JAC Advance Access published online on May 12, 2004
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkh243
© 2004 by The British Society for Antimicrobial Chemotherapy
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1 Microbiology Discipline,
School of Biomedical and Chemical Sciences, The University of Western
Australia,
35 Stirling Hwy, Crawley;
* To whom correspondence should be addressed. E-mail: khammer{at}cyllene.uwa.edu.au.
Objectives: The aim of this study
was to investigate the mechanism of action of tea tree oil and its
components against Candida albicans, Candida
glabrata and Saccharomyces cerevisiae. Methods: Yeast cells were treated with tea tree
oil or components, at one or more concentrations, for up to
6 h. During this time, alterations in permeability were assessed
by measuring the leakage of 260 nm absorbing materials and by the
uptake of Methylene Blue dye. Membrane fluidity was measured by
1,6-diphenyl-1,3,5-hexatriene fluorescence. The effects of tea tree
oil on glucose-induced medium acidification were quantified by measuring
the pH of cell suspensions in the presence of both tea tree oil
and glucose. Results: The treatment of C. albicans with
tea tree oil and components at concentrations of between 0.25 and 1.0% (v/v)
altered both permeability and membrane fluidity. Membrane fluidity
was also increased when C. albicans was
cultured for 24 h with 0.016%-0.06% (v/v)
tea tree oil, as compared with control cells. For all three organisms,
glucose-induced acidification of the external medium was inhibited
in a dose-dependent manner in the presence of 0.2%, 0.3% and
0.4% tea tree oil. Conclusions: Data from this study support the
hypothesis that tea tree oil and components exert their antifungal
actions by altering membrane properties and compromising membrane-associated
functions.
Revised March 5, 2004
Accepted March 22, 2004
Brief report
Antifungal effects of Melaleuca alternifolia (tea
tree) oil and
its components on Candida albicans, Candida
glabrata and Saccharomyces cerevisiae
2 Microbiology Discipline,
School of Biomedical and Chemical Sciences, The University of Western
Australia,
35 Stirling Hwy, Crawley; Division
of Microbiology and Infectious Diseases, Western Australian Centre
for Pathology and Medical Research, Queen Elizabeth II Medical Centre,
Nedlands, Western Australia, 6009
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