An A643V amino acid substitution in Upc2p contributes to azole resistance in well-characterized clinical isolates of Candida albicans

Antimicrob Agents Chemother. 2011 Feb;55(2):940-2. doi: 10.1128/AAC.00995-10. Epub 2010 Nov 15.

Abstract

The Candida albicans Upc2p transcription factor regulates ERG11, encoding the target of azole drugs. Gain-of-function mutations that contribute to resistance were recently identified in a series of sequential clinical isolates (N. Dunkel, T. T. Liu, K. S. Barker, R. Homayouni, J. Morschhauser, and P. D. Rogers, Eukaryot. Cell 7:1180-1190, 2008). In the present study, UPC2 was sequenced from a matched set of 17 isolates. An A643V substitution was present in all of the isolates in the series that overexpressed ERG11. Azole susceptibility, ergosterol levels, and expression of ERG genes were elevated in the A643V clinical isolates and in reconstructed strains.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Substitution*
  • Antifungal Agents / pharmacology*
  • Azoles / pharmacology*
  • Candida albicans / drug effects*
  • Candida albicans / genetics
  • Candida albicans / metabolism
  • Drug Resistance, Fungal / genetics*
  • Ergosterol / biosynthesis
  • Ergosterol / genetics
  • Fluconazole / pharmacology
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism
  • Gene Expression Regulation, Fungal*
  • Humans
  • Microbial Sensitivity Tests
  • Sequence Analysis, DNA
  • Trans-Activators / genetics*
  • Trans-Activators / metabolism

Substances

  • Antifungal Agents
  • Azoles
  • Fungal Proteins
  • Trans-Activators
  • Fluconazole
  • Ergosterol