Analyze Diet
Genome announcements2014; 2(5); e00797-14; doi: 10.1128/genomeA.00797-14

Complete genome sequence of equid herpesvirus 3.

Abstract: Equid herpesvirus 3 (EHV-3) is a member of the subfamily Alphaherpesvirinae that causes equine coital exanthema. Here, we report the first complete genome sequence of EHV-3. The 151,601-nt genome encodes 76 distinct genes like other equine alphaherpesviruses, but genetically, EHV-3 is significantly more divergent.
Publication Date: 2014-10-02 PubMed ID: 25278519PubMed Central: PMC4183863DOI: 10.1128/genomeA.00797-14Google 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.
  • Journal Article

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 article presents the complete genome sequencing of Equid Herpesvirus 3 (EHV-3), an alphaherpesvirinae subfamily member causing equine coital exanthema in horses. The study reveals unusual genetic divergence in the virus, even as it encodes 76 distinct genes, like other equine alphaherpesviruses.

Introduction to EHV-3

  • Equid Herpesvirus 3 (EHV-3) is a type of herpesvirus that infects members of the horse family (Equidae) and causes a disease known as equine coital exanthema.
  • This disease mostly affects the external genitalia of horses by causing lesions, and thus ultimately leads to infertility.
  • EHV-3 is part of the Alphaherpesvirinae subfamily, which contains viruses that typically cause respiratory and reproductive tract diseases in their hosts.

Genome sequencing of EHV-3

  • The main focus of this research article was to decode the complete genetic sequence of EHV-3. This is an important step as understanding its genomic structure can help in developing effective diagnostic methods and possible treatments.
  • The researchers successfully decoded the 151,601 nucleotide (nt) genome of EHV-3. A genome of this length is typically vast and complex, with its genetic material containing large amounts of information.
  • The EHV-3 genome was discovered to encode 76 distinct genes, like other equine alphaherpesviruses, pointing to shared genomic characteristics.

Genetic divergence of EHV-3

  • One of the significant findings from the genome sequencing was the considerable genetic divergence of EHV-3. This implies that the EHV-3 genome has significantly and unexpectedly evolved differently from other members of the equine alphaherpesviruses.
  • This genetic divergence is likely to impact the pathogenicity, virulence, and behavior of EHV-3 compared to its counterparts. This could mean that this virus might infect, replicate, or spread differently, which could affect the severity of the disease it causes and the way it should be treated.
  • An understanding of this divergence can be crucial in devising unique diagnostic tests and treatment options for the disease caused by EHV-3.

Cite This Article

APA
Sijmons S, Vissani A, Tordoya MS, Muylkens B, Thiry E, Maes P, Matthijnssens J, Barrandeguy M, Van Ranst M. (2014). Complete genome sequence of equid herpesvirus 3. Genome Announc, 2(5), e00797-14. https://doi.org/10.1128/genomeA.00797-14

Publication

ISSN: 2169-8287
NlmUniqueID: 101595808
Country: United States
Language: English
Volume: 2
Issue: 5
PII: e00797-14

Researcher Affiliations

Sijmons, Steven
  • Laboratory of Clinical Virology, Rega Institute for Medical Research, KU Leuven, Leuven, Belgium steven.sijmons@rega.kuleuven.be.
Vissani, Aldana
  • Instituto de Virología, CICVyA, INTA-Castelar, Buenos Aires, Argentina.
Tordoya, Maria Silva
  • Instituto de Virología, CICVyA, INTA-Castelar, Buenos Aires, Argentina.
Muylkens, Benoît
  • Veterinary Virology and Animal Viral Diseases, Department of Infectious and Parasitic Diseases, Faculty of Veterinary Medicine, University of Liège, Liège, Belgium.
Thiry, Etienne
  • Veterinary Virology and Animal Viral Diseases, Department of Infectious and Parasitic Diseases, Faculty of Veterinary Medicine, University of Liège, Liège, Belgium.
Maes, Piet
  • Laboratory of Clinical Virology, Rega Institute for Medical Research, KU Leuven, Leuven, Belgium.
Matthijnssens, Jelle
  • Laboratory of Clinical Virology, Rega Institute for Medical Research, KU Leuven, Leuven, Belgium.
Barrandeguy, Maria
  • Instituto de Virología, CICVyA, INTA-Castelar, Buenos Aires, Argentina.
Van Ranst, Marc
  • Laboratory of Clinical Virology, Rega Institute for Medical Research, KU Leuven, Leuven, Belgium.

References

This article includes 13 references
  1. Barrandeguy M, Thiry E. Equine coital exanthema and its potential economic implications for the equine industry.. Vet J 2012 Jan;191(1):35-40.
    doi: 10.1016/j.tvjl.2011.01.016pubmed: 21354835google scholar: lookup
  2. Telford EA, Watson MS, McBride K, Davison AJ. The DNA sequence of equine herpesvirus-1.. Virology 1992 Jul;189(1):304-16.
    doi: 10.1016/0042-6822(92)90706-Upubmed: 1318606google scholar: lookup
  3. Telford EA, Watson MS, Perry J, Cullinane AA, Davison AJ. The DNA sequence of equine herpesvirus-4.. J Gen Virol 1998 May;79 ( Pt 5):1197-203.
    pubmed: 9603335doi: 10.1099/0022-1317-79-5-1197google scholar: lookup
  4. Liu C, Guo W, Lu G, Xiang W, Wang X. Complete genomic sequence of an equine herpesvirus type 8 Wh strain isolated from China.. J Virol 2012 May;86(9):5407.
    doi: 10.1128/JVI.00445-12pmc: PMC3347380pubmed: 22492929google scholar: lookup
  5. Fukushi H, Yamaguchi T, Yamada S. Complete genome sequence of equine herpesvirus type 9.. J Virol 2012 Dec;86(24):13822.
    doi: 10.1128/JVI.02607-12pmc: PMC3503125pubmed: 23166237google scholar: lookup
  6. Hartley CA, Drummer HE, Studdert MJ. The nucleotide sequence of the glycoprotein G homologue of equine herpesvirus 3 (EHV3) indicates EHV3 is a distinct equid alphaherpesvirus.. Arch Virol 1999;144(10):2023-33.
    doi: 10.1007/s007050050723pubmed: 10550674google scholar: lookup
  7. Ehlers B, Borchers K, Grund C, Frölich K, Ludwig H, Buhk HJ. Detection of new DNA polymerase genes of known and potentially novel herpesviruses by PCR with degenerate and deoxyinosine-substituted primers.. Virus Genes 1999;18(3):211-20.
    doi: 10.1023/A:1008064118057pubmed: 10456789google scholar: lookup
  8. Kleiboeker SB, Chapman RK. Detection of equine herpesvirus 3 in equine skin lesions by polymerase chain reaction.. J Vet Diagn Invest 2004 Jan;16(1):74-9.
    doi: 10.1177/104063870401600113pubmed: 14974851google scholar: lookup
  9. Sijmons S, Thys K, Corthout M, Van Damme E, Van Loock M, Bollen S, Baguet S, Aerssens J, Van Ranst M, Maes P. A method enabling high-throughput sequencing of human cytomegalovirus complete genomes from clinical isolates.. PLoS One 2014;9(4):e95501.
  10. Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheeler transform.. Bioinformatics 2009 Jul 15;25(14):1754-60.
  11. Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R. The Sequence Alignment/Map format and SAMtools.. Bioinformatics 2009 Aug 15;25(16):2078-9.
  12. Zerbino DR, Birney E. Velvet: algorithms for de novo short read assembly using de Bruijn graphs.. Genome Res 2008 May;18(5):821-9.
    doi: 10.1101/gr.074492.107pmc: PMC2336801pubmed: 18349386google scholar: lookup
  13. Milne I, Stephen G, Bayer M, Cock PJ, Pritchard L, Cardle L, Shaw PD, Marshall D. Using Tablet for visual exploration of second-generation sequencing data.. Brief Bioinform 2013 Mar;14(2):193-202.
    doi: 10.1093/bib/bbs012pubmed: 22445902google scholar: lookup

Citations

This article has been cited 7 times.
  1. Losinno A, Vissani MA, Sanchez D, Damiani AM. Equid herpesvirus type 3 infection produces membrane-associated and secreted forms of glycoprotein G that are not required for efficient cell-to-cell spread of the virus in vitro.. Arch Virol 2023 Mar 28;168(4):122.
    doi: 10.1007/s00705-023-05727-4pubmed: 36977931google scholar: lookup
  2. Troncoso I, Calvanese R, Saravia F, Muñoz-Leal S, Zegpi NA, Ortega R. First molecular detection of Equine Herpesvirus type 3 (EHV-3) in Chile.. Vet Med Sci 2023 Mar;9(2):717-720.
    doi: 10.1002/vms3.976pubmed: 36253808google scholar: lookup
  3. Vissani MA, Damiani AM, Barrandeguy ME. Equine Coital Exanthema: New Insights on the Knowledge and Leading Perspectives for Treatment and Prevention.. Pathogens 2021 Aug 20;10(8).
    doi: 10.3390/pathogens10081055pubmed: 34451519google scholar: lookup
  4. Thorsteinsdóttir L, Guðmundsson GÖ, Jensson H, Torsteinsdóttir S, Svansson V. Isolation of equid alphaherpesvirus 3 from a horse in Iceland with equine coital exanthema.. Acta Vet Scand 2021 Feb 2;63(1):6.
    doi: 10.1186/s13028-021-00572-4pubmed: 33531030google scholar: lookup
  5. Câmara RJF, Bueno BL, Resende CF, Balasuriya UBR, Sakamoto SM, Reis JKPD. Viral Diseases that Affect Donkeys and Mules.. Animals (Basel) 2020 Nov 25;10(12).
    doi: 10.3390/ani10122203pubmed: 33255568google scholar: lookup
  6. Kirisawa R, Toishi Y, Akamatsu A, Soejima K, Miyashita T, Tsunoda N. Isolation of equine herpesvirus 3 (EHV-3) from equine coital exanthema of two stallions and sero-epidemiology of EHV-3 infection in Japan.. J Vet Med Sci 2017 Mar 23;79(3):636-643.
    doi: 10.1292/jvms.16-0518pubmed: 28132964google scholar: lookup
  7. Negussie H, Li Y, Tessema TS, Nauwynck HJ. Replication characteristics of equine herpesvirus 1 and equine herpesvirus 3: comparative analysis using ex vivo tissue cultures.. Vet Res 2016 Jan 15;47:19.
    doi: 10.1186/s13567-016-0305-5pubmed: 26768993google scholar: lookup