Analyze Diet
Equine veterinary journal1992; 24(1); 20-25; doi: 10.1111/j.2042-3306.1992.tb02772.x

Diagnosis of equid herpesviruses -1 and -4 by polymerase chain reaction.

Abstract: The polymerase chain reaction (PCR) is a sensitive technique used to detect DNA of viral pathogens. We have applied the technique to the detection of Equid herpesviruses-1 and -4 (EHV-1 and EHV-4) DNA within nasopharyngeal swab samples from horses. Ninety-eight samples from suspected field cases and in-contact horses were analysed. The assays were conducted blind and later decoded and compared with virus isolation data. Our results indicate that PCR is a sensitive and rapid technique for the diagnosis of EHV-1 and EHV-4 infection.
Publication Date: 1992-01-01 PubMed ID: 1313360DOI: 10.1111/j.2042-3306.1992.tb02772.xGoogle 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.
  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

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 presents the successful application of a technique known as the polymerase chain reaction (PCR) for the detection of Equid herpesviruses -1 and -4 (EHV-1 and EHV-4) in horses, indicating that this method is effective and efficient for diagnosing these infections.

Research Purpose and Approach

  • The study embarked on a mission to apply a widely recognised method called the polymerase chain reaction (PCR) to detect DNA of two types of Equid herpesviruses -1 and -4 (EHV-1 and EHV-4) which are among the most common viral pathogens in horses.
  • A total of 98 nasopharyngeal swab samples were obtained from horses, including those suspected of having EHV-1 or EHV-4 infections and those that were in close contact with the suspected cases.
  • To maintain the research’s objectivity and ensure the validity of the results, the PCR assays were conducted “blind”, meaning the researchers conducting the PCR tests did not know which samples were from suspected and in-contact horses.

Analysis Methodology and Findings

  • Once the PCR assays had been conducted, the samples were decoded and the results were compared with data obtained from traditional virus isolation methods.
  • The analysis shows that PCR was effective in detecting EHV-1 and EHV-4 in the samples. This suggested that PCR, a technique known for its sensitivity and rapidity, presented a viable means for diagnosing these types of infection in horses.
  • While the study did not indicate the specific rate of successful detection or the time taken by PCR as compared to traditional methods, the concluding remark indicates PCR’s relative superiority of being a more sensitive and rapid technique.

Conclusion

  • The findings from the study showcase the potential of PCR technique as a sensitive and rapid tool to diagnose Equid herpesviruses-1 and -4 infection in horses. The use of PCR could potentially enhance the speed of diagnosis, enabling faster medical treatment for infected horses and possibly controlling the spread of the virus among other horses.

Cite This Article

APA
Sharma PC, Cullinane AA, Onions DE, Nicolson L. (1992). Diagnosis of equid herpesviruses -1 and -4 by polymerase chain reaction. Equine Vet J, 24(1), 20-25. https://doi.org/10.1111/j.2042-3306.1992.tb02772.x

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 24
Issue: 1
Pages: 20-25

Researcher Affiliations

Sharma, P C
  • Department of Veterinary Pathology, University of Glasgow Veterinary School, UK.
Cullinane, A A
    Onions, D E
      Nicolson, L

        MeSH Terms

        • Animals
        • Base Sequence
        • DNA, Viral / analysis
        • Herpesviridae / genetics
        • Herpesviridae / isolation & purification
        • Herpesviridae Infections / diagnosis
        • Herpesviridae Infections / veterinary
        • Herpesvirus 1, Equid / genetics
        • Herpesvirus 1, Equid / isolation & purification
        • Horse Diseases / diagnosis
        • Horses
        • Molecular Sequence Data
        • Nasopharynx / microbiology
        • Nucleic Acid Hybridization
        • Oligonucleotide Probes / chemistry
        • Polymerase Chain Reaction
        • Sensitivity and Specificity

        Citations

        This article has been cited 7 times.
        1. Nielsen SS, Alvarez J, Bicout DJ, Calistri P, Canali E, Drewe JA, Garin-Bastuji B, Gonzales Rojas JL, Gortázar C, Herskin M, Michel V, Miranda Chueca MÁ, Roberts HC, Padalino B, Pasquali P, Spoolder H, Ståhl K, Calvo AV, Viltrop A, Winckler C, Carvelli A, Paillot R, Broglia A, Kohnle L, Baldinelli F, Van der Stede Y. Assessment of listing and categorisation of animal diseases within the framework of the Animal Health Law (Regulation (EU) No 2016/429): infection with Equine Herpesvirus-1. EFSA J 2022 Jan;20(1):e07036.
          doi: 10.2903/j.efsa.2022.7036pubmed: 35035581google scholar: lookup
        2. Rodriguez JM. Detection of animal pathogens by using the polymerase chain reaction (PCR). Vet J 1997 May;153(3):287-305.
          doi: 10.1016/s1090-0233(97)80063-9pubmed: 9232118google scholar: lookup
        3. Pfeffer M, Wiedmann M, Batt CA. Applications of DNA amplification techniques in veterinary diagnostics. Vet Res Commun 1995;19(5):375-407.
          doi: 10.1007/BF01839319pubmed: 8560754google scholar: lookup
        4. Belák S, Ballagi-Pordány A. Application of the polymerase chain reaction (PCR) in veterinary diagnostic virology. Vet Res Commun 1993;17(1):55-72.
          doi: 10.1007/BF01839180pubmed: 8396281google scholar: lookup
        5. Sinclair R, Binns MM, Chirnside ED, Mumford JA. Detection of antibodies against equine herpesvirus types 1 and 4 by using recombinant protein derived from an immunodominant region of glycoprotein B. J Clin Microbiol 1993 Feb;31(2):265-71.
          doi: 10.1128/jcm.31.2.265-271.1993pubmed: 8381809google scholar: lookup
        6. Yason CV, Harris LM, McKenna PK, Wadowska D, Kibenge FS. Establishment of conditions for the detection of bovine herpesvirus-1 by polymerase chain reaction using primers in the thymidine kinase region. Can J Vet Res 1995 Apr;59(2):94-101.
          pubmed: 7648533
        7. Rimstad E, Hyllseth B. Equine herpesviruses 1 and 4: amplification and differentiation by polymerase chain reaction. Acta Vet Scand 1994;35(3):303-6.
          doi: 10.1186/BF03548336pubmed: 7847200google scholar: lookup