Use of Drug Resistance Sequence Data for the Systematic Detection of Non‐B Human Immunodeficiency Virus Type 1 (HIV‐1) Subtypes: How to Create a Sentinel Site for Monitoring the Genetic Diversity of HIV‐1 at a Country Scale
Author(s) -
Nouara Yahi,
Jacques Fantini,
Christian Tourrès,
Natacha Tivoli,
Nathalie Koch,
Catherine Tamalet
Publication year - 2001
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/319859
Subject(s) - virology , protease , reverse transcriptase , biology , drug resistance , phylogenetic tree , sequence analysis , integrase , virus , genetics , lentivirus , coding region , polymerase chain reaction , gene , human immunodeficiency virus (hiv) , viral disease , enzyme , biochemistry
To assess the molecular epidemiology of human immunodeficiency virus type 1 (HIV-1), a screening method was developed for identification of non-B subtypes from sequence data obtained for resistance testing. The method is based on the evaluation of the percentage of divergence of a given sequence from the reference B subtype HXB2. Analysis of 1720 reverse-transcriptase (RT) and 1824 protease sequences stored in a database allowed for the determination of a threshold level of divergence from HXB2 above which a non-B subtype could be unambiguously characterized regardless of the pattern of resistance mutations (>8.6% for RT; >10.8% for protease). This conclusion was validated by phylogenetic analysis of RT, protease, and env genes. Overall, 72 (4.2%) and 73 (4.0%) non-B sequences were identified in the RT and protease coding regions, respectively. This method allows for the rapid detection of non-B subtypes among retrospective, recent, and future RT and/or protease sequence databases.
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