Analyze Diet
BMC veterinary research2018; 14(1); 230; doi: 10.1186/s12917-018-1554-5

Sero-epidemioloical survey on African horse sickness virus among horses in Khartoum State, Central Sudan.

Abstract: African horse sickness virus (AHSV) is an infectious non contagious insect-transmitted double-stranded (ds) RNA orbivirus of the family Reoviridae. AHSV causes an often fatal hemorrhagic infection with high mortality among selected breeds of Arabian horses. This study was conducted to avail some information with regard to the prevalence and associated risk factors of AHSV among ecotype breeds of horses in central Sudan. Methods: Sera were collected from 320 horses, which were selected randomly from four localities and employed in the study. A competitive enzyme-linked immunosorbent assay (cELISA) was used to screen sampled sera for AHSV-specific immunoglobulin G (Ig G) antibodies. Results: Seropositivity to AHSV Ig G was detected in 275 out of the 320 horse sera, thus accounting for a prevalence rate of 85.9%. Potential risk factors to AHSV infection were reported to be associated with horse breed (OR = 5.0, CI = 0.07-2.104, p-value = 0.039) and activity of the horse (OR = 3.21, CI = 0.72-1.48, p- value = 0.008). Conclusions: The high prevalence of AHSV in Khartoum State of Central Sudan necessitates the need for continuous surveillance for AHSV infection to prevent a possible disease outbreak in this region of the African continent.
Publication Date: 2018-08-01 PubMed ID: 30068335PubMed Central: PMC6090883DOI: 10.1186/s12917-018-1554-5Google 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.

This research investigated the prevalence and risk factors of the African horse sickness virus (AHSV) among various breeds of horses in central Sudan and found a high prevalence rate and certain risk factors.

Introduction

The research focuses on the African horse sickness virus (AHSKV), a deadly non- contagious virus, transmitted by insects that severely impacts certain breeds of Arabian horses. This study was carried out specifically in Khartoum State, located in central Sudan, to assess the commonality or prevalence of the AHSV and to identify the associated risk factors.

Methodology

  • 320 horses from different breeds from four different localities in central Sudan were included in the study.
  • Blood samples were taken from these horses and were analyzed for presence of AHSV-specific immunoglobulin G (Ig G) antibodies using a competitive enzyme-linked immunosorbent assay (cELISA) method. The Ig G antibodies indicate the body’s immune response to the virus.

Results

  • Out of 320 horses, 275 showed positive results for AHSV Ig G antibodies, indicating a prevalence rate of 85.9%. This high percentage suggests a widespread presence of the virus amongst the horse population.
  • Risk factors were identified and statistically linked to the presence of AHSV. Specifically, the breed of the horse and the activity level of the horse were significantly associated with the virus.

Conclusion

Due to the high prevalence rate, the research concludes that there is a need for a continuous surveillance for AHSV in central Sudan to prevent an outbreak of the disease. The identified risk factors should guide selective breeding and activity management to reduce the threat of AHSV.

Cite This Article

APA
Karamalla ST, Gubran AI, Adam IA, Abdalla TM, Sinada RO, Haroun EM, Aradaib IE. (2018). Sero-epidemioloical survey on African horse sickness virus among horses in Khartoum State, Central Sudan. BMC Vet Res, 14(1), 230. https://doi.org/10.1186/s12917-018-1554-5

Publication

ISSN: 1746-6148
NlmUniqueID: 101249759
Country: England
Language: English
Volume: 14
Issue: 1
Pages: 230

Researcher Affiliations

Karamalla, Siham T
  • Molecular Biology Laboratory (MBL), Department of Clinical Medicine, Faculty of Veterinary Medicine, University of Khartoum, P.O. Box 32, Khartoum North, Sudan.
Gubran, Ahmed I
  • Molecular Biology Laboratory (MBL), Department of Clinical Medicine, Faculty of Veterinary Medicine, University of Khartoum, P.O. Box 32, Khartoum North, Sudan.
Adam, Ibrahim A
  • Molecular Biology Laboratory (MBL), Department of Clinical Medicine, Faculty of Veterinary Medicine, University of Khartoum, P.O. Box 32, Khartoum North, Sudan.
Abdalla, Tamadur M
  • Molecular Biology Laboratory (MBL), Department of Clinical Medicine, Faculty of Veterinary Medicine, University of Khartoum, P.O. Box 32, Khartoum North, Sudan.
Sinada, Reem O
  • Molecular Biology Laboratory (MBL), Department of Clinical Medicine, Faculty of Veterinary Medicine, University of Khartoum, P.O. Box 32, Khartoum North, Sudan.
Haroun, Eltahir M
  • Scientific Research Directorate, Al-Mughtaribeen University, Khartoum, Sudan.
Aradaib, Imadeldin E
  • Molecular Biology Laboratory (MBL), Department of Clinical Medicine, Faculty of Veterinary Medicine, University of Khartoum, P.O. Box 32, Khartoum North, Sudan. aradaib@yahoo.com.
  • Scientific Research Directorate, Al-Mughtaribeen University, Khartoum, Sudan. aradaib@yahoo.com.
  • EBH Scientific Research Laboratory, Zamzam University College (ZUC), Khartoum, Sudan. aradaib@yahoo.com.

MeSH Terms

  • African Horse Sickness / epidemiology
  • African Horse Sickness / etiology
  • African Horse Sickness / virology
  • African Horse Sickness Virus
  • Animals
  • Antibodies, Bacterial / immunology
  • Enzyme-Linked Immunosorbent Assay / veterinary
  • Female
  • Horses / virology
  • Immunoglobulin G / immunology
  • Male
  • Prevalence
  • Risk Factors
  • Seroepidemiologic Studies
  • Sudan / epidemiology
  • Surveys and Questionnaires

Conflict of Interest Statement

Collection of blood from horses was performed by qualified veterinarians following proper physical restraint of animals to ensure both personnel and animal safety. Animal owners were explained the study purposes before procedures and upon agreeing to participate, they provided a written consent prior to study procedures and blood collection from their animals. The study received ethical clearance from the Research Board of the Faculty of Veterinary Medicine, University of Khartoum, Sudan. The risk factor information was obtained from the animal owners through the structured questionnaire form, which permitted the use of the blood samples for diagnostic and research purposes. Not applicable. The authors declare that they have no competing interests. Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

This article includes 29 references
  1. Borden EC, Shope RE, Murphy FA. Physicochemical and morphological relationships of some arthropod-borne viruses to bluetongue virus-anew taxonomic group. Physicochemical and serological studies.. J Gen Virol 1971;3:261–271.
    doi: 10.1099/0022-1317-13-2-261pubmed: 4333714google scholar: lookup
  2. Fenner F, Pereira HG, Porterfield JS. Family and generic names for virus approved by the International Committee on Taxonomy of Viruses.. Intervirology 1974;3:193–194.
    doi: 10.1159/000149755pubmed: 4443189google scholar: lookup
  3. Abuelzein EME, Mirghani ME, Ali BE. Observations on African horse sickness in donkeys in the Sudan.. Rev Sci Tech Off Int Epiz 1989;8:785–787.
    doi: 10.20506/rst.8.3.421pubmed: 32344953google scholar: lookup
  4. El-Hasnaoui H, el Harrak M, Zientara S, Laviada M, Hamblin C. Serological and virological responses in mules and donkeys following inoculation with African horse sickness virus serotype 4.. Arch Virol 1998;14:29–36.
    pubmed: 9785493
  5. Fassi-Fihri O, el Harrak M, Fass-Fehri MM. Clinical, virological and immune responses of normal and immunosuppressed donkeys (Equus asinus africanus) after inoculation with African horse sickness virus.. Arch Virol Suppl 1998;14:49–56.
    pubmed: 9785495
  6. Aradaib IE, Mohammed EHM, Ali NOM, Majid AA, Idris SH, Karrar AE. A simple and rapid method for detection of African horse sickness virus serogroup using RT-PCR.. Vet Res Comm 2006;30:319–324.
    doi: 10.1007/s11259-006-3262-zpubmed: 16437307google scholar: lookup
  7. Sailleau C, Hamblin C, Paweska JT, Zientara S. Identification and differentiation of nine African horse sickness virus serotypes by RT-PCR amplification of the serotype-specific genome segment 2.. J Gen Virol 2000;81:831–837.
    doi: 10.1099/0022-1317-81-3-831pubmed: 10675421google scholar: lookup
  8. Robin M, Page P, Archer D, Baylis M. African horse sickness: The potential for an outbreak in disease-free regions and current disease control and elimination techniques.. Equine Vet J 2016;48:659–669.
    doi: 10.1111/evj.12600pubmed: 27292229google scholar: lookup
  9. Becker E, Venter GJ, Greyling T, Molini U, van Hamburg H. Evidence of African horse sickness virus infection of Equus zebra hartmannae in the south-western Khomas Region, Namibia.. Transbound Emerg Dis 2018;65(1):278–80.
    pubmed: 28406577doi: 10.1111/tbed.12651google scholar: lookup
  10. Aradaib IE. PCR detection of African horse sickness virus based on genome segment three sequence analysis.. J Virol Method 2009;159:1–5.
  11. Mohammed EHM, Mellor PS. Further studies on bluetongue-related Orbiviruses in the Sudan.. Epidemiol & infect 1990;105:619–632.
    doi: 10.1017/S0950268800048263pmc: PMC2271820pubmed: 2174372google scholar: lookup
  12. Eisa M. The isolation and identification of type 9 African horse sickness virus in the Sudan.. Br Vet J 1974;130:606–610.
    doi: 10.1016/S0007-1935(17)35749-4pubmed: 4447879google scholar: lookup
  13. Ayelet G, Derso S, Jenberie S, Tigre W, Aklilu N, Gelaye E, Asmare K. Outbreak investigation and molecular characterization of African horse sickness virus circulating in selected areas of Ethiopia.. Acta Trop 2013;127:91–96.
  14. Bitew M, Andargie A, Bekele M, Jenberie S, Ayelet G, Gelaye E. Serological survey of African horse sickness in selected districts of Jimma zone, Southwestern Ethiopia.. Trop Anim Health Prod 2011;43:1543–1547.
    doi: 10.1007/s11250-011-9839-8pubmed: 21465102google scholar: lookup
  15. Hamblin C, Mertens PPC, Mellor PS, Burroughs NJ, Crowther JR. A serogroup specific enzyme-linked immunosorbent assay for the detection and identification of African horse sickness viruses.. J Virol Methods 1991;31:285–292.
    doi: 10.1016/0166-0934(91)90166-Wpubmed: 1864909google scholar: lookup
  16. Maree S, Paweska JT. Preparation of recombinant African horse sickness virus VP7 antigen via a simple method and validation of a VP7-based indirect ELISA for the detection of group-specific IgG antibodies in horse sera.. J Virol Methods 2005;125:55–65.
  17. Martinez-Torrecuadrada JL, Diaz-Laviada M, Roy P, Sanchez C, Vela C, Sanchez-Vizcaino JM, Casal JI. Serologic markers in early stages of African horse sickness virus infection.. J Clin Microbiol 1997;35:531–535.
    pmc: PMC229621pubmed: 9003637
  18. Martinez-Torrecuadrada JL, Iwata H, Venteo A, Casal I, Roy P. Expression and characterization of the two outer capsid proteins of African horsesickness virus: the role of VP2 in virus neutralization.. Virology 1994;202:348–359.
    doi: 10.1006/viro.1994.1351pubmed: 8009847google scholar: lookup
  19. Rodriguez M, Hooghuis H, Castano M. Current status of the diagnosis and control of African horse sickness.. Vet Res 1993;24:189–197.
    pubmed: 8343805
  20. Wade-Evans AM, Woolhouse T, O'Hara R, Hamblin C. The use of African horse sickness virus VP7 antigen, synthesised in bacteria, and anti-VP7 monoclonal antibodies in a competitive ELISA.. J Virol Method 1993;45:179–188.
    doi: 10.1016/0166-0934(93)90102-Wpubmed: 8113344google scholar: lookup
  21. Stone-Marschat M, Carville A, Skowronek A, Laegreid W. W: detection of African horse sickness virus by reverse transcription–PCR.. J Clin Microbiol 1994;32:697–700.
    pmc: PMC263109pubmed: 8195381
  22. Williams CF, Inoue T, Lucus AM, Zanotto PM, Roy R. The complete sequence of four structural proteins of African horse sickness virus serotype 6: evolutionary relationships within and between the orbiviruses.. Virus Res 1998;53:53–73.
    doi: 10.1016/S0168-1702(97)00131-7pubmed: 9617769google scholar: lookup
  23. Zientara S, Sailleau C, Moulay S, Plateau E, Cruciere C. Diagnosis and molecular epidemiology of the African horse sickness virus by the polymerase chain reaction and restriction patterns.. Vet Res 1993;24:385–395.
    pubmed: 8260960
  24. Zientara S, Sailleau C, Moulay S, Cruciere C. Differentiation of African horse sickness viruses by polymerase chain reaction and segments 10 restriction patterns.. Vet Microbiol 1995;47:365–375.
    doi: 10.1016/0378-1135(95)00104-2pubmed: 8748551google scholar: lookup
  25. Zientara S, Sailleau C, Moulay S, Wade-Evans A, Cruciere C. Application of the polymerase chain reaction to the detection of African horse sickness viruses.. J Virol Methods 1995;1995(53):47–54.
    doi: 10.1016/0166-0934(94)00175-Gpubmed: 7543488google scholar: lookup
  26. Zientara S, Sailleau C, Moulay S, Cruciere C, el- Harrak M, Laegreid WW, Hamblin C. Use of reverse transcriptase-polymerase chain reaction (RT-PCR) and dot-blot hybridization for the detection and identification of African horse sickness virus nucleic acids.. Arch Virol 1998;14:317–327.
    pubmed: 9785517
  27. Martin SW, Meek HA, Willeberg P. Veterinary Epidemiology: Principles and Methods. AMES: Iowa state University Press; 1987.
  28. Koekemoer JJ. Serotype-specific detection of African horsesickness virus by real-time PCR and the influence of genetic variations.. J Virol Methods 2008;154:104–110.
  29. Martin LA, Meyer AJ, O'Hara RS, Fu H, Mellor PS, Knowles NJ, Mertens PP. Phylogenetic analysis of African horse sickness virus segment 10: sequence variation, virulence characteristics and cell exit.. Arch Virol 1998;14:281–293.
    pubmed: 9785513