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dc.contributor.authorEscobar-Gutierrez, Alejandro-
dc.contributor.authorSoudeyns, Hugo-
dc.contributor.authorLarouche, Ariane-
dc.contributor.authorCarlos Carpio-Pedroza, Juan-
dc.contributor.authorMartinez-Guarneros, Armando-
dc.contributor.authorVazquez-Chacon, Carlos A.-
dc.contributor.authorFonseca-Coronado, Salvador-
dc.contributor.authorYamasaki, Lilian H. T.-
dc.contributor.authorRuiz-Tovar, Karina-
dc.contributor.authorCruz-Rivera, Mayra-
dc.date.accessioned2014-12-03T13:11:06Z-
dc.date.accessioned2016-10-25T20:12:10Z-
dc.date.available2014-12-03T13:11:06Z-
dc.date.available2016-10-25T20:12:10Z-
dc.date.issued2013-12-01-
dc.identifierhttp://dx.doi.org/10.1016/j.meegid.2013.10.005-
dc.identifier.citationInfection Genetics And Evolution. Amsterdam: Elsevier Science Bv, v. 20, p. 465-470, 2013.-
dc.identifier.issn1567-1348-
dc.identifier.urihttp://hdl.handle.net/11449/112858-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/112858-
dc.description.abstractGlobally, hepatitis C virus (HCV) infection affects approximately 130 million people and 3 million new infections occur annually. HCV is also recognized as an important cause of chronic liver disease in children. The absence of proofreading properties of the HCV RNA polymerase leads to a highly error prone replication process, allowing HCV to escape host immune response. The adaptive nature of HCV evolution dictates the outcome of the disease in many ways. Here, we investigated the molecular evolution of HCV in three unrelated children who acquired chronic HCV infection as a result of mother-to-child transmission, two of whom were also coinfected with HIV-1. The persistence of discrete HCV variants and their population structure were assessed using median joining network and Bayesian approaches. While patterns of viral evolution clearly differed between subjects, immune system dysfunction related to HIV coinfection or persistent HCV seronegativity stand as potential mechanisms to explain the lack of molecular evolution observed in these three cases. In contrast, treatment of HCV infection with PegIFN, which did not lead to sustained virologic responses in all 3 cases, was not associated with commensurate variations in the complexity of the variant spectrum. Finally, the differences in the degree of divergence suggest that the mode of transmission of the virus was not the main factor driving viral evolution. (C) 2013 Elsevier B. V. All rights reserved.en
dc.description.sponsorshipCanadian Institutes for Health Research (CIHR)/Health Canada Research Initiative on Hepatitis C-
dc.description.sponsorshipCANFAR-
dc.description.sponsorshipCanadian Foundation for AIDS Research-
dc.description.sponsorshipReseau SIDA-maladies infectieuses of the Fonds de la recherche du Quebec-sante (FRQS)-
dc.description.sponsorshipFondation CHU Sainte-Justine-
dc.description.sponsorshipFRQS-
dc.description.sponsorshipProyecto PAPIIT-
dc.description.sponsorshipDireccion General de Asuntos del Personal Academico-
dc.description.sponsorshipUniversidad Nacional Autonoma de Mexico y Fondo Sectorial de Investigacion en Salud y Seguridad Social-
dc.description.sponsorshipConsejo Nacional de Ciencia y Tecnologia-
dc.format.extent465-470-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectHepatitis C virusen
dc.subjectVertical transmissionen
dc.subjectMolecular evolutionen
dc.titleVertical transmission of hepatitis C virus: A tale of multiple outcomesen
dc.typeoutro-
dc.contributor.institutionInst Diagnost & Referencia Epidemiol-
dc.contributor.institutionCHU St Justine-
dc.contributor.institutionUniv Montreal-
dc.contributor.institutionUniv Nacl Autonoma Mexico-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationInst Diagnost & Referencia Epidemiol, Mexico City, DF, Mexico-
dc.description.affiliationCHU St Justine, Ctr Rech, Unite Immunopathol Virale, Montreal, PQ, Canada-
dc.description.affiliationUniv Montreal, Fac Med, Dept Microbiol Infectiol & Immunol, Montreal, PQ H3C 3J7, Canada-
dc.description.affiliationUniv Nacl Autonoma Mexico, Fac Estudios Super Cuautitlan, Unidad Invest Multidisciplinaria, Lab Inmunobiol Enfermedades Infecciosas, Mexico City, Estado De Mexic, Mexico-
dc.description.affiliationSao Paulo State Univ, Inst Biosci Language & Exact Sci, Dept Biol, Sao Jose Do Rio Preto, SP, Brazil-
dc.description.affiliationUniv Nacl Autonoma Mexico, Fac Med, Mexico City 04510, DF, Mexico-
dc.description.affiliationUnespSao Paulo State Univ, Inst Biosci Language & Exact Sci, Dept Biol, Sao Jose Do Rio Preto, SP, Brazil-
dc.description.sponsorshipIdCanadian Institutes for Health Research (CIHR)/Health Canada Research Initiative on Hepatitis CEOP-41537-
dc.description.sponsorshipIdCanadian Foundation for AIDS Research013515-
dc.description.sponsorshipIdProyecto PAPIITTA200112-
dc.description.sponsorshipIdUniversidad Nacional Autonoma de Mexico y Fondo Sectorial de Investigacion en Salud y Seguridad Social2012 C01-181585-
dc.identifier.doi10.1016/j.meegid.2013.10.005-
dc.identifier.wosWOS:000327701200058-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofInfection, Genetics and Evolution-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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