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HCV Genome-Wide Genetic Analyses in Context of Disease Progression and Hepatocellular Carcinoma

Hepatitis C virus (HCV) is a major cause of hepatitis and hepatocellular carcinoma (HCC) world-wide. Most HCV patients have relatively stable disease, but approximately 25% have progressive disease that often terminates in liver failure or HCC. HCV is highly variable genetically, with seven genotype...

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Autores principales: Donlin, Maureen J., Lomonosova, Elena, Kiss, Alexi, Cheng, Xiaohong, Cao, Feng, Curto, Teresa M., Di Bisceglie, Adrian, Tavis, John E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117537/
https://www.ncbi.nlm.nih.gov/pubmed/25079603
http://dx.doi.org/10.1371/journal.pone.0103748
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author Donlin, Maureen J.
Lomonosova, Elena
Kiss, Alexi
Cheng, Xiaohong
Cao, Feng
Curto, Teresa M.
Di Bisceglie, Adrian
Tavis, John E.
author_facet Donlin, Maureen J.
Lomonosova, Elena
Kiss, Alexi
Cheng, Xiaohong
Cao, Feng
Curto, Teresa M.
Di Bisceglie, Adrian
Tavis, John E.
author_sort Donlin, Maureen J.
collection PubMed
description Hepatitis C virus (HCV) is a major cause of hepatitis and hepatocellular carcinoma (HCC) world-wide. Most HCV patients have relatively stable disease, but approximately 25% have progressive disease that often terminates in liver failure or HCC. HCV is highly variable genetically, with seven genotypes and multiple subtypes per genotype. This variation affects HCV’s sensitivity to antiviral therapy and has been implicated to contribute to differences in disease. We sequenced the complete viral coding capacity for 107 HCV genotype 1 isolates to determine whether genetic variation between independent HCV isolates is associated with the rate of disease progression or development of HCC. Consensus sequences were determined by sequencing RT-PCR products from serum or plasma. Positions of amino acid conservation, amino acid diversity patterns, selection pressures, and genome-wide patterns of amino acid covariance were assessed in context of the clinical phenotypes. A few positions were found where the amino acid distributions or degree of positive selection differed between in the HCC and cirrhotic sequences. All other assessments of viral genetic variation and HCC failed to yield significant associations. Sequences from patients with slow disease progression were under a greater degree of positive selection than sequences from rapid progressors, but all other analyses comparing HCV from rapid and slow disease progressors were statistically insignificant. The failure to observe distinct sequence differences associated with disease progression or HCC employing methods that previously revealed strong associations with the outcome of interferon α-based therapy implies that variable ability of HCV to modulate interferon responses is not a dominant cause for differential pathology among HCV patients. This lack of significant associations also implies that host and/or environmental factors are the major causes of differential disease presentation in HCV patients.
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spelling pubmed-41175372014-08-04 HCV Genome-Wide Genetic Analyses in Context of Disease Progression and Hepatocellular Carcinoma Donlin, Maureen J. Lomonosova, Elena Kiss, Alexi Cheng, Xiaohong Cao, Feng Curto, Teresa M. Di Bisceglie, Adrian Tavis, John E. PLoS One Research Article Hepatitis C virus (HCV) is a major cause of hepatitis and hepatocellular carcinoma (HCC) world-wide. Most HCV patients have relatively stable disease, but approximately 25% have progressive disease that often terminates in liver failure or HCC. HCV is highly variable genetically, with seven genotypes and multiple subtypes per genotype. This variation affects HCV’s sensitivity to antiviral therapy and has been implicated to contribute to differences in disease. We sequenced the complete viral coding capacity for 107 HCV genotype 1 isolates to determine whether genetic variation between independent HCV isolates is associated with the rate of disease progression or development of HCC. Consensus sequences were determined by sequencing RT-PCR products from serum or plasma. Positions of amino acid conservation, amino acid diversity patterns, selection pressures, and genome-wide patterns of amino acid covariance were assessed in context of the clinical phenotypes. A few positions were found where the amino acid distributions or degree of positive selection differed between in the HCC and cirrhotic sequences. All other assessments of viral genetic variation and HCC failed to yield significant associations. Sequences from patients with slow disease progression were under a greater degree of positive selection than sequences from rapid progressors, but all other analyses comparing HCV from rapid and slow disease progressors were statistically insignificant. The failure to observe distinct sequence differences associated with disease progression or HCC employing methods that previously revealed strong associations with the outcome of interferon α-based therapy implies that variable ability of HCV to modulate interferon responses is not a dominant cause for differential pathology among HCV patients. This lack of significant associations also implies that host and/or environmental factors are the major causes of differential disease presentation in HCV patients. Public Library of Science 2014-07-31 /pmc/articles/PMC4117537/ /pubmed/25079603 http://dx.doi.org/10.1371/journal.pone.0103748 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Donlin, Maureen J.
Lomonosova, Elena
Kiss, Alexi
Cheng, Xiaohong
Cao, Feng
Curto, Teresa M.
Di Bisceglie, Adrian
Tavis, John E.
HCV Genome-Wide Genetic Analyses in Context of Disease Progression and Hepatocellular Carcinoma
title HCV Genome-Wide Genetic Analyses in Context of Disease Progression and Hepatocellular Carcinoma
title_full HCV Genome-Wide Genetic Analyses in Context of Disease Progression and Hepatocellular Carcinoma
title_fullStr HCV Genome-Wide Genetic Analyses in Context of Disease Progression and Hepatocellular Carcinoma
title_full_unstemmed HCV Genome-Wide Genetic Analyses in Context of Disease Progression and Hepatocellular Carcinoma
title_short HCV Genome-Wide Genetic Analyses in Context of Disease Progression and Hepatocellular Carcinoma
title_sort hcv genome-wide genetic analyses in context of disease progression and hepatocellular carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117537/
https://www.ncbi.nlm.nih.gov/pubmed/25079603
http://dx.doi.org/10.1371/journal.pone.0103748
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