Neospora spp. Seroprevalence and Risk Factors for Seropositivity in Apparently Healthy Horses and Pregnant Mares
Abstract
:Simple Summary
Abstract
1. Introduction
2. Materials and Methods
2.1. Experiment Design
2.2. Study Population
2.3. Anti-Neospora spp. Antibodies Detection by Indirect Fluorescent Antibody Test (IFAT)
2.4. Statistical Analysis
3. Results
3.1. Exposure to Neospora spp. in the First Study Population (Apparently Healthy Horses)
3.1.1. Seroprevalence of Neospora spp.
3.1.2. Risks Factors Associated with Neospora spp. Infection
3.2. Neospora spp. Exposure in Mares during and after Pregnancy
3.2.1. Seroprevalence to Neospora spp. and Pregnancy Follow up
3.2.2. Variations in Anti-Neospora Antibody Titers during and after Gestation
3.2.3. Risk Factors Associated with Neospora spp. Infection in Pregnant Mares
4. Discussion
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
- Dubey, J.P.; Schares, G.; Ortega-Mora, L.M. Epidemiology and control of neosporosis and Neospora caninum. Clin. Microbiol. Rev. 2007, 20, 323–367. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Donahoe, S.L.; Lindsay, S.A.; Krockenberger, M.; Phalen, D.; Šlapeta, J. A review of neosporosis and pathologic findings of Neospora caninum infection in wildlife. Int. J. Parasitol. Parasites Wildl. 2015, 4, 216–238. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Kligler, E.B.; Shkap, V.; Baneth, G.; Mildenberg, Z.; Steinman, A. Seroprevalence of Neospora spp. among asymptomatic horses, aborted mares and horses demonstrating neurological signs in Israel. Vet. Parasitol. 2007, 148, 109–113. [Google Scholar] [CrossRef] [PubMed]
- Pusterla, N. EPM’s Lesser-Known Cause: N. hughesi. Article, Diseases and Conditions, Equine Protozoal Myeloencephalitis (EPM), Horse Care, Neurologic Disease. The HORSE Your Guide to Equine Health Care. 2014. Available online: https://thehorse.com/149902/epms-lesser-known-cause-n-hughesi/ (accessed on 14 October 2014).
- Nematollahi, A.; Jaafari, R.; Moghaddam, G. Seroprevalence of Neospora caninum infection in dairy cattle in Tabriz, Northwest Iran. Iran. J. Parasitol. 2011, 6, 95. [Google Scholar]
- Gondim, L.F.; Lindsay, D.S.; McAllister, M.M. Canine and bovine Neospora caninum control sera examined for cross-reactivity using Neospora caninum and Neospora hughesi indirect fluorescent antibody tests. J. Parasitol. 2009, 95, 86–88. [Google Scholar] [CrossRef]
- Gupta, G.D.; Lakritz, J.; Kim, J.H.; Kim, D.Y.; Kim, J.K.; Marsh, A.E. Seroprevalence of Neospora, Toxoplasma gondii and Sarcocystis neurona antibodies in horses from Jeju island, South Korea. Vet. Parasitol. 2002, 106, 193–201. [Google Scholar] [CrossRef]
- Hoane, J.S.; Gennari, S.M.; Dubey, J.; Ribeiro, M.G.; Borges, A.S.; Yai, L.E.; Aguiar, D.M.; Cavalcante, G.T.; Bonesi, G.L.; Howe, D.K. Prevalence of Sarcocystis neurona and Neospora spp. infection in horses from Brazil based on presence of serum antibodies to parasite surface antigen. Vet. Parasitol. 2006, 136, 155–159. [Google Scholar] [CrossRef]
- Cheadle, M.A.; Lindsay, D.S.; Rowe, S.; Dykstra, C.C.; Williams, M.A.; Spencer, J.A.; Toivio-Kinnucan, M.A.; Lenz, S.D.; Newton, J.C.; Rolsma, M.D.; et al. Prevalence of antibodies to Neospora sp. in horses from Alabama and characterisation of an isolate recovered from a naturally infected horse [corrected]. Int. J. Parasitol. 1999, 29, 1537–1543. [Google Scholar] [CrossRef]
- Pitel, P.H.; Pronost, S.; Romand, S.; Thulliez, P.; Fortier, G.; Ballet, J.J. Prevalence of antibodies to Neospora caninum in horses in France. Equine Vet. J. 2001, 33, 205–207. [Google Scholar] [CrossRef]
- Vardeleon, D.; Marsh, A.E.; Thorne, J.G.; Loch, W.; Young, R.; Johnson, P.J. Prevalence of Neospora hughesi and Sarcocystis neurona antibodies in horses from various geographical locations. Vet. Parasitol. 2001, 95, 273–282. [Google Scholar] [CrossRef]
- Mazuz, M.L.; Mimoun, L.; Schvartz, G.; Tirosh-Levy, S.; Savitzki, I.; Edery, N.; Blum, S.E.; Baneth, G.; Pusterla, N.; Steinman, A. Detection of Neospora caninum infection in aborted equine fetuses in Israel. Pathogens 2020, 9, 962. [Google Scholar] [CrossRef]
- Dubey, J.P.; Schares, G. Neosporosis in animals—The last five years. Vet. Parasitol. 2011, 180, 90–108. [Google Scholar] [CrossRef]
- Dubey, J.P.; Buxton, D.; Wouda, W. Pathogenesis of bovine neosporosis. J. Comp. Pathol. 2006, 134, 267–289. [Google Scholar] [CrossRef]
- Antonello, A.M.; Pivoto, F.L.; Camillo, G.; Braunig, P.; Sangioni, L.A.; Pompermayer, E.; Vogel, F.S.F. The importance of vertical transmission of Neospora sp. in naturally infected horses. Vet. Parasitol. 2012, 187, 367–370. [Google Scholar] [CrossRef] [Green Version]
- Pusterla, N.; Conrad, P.A.; Packham, A.E.; Mapes, S.M.; Finno, C.J.; Gardner, I.A.; Wilson, W.D. Endogenous Transplacental Transmission of Neospora hughesi in Naturally Infected Horses. J. Parasitol. 2011, 97, 281–285. [Google Scholar] [CrossRef]
- Anderson, J.A.; Alves, D.A.; Cezar, C.C.; da Silva, A.F.; Murata, F.H.A.; Norris, J.; Howe, D.K.; Dubey, J.P. Histologically, immunohistochemically, ultrastructurally, and molecularly confirmed neosporosis abortion in an aborted equine fetus. Vet. Parasitol. 2019, 270, 20–24. [Google Scholar] [CrossRef]
- Bártová, E.; Sedlák, K.; Kobédová, K.; Budíková, M.; Atuman, Y.J.; Kamani, J. Seroprevalence and risk factors of Neospora spp. and Toxoplasma gondii infections among horses and donkeys in Nigeria, West Africa. Acta Parasitol. 2017, 62, 606–609. [Google Scholar] [CrossRef]
- de Araújo Valença, S.R.F.; Valença, R.M.B.; Junior, J.W.P.; de Albuquerque, P.P.F.; Neto, O.L.S.; Mota, R.A. Risk factors for occurrence of anti-Neospora spp. antibodies in horses from Alagoas, Brazil. J. Equine Vet. Sci. 2015, 35, 917–921. [Google Scholar] [CrossRef]
- Padilla-Díaz, K.J.; Medina-Esparza, L.; Cruz-Vazquez, C.; Vitela-Mendoza, I.; Gomez-Leyva, J.F.; Quezada-Tristan, T. Detection of anti-Neospora spp. antibodies associated with different risk factors in horses from Mexico. Rev. Mex. Cienc. Pecu. 2021, 12, 194–204. [Google Scholar] [CrossRef]
- Talafha, A.Q.; Abutarbush, S.M.; Rutley, D.L. Seroprevalence and potential risk factors associated with Neospora spp. infection among asymptomatic horses in Jordan. Korean J. Parasitol. 2015, 53, 163. [Google Scholar] [CrossRef] [Green Version]
- Silva, R.C.; Machado, G.P. Canine neosporosis: Perspectives on pathogenesis and management. Vet. Med. Res. Rep. 2016, 7, 59. [Google Scholar] [CrossRef]
- Schares, G.; Bärwald, A.; Staubach, C.; Ziller, M.; Klöss, D.; Schröder, R.; Labohm, R.; Dräger, K.; Fasen, W.; Hess, R.G.; et al. Potential risk factors for bovine Neospora caninum infection in Germany are not under the control of the farmers. Parasitology 2004, 129, 301. [Google Scholar] [CrossRef]
- McAllister, M.M.; Dubey, J.P.; Lindsay, D.S.; Jolley, W.R.; Wills, R.A.; McGuire, A.M. Rapid communication: Dogs are definitive hosts of Neospora caninum. Int. J. Parasitol. 1998, 28, 1473–1479. [Google Scholar] [CrossRef]
- Gondim, L.F.; McAllister, M.M.; Pitt, W.C.; Zemlicka, D.E. Coyotes (Canis latrans) are definitive hosts of Neospora caninum. Int. J. Parasitol. 2004, 34, 159–161. [Google Scholar] [CrossRef] [Green Version]
- King, J.S.; Šlapeta, J.; Jenkins, D.J.; Al-Qassab, S.E.; Ellis, J.T.; Windsor, P.A. Australian dingoes are definitive hosts of Neospora caninum. Int. J. Parasitol. 2010, 40, 945–950. [Google Scholar] [CrossRef] [PubMed]
- Eastick, F.A.; Elsheikha, H.M. Stress-driven stage transformation of Neospora caninum. Parasitol. Res. 2010, 106, 1009–1014. [Google Scholar] [CrossRef]
- Quinn, H.E.; Ellis, J.T.; Smith, N.C. Neospora caninum: A cause of immune-mediated failure of pregnancy? Trends Parasitol. 2002, 18, 391–394. [Google Scholar] [CrossRef]
Risk Factor | N | Cutoff Titer 1:50 | Cutoff Titer 1:200 | |||
---|---|---|---|---|---|---|
N Positive (%) | p Value | N Positive (%) | p Value | |||
Sex | Mare | 161 | 39 (24.2) | 0.580 | 14 (8.7) | 0.323 |
Gelding | 165 | 38 (23) | 8 (4.8) | |||
Stallion | 8 | 3 (37.5) | 0 (0) | |||
Breed | Mixed | 152 | 39 (25.7) | 0.107 | 9 (5.9) | 0.657 |
American | 76 | 16 (21.1) | 4 (5.3) | |||
Pony | 19 | 6 (31.6) | 2 (10.5) | |||
European | 20 | 3 (15) | 2 (10) | |||
Draft | 2 | 1 (33.3) | 0 (0) | |||
Arab | 44 | 14 (31.8) | 5 (11.4) | |||
Gaited | 13 | 0 (0) | 0 (0) | |||
Andalus | 1 | 1 (100) | 0 (0) | |||
Mixed vs. Pure-bred | Mixed | 152 | 39 (25.7) | 0.619 | 9 (5.9) | 0.597 |
Pure-bred | 176 | 41 (23.3) | 13 (7.4) | |||
Geographical area | North | 157 | 37 (23.6) | 0.645 | 9 (5.7) | 0.544 |
Center | 88 | 24 (27.3) | 8 (9.1) | |||
South | 89 | 19 (21.3) | 5 (5.6) | |||
Housing | Stall | 112 | 19 (17) | 0.033 | 4 (3.6) | 0.068 |
Stall and paddock | 86 | 30 (34.9) | 11 (12.8) | |||
Paddock | 78 | 18 (23.1) | 5 (6.4) | |||
Pasture | 58 | 13 (22.4) | 2 (3.4) |
Horse Serology Titer for Neospora spp. | N (%) * | Horse Age Mean | Standard Error (SE) | p Value |
---|---|---|---|---|
Negative | 250 (75.8) | 11.33 | 0.67 | |
Positive (cut-off titer 1:50) | 80 (24.2) | 13.06 | 0.38 | 0.026 |
Positive (cut-off titer 1:200) | 22 (6.7) | 13.14 | 1.08 | 0.265 |
Total ** | 330 | 11.7 | 0.332 |
Mare Serum Antibody Titers | Number of Mares | Pregnancy Outcome * | |
---|---|---|---|
During Pregnancy | After Parturition | ||
Negative | Negative | 19 | 17 normal parturitions 1 dystocia 1 absorption |
1:50 | 6 | normal parturition | |
1:100 | 5 | normal parturition | |
1:200 | 3 | normal parturition | |
1:50 | Negative | 21 | normal parturition |
1:50 | 10 | 9 normal parturitions 1 abortion during the 6th month | |
1:100 | 6 | normal parturition | |
1:200 | 2 | normal parturition | |
1:100 | Negative | 12 | normal parturition |
1:50 | 8 | 7 normal parturitions 1 abortion during the 7th month | |
1:100 | 7 | normal parturition | |
1:200 | 2 | normal parturition | |
1:200 | Negative | 3 | normal parturition |
1:50 | 1 | normal parturition | |
1:100 | 1 | 1 abortion during the 10th month | |
1:200 | 1 | normal parturition | |
Total | 107 |
Risk Factor * | Neospora spp. Seroprevalence in Pregnant Mares | Neospora spp. Seroprevalence in Mares after Parturition | |||||
---|---|---|---|---|---|---|---|
N1 | Positive (%) | p1 | N2 | Positive (%) | p2 | ||
Breed | Arab | 81 | 64 (79.0) | 0.005 | 61 | 37 (60.7) | 0.019 |
Mixed | 7 | 3 (42.9) | 6 | 2 (33.3) | |||
Other, pure-bred | 29 | 15 (51.7) | 19 | 5 (26.3) | |||
Housing | Stall | 57 | 39 (68.4) | 0.616 | 40 | 22 (55.0) | 0.264 |
Paddock ** | 87 | 56(64.4) | 64 | 28 (43.8) | |||
Pregnancies in the past | 0 | 18 | 10 (55.6) | 0.280 | 13 | 9 (69.2) | 0.654 |
1 | 18 | 14 (77.8) | 12 | 6 (50.0) | |||
2 or more | 32 | 24 (75.0) | 26 | 15 (57.7) | |||
Abortion history *** | No previous abortion | 83 | 54 (65.1) | 1.00 | 62 | 28 (45.2) | 0.824 |
Previous abortion | 14 | 9 (64.3) | 12 | 5 (41.7) | |||
Food storage condition | Open field | 51 | 32 (62.7) | 0.997 | 41 | 25 (61) | 0.099 |
Enclosed space | 59 | 37 (62.7) | 42 | 18 (42.9) | |||
Presence of cattle next to the farm | Yes | 27 | 21 (77.8) | 0.076 | 25 | 14 (56.0) | 0.314 |
No | 98 | 58 (59.2) | 70 | 31 (44.3) | |||
Presence of dogs in the farm | Yes | 114 | 72 (63.2) | 0.354 | 84 | 42 (50.0) | 0.070 |
No | 16 | 12 (75) | 13 | 3 (23.1) | |||
Food access by canids | Yes | 68 | 40 (58.8) | 0.187 | 55 | 30 (54.5) | 0.188 |
No | 54 | 38 (70.4) | 37 | 15 (40.5) | |||
Geographical location | North | 33 | 24 (72.7) | 0.635 | 28 56 23 | 14 (50.0) | 0.622 |
Center | 91 | 58 (63.7) | 25 (44.6) | ||||
South | 28 | 19 (67.9) | 13 (56.5) | ||||
Total | 152 | 101 (66.4) | 107 | 52 (48.6) |
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Mimoun, L.; Steinman, A.; Kliachko, Y.; Tirosh-Levy, S.; Schvartz, G.; Blinder, E.; Baneth, G.; Mazuz, M.L. Neospora spp. Seroprevalence and Risk Factors for Seropositivity in Apparently Healthy Horses and Pregnant Mares. Animals 2022, 12, 2699. https://doi.org/10.3390/ani12192699
Mimoun L, Steinman A, Kliachko Y, Tirosh-Levy S, Schvartz G, Blinder E, Baneth G, Mazuz ML. Neospora spp. Seroprevalence and Risk Factors for Seropositivity in Apparently Healthy Horses and Pregnant Mares. Animals. 2022; 12(19):2699. https://doi.org/10.3390/ani12192699
Chicago/Turabian StyleMimoun, Lea, Amir Steinman, Ynon Kliachko, Sharon Tirosh-Levy, Gili Schvartz, Elena Blinder, Gad Baneth, and Monica Leszkowicz Mazuz. 2022. "Neospora spp. Seroprevalence and Risk Factors for Seropositivity in Apparently Healthy Horses and Pregnant Mares" Animals 12, no. 19: 2699. https://doi.org/10.3390/ani12192699
APA StyleMimoun, L., Steinman, A., Kliachko, Y., Tirosh-Levy, S., Schvartz, G., Blinder, E., Baneth, G., & Mazuz, M. L. (2022). Neospora spp. Seroprevalence and Risk Factors for Seropositivity in Apparently Healthy Horses and Pregnant Mares. Animals, 12(19), 2699. https://doi.org/10.3390/ani12192699