Jpn. J. Infect. Dis., 58 (4), 235-237, 2005

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Short Communication

Differentiation of Candida albicans and Candida dubliniensis Using a Single-Enzyme PCR-RFLP Method

Hossein Mirhendi*, Koichi Makimura1, Kamiar Zomorodian, Nobuko Maeda2, Tomoko Ohshima2 and Hideyo Yamaguchi1

Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran, 1Department of Molecular Biology and Gene Diagnosis, Teikyo University Institute of Medical Mycology and Genome Research Center, Tokyo 192-0395 and 2Department of Oral Microbiology, School of Dental Medicine, Tsurumi University, Yokohama 230-8501, Japan

(Received November 30, 2004. Accepted April 20, 2005)


*Corresponding author: Mailing address: Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, P. O. Box: 14155-6446, Iran. Tel: +98-21-895-1583, Fax: +98-21-646-2267, E-mail: mirhendi@yahoo.com


SUMMARY: Candida dubliniensis is a novel Candida spp. that is similar to Candida albicans with respect to several phenotypic characteristics. However, they differ from each other with respect to epidemiology, pathogenesis, and the rapid development of resistance to fluconazole. In the present study, we used a single-enzyme PCR-restriction fragment length polymorphism (RFLP) technique to differentiate C. dubliniensis from C. albicans. The amplified ITS region of C. dubliniensis was digested once using the enzyme B1nI, whereas that of C. albicans remained intact. All standard strains tested were identified successfully by this method. None of 140 clinical isolates identified morphologically as C. albicans were recognized as C. dubliniensis based on their PCR-RFLP pattern. Our PCR-RFLP method easily differentiated C. dubliniensis from C. albicans, and this result was also demonstrated with standard strains.


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