Comparison of nucleic and amino acid sequences and phylogenetic analysis of the Gs protein of various equine arteritis virus isolates.
Abstract: The genetic variation in equine arteritis virus (EAV) Gs protein encoding gene was investigated. Nucleic and deduced amino acid sequences from eight different EAV isolates (one European, two American and five Canadian isolates) were compared with those of the Bucyrus reference strain. Nucleotide and amino acid identities between these isolates and the Bucyrus reference strain ranged from 92.3 to 96.4%, and 93.2 to 95.5%, respectively. However, phylogenetic tree analysis and estimation of genetic distances based on the Gs protein encoding gene sequences showed that the European prototype Vienna strain, the American 87AR-A1 isolate and all other North American EAV isolates could be classified into three genetically divergent groups. Our results showed that the Gs protein-encoding gene can be subjected on the basis of phylogenetic analysis to genetic variation, as previously shown for the other three EAV structural protein (M, N and GL)-encoding genes.
Publication Date: 1996-01-01 PubMed ID: 8938984DOI: 10.1007/BF00576983Google Scholar: Lookup
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research article focuses on understanding the genetic variation in the Gs protein gene of the Equine Arteritis Virus (EAV) by comparing it with the reference Bucyrus strain. The study also explores the genetic distinction in different EAV isolates utilizing nucleic and deduced amino acid sequences along with phylogenetic analysis.
Outline of the Research
- This scientific exploration digs into the genetic variance in the Gs protein of the equine arteritis virus (EAV), a pathogen majorly affecting horses.
- The investigation involves an in-depth comparative study of nucleic and predicted amino acid sequences from eight different EAV isolates.
- The isolates include: one from Europe, two from the United States, and five from Canada. The comparative study is carried out using the established Bucyrus strain as a reference.
Findings
- The researchers discovered that the nucleotide and amino acid similarities between the eight isolates and the Bucyrus reference strain fell between 92.3% and 96.4% for nucleotide identities, and 93.2% and 95.5% for amino acid identities.
- In spite of these similarities, the application of phylogenetic tree analysis and estimation of genetic distances based on the sequences of the Gs protein encoding gene showed distinct genetic divergences in these strains. Specifically, the European strain Vienna, the American strain 87AR-A1, and all the other North American EAV isolates could be separated into three significantly divergent groups.
Significance of the Results
- The outcomes of this study clearly indicate that the gene encoding the Gs protein in EAV is subject to genetic variance.
- This correlates with previous studies demonstrating genetic variation in other structural protein-encoding EAV genes – M, N, and GL.
- Consequently, this research adds value in understanding the genetic variations and the evolutionary trajectory of EAV, which could have implications in disease management and control strategies for horse populations.
Cite This Article
APA
Lepage N, St-Laurent G, Carman S, Archambault D.
(1996).
Comparison of nucleic and amino acid sequences and phylogenetic analysis of the Gs protein of various equine arteritis virus isolates.
Virus Genes, 13(1), 87-91.
https://doi.org/10.1007/BF00576983 Publication
Researcher Affiliations
- Unitersité du Québec à Montréal, Département des Sciences Biologiques, Québec, Canada.
MeSH Terms
- Amino Acid Sequence
- Animals
- Base Sequence
- Equartevirus / classification
- Equartevirus / genetics
- Equartevirus / isolation & purification
- Equidae / virology
- Evolution, Molecular
- GTP-Binding Protein alpha Subunits, Gs / genetics
- Genetic Variation
- Molecular Sequence Data
- Phylogeny
- Sequence Analysis, RNA
- Sequence Homology, Amino Acid
- Viral Proteins / genetics
References
This article includes 21 references
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