Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/57809
Title: Ketoconazole inhibits Malassezia furfur morphogenesis in vitro under filamentation optimized conditions
Authors: Sirida Youngchim
Joshua D. Nosanchuk
Siriporn Chongkae
Nongnuch Vanittanokom
Keywords: Medicine
Issue Date: 1-Jan-2017
Abstract: © 2016, Springer-Verlag Berlin Heidelberg. Malassezia furfur, a constituent of the normal human skin flora, is an etiological agent of pityriasis versicolor, which represents one of the most common human skin diseases. Under certain conditions, both exogenous and endogenous, the fungus can transition from a yeast form to a pathogenic mycelial form. To develop a standardized medium for reproducible production of the mycelial form of M. furfur to develop and optimize susceptibility testing for this pathogen, we examined and characterized variables, including kojic acid and glycine concentration, agar percentage, and pH, to generate a chemically defined minimal medium on which specific inoculums of M. furfur generated the most robust filamentation. Next, we examined the capacity of ketoconazole to inhibit the formation of M. furfur mycelial form. Both low and high, 0.01, 0.05 and 0.1 µg/ml concentrations of ketoconazole significantly inhibited filamentation at 11.9, 54.5 and 86.7%, respectively. Although ketoconazole can have a direct antifungal effect on both M. furfur yeast and mycelial cells, ketoconazole also has a dramatic impact on suppressing morphogenesis. Since mycelia typified the pathogenic form of Malassezia infection, the capacity of ketoconazole to block morphogenesis may represent an additional important effect of the antifungal.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84996968355&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/57809
ISSN: 1432069X
03403696
Appears in Collections:CMUL: Journal Articles

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