Evidence for extensive genotypic diversity and recombination of GB virus C (GBV‐C) in Germany
Identifieur interne : 000881 ( Main/Exploration ); précédent : 000880; suivant : 000882Evidence for extensive genotypic diversity and recombination of GB virus C (GBV‐C) in Germany
Auteurs : Markus Neibecker [Allemagne] ; Carolynne Schwarze-Zander [Allemagne] ; Jürgen K. Rockstroh [Allemagne] ; Ulrich Spengler [Allemagne] ; Jason T. Blackard [États-Unis]Source :
- Journal of Medical Virology [ 0146-6615 ] ; 2011-04.
English descriptors
- KwdEn :
- Accession numbers, Bayesian, Bootstrap, Chronic hepatitis, Genome, Genotype, Genotype distribution, Hepatitis, Intergenotypic recombination, Limited number, Muerhoff, Novel genotype, Outlier, Outlier group, Phylogenetic, Phylogenetic analysis, Positive subjects, Recombinant, Recombination, Untranslated region, Virol.
- Teeft :
- Accession numbers, Bayesian, Bootstrap, Chronic hepatitis, Genome, Genotype, Genotype distribution, Hepatitis, Intergenotypic recombination, Limited number, Muerhoff, Novel genotype, Outlier, Outlier group, Phylogenetic, Phylogenetic analysis, Positive subjects, Recombinant, Recombination, Untranslated region, Virol.
Abstract
Multiple genotypes of GB virus C (GBV‐C)—a non‐pathogenic flavivirus—have been identified to date, although they are not uniformly distributed worldwide. It has also been suggested that GBV‐C genotype may play a role in modulating HIV disease; however, the prevalence and genotype distribution of GBV‐C has not been adequately studied in most countries. Among 408 HIV positive subjects in Germany, 97 (23.8%) had detectable GBV‐C RNA. Based on sequencing of the 5′ untranslated region (5′‐UTR), the GBV‐C genotypes were 1 (n = 8; 8.2%), 2 (n = 81; 83.5%), and 3 (n = 2; 2.1%), as well as a unique genotype not previously reported (n = 6; 6.2%). Among 17 samples also sequenced in the envelope 2 (E2) region, 14 had concordant genotype results when comparing the 5′‐UTR and E2, while evidence of intergenotypic recombination was observed among E2 sequences from 3 individuals. These results suggest that genotypic diversity and viral recombination contribute to the overall genetic variability of GBV‐C. J. Med. Virol. 83:685–694, 2011. © 2011 Wiley‐Liss, Inc.
Url:
DOI: 10.1002/jmv.22029
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Multiple genotypes of GB virus C (GBV‐C)—a non‐pathogenic flavivirus—have been identified to date, although they are not uniformly distributed worldwide. It has also been suggested that GBV‐C genotype may play a role in modulating HIV disease; however, the prevalence and genotype distribution of GBV‐C has not been adequately studied in most countries. Among 408 HIV positive subjects in Germany, 97 (23.8%) had detectable GBV‐C RNA. Based on sequencing of the 5′ untranslated region (5′‐UTR), the GBV‐C genotypes were 1 (n = 8; 8.2%), 2 (n = 81; 83.5%), and 3 (n = 2; 2.1%), as well as a unique genotype not previously reported (n = 6; 6.2%). Among 17 samples also sequenced in the envelope 2 (E2) region, 14 had concordant genotype results when comparing the 5′‐UTR and E2, while evidence of intergenotypic recombination was observed among E2 sequences from 3 individuals. These results suggest that genotypic diversity and viral recombination contribute to the overall genetic variability of GBV‐C. J. Med. Virol. 83:685–694, 2011. © 2011 Wiley‐Liss, Inc.</div>
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