Antiretroviral Resistance and Genetic Diversity of Human Immunodeficiency Virus Type 1 Isolates from the Federal District, Central Brazil
In the context of universal access to antiretroviral therapy, the surveillance of human immunodeficiency virus type 1 (HIV-1) genetic diversity and resistance becomes pivotal. In this work our purpose was to describe the genetic variability; prevalence of drug-resistance mutations; and genotypic res...
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Published in | Memórias do Instituto Oswaldo Cruz Vol. 99; no. 8 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Fundação Oswaldo Cruz, Fiocruz
14.02.2005
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Subjects | |
Online Access | Get full text |
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Summary: | In the context of universal access to antiretroviral therapy, the
surveillance of human immunodeficiency virus type 1 (HIV-1) genetic
diversity and resistance becomes pivotal. In this work our purpose was
to describe the genetic variability; prevalence of drug-resistance
mutations; and genotypic resistance profiles in HIV-1 infected
individuals under antiretroviral treatment, from the Federal District,
Brasília, Central Brazil. The entire viral protease and codons 19
to 234 of the reverse transcriptase gene from 45 HIV-1 isolates were
amplified and sequenced for subtyping and genotyping. By phylogenetic
analysis, 96% of the samples clustered with subtype B and the remaining
4% with HIV-1 subtype F sequences. One major protease inhibitor
resistance-associated mutation, I50V, was detected in 38% of the
samples. Minor mutations were also found at the protease gene: L10I/V
(7%), K20M (2%), M36I (11%), L63P (20%), A71T (2%), and V77I (7%). Many
mutations associated with reduced susceptibility to nucleoside or
non-nucleoside reverse transcriptase inhibitors were detected: M41L
(11%), E44D (4%), D67N (11%), T69D (2%), K70R (11%), L74V (2%), L100I
(4%), K103N (18%), V118I (9%), Y181C (11%), M184V (18%), G190A (4%),
T215Y (4%), and K219E (4%). This study has shown that 84% of the
studied population from the Federal District, showing evidences of
therapy failure, presented viral genomic mutations associated with drug
resistance. The main antiretrovirals to which this population showed
resistance were the PI amprenavir (38%), the NNRTIs delavirdine,
nevirapine (31%), and efavirenz (24%), and the NRTIs lamivudine (18%),
abacavir, and zidovudine (13%). |
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ISSN: | 1678-8060 |