| Literature DB >> 22422573 |
Anna Bink1, Gilmer Govaert1, Davy Vandenbosch2, Soňa Kuchariková3,4, Tom Coenye2, Hans Nelis2, Patrick Van Dijck3,4, Bruno P A Cammue1, Karin Thevissen1.
Abstract
We investigated the molecular basis of the tolerance of Candida albicans biofilms to antifungals using the miconazole as a model compound, and translated the resulting data to other antifungals. Sessile cells of C. albicans Δefg1, lacking the transcription factor Efg1, showed increased susceptibility to miconazole, amphotericin B and caspofungin, whereas these sessile cells were equally resistant to fluconazole. The increased sensitivity to miconazole was, at least, partly due to an increased accumulation of miconazole in the cells as compared to wild-type or reintegrant Δefg1(EFG1) sessile cells. By using a rat biofilm model, we further confirmed the role of Efg1 in the tolerance of C. albicans biofilms to miconazole when grown in vivo.Entities:
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Year: 2012 PMID: 22422573 DOI: 10.1099/jmm.0.041020-0
Source DB: PubMed Journal: J Med Microbiol ISSN: 0022-2615 Impact factor: 2.472