In Vitro Antifungal Susceptibilities and Amplified Fragment Length Polymorphism Genotyping of a Worldwide Collection of 350 Clinical, Veterinary, and Environmental Cryptococcus gattii Isolates

F. Hagen, M.T. Illnait-Zaragozi, K.H. Bartlett, D. Swinne, E. Geertsen, C.H.W. Klaassen, T. Boekhout, J.F. Meis

    Research output: Contribution to journal/periodicalArticleScientificpeer-review

    Abstract

    The in vitro susceptibilities of a worldwide collection of 350 Cryptococcus gattii isolates to seven antifungal drugs, including the new triazole isavuconazole, were tested. With amplified fragment length polymorphism (AFLP) fingerprinting, human, veterinary, and environmental C. gattii isolates were subdivided into seven AFLP genotypes, including the interspecies hybrids AFLP8 and AFLP9. The majority of clinical isolates (n = 215) comprised genotypes AFLP4 (n = 76) and AFLP6 (n = 103). The clinical AFLP6 isolates had significantly higher geometric mean MICs for flucytosine and fluconazole than the clinical AFLP4 isolates. Of the seven antifungal compounds examined in this study, isavuconazole had the lowest MIC90 (0.125 mu g/ml) for all C. gattii isolates, followed by a 1 log(2) dilution step increase (MIC90, 0.25 mu g/ml) for itraconazole, voriconazole, and posaconazole. Amphotericin B had an acceptable MIC90 of 0.5 mu g/ml, but fluconazole and flucytosine had relatively high MIC(90)s of 8 mu g/ml.
    Original languageEnglish
    Pages (from-to)5139-5145
    JournalAntimicrobial Agents and Chemotherapy
    Volume54
    Issue number12
    DOIs
    Publication statusPublished - 2010

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