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Archives of virology. Supplementum1998; 14; 305-310; doi: 10.1007/978-3-7091-6823-3_26

Application of an indirect fluorescent antibody assay for the detection of African horse sickness virus antibodies.

Abstract: An indirect fluorescent antibody (IFA) technique was used to screen and quantify antibodies against African horse sickness virus (AHSV) in equine sera. Results obtained with the IFA assay were compared directly with those obtained with standard complement fixation (CF) and virus neutralisation (VN) tests using horse sera from experimental studies and samples from the field. Positive fluorescent antibody titres were detected from as early as 7 days after primary vaccination and persisted for at least six months. The IFA technique offers a clear advantage over CF tests, where the antibodies are often of shorter duration and where sera from donkeys and mules are frequently anticomplementary. The sensitivity and specificity of the IFA test compared with the VN test were 98% and 83.3%, respectively. The IFA test is rapid, relatively easy to perform and inexpensive, and can be recommended as an alternative assay for screening different species of equidae in AHSV control and surveillance programmes.
Publication Date: 1998-10-24 PubMed ID: 9785515DOI: 10.1007/978-3-7091-6823-3_26Google Scholar: Lookup
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  • Comparative Study
  • Journal Article

Summary

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The researchers applied an indirect fluorescent antibody technique for testing and measuring antibodies against African Horse Sickness Virus in horse blood serum. They found that this method offers notable advantages compared to the standard tests, being quicker, easier, less costly, and more effective.

Introduction

  • The research revolves around the use of an indirect fluorescent antibody (IFA) technique to detect and quantify antibodies against the African horse sickness virus (AHSV) in horse blood serum.
  • The technique was directly compared with the standard complement fixation (CF) test and the virus neutralisation (VN) test using serum samples both from experimental studies and from the field.

Results

  • With the IFA method, positive fluorescent antibody levels were detected as early as 7 days after the primary vaccination, and these levels persisted for at least six months.
  • The IFA technique was found to be superior to the CF test, which often reflects shorter-duration antibodies and frequently produces anticomplementary results with serum from donkeys and mules.
  • Comparing the sensitivity and specificity of the IFA test to the VN test, the results were that the IFA method had 98% sensitivity and 83.3% specificity.

Conclusion

  • The IFA test was concluded to be a rapid, relatively easy-to-perform, and inexpensive method for detecting antibodies against AHSV.
  • The researchers recommended it as an alternative assay for screening different equine species, thus providing a useful tool for controlling and monitoring AHSV.

Cite This Article

APA
el Hasnaoui H, el Harrak M, Tber A, Fikri A, Laghzaoui K, Bikour MH. (1998). Application of an indirect fluorescent antibody assay for the detection of African horse sickness virus antibodies. Arch Virol Suppl, 14, 305-310. https://doi.org/10.1007/978-3-7091-6823-3_26

Publication

ISSN: 0939-1983
NlmUniqueID: 9214275
Country: Austria
Language: English
Volume: 14
Pages: 305-310

Researcher Affiliations

el Hasnaoui, H
  • Laboratoire Régional d'Analyses et de Recherches Vétérinaires de Casablanca, Morocco.
el Harrak, M
    Tber, A
      Fikri, A
        Laghzaoui, K
          Bikour, M H

            MeSH Terms

            • African Horse Sickness / immunology
            • African Horse Sickness / prevention & control
            • African Horse Sickness Virus / immunology
            • Animals
            • Antibodies, Viral / blood
            • Complement Fixation Tests / veterinary
            • Equidae
            • Fluorescent Antibody Technique, Indirect / veterinary
            • Immunization, Secondary / veterinary
            • Neutralization Tests / veterinary
            • Reproducibility of Results
            • Sensitivity and Specificity
            • Vaccination / veterinary
            • Viral Vaccines / immunology

            Citations

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