Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy response

Detalhes bibliográficos
Autor(a) principal: Bittar, Cintia [UNESP]
Data de Publicação: 2010
Outros Autores: Jardim, Ana Carolina G. [UNESP], Yamasaki, Lilian H. T. [UNESP], de Queiroz, Artur T. L., Carareto, Claudia M. A. [UNESP], Pinho, Joao Renato R., de Carvalho-Mello, Isabel Maria V. G., Rahal, Paula [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1186/1471-2334-10-36
http://hdl.handle.net/11449/21647
Resumo: 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.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.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.Conclusions: Our study provides an overview of the genetic variability of complete NS5A protein in HCV genotype 3a.
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spelling Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy responseBackground: 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.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.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.Conclusions: Our study provides an overview of the genetic variability of complete NS5A protein in HCV genotype 3a.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Instituto Butantan, Viral Immunol Lab, BR-05503900 São Paulo, BrazilSão Paulo State Univ, UNESP, IBILCE,Dept Biol, Inst Biosci Language & Literature & Exact Sci, BR-15054010 São Paulo, BrazilUniv São Paulo, BR-05508900 São Paulo, BrazilUniv São Paulo, Fac Med, Dept Gastroenterol, Lab Hepatol & Gastroenterol,Inst Trop Med, BR-01246903 São Paulo, BrazilAlbert Einstein Israeli Hosp, Dept Clin Pathol, BR-05652000 São Paulo, BrazilSão Paulo State Univ, UNESP, IBILCE,Dept Biol, Inst Biosci Language & Literature & Exact Sci, BR-15054010 São Paulo, BrazilBiomed Central Ltd.Instituto ButantanUniversidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Albert Einstein Israeli HospBittar, Cintia [UNESP]Jardim, Ana Carolina G. [UNESP]Yamasaki, Lilian H. T. [UNESP]de Queiroz, Artur T. L.Carareto, Claudia M. A. [UNESP]Pinho, Joao Renato R.de Carvalho-Mello, Isabel Maria V. G.Rahal, Paula [UNESP]2014-05-20T14:01:16Z2014-05-20T14:01:16Z2010-02-23info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1-9application/pdfhttp://dx.doi.org/10.1186/1471-2334-10-36Bmc Infectious Diseases. London: Biomed Central Ltd., v. 10, p. 1-9, 2010.1471-2334http://hdl.handle.net/11449/2164710.1186/1471-2334-10-36WOS:000275622600001WOS000275622600001.pdf799108236267121234257729983192160000-0001-5693-61480000-0002-0298-1354Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBMC Infectious Diseases2.6201,576info:eu-repo/semantics/openAccess2023-12-13T06:21:52Zoai:repositorio.unesp.br:11449/21647Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:14:45.705984Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy response
title Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy response
spellingShingle Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy response
Bittar, Cintia [UNESP]
title_short Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy response
title_full Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy response
title_fullStr Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy response
title_full_unstemmed Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy response
title_sort Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy response
author Bittar, Cintia [UNESP]
author_facet Bittar, Cintia [UNESP]
Jardim, Ana Carolina G. [UNESP]
Yamasaki, Lilian H. T. [UNESP]
de Queiroz, Artur T. L.
Carareto, Claudia M. A. [UNESP]
Pinho, Joao Renato R.
de Carvalho-Mello, Isabel Maria V. G.
Rahal, Paula [UNESP]
author_role author
author2 Jardim, Ana Carolina G. [UNESP]
Yamasaki, Lilian H. T. [UNESP]
de Queiroz, Artur T. L.
Carareto, Claudia M. A. [UNESP]
Pinho, Joao Renato R.
de Carvalho-Mello, Isabel Maria V. G.
Rahal, Paula [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Instituto Butantan
Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
Albert Einstein Israeli Hosp
dc.contributor.author.fl_str_mv Bittar, Cintia [UNESP]
Jardim, Ana Carolina G. [UNESP]
Yamasaki, Lilian H. T. [UNESP]
de Queiroz, Artur T. L.
Carareto, Claudia M. A. [UNESP]
Pinho, Joao Renato R.
de Carvalho-Mello, Isabel Maria V. G.
Rahal, Paula [UNESP]
description 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.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.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.Conclusions: Our study provides an overview of the genetic variability of complete NS5A protein in HCV genotype 3a.
publishDate 2010
dc.date.none.fl_str_mv 2010-02-23
2014-05-20T14:01:16Z
2014-05-20T14:01:16Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/1471-2334-10-36
Bmc Infectious Diseases. London: Biomed Central Ltd., v. 10, p. 1-9, 2010.
1471-2334
http://hdl.handle.net/11449/21647
10.1186/1471-2334-10-36
WOS:000275622600001
WOS000275622600001.pdf
7991082362671212
3425772998319216
0000-0001-5693-6148
0000-0002-0298-1354
url http://dx.doi.org/10.1186/1471-2334-10-36
http://hdl.handle.net/11449/21647
identifier_str_mv Bmc Infectious Diseases. London: Biomed Central Ltd., v. 10, p. 1-9, 2010.
1471-2334
10.1186/1471-2334-10-36
WOS:000275622600001
WOS000275622600001.pdf
7991082362671212
3425772998319216
0000-0001-5693-6148
0000-0002-0298-1354
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv BMC Infectious Diseases
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application/pdf
dc.publisher.none.fl_str_mv Biomed Central Ltd.
publisher.none.fl_str_mv Biomed Central Ltd.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
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