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Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy response.
- Source :
-
BMC infectious diseases [BMC Infect Dis] 2010 Feb 23; Vol. 10, pp. 36. Date of Electronic Publication: 2010 Feb 23. - Publication Year :
- 2010
-
Abstract
- Background: The quasispecies nature of HCV may have important implications for viral persistence, pathogenicity and resistance to antiviral agents. The variability of one of the viral proteins, NS5A, is believed to be related to the response to IFN therapy, the standard treatment for infection. In this study we analyzed the quasispecies composition of NS5A protein in patients infected with HCV genotype 3a, before IFN therapy.<br />Methods: Viral RNA was isolated from samples of 12 patients: four sustained virological responders (SVR), four non-responders (NR), and four end-of-treatment responders (ETR). cDNA was synthesized, the NS5A region was amplified and the fragments obtained were cloned. Fifteen clones from each patient were sequenced with eight primers, generating 179 contigs.<br />Results: Higher values for substitution (either synonymous or non-synonymous) and for distance were found in the SVR group. However, the NR group showed relatively more non-synonymous mutations than the other groups, owing to the higher values of dN/dS in complete NS5A and most specific regions. Overall, NS5A protein is undergoing purifying selection, since all dN/dS ratios values are below 0.5.<br />Conclusions: Our study provides an overview of the genetic variability of complete NS5A protein in HCV genotype 3a.
- Subjects :
- Amino Acid Sequence
Amino Acid Substitution genetics
Cluster Analysis
Genotype
Hepacivirus genetics
Humans
Molecular Sequence Data
Phylogeny
Point Mutation
RNA, Viral genetics
Sequence Analysis, DNA
Treatment Outcome
Antiviral Agents therapeutic use
Genetic Variation
Hepacivirus classification
Hepacivirus isolation & purification
Hepatitis C, Chronic drug therapy
Hepatitis C, Chronic virology
Viral Nonstructural Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1471-2334
- Volume :
- 10
- Database :
- MEDLINE
- Journal :
- BMC infectious diseases
- Publication Type :
- Academic Journal
- Accession number :
- 20178583
- Full Text :
- https://doi.org/10.1186/1471-2334-10-36