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. 2007 Feb;45(2):380-5.
doi: 10.1128/JCM.01862-06. Epub 2006 Nov 22.

Development and clinical application of a panfungal PCR assay to detect and identify fungal DNA in tissue specimens

Anna Lau  1 , Sharon Chen, Tania Sorrell, Dee Carter, Richard Malik, Patricia Martin, Catriona Halliday
Affiliations

Development and clinical application of a panfungal PCR assay to detect and identify fungal DNA in tissue specimens

Anna Lau et al. J Clin Microbiol. 2007 Feb.

Abstract

Given the rise in the incidence of invasive fungal infections (IFIs) and the expanding spectrum of fungal pathogens, early and accurate identification of the causative pathogen is essential. We developed a panfungal PCR assay that targets the internal transcribed spacer 1 (ITS1) region of the ribosomal DNA gene cluster to detect fungal DNA in fresh and formalin-fixed, paraffin-embedded (PE) tissue specimens from patients with culture-proven (n=38) or solely histologically proven (n=24) IFIs. PCR products were sequenced and compared with sequences in the GenBank database to identify the causal pathogen. The molecular identification was correlated with results from histological examination and culture. The assay successfully detected and identified the fungal pathogen in 93.6% and 64.3% of culture-proven and solely histologically proven cases of IFI, respectively. A diverse range of fungal genera were identified, including species of Candida, Cryptococcus, Trichosporon, Aspergillus, Fusarium, Scedosporium, Exophiala, Exserohilum, Apophysomyces, Actinomucor, and Rhizopus. For five specimens, molecular analysis identified a pathogen closely related to that identified by culture. All PCR-negative specimens (n=10) were PE tissues in which fungal hyphae were visualized. The results support the use of the panfungal PCR assay in combination with conventional laboratory tests for accurate identification of fungi in tissue specimens.

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