Abstract
Changes in the drug susceptibility, gene lineage, and deduced amino acid sequences of the reverse transcriptase (RT) of human immunodeficiency virus type 1 (HIV-1) subtype E following 3'-azido-3'-deoxythymidine (AZT) monotherapy or AZT-2', 3'-dideoxyinosine combination therapy were examined with sequential virus isolates from a single family. The changes were compared to those reported for HIV-1 subtype B, revealing striking similarities in selected phenotype and amino acids independent of differences in the RT backbone sequences that constantly distinguish the two subtypes. Particularly, identical amino acid substitutions were present simultaneously at four different positions (D67N, K70R, T215F, and K219Q) for high-level AZT resistance. These data suggest that HIV-1 subtypes E and B evolve convergently at the phenotypic and amino acid levels when the nucleoside analogue RT inhibitors act as selective forces.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Amino Acid Substitution
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Anti-HIV Agents / therapeutic use*
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Base Sequence
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DNA, Viral
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Didanosine / therapeutic use*
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Drug Resistance, Microbial / genetics
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Evolution, Molecular*
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Female
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HIV Infections / drug therapy
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HIV Infections / virology*
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HIV Reverse Transcriptase / chemistry
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HIV Reverse Transcriptase / classification
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HIV Reverse Transcriptase / drug effects
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HIV Reverse Transcriptase / genetics*
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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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HIV-1 / isolation & purification
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Humans
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Male
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Molecular Sequence Data
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Protein Structure, Secondary
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Reverse Transcriptase Inhibitors / therapeutic use*
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Zidovudine / therapeutic use*
Substances
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Anti-HIV Agents
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DNA, Viral
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Reverse Transcriptase Inhibitors
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Zidovudine
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HIV Reverse Transcriptase
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Didanosine
Associated data
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GENBANK/AB038655
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GENBANK/AB038656
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GENBANK/AB038657
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GENBANK/AB038658
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GENBANK/AB038659
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GENBANK/AB038660
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GENBANK/AB038661