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Evidence of recombination in intrapatient populations of hepatitis C virus
Hepatitis C virus (HCV) is a major cause of liver disease worldwide and a potential cause of substantial morbidity and mortality in the future. HCV is characterized by a high level of genetic heterogeneity. Although homologous recombination has been demonstrated in many members of the family Flavivi...
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Published in: | PloS one 2008-09, Vol.3 (9), p.e3239-e3239 |
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creator | Sentandreu, Vicente Jiménez-Hernández, Nuria Torres-Puente, Manuela Bracho, María Alma Valero, Ana Gosalbes, María José Ortega, Enrique Moya, Andrés González-Candelas, Fernando |
description | Hepatitis C virus (HCV) is a major cause of liver disease worldwide and a potential cause of substantial morbidity and mortality in the future. HCV is characterized by a high level of genetic heterogeneity. Although homologous recombination has been demonstrated in many members of the family Flaviviridae, to which HCV belongs, there are only a few studies reporting recombination on natural populations of HCV, suggesting that these events are rare in vivo. Furthermore, these few studies have focused on recombination between different HCV genotypes/subtypes but there are no reports on the extent of intra-genotype or intra-subtype recombination between viral strains infecting the same patient. Given the important implications of recombination for RNA virus evolution, our aim in this study has been to assess the existence and eventually the frequency of intragenic recombination on HCV. For this, we retrospectively have analyzed two regions of the HCV genome (NS5A and E1-E2) in samples from two different groups: (i) patients infected only with HCV (either treated with interferon plus ribavirin or treatment naïve), and (ii) HCV-HIV co-infected patients (with and without treatment against HIV). The complete data set comprised 17712 sequences from 136 serum samples derived from 111 patients. Recombination analyses were performed using 6 different methods implemented in the program RDP3. Recombination events were considered when detected by at least 3 of the 6 methods used and were identified in 10.7% of the amplified samples, distributed throughout all the groups described and the two genomic regions studied. The resulting recombination events were further verified by detailed phylogenetic analyses. The complete experimental procedure was applied to an artificial mixture of relatively closely viral populations and the ensuing analyses failed to reveal artifactual recombination. From these results we conclude that recombination should be considered as a potentially relevant mechanism generating genetic variation in HCV and with important implications for the treatment of this infection. |
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HCV is characterized by a high level of genetic heterogeneity. Although homologous recombination has been demonstrated in many members of the family Flaviviridae, to which HCV belongs, there are only a few studies reporting recombination on natural populations of HCV, suggesting that these events are rare in vivo. Furthermore, these few studies have focused on recombination between different HCV genotypes/subtypes but there are no reports on the extent of intra-genotype or intra-subtype recombination between viral strains infecting the same patient. Given the important implications of recombination for RNA virus evolution, our aim in this study has been to assess the existence and eventually the frequency of intragenic recombination on HCV. For this, we retrospectively have analyzed two regions of the HCV genome (NS5A and E1-E2) in samples from two different groups: (i) patients infected only with HCV (either treated with interferon plus ribavirin or treatment naïve), and (ii) HCV-HIV co-infected patients (with and without treatment against HIV). The complete data set comprised 17712 sequences from 136 serum samples derived from 111 patients. Recombination analyses were performed using 6 different methods implemented in the program RDP3. Recombination events were considered when detected by at least 3 of the 6 methods used and were identified in 10.7% of the amplified samples, distributed throughout all the groups described and the two genomic regions studied. The resulting recombination events were further verified by detailed phylogenetic analyses. The complete experimental procedure was applied to an artificial mixture of relatively closely viral populations and the ensuing analyses failed to reveal artifactual recombination. From these results we conclude that recombination should be considered as a potentially relevant mechanism generating genetic variation in HCV and with important implications for the treatment of this infection.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0003239</identifier><identifier>PMID: 18800167</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acquired immune deficiency syndrome ; AIDS ; Algorithms ; Analysis ; Antiviral Agents - pharmacology ; Bioinformatics ; Biological evolution ; Biological response modifiers ; Cloning ; Computational Biology/Population Genetics ; Computers ; Genes ; Genetic diversity ; Genetic Variation ; Genetics and Genomics/Microbial Evolution and Genomics ; Genetics and Genomics/Population Genetics ; Genome ; Genomes ; Genomics ; Genotype ; Genotype & phenotype ; Genotypes ; Health aspects ; Hepacivirus - metabolism ; Hepatitis ; Hepatitis C ; Hepatitis C virus ; HIV ; Homologous recombination ; Homology ; Human immunodeficiency virus ; Identification methods ; In vivo methods and tests ; Infections ; Interferon ; Likelihood Functions ; Liver ; Liver diseases ; Models, Genetic ; Morbidity ; Mortality ; Natural populations ; Patients ; Phylogenetics ; Phylogeny ; Populations ; Public Health and Epidemiology/Infectious Diseases ; Recombination, Genetic ; Ribavirin ; Ribonucleic acid ; RNA ; RNA viruses ; Software ; Studies ; Virology/Immune Evasion ; Virology/Virus Evolution and Symbiosis ; Viruses</subject><ispartof>PloS one, 2008-09, Vol.3 (9), p.e3239-e3239</ispartof><rights>COPYRIGHT 2008 Public Library of Science</rights><rights>2008 Sentandreu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Sentandreu et al. 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c662t-144337b24b460e000ce897de79a68ae5107eb8d3dc7b9d51bcbe64c287fc91293</citedby><cites>FETCH-LOGICAL-c662t-144337b24b460e000ce897de79a68ae5107eb8d3dc7b9d51bcbe64c287fc91293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1312326206/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1312326206?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18800167$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Papavasiliou, Nina</contributor><creatorcontrib>Sentandreu, Vicente</creatorcontrib><creatorcontrib>Jiménez-Hernández, Nuria</creatorcontrib><creatorcontrib>Torres-Puente, Manuela</creatorcontrib><creatorcontrib>Bracho, María Alma</creatorcontrib><creatorcontrib>Valero, Ana</creatorcontrib><creatorcontrib>Gosalbes, María José</creatorcontrib><creatorcontrib>Ortega, Enrique</creatorcontrib><creatorcontrib>Moya, Andrés</creatorcontrib><creatorcontrib>González-Candelas, Fernando</creatorcontrib><title>Evidence of recombination in intrapatient populations of hepatitis C virus</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Hepatitis C virus (HCV) is a major cause of liver disease worldwide and a potential cause of substantial morbidity and mortality in the future. HCV is characterized by a high level of genetic heterogeneity. Although homologous recombination has been demonstrated in many members of the family Flaviviridae, to which HCV belongs, there are only a few studies reporting recombination on natural populations of HCV, suggesting that these events are rare in vivo. Furthermore, these few studies have focused on recombination between different HCV genotypes/subtypes but there are no reports on the extent of intra-genotype or intra-subtype recombination between viral strains infecting the same patient. Given the important implications of recombination for RNA virus evolution, our aim in this study has been to assess the existence and eventually the frequency of intragenic recombination on HCV. For this, we retrospectively have analyzed two regions of the HCV genome (NS5A and E1-E2) in samples from two different groups: (i) patients infected only with HCV (either treated with interferon plus ribavirin or treatment naïve), and (ii) HCV-HIV co-infected patients (with and without treatment against HIV). The complete data set comprised 17712 sequences from 136 serum samples derived from 111 patients. Recombination analyses were performed using 6 different methods implemented in the program RDP3. Recombination events were considered when detected by at least 3 of the 6 methods used and were identified in 10.7% of the amplified samples, distributed throughout all the groups described and the two genomic regions studied. The resulting recombination events were further verified by detailed phylogenetic analyses. The complete experimental procedure was applied to an artificial mixture of relatively closely viral populations and the ensuing analyses failed to reveal artifactual recombination. From these results we conclude that recombination should be considered as a potentially relevant mechanism generating genetic variation in HCV and with important implications for the treatment of this infection.</description><subject>Acquired immune deficiency syndrome</subject><subject>AIDS</subject><subject>Algorithms</subject><subject>Analysis</subject><subject>Antiviral Agents - pharmacology</subject><subject>Bioinformatics</subject><subject>Biological evolution</subject><subject>Biological response modifiers</subject><subject>Cloning</subject><subject>Computational Biology/Population Genetics</subject><subject>Computers</subject><subject>Genes</subject><subject>Genetic diversity</subject><subject>Genetic Variation</subject><subject>Genetics and Genomics/Microbial Evolution and Genomics</subject><subject>Genetics and Genomics/Population Genetics</subject><subject>Genome</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Genotype</subject><subject>Genotype & 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Nina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence of recombination in intrapatient populations of hepatitis C virus</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2008-09-18</date><risdate>2008</risdate><volume>3</volume><issue>9</issue><spage>e3239</spage><epage>e3239</epage><pages>e3239-e3239</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Hepatitis C virus (HCV) is a major cause of liver disease worldwide and a potential cause of substantial morbidity and mortality in the future. HCV is characterized by a high level of genetic heterogeneity. Although homologous recombination has been demonstrated in many members of the family Flaviviridae, to which HCV belongs, there are only a few studies reporting recombination on natural populations of HCV, suggesting that these events are rare in vivo. Furthermore, these few studies have focused on recombination between different HCV genotypes/subtypes but there are no reports on the extent of intra-genotype or intra-subtype recombination between viral strains infecting the same patient. Given the important implications of recombination for RNA virus evolution, our aim in this study has been to assess the existence and eventually the frequency of intragenic recombination on HCV. For this, we retrospectively have analyzed two regions of the HCV genome (NS5A and E1-E2) in samples from two different groups: (i) patients infected only with HCV (either treated with interferon plus ribavirin or treatment naïve), and (ii) HCV-HIV co-infected patients (with and without treatment against HIV). The complete data set comprised 17712 sequences from 136 serum samples derived from 111 patients. Recombination analyses were performed using 6 different methods implemented in the program RDP3. Recombination events were considered when detected by at least 3 of the 6 methods used and were identified in 10.7% of the amplified samples, distributed throughout all the groups described and the two genomic regions studied. The resulting recombination events were further verified by detailed phylogenetic analyses. The complete experimental procedure was applied to an artificial mixture of relatively closely viral populations and the ensuing analyses failed to reveal artifactual recombination. From these results we conclude that recombination should be considered as a potentially relevant mechanism generating genetic variation in HCV and with important implications for the treatment of this infection.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>18800167</pmid><doi>10.1371/journal.pone.0003239</doi><tpages>e3239</tpages><oa>free_for_read</oa></addata></record> |
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recordid | cdi_plos_journals_1312326206 |
source | Open Access: PubMed Central; Publicly Available Content Database |
subjects | Acquired immune deficiency syndrome AIDS Algorithms Analysis Antiviral Agents - pharmacology Bioinformatics Biological evolution Biological response modifiers Cloning Computational Biology/Population Genetics Computers Genes Genetic diversity Genetic Variation Genetics and Genomics/Microbial Evolution and Genomics Genetics and Genomics/Population Genetics Genome Genomes Genomics Genotype Genotype & phenotype Genotypes Health aspects Hepacivirus - metabolism Hepatitis Hepatitis C Hepatitis C virus HIV Homologous recombination Homology Human immunodeficiency virus Identification methods In vivo methods and tests Infections Interferon Likelihood Functions Liver Liver diseases Models, Genetic Morbidity Mortality Natural populations Patients Phylogenetics Phylogeny Populations Public Health and Epidemiology/Infectious Diseases Recombination, Genetic Ribavirin Ribonucleic acid RNA RNA viruses Software Studies Virology/Immune Evasion Virology/Virus Evolution and Symbiosis Viruses |
title | Evidence of recombination in intrapatient populations of hepatitis C virus |
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