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Journal of Clinical Microbiology, July 1998, p. 2093-2095, Vol. 36, No. 7
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Simple, Inexpensive, Reliable Method for Differentiation of Candida dubliniensis from Candida albicans

Emmanuelle Pinjon,1 Derek Sullivan,1 Ira Salkin,2,* Diarmuid Shanley,1 and David Coleman1

Department of Oral Medicine and Pathology, School of Dental Science and Dublin Dental Hospital, Trinity College, University of Dublin, Dublin 2, Republic of Ireland,1 and Wadsworth Center, New York State Department of Health, Albany, New York2

Received 13 February 1998/Accepted 21 April 1998

Candida dubliniensis is a recently described pathogenic species which shares many phenotypic features with Candida albicans, including the ability to form germ tubes and chlamydospores. These similarities have caused significant problems in the identification of C. dubliniensis by the average clinical mycology laboratory. To facilitate the differentiation of these species, we investigated the growth of 120 isolates of C. dubliniensis and 98 C. albicans isolates at 42 and 45°C on Emmons' modified Sabouraud glucose agar (SGA) and 10 isolates of each species in yeast-peptone-dextrose broth. None of the C. dubliniensis isolates grew on the agar or in the broth medium at 45°C, while 11 isolates were capable of growing on SGA at 42°C. In contrast, all of the C. albicans isolates but one grew at 45°C on or in either medium. These reproducible results clearly demonstrate that the incubation of isolates suspected to be C. dubliniensis or C. albicans at 45°C provides a simple, reliable, and inexpensive method for the differentiation of the two species.


* Corresponding author. Mailing address: Wadsworth Center, New York State Department of Health, Albany, NY 12201-0509. Phone: (518) 485-5386. Fax: (518) 485 5414. E-mail: ifs02{at}health.state.ny.us.


Journal of Clinical Microbiology, July 1998, p. 2093-2095, Vol. 36, No. 7
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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