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Gag drug resistance mutations in HIV-1 subtype C patients, failing a protease inhibitor inclusive treatment regimen, with detectable lopinavir levels

The development of antiretroviral (ARV) drugs and their use in human immunodeficiency virus type 1 (HIV-1) has led to the effective control of HIV replication in infected patients. However the emergence of resistant HIV-1 strains still remains a problem. Literature has shown that mutations may accum...

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Autores principales: Kelly Pillay, Sameshnee, Singh, Urisha, Singh, Avashna, Gordon, Michelle, Ndungu, Thumbi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International AIDS Society 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225273/
https://www.ncbi.nlm.nih.gov/pubmed/25397528
http://dx.doi.org/10.7448/IAS.17.4.19784
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author Kelly Pillay, Sameshnee
Singh, Urisha
Singh, Avashna
Gordon, Michelle
Ndungu, Thumbi
author_facet Kelly Pillay, Sameshnee
Singh, Urisha
Singh, Avashna
Gordon, Michelle
Ndungu, Thumbi
author_sort Kelly Pillay, Sameshnee
collection PubMed
description The development of antiretroviral (ARV) drugs and their use in human immunodeficiency virus type 1 (HIV-1) has led to the effective control of HIV replication in infected patients. However the emergence of resistant HIV-1 strains still remains a problem. Literature has shown that mutations may accumulate in the protease (PR) and gag regions of HIV-1 patients who fail therapy with protease inhibitor (PI) drugs [1, 2]. Gag mutations have also been found to play an important role in the evolution of PI resistance [2]. Despite this, the standard genotypic drug-resistance test examines mutations in the reverse transcriptase (RT) and PR region of HIV-1 and not gag [3]. This study investigated the frequency of gag drug resistance mutations in the absence of major PI mutations in HIV-1 subtype C patients, failing a PI inclusive treatment regimen. Sixty-eight samples were retrieved from patients that were classified as second line treatment failures as they had a viral load greater than 1000 copies\mL, as well as detectable lopinavir (LPV) levels. The gag and protease region of these patients were genotyped. Mutations in the gag and protease region were assessed using the REga Db sequencing tool and the CPR programme on the Stanford University HIV drug resistance database. The mean LPV level of these samples was 11.66 µg/mL. 69.11% (n=46) of the patients have no major PI mutations in protease. The following mutations that are associated with PI exposure were present in the data set: G62R (n=6), H219Q (n=11), S737T (n=8), I389T (n=8) and Q474L (n=7). Predictably, mutations that are associated with PI resistance were found, which are generally located in the p7/p1 and p1/p6 cleavage site. These mutations are K436R (n=4), I437V (n=1), L449P (n=5), R452K (n=4) and P453L\T (n=9). These results contribute to the knowledge of resistance mutations in gag and their impact on PI resistance.
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spelling pubmed-42252732014-11-12 Gag drug resistance mutations in HIV-1 subtype C patients, failing a protease inhibitor inclusive treatment regimen, with detectable lopinavir levels Kelly Pillay, Sameshnee Singh, Urisha Singh, Avashna Gordon, Michelle Ndungu, Thumbi J Int AIDS Soc Poster Sessions – Abstract P252 The development of antiretroviral (ARV) drugs and their use in human immunodeficiency virus type 1 (HIV-1) has led to the effective control of HIV replication in infected patients. However the emergence of resistant HIV-1 strains still remains a problem. Literature has shown that mutations may accumulate in the protease (PR) and gag regions of HIV-1 patients who fail therapy with protease inhibitor (PI) drugs [1, 2]. Gag mutations have also been found to play an important role in the evolution of PI resistance [2]. Despite this, the standard genotypic drug-resistance test examines mutations in the reverse transcriptase (RT) and PR region of HIV-1 and not gag [3]. This study investigated the frequency of gag drug resistance mutations in the absence of major PI mutations in HIV-1 subtype C patients, failing a PI inclusive treatment regimen. Sixty-eight samples were retrieved from patients that were classified as second line treatment failures as they had a viral load greater than 1000 copies\mL, as well as detectable lopinavir (LPV) levels. The gag and protease region of these patients were genotyped. Mutations in the gag and protease region were assessed using the REga Db sequencing tool and the CPR programme on the Stanford University HIV drug resistance database. The mean LPV level of these samples was 11.66 µg/mL. 69.11% (n=46) of the patients have no major PI mutations in protease. The following mutations that are associated with PI exposure were present in the data set: G62R (n=6), H219Q (n=11), S737T (n=8), I389T (n=8) and Q474L (n=7). Predictably, mutations that are associated with PI resistance were found, which are generally located in the p7/p1 and p1/p6 cleavage site. These mutations are K436R (n=4), I437V (n=1), L449P (n=5), R452K (n=4) and P453L\T (n=9). These results contribute to the knowledge of resistance mutations in gag and their impact on PI resistance. International AIDS Society 2014-11-02 /pmc/articles/PMC4225273/ /pubmed/25397528 http://dx.doi.org/10.7448/IAS.17.4.19784 Text en © 2014 Kelly Pillay S et al; licensee International AIDS Society http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Poster Sessions – Abstract P252
Kelly Pillay, Sameshnee
Singh, Urisha
Singh, Avashna
Gordon, Michelle
Ndungu, Thumbi
Gag drug resistance mutations in HIV-1 subtype C patients, failing a protease inhibitor inclusive treatment regimen, with detectable lopinavir levels
title Gag drug resistance mutations in HIV-1 subtype C patients, failing a protease inhibitor inclusive treatment regimen, with detectable lopinavir levels
title_full Gag drug resistance mutations in HIV-1 subtype C patients, failing a protease inhibitor inclusive treatment regimen, with detectable lopinavir levels
title_fullStr Gag drug resistance mutations in HIV-1 subtype C patients, failing a protease inhibitor inclusive treatment regimen, with detectable lopinavir levels
title_full_unstemmed Gag drug resistance mutations in HIV-1 subtype C patients, failing a protease inhibitor inclusive treatment regimen, with detectable lopinavir levels
title_short Gag drug resistance mutations in HIV-1 subtype C patients, failing a protease inhibitor inclusive treatment regimen, with detectable lopinavir levels
title_sort gag drug resistance mutations in hiv-1 subtype c patients, failing a protease inhibitor inclusive treatment regimen, with detectable lopinavir levels
topic Poster Sessions – Abstract P252
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225273/
https://www.ncbi.nlm.nih.gov/pubmed/25397528
http://dx.doi.org/10.7448/IAS.17.4.19784
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