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ABSTRACT: Background
In this work, we investigated the genetic diversity of HIV-1 and the presence of mutations conferring antiretroviral drug resistance in 50 drug-naïve infected persons in the Republic of Congo (RoC). Samples were obtained before large-scale access to HAART in 2002 and 2004.Methods
To assess the HIV-1 genetic recombination, the sequencing of the pol gene encoding a protease and partial reverse transcriptase was performed and analyzed with updated references, including newly characterized CRFs. The assessment of drug resistance was conducted according to the WHO protocol.Results
Among the 50 samples analyzed for the pol gene, 50% were classified as intersubtype recombinants, charring complex structures inside the pol fragment. Five samples could not be classified (noted U). The most prevalent subtypes were G with 10 isolates and D with 11 isolates. One isolate of A, J, H, CRF05, CRF18 and CRF37 were also found. Two samples (4%) harboring the mutations M230L and Y181C associated with the TAMs M41L and T215Y, respectively, were found.Conclusion
This first study in the RoC, based on WHO classification, shows that the threshold of transmitted drug resistance before large-scale access to antiretroviral therapy is 4%.
SUBMITTER: Niama FR
PROVIDER: S-EPMC5498887 | biostudies-literature | 2017 Jul
REPOSITORIES: biostudies-literature

Niama Fabien Roch FR Vidal Nicole N Diop-Ndiaye Halimatou H Nguimbi Etienne E Ahombo Gabriel G Diakabana Philippe P Bayonne Kombo Édith Sophie ÉS Mayengue Pembe Issamou PI Kobawila Simon-Charles SC Parra Henri Joseph HJ Toure-Kane Coumba C
BMC research notes 20170705 1
<h4>Background</h4>In this work, we investigated the genetic diversity of HIV-1 and the presence of mutations conferring antiretroviral drug resistance in 50 drug-naïve infected persons in the Republic of Congo (RoC). Samples were obtained before large-scale access to HAART in 2002 and 2004.<h4>Methods</h4>To assess the HIV-1 genetic recombination, the sequencing of the pol gene encoding a protease and partial reverse transcriptase was performed and analyzed with updated references, including ne ...[more]