Abstract
Subtype-dependent selection of HIV-1 reverse transcriptase resistance mutation K65R was previously observed in cell culture and small clinical investigations. We compared K65R prevalence across subtypes A, B, C, F, G, and CRF02_AG separately in a cohort of 3,076 patients on combination therapy including tenofovir. K65R selection was significantly higher in HIV-1 subtype C. This could not be explained by clinical and demographic factors in multivariate analysis, suggesting subtype sequence-specific K65R pathways.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenine / analogs & derivatives*
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Adenine / therapeutic use
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Adult
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Anti-HIV Agents / therapeutic use*
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Drug Resistance, Viral / genetics
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Drug Therapy, Combination
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Female
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Genetic Variation
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HIV Infections / drug therapy
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HIV Infections / virology
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HIV Reverse Transcriptase / genetics*
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HIV-1 / classification
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HIV-1 / drug effects
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HIV-1 / enzymology
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HIV-1 / genetics
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Humans
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Male
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Middle Aged
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Molecular Sequence Data
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Organophosphonates / therapeutic use*
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RNA-Directed DNA Polymerase / genetics
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Reverse Transcriptase Inhibitors / pharmacology
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Reverse Transcriptase Inhibitors / therapeutic use*
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Tenofovir
Substances
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Anti-HIV Agents
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Organophosphonates
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Reverse Transcriptase Inhibitors
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Tenofovir
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reverse transcriptase, Human immunodeficiency virus 1
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HIV Reverse Transcriptase
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RNA-Directed DNA Polymerase
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Adenine
Associated data
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GENBANK/KC218938
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GENBANK/KC222012