyzoites of N. caninum as antigen and employing two common serologic methods, IFAT and immunoblot. Sera from 500 donkeys were obtained from 30 municipalities in Bahia state and tested by IFAT. Two of 500 sera were positive for Neospora spp. by IFAT with antibody titers of 100, and recognized a 37kDa antigen in immunoblot. Approximately 22% of the samples showed strong apical reactions and/or incomplete fluorescence, what may cause confusion in the interpretation of IFAT. We concluded that Neospora spp. are possibly of minor importance for Brazilian donkeys. Future studies are necessary to prove that Neospora spp. can naturally infect donkeys.

Key words: Neospora ; Equus asinus ; donkeys; antibodies

RESUMO

Asininos (Equus asinus) são próximos filogeneticamente a equinos e podem ser infectados por vários patógenos de cavalos. Neospora caninum e Neospora hughesi são parasitos protozoários que infectam equinos, porém não foram confirmados em asininos até o momento. O objetivo deste estudo foi avaliar a exposição de asininos (Equus asinus) a Neospora spp., usando-se taquizoítos de N. caninum como antígeno e empregando-se duas técnicas sorológicas comuns para esta finalidade, reação de imunofluorescência indireta (RIFI) e immunoblot. Soros de 500 asininos, obtidos em 30 municípios no Estado da Bahia, foram testados por meio da RIFI. Dois dos 500 soros foram positivos para Neospora spp. pela RIFI com títulos de anticorpos de 100, e reconheceram um antígeno de 37kDa no immunoblot. Aproximadamente, 22% das amostras apresentaram fortes reações apicais e/ou fluorescência incompleta, o que pode causar confusão na interpretação da RIFI. Conclui-se que Neospora spp. são, possivelmente, de pouca importância para asininos brasileiros. Estudos posteriores são necessários para provar que Neospora spp. podem causar infecção natural em asininos.

Palavras-Chave: Neospora ; Equus asinus ; asininos; anticorpos

Introduction

Neospora caninum is a protozoan parasite that causes a great economic impact in cattle industry worldwide (REICHEL et al., 2013). The parasite is commonly transmitted to herbivores via transplacental infection or through ingestion of oocysts shed in the feces from definitive hosts (DH). There are four canid species identified as DH of N. caninum, which are domestic dogs (MCALLISTER et al., 1998), coyotes (GONDIM et al., 2004), Australian dingoes (KING et al., 2010) and grey wolves (DUBEY et al., 2011). A great number of mammalian species, including horses, may serve as intermediate hosts for N. caninum. Some of these hosts may present neosporosis (GOODSWEN et al., 2013).

A second species was proposed in the genus Neospora (N. hughesi), isolated from a horse with neurological disease. Its classification was based on molecular, antigenic and ultrastructural differences from N. caninum (MARSH et al., 1998). Therefore, the equine protozoal mieloencephalitis (EPM), a serious neurologic disease of horses, which had Sarcocystis neurona as its sole agent (DUBEY et al., 1991), was shown to have Neospora hughesi (N. hughesi) as a second etiologic agent. Walsh et al. (2000) tested whether dogs could serve as definitive hosts for N. hughesi. Two dogs were fed brains from N. hughesi-experimentally infected mice. The dogs did not excrete Neospora-like oocysts in their feces. These authors concluded that dogs do not appear to be definitive hosts of the parasite. So far, no animal has been identified as DH of N. hughesi.

Horses are infected by both N. caninum and N. hughesi. The former may cause abortion in horses and the latter was only associated with neurologic disease in this animal species (MARSH et al., 1998; PITEL et al., 2003). However, no serologic test has been proved to differentiate infections caused by N. caninum and N. hughesi (GONDIM et al., 2009).

Donkeys (Equus asinus) are closely related to horses and are affected by several microorganisms that are commonly found in equines, including the protozoa Theileria equi and Babesia caballi (MACHADO et al., 2012). In two publications, donkeys from Italy and Iran were reported to be exposed to Nesporaspp. based on the detection of anti-Neospora sp. antibodies (GHAREKHANI et al., 2013; MACHAČOVÁ et al., 2013). In each of these reports, a single serologic method was used to test the animal sera. Up to this date, there is no confirmation of Neospora DNA or detection of any Neospora stages (tachyzoites or encysted bradzyoites) in tissues from donkeys.

The aim of this study was to test whether donkeys raised in Bahia state, Brazil, are exposed to Neospora sp. through two serologic tests.

Materials and Methods

Animals

The sample size for this study was calculated according to the reported population of donkeys (271.401) in Bahia state, (Brazilian Agency of Geography and Statistics – IBGE (2010). At the time the experiment was planned, no epidemiological data were available for Neospora sp. in donkeys. Therefore, an expected frequency for Neospora spp. antibodies in horses (2.5%) (HOANE et al., 2006) was used for the sample size estimation. A confidence interval of 95% and precision of 5% were used in the sample calculation. Values of p<0.05 were considered significant.

Bahia state has a country-like territorial extension (564,733,177 km2) which is larger than countries such as France and Germany. It possesses the largest population of donkeys in Brazil, corresponding to 271.401 animals (IBGE, 2010).

A total of 500 sera from donkeys were obtained between the years of 2009 and 2012. The animals were originated from 30 municipalities distributed in the state of Bahia (Figure 1). Most animals (275) were 5 to 10 years old, 159 were below 5 years old, and 66 animals had ages above 10 years. Males and females corresponded to 191 and 309 donkeys, respectively. Sera from 173 animals were obtained in a donkey breeding farm in the municipality of Valente, Bahia, which sells donkeys for several regions in Bahia and to other Brazilian states, mainly for the production of hybrids (mules). The remaining sera (327 samples) were originated from 29 municipalities.

Figure 1 Serum samples from donkeys were obtained in 30 municipalities in Bahia state, Brazil, during the years of 2009 and 2012. 

Cell culture and antigen preparation for IFAT

Tachyzoites of N. caninum (NC-Bahia strain) were used as antigen for IFAT reactions. The parasites were maintained in monolayers of VERO cells, cultured with RPMI-1650 + L-glutamin (Invitrogen/Gibco®, New York, USA), supplemented with antibiotic-antimycotic:100 units/mL of penicillin, 100 µg/mL of streptomycin and 0.25 µg/mL of Fungizone®-amphotericin B (Gibco®, USA), 10% of inactivate calf serum (Invitrogen/Gibco®, Auck-land, NZ) at 37 °C in 5% CO2. Tachyzoites were harvested with a cell scraper when approximately 2/3 of cell mono-layer was disrupted by the parasites. The harvested suspensions were centrifuged at 1000 × g for 10 min at 4 °C, resuspended in filtered phosphate buffered saline (PBS) pH 7.2, passed through a 22-Gauge needle and purified using a 5µl-syringe filter. The filtered zoites were washed three times with sterile PBS (pH 7.2), placed in 5mm-well slides, and fixed by methanol for 5 min. The slides were stored at –20 °C no more than 2 months until used.

Indirect immunofluorescence antibody test (IFAT)

The samples were analyzed in a second time by a different person. The number of sera included in the analysis was 499, because one of the 500 samples was in small amount and in insufficient for other tests. At this time, NC-1 tachyzoites were used as antigens and the samples were examined according to methods described by Schares et al. (1999). Positive and negative controls from a N. caninum-positive bovine were used in each antigen slide.

1D SDS PAGE and immunoblot using N. caninum antigen

Tachyzoites of the N. caninum strain NC-1 (DUBEY et al., 1988) were cultured similarly as described above, but Marc-145 was employed as host cells with DMEM as culture medium. The parasites were separated from the host cells using 5µm filter and pelleted by centrifugation. A pellet containing 4.8 × 108 tachyzoites was used for antigen preparation. The SDS PAGE and immunoblot were performed according to Schares et al. (1998). The parasites were mixed with a sample buffer (2% SDS, 10% glycerol, 62 mM TrisHCl, pH 6.8), heated at 97 °C for 10 min, and centrifuged for 13,000g for 10 min at 4 °C. The supernatant containing antigen and a protein marker were run on a SDS-polyacrilamide gel (12.5%) and transferred to a Polyvinylidene difluoride (PVDF) membrane. The membrane was blocked with PBS Tween (PBS-T) (0.05% Tween 20) containing 2% of gelatin (PBS-T-Gelatin), and cut in stripes of approximately 2mm of width.

The donkey sera (499 samples) were diluted 1:100 and incubated with the antigen stripes at room temperature under agitation for 1h. Positive and negative controls from bovine were included in each analysis at 1:500 dilutions. The membranes were washed 5 times in PBS-T, and a peroxidase conjugate anti-donkey IgG in PBS-T-Gelatin was added to the reactions. A peroxidase anti-bovine IgG conjugate was employed for the bovine sera. The membranes were incubated for 1h, washed 3 times with PBS-T, 3 times with PBS, then incubated with 4-Chloro-1-naftol in methanol (1:4 in PBS with 0.1% H2O2) as substrate. When the reactive bands were clearly seen, the reactions were stopped by adding water into the wells.

Results

Antibodies against Neospora spp. were initially detected by IFAT in 21.6% (108/500) of the donkeys. A second analysis was performed by a second veterinarian who noted that most positive reactions were in fact strong apical reactions and/or incomplete fluorescence around the surface of the tachyzoites. The number of true positive samples in the second analysis was 2/500 (0.4%). These reactions were characterized by complete fluorescence in the periphery of the tachyzoites. Both reactive samples had antibody titers of 100.

Immunoblot using non-reduced antigen of N. caninum was performed in all samples from donkeys. The two reactive samples observed by IFAT showed reactions against a 37kDa antigen (Figure 2).

Figure 2 Immunoblot using serum from a Neospora caninum-infected bovine (1), a negative control serum from bovine (2), and serum from a donkey which tested positive by IFAT for Neospora spp. with an antibody titer of 100 (3). Note the weak positive reaction of a band at approximately 37kDa. 

Discussion

In the current study, we tested the exposure of 500 donkeys to Neospora spp. Donkeys are closely related to horses and may be potentially infected by N. caninum and N. hughesi, which cause disease in horses (MARSH et al., 1998; PITEL et al., 2003). The donkey sera were analyzed by IFAT and immunoblot. Donkeys exhibited a low frequency of antibodies against Neospora sp. by IFAT. When tested by immunoblot using non-reduced antigen from N. caninum, two serum samples reacted against a 37kDa antigen.

It is important to note that 21.6% of the samples in the initial analysis were incorrectly interpreted as positive by IFAT. The examination of the tested sera by a second veterinarian revealed that most reactions assumed as positive in the first analysis were in fact apical and/or incomplete reactions, what caused confusion in the classification of the positive results. After immunoblot, two sera with IFAT titers of 100 recognized a 37kDa antigen, regarded as one of the immunodominant antigens of N. caninum (BARTA & DUBEY, 1992).

Neospora caninum is spread in cattle in Bahia state and has also been isolated from a naturally-infected dog in the same region (GONDIM et al., 2001; GONDIM et al., 1999). In the current study, the low frequency of antibodies observed in donkeys bred in Bahia, where dogs are commonly raised close to donkeys, is suggestive that Neospora spp. are of minor importance for this animal species. In a study performed in Italy, 11.8% of 238 donkeys were positive for Neospora spp. using a commercial competitive-inhibition ELISA (cELISA, VMRD, Inc., Pullman, WA, USA) for N. caninum (MACHAČOVÁ et al., 2013). In another study conducted in Iran, 100 sera from donkeys were tested by a Neospora modified agglutination test (N-MAT) and revealed 52% of reactive samples. Despite both techniques (cELISA and N-MAT) that were employed in the studies from Italy and Iran have been tested using other animal species (reviewed by BJORKMAN & UGGLA, 1999), they had not been tested before with sera from donkeys. It is uncertain whether the positive reactions truly represent exposure to Neospora spp. or are due to potential cross-reactivity to other cyst-forming coccidian from donkeys.

In the present work, the combination of IFAT and immunoblot using antigens derived from N. caninum tachyzoites is suggestive that only two of the 500 tested Brazilian donkeys were exposed to Neospora spp. However, Neospora spp. have never been reported in donkeys and the putative detection of antibodies to Neospora spp. in our study does not prove that the animals were infected by the parasites.

Four immunodominant antigens have been identified in immunoblot for N. caninum (16/17, 29, 37 and 46kDa) using non-reduced antigen from tachyzoites (BARTA & DUBEY, 1992). Sondgen et al. (2001) performed immunoblot using fetal fluids from aborted bovine fetuses and non-reduced antigen from N. caninum tachyzoites. These authors observed that the 37kDa, followed by the 29kDa antigens were the most frequently identified antigens by Neospora-positive animals.

We conclude that, up to this date, there is no strong serologic evidence that Neospora spp. is able to infect donkeys. We used a quite large sample size and two serologic techniques, but only two animals were reactive with low antibody titers by IFAT. In addition, their sera recognized only one N. caninum immunodominant antigen of 37kDa by immunoblot. Further studies are necessary to confirm whether N. caninum and N. hughesi are able to infect donkeys.

Acknowledgements

This study was supported by Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) from Brazil, and partially granted by funds from the Alexander von Humboldt Foundation, Germany. We thank to Müller R. Andrade and Rogério F. Jesus for excellent technical assistance. We are thankful to Marta M. Nascimento for helping with the geographical data.

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Received: May 06, 2015; Accepted: June 01, 2015

*Corresponding author: Luís Fernando Pita Gondim. Departamento de Anatomia, Escola de Medicina Veterinária e Zootecnia, Patologia e Clínicas, Universidade Federal da Bahia - UFBA, Av. Adhemar de Barros, 500, Ondina, CEP 40170-110, Salvador, BA, Brasil. e-mail: pita@ufba.br

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