Basis of cerulenin resistance of two strains of Candida albicans

Microbiology (Reading). 1995 Jul:141 ( Pt 7):1553-8. doi: 10.1099/13500872-141-7-1553.

Abstract

The basis of cerulenin resistance of Candida albicans strains 4918-2 and 4918-10 has been investigated. Parasexual genetic analyses established that cerulenin resistance to concentrations of at least 5 micrograms ml-1 is dominant in both strains. The results also showed that strain 4918-2 is heterozygous for resistance, while the change from resistance to sensitivity of strain 4918-10 is reversible. Experiments to define the mechanism(s) responsible for resistance focused on cerulenin uptake and fatty-acid synthase activity. Cerulenin uptake by strains 4918-2 and 4918-10 was 24% of that of the wild-type (strain 4918). Uptake was restored in UV-induced cerulenin-sensitive segregants of strains 4918-2 and 4918-10, and varied from 63% to 200% of parental values. Fatty-acid synthase from strains 4918-2 and 4918-10 was resistant to cerulenin as judged by differences in the inactivation of the enzyme by the agent. However, inactivation kinetics of fatty-acid synthase of cerulenin-sensitive segregants did not revert to the parental inactivation profile. Further investigation showed that nine out of ten segregants were resistant to cerulenin at concentrations between 1 and 4 micrograms ml-1 while strain 4918 was sensitive to cerulenin at all concentrations tested. Thus, the results suggest that alteration of fatty-acid synthase and changes in permeability contribute to total cerulenin resistance of each strain.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Candida albicans / drug effects
  • Candida albicans / genetics*
  • Candida albicans / metabolism
  • Candida albicans / radiation effects
  • Cell Membrane Permeability
  • Cerulenin / metabolism*
  • Cerulenin / pharmacology*
  • Drug Resistance, Microbial
  • Fatty Acid Synthases / antagonists & inhibitors
  • Fatty Acid Synthases / genetics
  • Fatty Acid Synthases / metabolism*
  • Heterozygote
  • Kinetics
  • Microbial Sensitivity Tests
  • Recombination, Genetic
  • Time Factors
  • Ultraviolet Rays

Substances

  • Cerulenin
  • Fatty Acid Synthases