Increased ability for selection of zidovudine resistance in a distinct class of wild-type HIV-1 from drug-naive persons

Proc Natl Acad Sci U S A. 2001 Nov 20;98(24):13907-12. doi: 10.1073/pnas.241300698. Epub 2001 Nov 6.

Abstract

Transmission of HIV-1 with reduced susceptibility to antiretroviral drugs raises public health concerns. Through surveillance of drug-resistant HIV-1 in 603 treatment-naive, recently diagnosed HIV-1-infected persons, we identified a distinct group of viruses that have mutations at codon 215 of the reverse transcriptase (RT) gene that are different from either the wild-type (WT) T or the zidovudine (AZT)-selected T215Y/F. These mutations included 215D/C/S and were found in 20 patients (3.3%). The 215D, 215C, and 215S mutations differ from 215Y by a 1-nt change compared with 2 nt for the WT T215 and likely represent revertants of 215Y. These viruses all were found to have WT susceptibility to AZT, and all replicated efficiently as WT HIV-1(T215). However, differences in fitness among HIV-1(215D), HIV-1(215C), and HIV-1(215S) were seen when RT backgrounds were changed, demonstrating a role of the RT background in the selection of these revertants. In vitro selection with AZT showed that HIV-1(215D) and HIV-1(215C) acquired 215Y more rapidly than did WT HIV-1(T215), likely reflecting the need for only 1-nt change to evolve to 215Y. Our study demonstrates that HIV-1 with unusual mutations at codon 215 replicate efficiently, have WT susceptibility, and are commonly found in treatment-naive persons. The increased ability for selecting resistance mutations defines this class of WT HIV-1 and highlights the higher potential of these viruses to compromise the efficacy of antiretroviral therapy.

MeSH terms

  • Anti-HIV Agents / pharmacology*
  • Anti-HIV Agents / therapeutic use
  • Base Sequence
  • DNA, Viral
  • Didanosine / pharmacology
  • Dideoxynucleosides / pharmacology
  • Drug Resistance, Viral / genetics*
  • Evolution, Molecular
  • HIV Infections / drug therapy
  • HIV Infections / virology*
  • HIV Reverse Transcriptase / genetics*
  • HIV-1 / drug effects
  • HIV-1 / enzymology*
  • HIV-1 / genetics
  • Humans
  • Molecular Sequence Data
  • Mutagenesis
  • Recombination, Genetic
  • Reverse Transcriptase Inhibitors / pharmacology*
  • Reverse Transcriptase Inhibitors / therapeutic use
  • Stavudine / pharmacology
  • Virus Replication / genetics
  • Zalcitabine / pharmacology
  • Zidovudine / pharmacology*
  • Zidovudine / therapeutic use

Substances

  • Anti-HIV Agents
  • DNA, Viral
  • Dideoxynucleosides
  • Reverse Transcriptase Inhibitors
  • Zidovudine
  • Zalcitabine
  • Stavudine
  • HIV Reverse Transcriptase
  • Didanosine
  • abacavir

Associated data

  • GENBANK/AF415228
  • GENBANK/AF415229
  • GENBANK/AF415230
  • GENBANK/AF415231
  • GENBANK/AF415232
  • GENBANK/AF415233
  • GENBANK/AF415234