Molecular and phenotypic identification of the yeast pathogen Candida dubliniensis

• Published in: Journal of molecular medicine (Berlin, Germany) Vol. 78; no. 9; pp. 521 - 529
• Main Authors: KURZAI, Oliver, KORTING, Hans-Christian, HARMSEN, Dag, BAUTSCH, Wilfried, MOLITOR, Michael, FROSCH, Matthias, MÜHLSCHLEGEL, Fritz A
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01.01.2000
• Subjects: AIDS-Related Opportunistic Infections - microbiology; Biological and medical sciences; Candida - classification; Candida - genetics; Candida - physiology; Candida albicans; Candida dubliniensis; Candidiasis - microbiology; Carbohydrate Metabolism; DNA, Fungal - analysis; DNA, Fungal - genetics; DNA, Ribosomal Spacer - genetics; Genes, rRNA; Human immunodeficiency virus; Humans; Investigative techniques, diagnostic techniques (general aspects); Medical sciences; Miscellaneous. Technology; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques; Phenotype; Polymerase Chain Reaction; RNA, Ribosomal - genetics; Sequence Analysis, DNA; Temperature; Human; Identification; Fungi; Polymerase chain reaction; Phenotype; Microbiological investigation; Mycological investigation; Candida; Fungi Imperfecti; Diagnosis; Technique; Molecular biology; Thallophyta
• ISSN: 0946-2716; 1432-1440
• DOI: 10.1007/s001090000142

Candida dubliniensis is an emerging yeast pathogen generally misclassified as Candida albicans by standard diagnostic procedures. This study examined the efficiency of molecular identification, based on a discriminative PCR test, in a prospective study on the prevalence of C. dubliniensis among 103 oropharyngeal isolates from HIV-infected individuals or transplant recipients, and 30 vaginal isolates. All of the isolates had been classified as C. albicans by standard laboratory procedures. The PCR was evaluated in a blinded fashion against classification achieved by sequencing rDNA. Sequencing results corresponded 100% to the results of the discriminative PCR, indicating the validity of this rapid test. Twenty-one C. dubliniensis isolates were identified, all of them from HIV-infected individuals (prevalence 30%). The internal transcribed spacer regions of the C. dubliniensis isolates were sequenced. Phenotypic features of C. dubliniensis, namely abundant chlamydospore formation, atypical color on CHROMagar, growth defect at 45 degrees C, and colony morphology on Staib agar, were evaluated in a blinded fashion with respect to their discriminative potential, facilitating the design of further epidemiological studies. Carbohydrate assimilation patterns were determined for C. dubliniensis with a novel automated system showing that, in contrast to previous reports, C. dubliniensis is able to utilize D-xylose and trehalose. In evaluating these tests we present a rational approach to identification of the new species and characterization of C. dubliniensis isolates.