Impact of nelfinavir resistance mutations on in vitro phenotype, fitness, and replication capacity of human immunodeficiency virus type 1 with subtype B and C proteases

Antimicrob Agents Chemother. 2004 Sep;48(9):3552-5. doi: 10.1128/AAC.48.9.3552-3555.2004.

Abstract

Human immunodeficiency virus type 1 subtype B and C proteases were manipulated to contain 90M, 88D, or 89L, and their in vitro biological properties were studied. We showed that D30N has significantly more impact in subtype C than in subtype B counterparts, accounting for the reported low prevalence of this mutation in patients failing nelfinavir-based regimens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Cloning, Molecular
  • DNA Primers
  • Drug Resistance, Viral
  • HIV Infections / virology
  • HIV Protease / genetics*
  • HIV Protease Inhibitors / pharmacology*
  • HIV-1 / drug effects*
  • HIV-1 / enzymology*
  • HIV-1 / genetics
  • Humans
  • Isoenzymes / genetics
  • Mutation / genetics*
  • Nelfinavir / pharmacology*
  • Phenotype
  • RNA, Viral / genetics
  • Recombinant Fusion Proteins / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transfection
  • Virus Replication / drug effects

Substances

  • DNA Primers
  • HIV Protease Inhibitors
  • Isoenzymes
  • RNA, Viral
  • Recombinant Fusion Proteins
  • HIV Protease
  • Nelfinavir