Development of Melting-Curve-Based Real-Time PCR for Differentiating Medically Important Candida Species

<i>Candida</i> species are the primary fungal pathogens of invasive infections associated with high morbidity and mortality. The identification of these microorganisms is critical for therapeutic management and control of hospital infection. Herein, assays targeting the Intergenic Spacer 2 (IGS2) and Internal Transcribed Spacer 1 (ITS1) from the rDNA locus were developed to differentiate <i>Candida</i> species. Based on consensus nucleotide sequences, specific primers and positive controls were designed, and standard PCR and real-time PCR (qPCR) assays were performed. All primers resulted in specific amplification of the molecular targets of each species with no amplifications of the negative template control. Furthermore, the primers were highly specific when tested with a range of fungal DNAs and no cross-reactivity was observed among <i>Candida</i> species. The assays presented a limit of detection (LoD) of 10 copies of positive control per reaction for all specific primers designed. Overall, our results showed that qPCR assays employing primers targeting the regions IGS2 and ITS1 completely differentiated between <i>Candida albicans</i>, <i>Candida auris</i>, <i>Candida parapsilosis</i>, <i>Candida tropicalis</i>, and <i>Nakazeomyces glabratus</i>, with great accuracy and no amplification of DNA from other fungal species.