Analyze Diet
Folia parasitologica2024; 71; 2024.022; doi: 10.14411/fp.2024.022

Seroepidemiological study of Neospora caninum in equids using c-ELISA in Erbil Province, Iraq.

Abstract: Equine neosporosis is an intracellular protozoan disease with a global distribution, affecting a diverse range of warm-blooded animals. Neospora caninum Dubey, Carpenter, Speer, Topper et Uggla, 1988 is associated with foetal loss, neurological disease and abortion in equids. No information was available regarding equine N. caninum infection among equids in Iraq. Thus, the aim of this study was to determine the prevalence rate of N. caninum in equines by using a competitive enzyme-linked immunosorbent assay (c-ELISA). A total of 329 blood samples randomly selected from equines, comprising 268 horses and 61 donkeys were examined. The seroprevalence rate of N. caninum was determined as 46% (28/61) for donkeys and 24% (64/268) for horses. The prevalence of N. caninum indicated a significantly higher risk of infection in donkeys compared to horses (P < 0.001). However, the odds of N. caninum infection in draught equids were 8.2 times greater than other equids with a significant difference (P < 0.001). The current study revealed no significant differences in the prevalence of N. caninum across various genders, breeds, clinical statuses, disease histories and among equids that had contact with dogs. While outdoor feeding and mixed (grazing), showed a significant difference (P = 0.003) and (P = 0.75), respectively, in the presence of antibodies against N. caninum compared to indoor feeding (stable). Moreover, the odds of infection in equids with a history of late abortion were 4.8 times higher than those without such a history of abortion (2.20-10.56) with statistical significance (P < 0.001).
Publication Date: 2024-11-25 PubMed ID: 39632700DOI: 10.14411/fp.2024.022Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The study investigates the prevalence of the parasitic disease, neosporosis, in horses and donkeys in Erbil, Iraq, using a laboratory technique called competitive enzyme-linked immunosorbent assay (c-ELISA). The research reveals higher infection in donkeys compared to horses, and found a greater risk of infection in draught equids compared to other types.

Objective of the Study

  • The primary goal of this research was to determine the prevalence of the Neospora caninum parasite in equids (horses and donkeys) in Erbil, Iraq. This study was prompted by the lack of information about how frequently N. caninum infects horses and donkeys in this region.
  • The researchers chose to use the competitive enzyme-linked immunosorbent assay (c-ELISA) to detect the disease. This is a specific type of blood test designed to identify antibodies produced by the immune system in response to N. caninum.

Methodology and Findings

  • The study examined the blood samples from 329 equids – 268 horses and 61 donkeys. They found that 24% of horses and 46% of donkeys were infected with N. caninum. Thus, the data indicates a higher risk of infection in donkeys than in horses.
  • The study also looked at the infection rate in ‘draught equids’, or animals used for hard physical work like pulling loads. The results showed the odds of infection in these animals were 8.2 times greater compared to other animals. The researchers suspect that this could be due to their increased exposure to the parasite due to their work environments.
  • The research did not find significant differences in the prevalence of the disease across various genders, breeds, or clinical statuses. There were no discrepancies observed between equids that had contact with dogs either, despite dogs being known carriers of the disease.
  • However, the method of feeding did show a significant difference. Outdoor feeding and mixed grazing were associated with higher antibody presence against N. caninum compared to stable feeding (indoor feeding).
  • The study reported the odds of infection were 4.8 times higher in equids with a history of late abortions than in those with no history of abortions, indicating N. caninum may play a role in reproductive failures.

Significance of the Study

  • This study fills a gap in knowledge about the prevalence of N. caninum in equids in Erbil, Iraq, highlighting the higher susceptibility of donkeys and draught animals.
  • The findings can guide better management and preventive strategies for equids, especially those at higher risk of infection.
  • Furthermore, the association of N. caninum infection with reproductive failures can provide a basis for further studies into the parasite’s role in equine reproduction issues.

Cite This Article

APA
Jabar Aziz K, Mikaeel FB, Azeez SH, Bilal SJ. (2024). Seroepidemiological study of Neospora caninum in equids using c-ELISA in Erbil Province, Iraq. Folia Parasitol (Praha), 71, 2024.022. https://doi.org/10.14411/fp.2024.022

Publication

ISSN: 1803-6465
NlmUniqueID: 0065750
Country: Czech Republic
Language: English
Volume: 71
PII: 2024.022

Researcher Affiliations

Jabar Aziz, Khalid
  • College of Veterinary Medicine, Salahaddin University-Erbil, Erbil, Iraq.
Mikaeel, Farhad Buzo
  • College of Veterinary Medicine, University of Duhok, Duhok, Iraq.
Azeez, Sarhang Hasan
  • College of Education, Biology Department, Salahaddin University-Erbil, Erbil, Iraq.
Bilal, Samir Jawdat
  • College of Agricultural Engineering Sciences, Department of Fish Resources and Aquatic Animals, Salahaddin University-Erbil, Erbil, Iraq *Address for correspondence: Khalid Jabar Aziz, College of Veterinary Medicine, Salahaddin University-Erbil, Erbil, Iraq; Email: khalid.aziz1@su.edu.krd; ORCID: 0000-0002-6662-3863.

MeSH Terms

  • Animals
  • Neospora / isolation & purification
  • Coccidiosis / veterinary
  • Coccidiosis / epidemiology
  • Coccidiosis / parasitology
  • Iraq / epidemiology
  • Seroepidemiologic Studies
  • Equidae / parasitology
  • Enzyme-Linked Immunosorbent Assay / veterinary
  • Horse Diseases / epidemiology
  • Horse Diseases / parasitology
  • Horses
  • Female
  • Male
  • Antibodies, Protozoan / blood
  • Prevalence

References

This article includes 36 references
  1. Alshammari A, Gattan HS, Marzok M, Selim A. Seroprevalence and risk factors for Neospora spp. infection in equine in Egypt. Sci. Rep. 13: 20242.
    pubmed: 37981658doi: 10.1038/s41598-023-47601-ygoogle scholar: lookup
  2. Bártová E, Machačová T, Sedlák K, Budíková M, Mariani U, Veneziano V. Seroprevalence of antibodies of Neospora spp. and Toxoplasma gondii in horses from southern Italy. Folia Parasitol. 62: 043.
    pubmed: 26278845doi: 10.14411/fp.2015.043google scholar: lookup
  3. Bártová E, Sedlák K, Syrová M, Literák I. Neospora spp. and Toxoplasma gondii antibodies in horses in the Czech Republic. Parasitol. Res. 107: 783-785.
    pubmed: 20532561doi: 10.1007/s00436-010-1929-4google scholar: lookup
  4. Ciaramella P, Corona M, Cortese L, Piantedosi D, Santoro D, Di Loria A, Rigato R. Seroprevalence of Neospora spp. in asymptomatic horses in Italy. Vet. Parasitol. 123: 11-15.
    pubmed: 15265566doi: 10.1016/j.vetpar.2004.05.022google scholar: lookup
  5. Cruz I, Vinhas AR, Dubey JP, Cardoso L, Cotovio M, Lopes AP. First report of antibodies to Neospora spp. in horses from Portugal. Rev. Bras. Parasitol. Vet. 28: 161-163.
    pubmed: 30892382doi: 10.1590/s1984-296120180081google scholar: lookup
  6. Dangoudoubiyam S, Oliveira JB, Víquez C, Gómez-García A, González O, Romero JJ, Kwok OC, Dubey JP, Howe DK. Detection of antibodies against Sarcocystis neurona, Neospora spp., and Toxoplasma gondii in horses from Costa Rica. J. Parasitol. 97: 522-524.
    pubmed: 21506839doi: 10.1645/GE-2722.1google scholar: lookup
  7. Dubey JP. Review of Neospora caninum and neosporosis in animals. Kor. J. Parasitol. 41: 1.
    pubmed: 12666725doi: 10.3347/kjp.2003.41.1.1google scholar: lookup
  8. Dubey JP, Hemphill A, Calero-Bernal R, Schares G. Neosporosis in Animals. CRC Press Boca Raton, 548 pp..
    doi: 10.1201/9781315152561google scholar: lookup
  9. Dubey JP, Lindsay DS. A review of Neospora caninum and neosporosis. Vet. Parasitol. 67: 1-59.
    pubmed: 9011014doi: 10.1016/S0304-4017(96)01035-7google scholar: lookup
  10. Dubey JP, Mitchell SM, Morrow JK, Rhyan JC, Stewart LM, Granstrom DE, Romand S, Thulliez P, Saville WJ, Lindsay DS. Prevalence of antibodies to Neospora caninum, Sarcocystis neurona, and Toxoplasma gondii in wild horses from central Wyoming. J. Parasitol. 89: 716-720.
    pubmed: 14533680doi: 10.1645/GE-66Rgoogle scholar: lookup
  11. Dubey JP, Schares G. Neosporosis in animals-the last five years. Vet. Parasitol. 180: 90-108.
    pubmed: 21704458doi: 10.1016/j.vetpar.2011.05.031google scholar: lookup
  12. Dubey JP, Schares G, Ortega-Mora L. Epidemiology and control of neosporosis and Neospora caninum. Clin. Microbiol. Rev. 20: 323-67.
    pubmed: 17428888doi: 10.1128/CMR.00031-06google scholar: lookup
  13. Gennari SM, Pena HF DJ, Lindsay DS, Lopes MG, Soares HS, Cabral AD, Vitaliano SN, Amaku M. Prevalence of antibodies against Neospora spp. and Sarcocystis neurona in donkeys from northeastern Brazil. Rev. Bras. Parasitol. Vet. 25: 109-111.
    pubmed: 26982557doi: 10.1590/S1984-29612016003google scholar: lookup
  14. Gharekhani J, Heidari H. Serology based comprehensive study of Neospora infection in domestic animals in Hamedan province, Iran. J. Adv. Vet. Anim. Res. 1: 119-124.
    doi: 10.5455/javar.2014.a23google scholar: lookup
  15. Gharekhani J, Tavoosidana GR, Naderisefat GR. Seroprevalence of Neospora infection in horses and donkeys in Hamedan province, Western Iran. Vet. World 6: 620.
  16. Hiasa J, Kohara J, Nishimura M, Xuan X, Tokimitsu H, Nishikawa Y. ELISAs based on rNcGRA7 and rNcSAG1 antigens as an indicator of Neospora caninum activation. Vet. Parasitol. 187: 379-385.
    pubmed: 22365337doi: 10.1016/j.vetpar.2012.01.036google scholar: lookup
  17. Hoane JS, Gennari SM, Dubey JP, Ribeiro MG, Borges AS, Yai LE, Aguiar DM, Cavalcante GT, Bonesi GL, Howe DK. Prevalence of Sarcocystis neurona and Neospora spp. infection in horses from Brazil based on presence of serum antibodies to parasite surface antigen. Vet. Parasitol. 136: 155-159.
    pubmed: 16310955doi: 10.1016/j.vetpar.2005.10.023google scholar: lookup
  18. Jakubek EB, Lundén A, Uggla A. Seroprevalences of Toxoplasma gondii and Neospora sp. infections in Swedish horses. Vet. Parasitol. 138: 194-199.
    pubmed: 16517077doi: 10.1016/j.vetpar.2006.02.002google scholar: lookup
  19. Javanmardi E, Majidiani H, Shariatzadeh SA, Anvari D, Shamsinia S, Ghasemi E, Kordi B, Shams M. Global seroprevalence of Neospora spp. in horses and donkeys: a systematic review and meta-analysis. Vet. Parasitol. 288: 109299.
    pubmed: 33227673doi: 10.1016/j.vetpar.2020.109299google scholar: lookup
  20. Karatepe M, Karatepe B. Investigation of seroprevalence of Neospora spp. in horses in Niğde province (Turkey). Kafkas Univ. Vet. Fak. Derg. A39-A42.
  21. 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. 148: 109-113.
    pubmed: 17614202doi: 10.1016/j.vetpar.2007.06.002google scholar: lookup
  22. Leszkowicz Mazuz M, Mimoun L, Schvartz G, Tirosh-Levy S, Savitzki I, Edery N, Blum SE, Baneth G, Pusterla N, Steinman A. Detection of Neospora caninum infection in aborted equine fetuses in Israel. Pathogens 9: 962.
    pubmed: 33228059doi: 10.3390/pathogens9110962google scholar: lookup
  23. Marsh AE, Howe DK, Wang G, Barr BC, Cannon N, Conrad PA. Differentiation of Neospora hughesi from Neospora caninum based on their immunodominant surface antigen, SAG1 and SRS2. Int. J. Parasitol. 29: 1575-1582.
    pubmed: 10608444doi: 10.1016/S0020-7519(99)00120-4google scholar: lookup
  24. Pagmadulam B, Myagmarsuren P, Fereig RM, Igarashi M, Yokoyama N, Battsetseg B, Nishikawa Y. Seroprevalence of Toxoplasma gondii and Neospora caninum infections in cattle in Mongolia. Vet. Parasitol. Reg. Stud. Rep. 14: 11-17.
    pubmed: 31014714doi: 10.1016/j.vprsr.2018.08.001google scholar: lookup
  25. Pitel PH, Pronost S, Chatagnon G, Tainturier D, Fortier G, Ballet JJ. Neosporosis in bovine dairy herds from the west of France: detection of Neospora caninum DNA in aborted fetuses, seroepidemiology of N. caninum in cattle and dogs. Vet. Parasitol. 102: 269-277.
    pubmed: 11731070doi: 10.1016/S0304-4017(01)00544-1google scholar: lookup
  26. Santolaria Blasco P, Almería S, Martínez Bello D, Nogareda C, Mezo M, Gonzalez Warleta M, Pabón M, López Gatius F, Yániz JL, Castro Hermida JA. Different humoral mechanisms against Neospora caninum infection in purebreed and crossbreed beef/dairy cattle pregnancies. Vet. Parasitol. 178: 70-76.
    pubmed: 21216103doi: 10.1016/j.vetpar.2010.12.018google scholar: lookup
  27. Saqib M, Hussain MH, Sajid MS, Mansoor MK, Asi MN, Fadya AA, Zohaib A, Sial AUR, Muhammad G, Ullah I. Sero-epidemiology of equine toxoplasmosis using a latex agglutination test in the three metropolises of Punjab, Pakistan. Trop. Biomed. 32: 276-285.
  28. Selim A, Marawan MA, Ali A-F, Manaa E, AbouelGhaut HA. Seroprevalence of bovine leukemia virusin cattle, buffalo, and camel in Egypt. Trop. Anim. Health Prod. 52: 1207-1210.
    pubmed: 31686339doi: 10.1007/s11250-019-02105-8google scholar: lookup
  29. 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. 40: 100.
    doi: 10.29261/pakvetj/2020.008google scholar: lookup
  30. Talafha AQ, Abutarbush SM, Rutley DL. Seroprevalence and potential risk factors associated with Neospora spp. infection among asymptomatic horses in Jordan. Kor. J. Parasitol. 53: 163.
    pubmed: 25925174doi: 10.3347/kjp.2015.53.2.163google scholar: lookup
  31. Tirosh-Levy S, Steinman A, Minderigiu A, Arieli O, Savitski I, Fleiderovitz L, Edery N, Schvartz G, Leszkowicz Mazuz M. High exposure to Toxoplasma gondii and Neospora spp. in donkeys in Israel: serological survey and case reports. Animals 10: 1921.
    pubmed: 33086723doi: 10.3390/ani10101921google scholar: lookup
  32. Vanleeuwen JA, Haddad JP, Dohoo IR, Keefe GP, Tiwari A, Scott HM. Risk factors associated with Neospora caninum seropositivity in randomly sampled Canadian dairy cows and herds. Prev. Vet. Med. 93: 129-138.
  33. Vardeleon D, Marsh AE, Thorne JG, Loch W, Young R, Johnson PJ. Prevalence of Neospora hughesi and Sarcocystis neurona antibodies in horses from various geographical locations. Vet. Parasitol. 95: 273-282.
    pubmed: 11223207doi: 10.1016/S0304-4017(00)00393-9google scholar: lookup
  34. Veronesi F, Diaferia M, Mandara MT, Marenzoni ML, Cittadini F, Piergili Fioretti D. Neospora spp. infection associated with equine abortion and/or stillbirth rate. Vet. Res. Commun. 32: 223-226.
    pubmed: 18696243doi: 10.1007/s11259-008-9155-6google scholar: lookup
  35. de Waal T. Advances in diagnosis of protozoan diseases. Vet. Parasitol. 189: 65-74.
    pubmed: 22503386doi: 10.1016/j.vetpar.2012.03.033google scholar: lookup
  36. Zhou M, Cao S, Sevinc F, Sevinc M, Ceylan O, Liu M. Enzyme-linked immunosorbent assays using recombinant TgSAG2 and NcSAG1 to detect Toxoplasma gondii and Neospora caninum-specific antibodies in domestic animals in Turkey. J. Vet. Med. Sci. 78: 1877-1881.
    pubmed: 27523504doi: 10.1292/jvms.16-0234google scholar: lookup

Citations

This article has been cited 0 times.