Journal Article

Squalene epoxidase encoded by <i>ERG1</i> affects morphogenesis and drug susceptibilities of <i>Candida albicans</i>

Ritu Pasrija, Shankarling Krishnamurthy, Tulika Prasad, Joachim F. Ernst and Rajendra Prasad

in Journal of Antimicrobial Chemotherapy

Published on behalf of British Society for Antimicrobial Chemotherapy

Volume 55, issue 6, pages 905-913
Published in print June 2005 | ISSN: 0305-7453
Published online April 2005 | e-ISSN: 1460-2091 | DOI:
Squalene epoxidase encoded by ERG1 affects morphogenesis and drug susceptibilities of Candida albicans

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Objectives: Functional characterization of the erg1 mutant of ergosterol biosynthesis of Candida albicans.

Methods: We disrupted the ERG1 gene of C. albicans, which encodes squalene epoxidase (EC Since the disruption of both alleles of ERG1 was lethal, the second allele of a heterozygous disruptant was placed under the control of a regulable promoter, MET3p, which is repressed by methionine and cysteine.

Results: The reverse-phase HPLC analysis of sterol, extracted from the conditional mutant strain, showed a total lack of ergosterol and instead accumulation of squalene. This imbalance in sterol composition led to defects in growth and increased susceptibilities to drugs including fluconazole, ketoconazole, cycloheximide, nystatin, amphotericin B and terbinafine. Reduced drug efflux activity of the erg1 mutant was associated with poor surface localization of Cdr1p, suggesting that enhanced passive diffusion and reduced efflux mediated by the ABC (ATP binding cassette) transporter Cdr1p increases drug susceptibility. Additionally, conditional erg1 mutant strains were unable to form hyphae in various media.

Conclusions: Taken together, our results demonstrate that the absence of ergosterol, which is one of the constituents of membrane microdomains (rafts), has a direct effect on drug susceptibility and morphogenesis of C. albicans.

Keywords: regulable promoter; hyphae; drug resistance; Cdr1p; ergosterol; dimorphism

Journal Article.  4987 words.  Illustrated.

Subjects: Medical Oncology ; Critical Care

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