Distribution and genetic analysis of TTV and TTMV major phylogenetic groups in French blood donors
TTV and TTMV (recently assigned to the floating genus Anellovirus) infect human populations (including healthy individuals) at high prevalence (>80%). They display notably high levels of genetic diversity, but very little is known regarding the distribution of Anellovirus genetic groups in human...
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Published in | Journal of medical virology Vol. 78; no. 2; pp. 298 - 304 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.02.2006
Wiley-Liss Wiley-Blackwell |
Subjects | |
Online Access | Get full text |
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Summary: | TTV and TTMV (recently assigned to the floating genus Anellovirus) infect human populations (including healthy individuals) at high prevalence (>80%). They display notably high levels of genetic diversity, but very little is known regarding the distribution of Anellovirus genetic groups in human populations. We analyzed the distribution of the major genetic groups of TTV and TTMV in healthy voluntary blood donors using group‐independent and group‐specific PCR amplifications systems, combined with sequence determination and phylogenetic analysis. Analysis of Anellovirus groups revealed a non‐random pattern of group distribution with a predominant prevalence of TTV phylogenetic groups 1, 3, and 5, and of TTMV group 1. Multiple co‐infections were observed. In addition, TTMV sequences exhibiting a high genetic divergence with reference sequences were identified. This study provided the first picture of the genetic distribution of the major phylogenetic groups of members of the genus Anellovirus in a cohort of French voluntary blood donors. Obtaining such data from a reference population comprising healthy individuals was an essential step that will allow the subsequent comparative analysis of cohorts including patients with well‐characterized diseases, in order to identify any possible relationship between Anellovirus infection and human diseases. J. Med. Virol. 78:298–304, 2006. © 2005 Wiley‐Liss, Inc. |
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Bibliography: | istex:C6FEC931C65A5E425CD275F27991A1F66A5667D0 ark:/67375/WNG-QWJBCGK9-L ArticleID:JMV20539 Etablissement Français du Sang (Paris, France) The GenBank accession numbers of the TTMV sequences reported in this article are: DQ221102 for F1TL1, DQ221103 for H1TL1, DQ221104 for D2TL3, and DQ223687-DQ223717 for the sequences of 31 clones (NCR region). The GenBank accession numbers of the TTMV sequences reported in this article are: DQ221102 for F1TL1, DQ221103 for H1TL1, DQ221104 for D2TL3, and DQ223687‐DQ223717 for the sequences of 31 clones (NCR region). ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0146-6615 1096-9071 |
DOI: | 10.1002/jmv.20539 |