Scientific reports2023; 13(1); 20242; doi: 10.1038/s41598-023-47601-y

Seroprevalence and risk factors for Neospora spp. infection in equine in Egypt.

Abstract: Neospora infections in equine are associated with reproductive disorders and neurological diseases. Nevertheless, Egypt has no epidemiological information on this parasite in equine. This study determined the prevalence of Neospora spp. infection in 325 equines from three Egyptian governorates located at Northern Egypt using cELISA. The prevalence of antibodies against Neospora spp. was 19% (95% CI: 14.09-25.05) in horse, 34.1% (95%CI: 24.92-44.69) in donkey and 26.7% (95% CI: 15.97-41.04) in mule. In comparison to horse, donkey had a considerably higher chance of contracting Neospora spp. infection (OR = 1.80, 95% CI: 0.78-4.13; P = 0.016). The risk was also higher in freely grazing animals (OR = 3.49, 95% CI: 0.95-12.78; P = 0.059). Moreover, yearling animals (12-24 months) (OR = 5.03, 95% CI: 1.51-16.80; P = 0.009) and those with natural breeding (OR = 11.80, 95% CI: 3.24-42.99, P < 0.0001) and a history of early abortion (OR = 7.04, 95% CI: 3.01-16.47; P < 0.0001) also showed a greater risk of seropositivity. The risk of Neospora infection increased significantly in equines contacted with dogs (OR = 5.16, 95% CI: 1.76-15.10; P = 0.003). This the first serological study to determine the seroprevalence of Neospora spp. in equine in Egypt. Further studies are necessary to identify the species of Neospora and to understand the role of above-mentioned risk factors in spreading of infection.
Publication Date: 2023-11-19 PubMed ID: 37981658PubMed Central: PMC10658168DOI: 10.1038/s41598-023-47601-yGoogle Scholar: Lookup
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  • Journal Article

Summary

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This study explores the prevalence and risk factors of Neospora infection, a parasite linked to reproductive and neurological issues, in horses, donkeys, and mules in Northern Egypt. Results showed varying rates of the infection in different animals, with donkeys showing higher chances of infection. Several risk factors associated with increased prevalence were identified.

Study Overview and Objectives

  • The study wanted to assess the prevalence of Neospora spp. infections in equines in Egypt, a topic on which no previous epidemiological information existed.
  • Neospora infections can lead to severe reproductive and neurological diseases, potentially affecting the health and productivity of equines.
  • The study employed competitive enzyme-linked immunosorbent assay (cELISA) for detecting Neospora infections in equines across three Egyptian governorates.

Key Findings

  • The overall prevalence of Neospora spp. infection was found to be 19% in horses, 34.1% in donkeys, and 26.7% in mules.
  • The infection was much higher in donkeys as compared to horses, with an odds ratio of 1.80.
  • Freely grazing animals were found to have a significantly higher risk of infection, with an odds ratio of 3.49.
  • Young animals between 12 to 24 months (yearlings) and those with natural breeding practices were at greater risk of infection.
  • Those equines having a history of early abortion also showed a higher risk.
  • Significantly, the risk of Neospora infection was found to be higher in equines that had contacts with dogs.

Implications of the Findings

  • The study offers initial insights into the prevalence of Neospora infections in equines in Egypt, a topic previously unexplored.
  • These findings can help in adopting informed precautions and prevention measures directed towards identified high-risk groups – namely, donkeys, young animals, freely grazing animals, naturally bred ones, and those equines with a history of early abortion.
  • Moreover, the finding on the link between Neospora infection and contact with dogs suggests a useful clue for future studies to investigate the role of dogs in spreading the infection.
  • The authors recommend further research to identify the precise species of Neospora and to better understand the role of the identified risk factors in spreading the infection.

Cite This Article

APA
Alshammari A, Gattan HS, Marzok M, Selim A. (2023). Seroprevalence and risk factors for Neospora spp. infection in equine in Egypt. Sci Rep, 13(1), 20242. https://doi.org/10.1038/s41598-023-47601-y

Publication

ISSN: 2045-2322
NlmUniqueID: 101563288
Country: England
Language: English
Volume: 13
Issue: 1
Pages: 20242
PII: 20242

Researcher Affiliations

Alshammari, Ayed
  • Department of Biology, College of Science, University of Hafr Al-Batin, Hafr Al-Batin, Saudi Arabia.
Gattan, Hattan S
  • Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King AbdulAziz University, Jeddah, Saudi Arabia.
  • Special Infectious Agents Unit, King Fahad Medical Research Center, King AbdulAziz University, Jeddah, Saudi Arabia.
Marzok, Mohamed
  • Department of Clinical Sciences, College of Veterinary Medicine, King Faisal University, 31982, Al-Ahsa, Saudi Arabia. mmarzok@kfu.edu.sa.
  • Department of Surgery, Faculty of Veterinary Medicine, Kafr El Sheikh University, Kafr El Sheikh, Egypt. mmarzok@kfu.edu.sa.
Selim, Abdelfattah
  • Department of Animal Medicine (Infectious Diseases), Faculty of Veterinary Medicine, Benha University, Toukh, 13736, Egypt. Abdelfattah.selim@fvtm.bu.edu.eg.

MeSH Terms

  • Female
  • Pregnancy
  • Horses
  • Animals
  • Dogs
  • Neospora
  • Seroepidemiologic Studies
  • Egypt / epidemiology
  • Risk Factors
  • Equidae

Conflict of Interest Statement

The authors declare no competing interests.

References

This article includes 64 references
  1. Dubey J, Schares G, Ortega-Mora L. Epidemiology and control of neosporosis and Neospora caninum. Clin. Microbiol. Rev. 2007;20:323u2013367. doi: 10.1128/CMR.00031-06.
    doi: 10.1128/CMR.00031-06pmc: PMC1865591pubmed: 17428888google scholar: lookup
  2. Vardeleon D, et al. Prevalence of Neospora hughesi and Sarcocystis neurona antibodies in horses from various geographical locations. Vet. Parasitol. 2001;95:273u2013282. doi: 10.1016/S0304-4017(00)00393-9.
    doi: 10.1016/S0304-4017(00)00393-9pubmed: 11223207google scholar: lookup
  3. Khan A, Shaik JS, Sikorski P, Dubey JP, Grigg ME. Neosporosis: An overview of its molecular epidemiology and pathogenesis. Engineering. 2020;6:10u201319. doi: 10.1016/j.eng.2019.02.010.
    doi: 10.1016/j.eng.2019.02.010google scholar: lookup
  4. Antonello AM, et al. The importance of vertical transmission of Neospora sp. in naturally infected horses. Vet. Parasitol. 2012;187:367u2013370. doi: 10.1016/j.vetpar.2012.02.005.
    doi: 10.1016/j.vetpar.2012.02.005pubmed: 22436425google scholar: lookup
  5. Kligler EB, 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;148:109u2013113. doi: 10.1016/j.vetpar.2007.06.002.
    doi: 10.1016/j.vetpar.2007.06.002pubmed: 17614202google scholar: lookup
  6. Villalobos EMC, et al. Association between the presence of serum antibodies against Neospora spp. and fetal loss in equines. Vet. Parasitol. 2006;142:372u2013375. doi: 10.1016/j.vetpar.2006.07.016.
    doi: 10.1016/j.vetpar.2006.07.016pubmed: 16962708google scholar: lookup
  7. Pusterla N, et al. Endogenous transplacental transmission of Neospora hughesi in naturally infected horses. J. Parasitol. 2011;97:281u2013285. doi: 10.1645/ge-2657.1.
    doi: 10.1645/ge-2657.1pubmed: 21506870google scholar: lookup
  8. Dubey JP. Review of Neospora caninum and neosporosis in animals. Korean J. Parasitol. 2003;41:1u201316. doi: 10.3347/kjp.2003.41.1.1.
    doi: 10.3347/kjp.2003.41.1.1pmc: PMC2717477pubmed: 12666725google scholar: lookup
  9. Wobeser BK, Godson DL, Rejmanek D, Dowling P. Equine protozoal myeloencephalitis caused by Neospora hughesi in an adult horse in Saskatchewan. Can. Vet. J. 2009;50:851u2013853.
    pmc: PMC2711471pubmed: 19881924
  10. Nematollahi A, Jaafari R, Moghaddam G. Seroprevalence of Neospora caninum infection in dairy cattle in Tabriz, Northwest Iran. Iran. J. Parasitol. 2011;6:95.
    pmc: PMC3279911pubmed: 22347319
  11. Gondim LF, Lindsay DS, McAllister MM. Canine and bovine Neospora caninum control sera examined for cross-reactivity using Neospora caninum and Neospora hughesi indirect fluorescent antibody tests. J. Parasitol. 2009;95:86u201388. doi: 10.1645/GE-1710.1.
    doi: 10.1645/GE-1710.1pubmed: 18613752google scholar: lookup
  12. Gupta G, et al. Seroprevalence of Neospora, Toxoplasma gondii and Sarcocystis neurona antibodies in horses from Jeju island, South Korea. Vet. Parasitol. 2002;106:193u2013201. doi: 10.1016/S0304-4017(02)00064-X.
    doi: 10.1016/S0304-4017(02)00064-Xpubmed: 12062508google scholar: lookup
  13. Cheadle M, 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;29:1537u20131543. doi: 10.1016/S0020-7519(99)00140-X.
    doi: 10.1016/S0020-7519(99)00140-Xpubmed: 10608440google scholar: lookup
  14. Hoane JS, et al. 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;136:155u2013159. doi: 10.1016/j.vetpar.2005.10.023.
    doi: 10.1016/j.vetpar.2005.10.023pubmed: 16310955google scholar: lookup
  15. Pitel PH, et al. Prevalence of antibodies to Neospora caninum in horses in France. Equine Vet. J. 2001;33:205u2013207. doi: 10.1111/j.2042-3306.2001.tb00602.x.
  16. Reisberg K, Selim AM, Gaede W. Simultaneous detection of Chlamydia spp., Coxiella burnetii, and Neospora caninum in abortion material of ruminants by multiplex real-time polymerase chain reaction. J. Vet. Diagn. Investig. 2013;25:614u2013619. doi: 10.1177/1040638713497483.
    doi: 10.1177/1040638713497483pubmed: 23942900google scholar: lookup
  17. Selim A, Manaa E, Khater H. Molecular characterization and phylogenetic analysis of lumpy skin disease in Egypt. Compar. Immunol. Microbiol. Infect. Dis. 2021;79:101699. doi: 10.1016/j.cimid.2021.101699.
    doi: 10.1016/j.cimid.2021.101699pubmed: 34461343google scholar: lookup
  18. Selim AM, Elhaig MM, Gaede W. Development of multiplex real-time PCR assay for the detection of Brucella spp., Leptospira spp. and Campylobacter foetus. Vet. Ital. 2014;50:75.
    pubmed: 25546064
  19. Selim A, Abdelrahman A, Thiu00e9ry R, Sidi-Boumedine K. Molecular typing of Coxiella burnetii from sheep in Egypt. Compar. Immunol. Microbiol. Infect. Dis. 2019;67:101353. doi: 10.1016/j.cimid.2019.101353.
    doi: 10.1016/j.cimid.2019.101353pubmed: 31605891google scholar: lookup
  20. Waldner CL, Henderson J, Wu J, Breker K, Chow E. Reproductive performance of a cow-calf herd following a Neospora caninum-associated abortion epidemic. Can. Vet. J. 2001;42:355.
    pmc: PMC1476502pubmed: 11360856
  21. Wu JT, Dreger S, Chow EY, Bowlby EE. Validation of 2 commercial Neospora caninum antibody enzyme linked immunosorbent assays. Can. J Vet. Res. 2002;66:264.
    pmc: PMC227014pubmed: 12418782
  22. El-Ghaysh A, Khalil F, Hilali M, Nassar A. Serological diagnosis of Neospora caninum infection in some domestic animals from Egypt. Vet. Med. J.-Giza. 2003;51:355u2013362.
  23. Selim A, Khater H, Almohammed HI. A recent update about seroprevalence of ovine neosporosis in Northern Egypt and its associated risk factors. Sci. Rep. 2021;11:14043. doi: 10.1038/s41598-021-93596-9.
    doi: 10.1038/s41598-021-93596-9pmc: PMC8263615pubmed: 34234210google scholar: lookup
  24. Selim A, Abdelhady A. Neosporosis among Egyptian camels and its associated risk factors. Trop. Anim. Health Prod. 2020;52:3381u20133385. doi: 10.1007/s11250-020-02370-y.
    doi: 10.1007/s11250-020-02370-ypubmed: 32929587google scholar: lookup
  25. Ibrahim HM, et al. Prevalence of Neospora caninum and Toxoplasma gondii antibodies in Northern Egypt. Am. J. Trop. Med. Hygiene. 2009;80:263u2013267. doi: 10.4269/ajtmh.2009.80.263.
    doi: 10.4269/ajtmh.2009.80.263pubmed: 19190225google scholar: lookup
  26. Metwally S, Hamada R, Sobhy K, Frey CF, Fereig RM. Seroprevalence and risk factors analysis of Neospora caninum and Toxoplasma gondii in cattle of Beheira, Egypt. Front. Vet. Sci. 2023;10:1122092. doi: 10.3389/fvets.2023.1122092.
    doi: 10.3389/fvets.2023.1122092pmc: PMC9968803pubmed: 36861008google scholar: lookup
  27. Nazir MM, et al. Prevalence and risk factors for IgG antibodies to Neospora spp. in three types of equids from Southern Punjab, Pakistan. Acta Trop. 2018;188:240u2013243. doi: 10.1016/j.actatropica.2018.09.007.
  28. Selim AM, Elhaig MM, Moawed SA, El-Nahas E. Modeling the potential risk factors of bovine viral diarrhea prevalence in Egypt using univariable and multivariable logistic regression analyses. Vet. World. 2018;11:259. doi: 10.14202/vetworld.2018.259-267.
  29. Said MB, et al. Molecular epidemiological survey, genetic characterization and phylogenetic analysis of Anaplasma ovis infecting sheep in Northern Egypt. Acta Trop. 2022;229:106370. doi: 10.1016/j.actatropica.2022.106370.
  30. Selim A, et al. Prevalence and animal level risk factors associated with Trypanosoma evansi infection in dromedary camels. Sci. Rep. 2022;12:8933. doi: 10.1038/s41598-022-12817-x.
    doi: 10.1038/s41598-022-12817-xpmc: PMC9142598pubmed: 35624132google scholar: lookup
  31. Selim A, Attia KA, Alsubki RA, Kimiko I, Sayed-Ahmed MZ. Cross-sectional survey on Mycobacterium avium Subsp. paratuberculosis in Dromedary Camels: Seroprevalence and risk factors. Acta Trop. 2022;226:106261. doi: 10.1016/j.actatropica.2021.106261.
  32. Selim A, Manaa EA, Alanazi AD, Alyousif MS. Seroprevalence, risk factors and molecular identification of bovine leukemia virus in Egyptian cattle. Animals. 2021;11:319. doi: 10.3390/ani11020319.
    doi: 10.3390/ani11020319pmc: PMC7912176pubmed: 33513908google scholar: lookup
  33. Hosmer DW, Lemeshow S, Sturdivant RX. Introduction to the logistic regression model. Appl. Logist. Regress. 2000;2:1u201330.
  34. McCann CM, et al. Lack of serologic evidence of Neospora caninum in humans, England. Emerg. Infect. Dis. 2008;14:978. doi: 10.3201/eid1406.071128.
    doi: 10.3201/eid1406.071128pmc: PMC2600293pubmed: 18507920google scholar: lookup
  35. Dubey J, Hemphill A, Calero-Bernal R, Schares G. Neosporosis in Animals. CRC Press; 2017.
  36. Jakubek E-B, Lundu00e9n A, Uggla A. Seroprevalences of Toxoplasma gondii and Neospora sp. infections in Swedish horses. Vet. Parasitol. 2006;138:194u2013199. doi: 10.1016/j.vetpar.2006.02.002.
    doi: 10.1016/j.vetpar.2006.02.002pubmed: 16517077google scholar: lookup
  37. Javanmardi E, et al. Global seroprevalence of Neospora spp. in horses and donkeys: A systematic review and meta-analysis. Vet. Parasitol. 2020;288:109299. doi: 10.1016/j.vetpar.2020.109299.
    doi: 10.1016/j.vetpar.2020.109299pubmed: 33227673google scholar: lookup
  38. Selim A. Chlamydophila abortus infection in small ruminants: A review. Asian J. Anim. Vet. Adv. 2016;11:587u2013593. doi: 10.3923/ajava.2016.587.593.
  39. Bu00e1rtovu00e1 E, Sedlu00e1k K, Syrovu00e1 M, Literu00e1k I. Neospora spp. and Toxoplasma gondii antibodies in horses in the Czech Republic. Parasitol. Res. 2010;107:783u2013785. doi: 10.1007/s00436-010-1929-4.
    doi: 10.1007/s00436-010-1929-4pubmed: 20532561google scholar: lookup
  40. Moura ABD, et al. Neospora spp. antibodies in horses from two geographical regions of the state of Santa Catarina, Brazil. Rev. Bras. Parasitol. Vet. 2013;22:597u2013601. doi: 10.1590/S1984-29612013000400023.
  41. Patitucci A, Pu00e9rez M, Carcamo C, Baeza L. Presencia de anticuerpos sericos contra Neospora caninum en equinos en Chile. Arch. Med. Vet. 2004;36:203u2013206. doi: 10.4067/S0301-732X2004000200011.
  42. Ciaramella P, et al. Seroprevalence of Neospora spp. in asymptomatic horses in Italy. Vet. Parasitol. 2004;123:11u201315. doi: 10.1016/j.vetpar.2004.05.022.
    doi: 10.1016/j.vetpar.2004.05.022pubmed: 15265566google scholar: lookup
  43. Dangoudoubiyam S, et al. Detection of antibodies against Sarcocystis neurona, Neospora spp., and Toxoplasma gondii in horses from Costa Rica. J. Parasitol. 2011;97:522u2013524. doi: 10.1645/GE-2722.1.
    doi: 10.1645/GE-2722.1pubmed: 21506839google scholar: lookup
  44. Piantedosi D, et al. Seroprevalence of Neospora spp. in asymptomatic horses in Italy. Ippologia. 2009;20:3u20138.
    pubmed: 15265566
  45. Pitel P-H, et al. Investigation of Neospora sp. antibodies in aborted mares from Normandy, France. Vet. Parasitol. 2003;118:1u20136. doi: 10.1016/j.vetpar.2003.10.007.
    doi: 10.1016/j.vetpar.2003.10.007pubmed: 14651869google scholar: lookup
  46. Galvu00e3o CMMDQ, et al. Brazilian donkeys (Equus asinus) have a low exposure to Neospora spp. Rev. Bras. Parasitol. Vet. 2015;24:340u2013344. doi: 10.1590/S1984-29612015057.
    doi: 10.1590/S1984-29612015057pubmed: 26444065google scholar: lookup
  47. Gennari SM, et al. Prevalence of antibodies against Neospora spp. and Sarcocystis neurona in donkeys from northeastern Brazil. Rev. Brasil. Parasitol. Vet. 2016;25:109u2013111. doi: 10.1590/S1984-29612016003.
    doi: 10.1590/S1984-29612016003pubmed: 26982557google scholar: lookup
  48. Alvarado-Esquivel C, et al. Seroepidemiology of Sarcocystis neurona and Neospora hughesi infections in domestic donkeys (Equus asinus) in Durango, Mexico. Parasite. 2017;24:27. doi: 10.1051/parasite/2017030.
    doi: 10.1051/parasite/2017030pmc: PMC5520387pubmed: 28730993google scholar: lookup
  49. Cong W, et al. Prevalence of Neospora spp. in donkeys in China. Parasite. 2018;25:16. doi: 10.1051/parasite/2018018.
    doi: 10.1051/parasite/2018018pmc: PMC5859821pubmed: 29557777google scholar: lookup
  50. Gharekhani J, Tavoosidana G-R, Naderisefat G-R. Seroprevalence of Neospora infection in horses and donkeys in Hamedan province, Western Iran. Vet. World. 2013;6:620. doi: 10.5455/vetworld.2013.620-622.
  51. Machau010dovu00e1 T, et al. Seroprevalence and risk factors of Neospora spp. in donkeys from Southern Italy. Vet. Parasitol. 2013;198:201u2013204. doi: 10.1016/j.vetpar.2013.08.013.
    doi: 10.1016/j.vetpar.2013.08.013pubmed: 24050943google scholar: lookup
  52. Abd-Elmohsen M, Selim A, Abd-Elmoneim AE. Prevalence and molecular characterization of Lumpy Skin Disease in cattle. Benha Vet. Med. J. 2019;37:144u2013147.
  53. Elhaig MM, Selim A, Mandour AS, Schulz C, Hoffmann B. Prevalence and molecular characterization of peste des petits ruminants virus from Ismailia and Suez, Northeastern Egypt, 2014u20132016. Small Ruminant Res. 2018;169:94u201398. doi: 10.1016/j.smallrumres.2018.07.001.
  54. Selim A, Abdelhady A. The first detection of anti-West Nile virus antibody in domestic ruminants in Egypt. Trop. Anim. Health Prod. 2020;52:3147u20133151. doi: 10.1007/s11250-020-02339-x.
    doi: 10.1007/s11250-020-02339-xpubmed: 32588359google scholar: lookup
  55. Selim A, Ali A-F, Ramadan E. Prevalence and molecular epidemiology of Johneu2019s disease in Egyptian cattle. Acta Trop. 2019;195:1u20135. doi: 10.1016/j.actatropica.2019.04.019.
  56. Selim A, Attia K, Ramadan E, Hafez YM, Salman A. Seroprevalence and molecular characterization of Brucella species in naturally infected cattle and sheep. Prevent. Vet. Med. 2019;171:104756. doi: 10.1016/j.prevetmed.2019.104756.
  57. Baz MM, Selim A, Radwan IT, Alkhaibari AM, Khater HF. Larvicidal and adulticidal effects of some Egyptian oils against Culex pipiens. Sci. Rep. 2022;12:4406. doi: 10.1038/s41598-022-08223-y.
    doi: 10.1038/s41598-022-08223-ypmc: PMC8924206pubmed: 35292687google scholar: lookup
  58. Selim A, Elhaig M, Taha S, Nasr E. Antibacterial activity of silver nanoparticles against field and reference strains of Mycobacterium tuberculosis, Mycobacterium bovis and multiple-drug-resistant tuberculosis strains. Rev. Sci. Tech. OIE. 2018;37:823u2013830. doi: 10.20506/rst.37.3.2888.
    doi: 10.20506/rst.37.3.2888pubmed: 30964466google scholar: lookup
  59. Karatepe M, Karatepe B. Investigation of seroprevalence of Neospora spp. in horses in Niu011fde province (Turkey) Kafkas u00dcniv. Vet. Faku00fcltesi Derg. 2012;18:859.
  60. Bu00e1rtovu00e1 E, et al. Seroprevalence of antibodies of Neospora spp. and Toxoplasma gondii in horses from southern Italy. Folia Parasitol. 2015;62:1. doi: 10.14411/fp.2015.043.
    doi: 10.14411/fp.2015.043pubmed: 26278845google scholar: lookup
  61. Talafha AQ, Abutarbush SM, Rutley DL. Seroprevalence and potential risk factors associated with Neospora spp. infection among asymptomatic horses in Jordan. Korean J. Parasitol. 2015;53:163. doi: 10.3347/kjp.2015.53.2.163.
    doi: 10.3347/kjp.2015.53.2.163pmc: PMC4416377pubmed: 25925174google scholar: lookup
  62. Selim A, Marawan MA, Ali A-F, Manaa E, AbouelGhaut HA. Seroprevalence of bovine leukemia virus in cattle, buffalo, and camel in Egypt. Trop. Anim. Health Prod. 2020;52:1207u20131210. doi: 10.1007/s11250-019-02105-8.
    doi: 10.1007/s11250-019-02105-8pubmed: 31686339google scholar: lookup
  63. Selim A, Radwan A, Arnaout F, Khater H. The recent update of the situation of West Nile fever among equids in Egypt after three decades of missing information. Pak. Vet. J. 2020;40:100.
  64. de-Arau00fajo-Valenu00e7a SRF, et al. Risk factors for occurrence of anti-Neospora spp. antibodies in horses from Alagoas, Brazil. J. Equine Vet. Sci. 2015;35:917u2013921. doi: 10.1016/j.jevs.2015.08.014.

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