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Prevalence, genetic diversity and antiretroviral drugs resistance-associated mutations among untreated HIV-1-infected pregnant women in Gabon, central Africa

BACKGROUND: In Africa, the wide genetic diversity of HIV has resulted in emergence of new strains, rapid spread of this virus in sub-Saharan populations and therefore spread of the HIV epidemic throughout the continent. METHODS: To determine the prevalence of antibodies to HIV among a high-risk popu...

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Autores principales: Caron, Mélanie, Lekana-Douki, Sonia Etenna, Makuwa, Maria, Obiang-Ndong, Guy-Patrick, Biba, Olivia, Nkoghé, Dieudonné, Kazanji, Mirdad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359209/
https://www.ncbi.nlm.nih.gov/pubmed/22433277
http://dx.doi.org/10.1186/1471-2334-12-64
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author Caron, Mélanie
Lekana-Douki, Sonia Etenna
Makuwa, Maria
Obiang-Ndong, Guy-Patrick
Biba, Olivia
Nkoghé, Dieudonné
Kazanji, Mirdad
author_facet Caron, Mélanie
Lekana-Douki, Sonia Etenna
Makuwa, Maria
Obiang-Ndong, Guy-Patrick
Biba, Olivia
Nkoghé, Dieudonné
Kazanji, Mirdad
author_sort Caron, Mélanie
collection PubMed
description BACKGROUND: In Africa, the wide genetic diversity of HIV has resulted in emergence of new strains, rapid spread of this virus in sub-Saharan populations and therefore spread of the HIV epidemic throughout the continent. METHODS: To determine the prevalence of antibodies to HIV among a high-risk population in Gabon, 1098 and 2916 samples were collected from pregnant women in 2005 and 2008, respectively. HIV genotypes were evaluated in 107 HIV-1-positive samples to determine the circulating subtypes of strains and their resistance to antiretroviral drugs (ARVs). RESULTS: The seroprevalences were 6.3% in 2005 and 6.0% in 2008. The main subtype was recombinant CRF02_AG (46.7%), followed by the subtypes A (19.6%), G (10.3%), F (4.7%), H (1.9%) and D (0.9%) and the complex recombinants CRF06_cpx (1.9%) and CRF11_cpx (1.9%); 12.1% of subtypes could not be characterized. Analysis of ARVs resistance to the protease and reverse transcriptase coding regions showed mutations associated with extensive subtype polymorphism. In the present study, the HIV strains showed reduced susceptibility to ARVs (2.8%), particularly to protease inhibitors (1.9%) and nucleoside reverse transcriptase inhibitors (0.9%). CONCLUSIONS: The evolving genetic diversity of HIV calls for continuous monitoring of its molecular epidemiology in Gabon and in other central African countries.
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spelling pubmed-33592092012-05-24 Prevalence, genetic diversity and antiretroviral drugs resistance-associated mutations among untreated HIV-1-infected pregnant women in Gabon, central Africa Caron, Mélanie Lekana-Douki, Sonia Etenna Makuwa, Maria Obiang-Ndong, Guy-Patrick Biba, Olivia Nkoghé, Dieudonné Kazanji, Mirdad BMC Infect Dis Research Article BACKGROUND: In Africa, the wide genetic diversity of HIV has resulted in emergence of new strains, rapid spread of this virus in sub-Saharan populations and therefore spread of the HIV epidemic throughout the continent. METHODS: To determine the prevalence of antibodies to HIV among a high-risk population in Gabon, 1098 and 2916 samples were collected from pregnant women in 2005 and 2008, respectively. HIV genotypes were evaluated in 107 HIV-1-positive samples to determine the circulating subtypes of strains and their resistance to antiretroviral drugs (ARVs). RESULTS: The seroprevalences were 6.3% in 2005 and 6.0% in 2008. The main subtype was recombinant CRF02_AG (46.7%), followed by the subtypes A (19.6%), G (10.3%), F (4.7%), H (1.9%) and D (0.9%) and the complex recombinants CRF06_cpx (1.9%) and CRF11_cpx (1.9%); 12.1% of subtypes could not be characterized. Analysis of ARVs resistance to the protease and reverse transcriptase coding regions showed mutations associated with extensive subtype polymorphism. In the present study, the HIV strains showed reduced susceptibility to ARVs (2.8%), particularly to protease inhibitors (1.9%) and nucleoside reverse transcriptase inhibitors (0.9%). CONCLUSIONS: The evolving genetic diversity of HIV calls for continuous monitoring of its molecular epidemiology in Gabon and in other central African countries. BioMed Central 2012-03-20 /pmc/articles/PMC3359209/ /pubmed/22433277 http://dx.doi.org/10.1186/1471-2334-12-64 Text en Copyright ©2012 Caron et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Caron, Mélanie
Lekana-Douki, Sonia Etenna
Makuwa, Maria
Obiang-Ndong, Guy-Patrick
Biba, Olivia
Nkoghé, Dieudonné
Kazanji, Mirdad
Prevalence, genetic diversity and antiretroviral drugs resistance-associated mutations among untreated HIV-1-infected pregnant women in Gabon, central Africa
title Prevalence, genetic diversity and antiretroviral drugs resistance-associated mutations among untreated HIV-1-infected pregnant women in Gabon, central Africa
title_full Prevalence, genetic diversity and antiretroviral drugs resistance-associated mutations among untreated HIV-1-infected pregnant women in Gabon, central Africa
title_fullStr Prevalence, genetic diversity and antiretroviral drugs resistance-associated mutations among untreated HIV-1-infected pregnant women in Gabon, central Africa
title_full_unstemmed Prevalence, genetic diversity and antiretroviral drugs resistance-associated mutations among untreated HIV-1-infected pregnant women in Gabon, central Africa
title_short Prevalence, genetic diversity and antiretroviral drugs resistance-associated mutations among untreated HIV-1-infected pregnant women in Gabon, central Africa
title_sort prevalence, genetic diversity and antiretroviral drugs resistance-associated mutations among untreated hiv-1-infected pregnant women in gabon, central africa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359209/
https://www.ncbi.nlm.nih.gov/pubmed/22433277
http://dx.doi.org/10.1186/1471-2334-12-64
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