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The Journal of general virology2015; 97(1); 169-178; doi: 10.1099/jgv.0.000332

Genetic variation and dynamics of infections of equid herpesvirus 5 in individual horses.

Abstract: Equid herpesvirus 5 (EHV-5) is related to the human Epstein-Barr virus (human herpesvirus 4) and has frequently been observed in equine populations worldwide. EHV-5 was previously assumed to be low to non-pathogenic; however, studies have also related the virus to the severe lung disease equine multinodular pulmonary fibrosis (EMPF). Genetic information of EHV-5 is scanty: the whole genome was recently described and only limited nucleotide sequences are available. In this study, samples were taken twice 1 year apart from eight healthy horses at the same professional training yard and samples from a ninth horse that was diagnosed with EMPF with samples taken pre- and post-mortem to analyse partial glycoprotein B (gB) gene of EHV-5 by using next-generation sequencing. The analysis resulted in 27 partial gB gene sequences, 11 unique sequence types and five amino acid sequences. These sequences could be classified within four genotypes (I-IV) of the EHV-5 gB gene based on the degree of similarity of the nucleotide and amino acid sequences, and in this work horses were shown to be identified with up to three different genotypes simultaneously. The observations showed a range of interactions between EHV-5 and the host over time, where the same virus persists in some horses, whereas others have a more dynamic infection pattern including strains from different genotypes. This study provides insight into the genetic variation and dynamics of EHV-5, and highlights that further work is needed to understand the EHV-5 interaction with its host.
Publication Date: 2015-10-30 PubMed ID: 26518010DOI: 10.1099/jgv.0.000332Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research study delves into the behaviour and variation of equid herpesvirus 5 (EHV-5) in horses, drawing upon empirical data gathered from nine horses over a one-year period. The study uniquely provides a deeper understanding of the genetic variations and dynamics of EHV-5 infections in horses.

Objective of the research

  • The research aims to grasp complexities surrounding EHV-5, a virus akin to the human Epstein-Barr virus.
  • Despite previously being regarded as low to non-pathogenic, EHV-5 has been increasingly associated with severe lung disease equine multinodular pulmonary fibrosis (EMPF), stirring a need for deeper comprehension of its genetics and disease dynamics.

Methodology employed

  • This study involved observations and tests conducted on two different sessions a year apart on eight healthy horses from the same professional training yard, and another horse suffering from EMPF. The latter set of samples were taken pre- and post-mortem.
  • The researchers inspected the partial glycoprotein B (gB) gene of the EHV-5 virus using next-generation sequencing methods.

Key findings

  • The team successfully extracted 27 partial gB gene sequences, 11 unique sequence types, and five amino acid sequences following analysis.
  • The sequences were categorized into four genotypes (I-IV) of the gB gene, which took into consideration the degree of similarity in nucleotide and amino acid sequences.
  • The study showed that horses could present themselves with up to three different genotypes simultaneously, highlighting the complexity and variation in EHV-5 infections.
  • The research also indicated a wide spectrum of interactions between EHV-5 and the host over time. Some horses showed persistent infection with the same virus, while others displayed a more dynamic infection pattern fluctuating between strains from different genotypes.

Conclusion and future work

  • The study offers a valuable peek into the genetic variation and dynamic nature of EHV-5 infections in horses, enabling a better understanding of the relationships and interactions between the virus and its equine host.
  • The authors recommend further exploration in the area to entirely comprehend the interaction between the EHV-5 virus and its host, as their research mainly used a limited set of nucleotide sequences.

Cite This Article

APA
Back H, Ullman K, Leijon M, Söderlund R, Penell J, Ståhl K, Pringle J, Valarcher JF. (2015). Genetic variation and dynamics of infections of equid herpesvirus 5 in individual horses. J Gen Virol, 97(1), 169-178. https://doi.org/10.1099/jgv.0.000332

Publication

ISSN: 1465-2099
NlmUniqueID: 0077340
Country: England
Language: English
Volume: 97
Issue: 1
Pages: 169-178

Researcher Affiliations

Back, Helena
  • Department of Virology, Immunobiology and Parasitology, National Veterinary Institute, Uppsala, Sweden.
Ullman, Karin
  • Department of Virology, Immunobiology and Parasitology, National Veterinary Institute, Uppsala, Sweden.
Leijon, Mikael
  • Department of Virology, Immunobiology and Parasitology, National Veterinary Institute, Uppsala, Sweden.
Söderlund, Robert
  • Department of Bacteriology, National Veterinary Institute, Uppsala, Sweden.
Penell, Johanna
  • Department of Veterinary Epidemiology and Public Health, University of Surrey, Guildford, UK.
Ståhl, Karl
  • Department of Disease Control and Epidemiology, National Veterinary Institute, Uppsala, Sweden.
Pringle, John
  • Department of Clinical Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Valarcher, Jean-François
  • Department of Virology, Immunobiology and Parasitology, National Veterinary Institute, Uppsala, Sweden.
  • Department of Clinical Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.

MeSH Terms

  • Animals
  • Carrier State / veterinary
  • Carrier State / virology
  • Cluster Analysis
  • Coinfection / veterinary
  • Coinfection / virology
  • DNA, Viral / chemistry
  • DNA, Viral / genetics
  • Genetic Variation
  • Genotype
  • Herpesviridae / classification
  • Herpesviridae / genetics
  • Herpesviridae / isolation & purification
  • Herpesviridae Infections / veterinary
  • Herpesviridae Infections / virology
  • Horse Diseases / virology
  • Horses
  • Molecular Sequence Data
  • Phylogeny
  • Sequence Analysis, DNA
  • Sequence Homology

Citations

This article has been cited 7 times.
  1. Stasiak K, Dunowska M, Rola J. Kinetics of the Equid Herpesvirus 2 and 5 Infections among Mares and Foals from Three Polish National Studs. Viruses 2022 Mar 29;14(4).
    doi: 10.3390/v14040713pubmed: 35458443google scholar: lookup
  2. Stasiak K, Dunowska M, Trewick S, Rola J. Genetic Variation in the Glycoprotein B Sequence of Equid Herpesvirus 5 among Horses of Various Breeds at Polish National Studs. Pathogens 2021 Mar 9;10(3).
    doi: 10.3390/pathogens10030322pubmed: 33803246google scholar: lookup
  3. Easton-Jones CA, Madigan JE, Barnum S, Maxwell LK, Taylor SD, Arnesen T, Pusterla N. Effect of valacyclovir on EHV-5 viral kinetics in horses with equine multinodular pulmonary fibrosis. J Vet Intern Med 2018 Sep;32(5):1763-1767.
    doi: 10.1111/jvim.15230pubmed: 30221792google scholar: lookup
  4. Stasiak K, Dunowska M, Rola J. Prevalence and sequence analysis of equid herpesviruses from the respiratory tract of Polish horses. Virol J 2018 Jul 11;15(1):106.
    doi: 10.1186/s12985-018-1018-3pubmed: 29996858google scholar: lookup
  5. Tashiro J, Rubio GA, Limper AH, Williams K, Elliot SJ, Ninou I, Aidinis V, Tzouvelekis A, Glassberg MK. Exploring Animal Models That Resemble Idiopathic Pulmonary Fibrosis. Front Med (Lausanne) 2017;4:118.
    doi: 10.3389/fmed.2017.00118pubmed: 28804709google scholar: lookup
  6. Stasiak K, Dunowska M, Rola J. Genetic Diversity of Equid Herpesvirus 5 in Temporal Samples from Mares and Their Foals at Three Polish National Studs. Int J Mol Sci 2025 Aug 27;26(17).
    doi: 10.3390/ijms26178298pubmed: 40943220google scholar: lookup
  7. James K, Chappell DE, Craig B, Pariseau C, Wright C, van Harreveld P, Barnum S, Pusterla N. Investigation of Selected Prevalence Factors Associated with EHV-2 and/or EHV-5 Infection in Horses with Acute Onset of Fever and Respiratory Signs. Viruses 2025 Apr 25;17(5).
    doi: 10.3390/v17050612pubmed: 40431624google scholar: lookup