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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/21647
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dc.contributor.authorBittar, Cintia-
dc.contributor.authorJardim, Ana Carolina G.-
dc.contributor.authorYamasaki, Lilian H. T.-
dc.contributor.authorde Queiroz, Artur T. L.-
dc.contributor.authorCarareto, Claudia M. A.-
dc.contributor.authorPinho, Joao Renato R.-
dc.contributor.authorde Carvalho-Mello, Isabel Maria V. G.-
dc.contributor.authorRahal, Paula-
dc.date.accessioned2014-05-20T14:01:16Z-
dc.date.available2014-05-20T14:01:16Z-
dc.date.issued2010-02-23-
dc.identifierhttp://dx.doi.org/10.1186/1471-2334-10-36-
dc.identifier.citationBmc Infectious Diseases. London: Biomed Central Ltd., v. 10, p. 1-9, 2010.-
dc.identifier.issn1471-2334-
dc.identifier.urihttp://hdl.handle.net/11449/21647-
dc.description.abstractBackground: 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.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.format.extent1-9-
dc.language.isoeng-
dc.publisherBiomed Central Ltd.-
dc.sourceWeb of Science-
dc.titleGenetic diversity of NS5A protein from hepatitis C virus genotype 3a and its relationship to therapy responseen
dc.typeoutro-
dc.contributor.institutionInstituto Butantan-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionAlbert Einstein Israeli Hosp-
dc.description.affiliationInstituto Butantan, Viral Immunol Lab, BR-05503900 São Paulo, Brazil-
dc.description.affiliationSão Paulo State Univ, UNESP, IBILCE,Dept Biol, Inst Biosci Language & Literature & Exact Sci, BR-15054010 São Paulo, Brazil-
dc.description.affiliationUniv São Paulo, BR-05508900 São Paulo, Brazil-
dc.description.affiliationUniv São Paulo, Fac Med, Dept Gastroenterol, Lab Hepatol & Gastroenterol,Inst Trop Med, BR-01246903 São Paulo, Brazil-
dc.description.affiliationAlbert Einstein Israeli Hosp, Dept Clin Pathol, BR-05652000 São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, UNESP, IBILCE,Dept Biol, Inst Biosci Language & Literature & Exact Sci, BR-15054010 São Paulo, Brazil-
dc.identifier.doi10.1186/1471-2334-10-36-
dc.identifier.wosWOS:000275622600001-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000275622600001.pdf-
dc.relation.ispartofBMC Infectious Diseases-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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