Genetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy response
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , , , , |
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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Repositório Institucional da UNESP |
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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 2.620 1,576 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1-9 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 instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
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1808129178570063872 |