Variability of non-structural proteins of equine arteritis virus during persistent infection of the stallion.
Abstract: The genetic stability of ORF1a encoding non-structural proteins nsp1, nsp2, nsp3 and nsp4 of equine arteritis virus (EAV) has been analysed for nearly seven years in a persistently infected stallion of the Malopolska breed. Between November 2004 and June 2011, 11 semen samples were collected. Viral RNA extracted from semen of this carrier stallion was amplified, sequenced and compared with the sequences of the other known strains of EAV. Sequence analysis of ORF1a showed 84 synonymous and 16 non-synonymous mutations. The most variable part of ORF1a was the region encoding nsp2 protein with 13 non-synonymous substitutions. The degree of amino acid identity between isolates ranged from 98.91 to 100%. Only single non-synonymous mutations were detected in nsp1 (one substitution) and nsp4 (two substitutions). The most stable was nsp3 in which no amino acid substitutions were observed during the whole period of observation.
Publication Date: 2015-07-15 PubMed ID: 26172173DOI: 10.1515/pjvs-2015-0033Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This study investigates the stability of certain non-structural proteins found in the equine arteritis virus (EAV) during a lengthy persistent infection in a stallion. The findings indicate varying degrees of genetic stability between these proteins, with nsp3 being the most stable with no observed amino acid substitutions.
Research Background and Methodology
- The study focuses on the equine arteritis virus (EAV), known to cause respiratory disease and other ailments in horses. Specifically, research scrutinizes the genetic stability of certain non-structural proteins (nsp1, nsp2, nsp3, nsp4) during a prolonged, persistent infection in a stallion of the Malopolska breed.
- Over the course of nearly seven years (from November 2004 to June 2011), 11 semen samples were collected from this persistently infected stallion.
- Researchers extracted the viral RNA from these semen samples and amplified it for analysis. They then sequenced the amplified RNA and compared the resulting sequences with those of other known strains of EAV.
Findings
- Upon analysis of the ORF1a sequence, which encodes the non-structural proteins under investigation, the researchers identified a total of 84 synonymous and 16 non-synonymous mutations.
- The nsp2 protein was found to be the most variable part of ORF1a, showing 13 non-synonymous substitutions.
- They found that the degree of amino acid identity between different isolates of the virus ranged from 98.91% to 100%.
- Meanwhile, very few non-synonymous mutations were found in the nsp1 (one substitution) and nsp4 (two substitutions) proteins.
- The most stable protein examined was nsp3. Researchers noted no amino acid substitutions in this protein throughout the entire observation period.
Implications
- The findings of this study provide important insights into the genetic stability of these non-structural proteins (nsp1, nsp2, nsp3, nsp4) of EAV during a persistent infection.
- Understanding the genetic stability and variation of these proteins can help elucidate the virus’s mechanisms of persistence, potentially aiding in the development of more effective treatment and control methods for EAV.
Cite This Article
APA
Socha W, Rola J, Żmudziński JF.
(2015).
Variability of non-structural proteins of equine arteritis virus during persistent infection of the stallion.
Pol J Vet Sci, 18(2), 255-259.
https://doi.org/10.1515/pjvs-2015-0033 Publication
Researcher Affiliations
MeSH Terms
- Amino Acid Sequence
- Animals
- Arterivirus Infections / veterinary
- Arterivirus Infections / virology
- Equartevirus / genetics
- Equartevirus / metabolism
- Gene Expression Regulation, Viral / physiology
- Genome, Viral
- Horse Diseases / virology
- Horses
- Male
- Phylogeny
- RNA, Viral / genetics
- RNA, Viral / metabolism
- Reverse Transcriptase Polymerase Chain Reaction / veterinary
- Viral Nonstructural Proteins / genetics
- Viral Nonstructural Proteins / metabolism
Citations
This article has been cited 2 times.- Jian Z, Ma R, Zhu L, Deng H, Li F, Zhao J, Deng L, Lai S, Sun X, Tang H, Xu Z. Evasion of interferon-mediated immune response by arteriviruses. Front Immunol 2022;13:963923.
- Chen J, Wang D, Sun Z, Gao L, Zhu X, Guo J, Xu S, Fang L, Li K, Xiao S. Arterivirus nsp4 Antagonizes Interferon Beta Production by Proteolytically Cleaving NEMO at Multiple Sites. J Virol 2019 Jun 15;93(12).
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