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Veterinary microbiology1994; 39(3-4); 275-283; doi: 10.1016/0378-1135(94)90164-3

Epidemiological investigation of equid herpesvirus-4 (EHV-4) excretion assessed by nasal swabs taken from thoroughbred foals.

Abstract: Equid herpesvirus-4 (EHV-4) was detected in nasal swabs taken from foals using a PCR based test and this information used to study the epidemiology of EHV-4 disease on three Australian Thoroughbred stud farms in NSW in 1992. There was a very high level of agreement (kappa value of 0.84) between the PCR results and virus isolation using cell culture techniques. There was a strong seasonal distribution of EHV-4 shedding. Twenty-five of 26 positive samples were collected in January and March with the remaining positive sample collected in February. Foals with clinical signs of upper respiratory tract infection per se were no more likely to be shedders of EHV-4 (odds ratio [OR] 1.4, 95% confidence limits [CL] 0.5-3.8). However, EHV-4 was more likely to be isolated from foals exhibiting copious serous or mucopurulent nasal discharge than those with no clinical signs (OR 4.6, 95% CL 1.1-19.0 and OR 2.5, 95% CL 0.8-8.0, respectively). The month of the year was more important than weaning or age as a risk factor for excretion of EHV-4. Male foals and those with a history of respiratory disease that had required veterinary treatment were more likely to shed EHV-4.
Publication Date: 1994-04-01 PubMed ID: 8042275DOI: 10.1016/0378-1135(94)90164-3Google Scholar: Lookup
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  • Journal Article

Summary

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The research article discusses a study into the spread and occurrence of the Equid herpesvirus-4 (EHV-4) in thoroughbred foals on three stud farms in Australia. The study used nasal swabs to detect the presence of the virus and analyzed the impact of factors such as time of year, symptoms, and the foal’s history of respiratory disease on the likelihood of the virus being present.

Methodology and Findings

  • The study detected the EHV-4 virus in thoroughbred foals by nasal swabs, using the PCR (Polymerase Chain Reaction) test, an effective method of examining viral DNA.
  • There was a strong correlation between PCR test results and virus isolation via cell culture techniques, indicating that the nasal swab PCR test is a reliable method for examining the equine herpesvirus.
  • The study observed a strong correlation between excretion of EHV-4 and certain months of the year – namely January, February, and March. This suggests that EHV-4 has a seasonal pattern.
  • The research also revealed that foals exhibiting heavy serous or mucopurulent nasal discharge – indicative of an upper respiratory tract infection – were more likely to be diagnosed with EHV-4.

Implications of the Research

  • The identification of risk factors in the study, such as time of year and respiratory symptoms, can inform prevention and early detection strategies. This can lead to reduced virus circulation, potentially mitigating equine health problems associated with EHV-4.
  • The study’s confirmation of PCR nasal swab tests as a reliable method for detecting EHV-4 provides assurance for their use in future equine health screening.
  • The finding that male foals and those with a history of respiratory issues are more likely to shed the EHV-4 virus could direct more focused surveillance and intervention strategies in the future.

Limitations and Further Research

  • The study was conducted on three stud farms in one specific geographical location (NSW, Australia) during 1992. Future research may seek to confirm these findings in varied locations and more recently to ensure widespread relevance.
  • The study serves as a basis for further research into the biology and epidemiology of EHV-4 to gain a fuller understanding of the virus’s behavior, evolution, and impact across differing climates and horse breeds.

Cite This Article

APA
Gilkerson J, Jorm LR, Love DN, Lawrence GL, Whalley JM. (1994). Epidemiological investigation of equid herpesvirus-4 (EHV-4) excretion assessed by nasal swabs taken from thoroughbred foals. Vet Microbiol, 39(3-4), 275-283. https://doi.org/10.1016/0378-1135(94)90164-3

Publication

ISSN: 0378-1135
NlmUniqueID: 7705469
Country: Netherlands
Language: English
Volume: 39
Issue: 3-4
Pages: 275-283

Researcher Affiliations

Gilkerson, J
  • Department of Veterinary Pathology, University of Sydney, NSW, Australia.
Jorm, L R
    Love, D N
      Lawrence, G L
        Whalley, J M

          MeSH Terms

          • Age Factors
          • Animals
          • Base Sequence
          • DNA Primers / chemistry
          • DNA, Viral / analysis
          • Female
          • Herpesviridae / genetics
          • Herpesviridae / isolation & purification
          • Herpesviridae Infections / epidemiology
          • Herpesviridae Infections / microbiology
          • Herpesviridae Infections / veterinary
          • Horse Diseases / epidemiology
          • Horse Diseases / microbiology
          • Horses
          • Male
          • Molecular Sequence Data
          • Nasal Mucosa / microbiology
          • New South Wales / epidemiology
          • Polymerase Chain Reaction
          • Risk Factors
          • Seasons
          • Sex Factors

          Citations

          This article has been cited 5 times.
          1. El-Hage C, Mekuria Z, Dynon K, Hartley C, McBride K, Gilkerson J. Association of Equine Herpesvirus 5 with Mild Respiratory Disease in a Survey of EHV1, -2, -4 and -5 in 407 Australian Horses. Animals (Basel) 2021 Nov 30;11(12).
            doi: 10.3390/ani11123418pubmed: 34944194google scholar: lookup
          2. Pearson W, Omar S, Clarke AF. Low-dose ginseng (Panax quinquefolium) modulates the course and magnitude of the antibody response to vaccination against equid herpesvirus I in horses. Can J Vet Res 2007 Jul;71(3):213-7.
            pubmed: 17695597
          3. Nelson RJ, Demas GE, Klein SL, Kriegsfeld LJ. The influence of season, photoperiod, and pineal melatonin on immune function. J Pineal Res 1995 Nov;19(4):149-65.
          4. 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
          5. Hardefeldt L, Thomas K, Page S, Norris J, Browning G, El Hage C, Stewart A, Gilkerson J, Muscatello G, Verwilghen D, van Galen G, Bauquier J, Cuming R, Reynolds B, Whittaker C, Wilkes E, Clulow J, Burden C, Begg L. Antimicrobial prescribing guidelines for horses in Australia. Aust Vet J 2025 Dec;103(12):781-889.
            doi: 10.1111/avj.70003pubmed: 40903020google scholar: lookup