The development and validation of a rapid genetic method for species identification and genotyping of medically important fungal pathogens using high-resolution melting curve analysis

• Published in: Molecular oral microbiology Vol. 29; no. 3; pp. 117 - 130
• Main Authors: Alnuaimi, A.D., Wiesenfeld, D., O'Brien-Simpson, N.M., Reynolds, E.C., Peng, B., McCullough, M.J.
• Format: Journal Article
• Language: English
• Published: Denmark Blackwell Publishing Ltd 01-06-2014; Wiley Subscription Services, Inc
• Subjects: Candida - classification; Candida - genetics; Candida albicans; Candida dubliniensis; Candida genotyping; Candida glabrata; Candida guilliermondii; Candida krusei; Candida lusitaniae; Candida parapsilosis; Candida tropicalis; Dentistry; DNA, Fungal - chemistry; DNA, Ribosomal - chemistry; Feasibility Studies; Genotype; high-resolution melting curve analysis; Humans; Nucleic Acid Denaturation; rapid identification; Real-Time Polymerase Chain Reaction; Species Specificity; Candida albicans; high-resolution melting curve analysis; rapid identification; Candida genotyping
• DOI: 10.1111/omi.12050
• EISSN: 2041-1014
• ISSN: 2041-1006

Summary
Accurate, rapid and economical fungal species identification has been a major aim in mycology. In this study, our goal was to examine the feasibility of a high‐resolution melting curve analysis (HRMA) of internal transcribed regions ITS1 and ITS2 in ribosomal DNA (rDNA) for a rapid, simple and inexpensive differentiation of eight clinically relevant Candida species (Candida albicans, Candida glabrata, Candida parapsilosis, Candida krusei, Candida tropicalis, Candida guilliermondii, Candida dubliniensis and Candida lusitaniae). In addition, for the first time, we tested the applicability of HRMA to classify C. albicans strains into four previously described genotypes (A, B, C and D) using a primer set that spans the transposable intron region of 25S of rDNA. Type and unknown clinical oral isolates were used in this study and the melting curve analysis was compared with both amplicons' sequencing and agarose gel electrophoresis analysis. Real‐time PCR and subsequent HRMA of the two described rDNA regions generated distinct melting curve profiles that were in accord with sequencing and gel electrophoresis analysis, highly reproducible, and characteristic of each of the eight Candida species and C. albicans genotypes. Moreover, results were obtained in 4 h and without the need for any post‐amplification handling, so reducing time and cost. Owing to its simplicity and speed, this technique is a good fit for genotypic analysis of hundreds of clinical strains in large epidemiological settings.