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Journal of equine veterinary science2023; 130; 104916; doi: 10.1016/j.jevs.2023.104916

Comprehensive Analysis of Equid Herpesvirus Recombination: An Insight Into the Repeat Regions.

Abstract: High-throughput sequencing of genomes has expanded our knowledge of the Alphaherpesvirinae, a widely extended subfamily of DNA viruses that recombine to increase their genetic diversity. It has been acknowledged that equid herpesvirus 1 (EHV-1) and equid herpesvirus 4 (EHV-4), two alphaherpesviruses with an economic impact on the horse industry, can recombine. This work aimed to analyze interspecific recombination between all equid alphaherpesvirus species, using genomes of EHV-1, EHV-3, EHV-4, EHV-6, EHV-8, and EHV-9 available in GenBank. 14 events of recombination by RDP4 and Simplot between EHV-1 x EHV-4, EHV-1 x EHV-9, EHV-8 x EHV-1, and EHV-8 x EHV-9 were identified. Ten out of 14 events involved ORF64, a double-copy gene located at the repeat regions that codifies for the infected cell protein 4 (ICP4). Among the ICP4, recombination can be found between EHV-1 X EHV-9, EHV-8 X EHV-9, and EHV-1 X EHV-4, the former affects zebra-borne genotypes, a type of EHV-1 that infect wild equids, and the latter match with previous breakpoints reported in fields isolates. Consequently, these findings strongly suggest that ICP4 is a hotspot for recombination. This work describes novel recombination events and is the first genome-wide recombination analysis using all available equid alphaherpesvirus species genomes.
Publication Date: 2023-09-11 PubMed ID: 37704182DOI: 10.1016/j.jevs.2023.104916Google Scholar: Lookup
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  • Journal Article

Summary

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This study investigates the genetic recombination of equid herpesviruses, a subfamily of viruses which can recombine to increase their diversity and affect horses. The study identifies specific genes that are hotspot for recombination among different types of these herpesviruses.

Detailed Overview

The body of the study focuses on the comprehensive analysis of recombination in the equid herpesvirus strains. The strains analyzed include EHV-1, EHV-3, EHV-4, EHV-6, EHV-8, and EHV-9.

  • Using high-throughput sequencing of genomes, the authors expanded the understanding of the Alphaherpesvirinae subfamily. These are DNA viruses known for their ability to recombine and hence increase their genetic diversity.
  • It was already known that EHV-1 and EHV-4, both of which impact the horse industry economically, could recombine.
  • In this study, the aim was to scrutinize the interspecific recombination among all equid alphaherpesvirus species. The genomes for these virus species available in GenBank, an open access database, were used for the study.
  • In total, 14 recombination events were identified by researchers using RDP4 and Simplot between EHV-1 x EHV-4, EHV-1 x EHV-9, EHV-8 x EHV-1, and EHV-8 x EHV-9.

Key Findings

The key revelations from the study highlight particular genes as hotspots for recombination, presenting an insightful picture of the impact of recombination on these viruses.

  • Out of the 14 identified recombination events, 10 involved ORF64. This gene is a double-copy gene located at the repeat regions, and it codifies for the infected cell protein 4 (ICP4).
  • Regarding ICP4, recombination occurred among EHV-1 X EHV-9, EHV-8 X EHV-9, and EHV-1 X EHV-4. Interesting to note is that recombination in EHV-1 X EHV-9 affects zebra-borne genotypes – a subtype of EHV-1 that infects wild equids.
  • The recombination found in EHV-1 X EHV-4 matched with breakpoints reported previously in field isolates.
  • These findings suggest that the ICP4 is a frequent site for recombination events.

In conclusion, this research describes new recombination events and is the first to conduct a genome-wide recombination analysis using all available equid alphaherpesvirus species genomes.

Cite This Article

APA
Tau RL, Ferreccio C, Bachir N, Torales F, Romera SA, Maidana SS. (2023). Comprehensive Analysis of Equid Herpesvirus Recombination: An Insight Into the Repeat Regions. J Equine Vet Sci, 130, 104916. https://doi.org/10.1016/j.jevs.2023.104916

Publication

ISSN: 0737-0806
NlmUniqueID: 8216840
Country: United States
Language: English
Volume: 130
Pages: 104916
PII: S0737-0806(23)00732-3

Researcher Affiliations

Tau, Rocío Lucía
  • Institute of Virology and Technological Innovations, IVIT (INTA-CONICET), Dr Nicolas Repetto and De los Reseros, CP 1686, Hurlingham, Buenos Aires, Argentina. Electronic address: tau.rocio@inta.gob.ar.
Ferreccio, Carola
  • Institute of Virology and Technological Innovations, IVIT (INTA-CONICET), Dr Nicolas Repetto and De los Reseros, CP 1686, Hurlingham, Buenos Aires, Argentina; Chair of immunology, University of Salvador (USAL), Champagnat 1599, CP 1630, Pilar, Buenos Aires, Argentina.
Bachir, Natalia
  • Institute of Virology and Technological Innovations, IVIT (INTA-CONICET), Dr Nicolas Repetto and De los Reseros, CP 1686, Hurlingham, Buenos Aires, Argentina.
Torales, Fatima
  • Institute of Virology and Technological Innovations, IVIT (INTA-CONICET), Dr Nicolas Repetto and De los Reseros, CP 1686, Hurlingham, Buenos Aires, Argentina.
Romera, Sonia Alejandra
  • Institute of Virology and Technological Innovations, IVIT (INTA-CONICET), Dr Nicolas Repetto and De los Reseros, CP 1686, Hurlingham, Buenos Aires, Argentina; Chair of immunology, University of Salvador (USAL), Champagnat 1599, CP 1630, Pilar, Buenos Aires, Argentina.
Maidana, Silvina Soledad
  • Institute of Virology and Technological Innovations, IVIT (INTA-CONICET), Dr Nicolas Repetto and De los Reseros, CP 1686, Hurlingham, Buenos Aires, Argentina; Chair of immunology, University of Salvador (USAL), Champagnat 1599, CP 1630, Pilar, Buenos Aires, Argentina.

Conflict of Interest Statement

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Citations

This article has been cited 4 times.
  1. Tallmadge RL, Laverack M, Lejeune M, Crossley B, Diel DG. A multiplex real-time PCR assay for detection of equid herpesvirus 1 and 4. Sci Rep 2025 Oct 31;15(1):38201.
    doi: 10.1038/s41598-025-22043-wpubmed: 41173927google scholar: lookup
  2. Paredes-Galarza BS, Campos FS, Oliveira MT, Prandi BA, de Souza UJB, Junqueira DM, Martin DP, Spilki FR, Franco AC, Roehe PM. Recombination Between Bubaline Alphaherpesvirus 1 and Bovine Alphaherpesvirus 1 as a Possible Origin of Bovine Alphaherpesvirus 5. Viruses 2025 Jan 30;17(2).
    doi: 10.3390/v17020198pubmed: 40006953google scholar: lookup
  3. Ruan L, Li L, Yang R, You A, Khan MZ, Yu Y, Chen L, Li Y, Liu G, Wang C, Wang T. Equine Herpesvirus-1 Induced Respiratory Disease in Dezhou Donkey Foals: Case Study from China, 2024. Vet Sci 2025 Jan 14;12(1).
    doi: 10.3390/vetsci12010056pubmed: 39852931google scholar: lookup
  4. Tau RL, Marandino AE, Panzera Y, Alamos F, Vissani MA, Romera SA, Pérez R, Maidana SS. The complete genome of equid herpesvirus-1 (EHV-1) field isolates from Argentina reveals an interspecific recombinant strain. Virus Genes 2024 Oct;60(5):559-562.
    doi: 10.1007/s11262-024-02093-4pubmed: 39028407google scholar: lookup