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Veterinary microbiology1993; 37(1-2); 147-161; doi: 10.1016/0378-1135(93)90189-e

The effect of EHV-1 infection upon circulating leucocyte populations in the natural equine host.

Abstract: It has been suggested that EHV-1 infection may perturb immune responsiveness in the natural equine host. The mechanism underlying this phenomenon is not clear, but disturbances of circulating leucocyte populations could contribute. In order to objectively assess the nature of the haematological changes provoked by EHV-1 infection, two groups of conventionally-maintained Welsh mountain ponies were challenge-infected intra-nasally with the Ab4 isolate of EHV-1. These groups were controlled by similarly-sized groups of non-infected ponies. All data generated was subjected to rigorous statistical analysis. Whole leucocyte count, neutrophil count, lymphocyte count, pan T cell count (RVC1 + cells-putative CD5 homologue), T cell subset count (RVC3 + cell-putative CD8 homologue), RVC2 + cells (putatively class II MHC+) and B cell count were recorded in experimental and control subjects at frequent intervals post-infection via flow cytometry. The principal abnormalities post-infection were T cell lymphopaenia, neutropaenia and the appearance of blastic cells of undetermined lineage. This study underlined the variability of EHV-1 infection in the natural, outbred equine host.
Publication Date: 1993-10-01 PubMed ID: 8296444DOI: 10.1016/0378-1135(93)90189-eGoogle Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research investigates the impact of EHV-1 infection on the immune system of horses, focusing on how it alters the composition of circulating white blood cells (leucocytes). The study details the changes to various leucocyte subsets following EHV-1 infection and highlights the variability of the infection in real-world conditions.

Objective and Methodology

  • The research aimed to understand the effect of Equine Herpesvirus 1 (EHV-1) infection on the immune system of horses, specifically the changes it induces to the population of circulating white blood cells (leucocytes).
  • To achieve this, the researchers challenged two groups of conventionally-maintained Welsh mountain ponies with an intra-nasal infection of the Ab4 isolate of EHV-1.
  • The effects of this infection were compared against similar-sized groups of non-infected, control ponies.
  • All collected data was subjected to thorough statistical evaluation to ensure the validity of the findings.

Data Collection and Indicators

  • Several indicators were used to ascertain the changes in pony health following EHV-1 infection. These included total leucocyte count, neutrophil count, lymphocyte count, pan T cell count, T cell subset count, RVC2+ cells, and B cell count.
  • These factors were measured at frequent intervals after the infection was introduced, using flow cytometry, an advanced technology that allows for detailed analysis of individual cells.

Findings

  • Critical irregularities following the infection were noted in the T cell lymphopaenia (a decrease in T-cell lymphocytes), neutropenia (lower neutrophil count), and the emergence of blastic cells of undetermined lineage.
  • These changes occur due to the EHV-1 infection disrupting the balance of circulating leucocyte populations, indicating a suppression of immune response in the infected equine hosts.
  • The research emphasizes the variability of the effects of EHV-1 infection among the inherently diverse equine population, suggesting that immune response can differ substantially in individual cases.

Cite This Article

APA
McCulloch J, Williamson SA, Powis SJ, Edington N. (1993). The effect of EHV-1 infection upon circulating leucocyte populations in the natural equine host. Vet Microbiol, 37(1-2), 147-161. https://doi.org/10.1016/0378-1135(93)90189-e

Publication

ISSN: 0378-1135
NlmUniqueID: 7705469
Country: Netherlands
Language: English
Volume: 37
Issue: 1-2
Pages: 147-161

Researcher Affiliations

McCulloch, J
  • Department of Veterinary Pathology, Royal Veterinary College, London, UK.
Williamson, S A
    Powis, S J
      Edington, N

        MeSH Terms

        • Animals
        • Antigens, Surface / blood
        • Flow Cytometry / veterinary
        • Herpesviridae Infections / blood
        • Herpesviridae Infections / immunology
        • Herpesviridae Infections / veterinary
        • Herpesvirus 1, Equid
        • Horse Diseases / blood
        • Horse Diseases / immunology
        • Horses
        • Leukocyte Count / veterinary
        • Lymphocytes
        • Neutrophils

        Citations

        This article has been cited 5 times.
        1. Zarski LM, Giessler KS, Jacob SI, Weber PSD, McCauley AG, Lee Y, Soboll Hussey G. Identification of Host Factors Associated with the Development of Equine Herpesvirus Myeloencephalopathy by Transcriptomic Analysis of Peripheral Blood Mononuclear Cells from Horses. Viruses 2021 Feb 24;13(3).
          doi: 10.3390/v13030356pubmed: 33668216google scholar: lookup
        2. Zarski LM, Weber PSD, Lee Y, Soboll Hussey G. Transcriptomic Profiling of Equine and Viral Genes in Peripheral Blood Mononuclear Cells in Horses during Equine Herpesvirus 1 Infection. Pathogens 2021 Jan 7;10(1).
          doi: 10.3390/pathogens10010043pubmed: 33430330google scholar: lookup
        3. Giessler KS, Samoilowa S, Soboll Hussey G, Kiupel M, Matiasek K, Sledge DG, Liesche F, Schlegel J, Fux R, Goehring LS. Viral Load and Cell Tropism During Early Latent Equid Herpesvirus 1 Infection Differ Over Time in Lymphoid and Neural Tissue Samples From Experimentally Infected Horses. Front Vet Sci 2020;7:621.
          doi: 10.3389/fvets.2020.00621pubmed: 33102556google scholar: lookup
        4. Oladunni FS, Horohov DW, Chambers TM. EHV-1: A Constant Threat to the Horse Industry. Front Microbiol 2019;10:2668.
          doi: 10.3389/fmicb.2019.02668pubmed: 31849857google scholar: lookup
        5. Sutton GA, Viel L, Carman PS, Boag BL. Pathogenesis and clinical signs of equine herpesvirus-1 in experimentally infected ponies in vivo. Can J Vet Res 1998 Jan;62(1):49-55.
          pubmed: 9442940