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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/75169
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dc.contributor.authorBittar, Cíntia-
dc.contributor.authorJardim, Ana Carolina Gomes-
dc.contributor.authorYamasaki, Lilian Hiromi Tomonari-
dc.contributor.authorCarareto, Claudia Márcia Aparecida-
dc.contributor.authorPinho, João Renato Rebello-
dc.contributor.authorLemey, Philippe-
dc.contributor.authorde Carvalho-Mello, Isabel Maria Vicente Guedes-
dc.contributor.authorRahal, Paula-
dc.date.accessioned2014-05-27T11:29:00Z-
dc.date.accessioned2016-10-25T18:47:42Z-
dc.date.available2014-05-27T11:29:00Z-
dc.date.available2016-10-25T18:47:42Z-
dc.date.issued2013-04-25-
dc.identifierhttp://dx.doi.org/10.1371/journal.pone.0062393-
dc.identifier.citationPLoS ONE, v. 8, n. 4, 2013.-
dc.identifier.issn1932-6203-
dc.identifier.urihttp://hdl.handle.net/11449/75169-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/75169-
dc.description.abstractBackground:Hepatitis C is a disease spread throughout the world. Hepatitis C virus (HCV), the etiological agent of this disease, is a single-stranded positive RNA virus. Its genome encodes a single precursor protein that yields ten proteins after processing. NS5A, one of the non-structural viral proteins, is most associated with interferon-based therapy response, the approved treatment for hepatitis C in Brazil. HCV has a high mutation rate and therefore high variability, which may be important for evading the immune system and response to therapy. The aim of this study was to analyze the evolution of NS5A quasispecies before, during, and after treatment in patients infected with HCV genotype 3a who presented different therapy responses.Methods:Viral RNA was extracted, cDNA was synthesized, the NS5A region was amplified and cloned, and 15 clones from each time-point were sequenced. The sequences were analyzed for evolutionary history, genetic diversity and selection.Results:This analysis shows that the viral population that persists after treatment for most non-responder patients is present in before-treatment samples, suggesting it is adapted to evade treatment. In contrast, the population found in before treatment samples from most end-of-treatment responder patients either are selected out or appears in low frequency after relapse, therefore changing the population structure. The exceptions illustrate the uniqueness of the evolutionary process, and therefore the treatment resistance process, in each patient.Conclusion:Although evolutionary behavior throughout treatment showed that each patient presented different population dynamics unrelated to therapy outcome, it seems that the viral population from non-responders that resists the treatment already had strains that could evade therapy before it started. © 2013 Bittar et al.en
dc.language.isoeng-
dc.sourceScopus-
dc.subjectcomplementary DNA-
dc.subjectnonstructural protein 5A-
dc.subjectvirus RNA-
dc.subjectcontrolled study-
dc.subjectgenetic distance-
dc.subjectgenetic selection-
dc.subjectgenetic variability-
dc.subjectgenotyping technique-
dc.subjectHepatitis C virus-
dc.subjecthuman-
dc.subjectmicrobial population dynamics-
dc.subjectmolecular evolution-
dc.subjectmolecular phylogeny-
dc.subjectnonhuman-
dc.subjectnucleotide sequence-
dc.subjectpopulation structure-
dc.subjectRNA sequence-
dc.subjectsequence analysis-
dc.subjectstop codon-
dc.subjectunindexed sequence-
dc.subjectvirus cell interaction-
dc.subjectvirus genome-
dc.titleOn Hepatitis C Virus Evolution: The Interaction between Virus and Host towards Treatment Outcomeen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionAlbert Einstein Israeli Hospital-
dc.contributor.institutionKatholieke Universiteit Leuven - Lab. of Clinical and Epidemiological Virology (Rega Institute)-
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)-
dc.description.affiliationDepartment of Biology UNESP - São Paulo State University - IBILCE- - Institute of Bioscience Language and Literature and Exact Science, São José do Rio Preto, São Paulo-
dc.description.affiliationDepartment of Gastroenterology - Laboratory of Hepatology and Gastroenterology Institute of Tropical Medicine USP - São Paulo University - Faculty of Medicine, São Paulo, São Paulo-
dc.description.affiliationDepartment of Clinical Pathology Albert Einstein Israeli Hospital, São Paulo, São Paulo-
dc.description.affiliationKatholieke Universiteit Leuven - Lab. of Clinical and Epidemiological Virology (Rega Institute), Leuven-
dc.description.affiliationDepartamento de Medicina - Disciplina de Gastroenterologia Laboratório de Hepatologia Molecular Aplicada Universidade Federal de São Paulo - Escola Paulista de Medicina, São Paulo, São Paulo-
dc.description.affiliationUnespDepartment of Biology UNESP - São Paulo State University - IBILCE- - Institute of Bioscience Language and Literature and Exact Science, São José do Rio Preto, São Paulo-
dc.identifier.doi10.1371/journal.pone.0062393-
dc.identifier.wosWOS:000318341400053-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-84876704094.pdf-
dc.relation.ispartofPLOS ONE-
dc.identifier.scopus2-s2.0-84876704094-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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