# Dual-Emission FRET-PCR Outperforms SYBR Green and EvaGreen for Accurate Discrimination of Primary Canine Dermatophytes: Microsporum canis, Nannizzia gypsea, and Trichophyton mentagrophytes

**Authors:** Nneka Vivian Iduu, Rae Kantzler, Donna Raiford, Brenda Bixler, Kelly Chenoweth, Chengming Wang

PMC · DOI: 10.3390/jof11100708 · Journal of Fungi · 2025-09-30

## TL;DR

A new PCR method called FRET-qPCR is more accurate and sensitive than existing methods for identifying three common dog fungal infections.

## Contribution

FRET-qPCR outperforms SYBR Green and EvaGreen for detecting and differentiating three canine dermatophytes with high specificity and sensitivity.

## Key findings

- FRET-qPCR achieved a detection limit of one gene copy per reaction.
- FRET-qPCR showed 100% specificity and distinct melting profiles for each dermatophyte species.
- SYBR Green and EvaGreen had reduced sensitivity and cross-reactivity with non-target fungi.

## Abstract

Conventional diagnosis of dermatophytosis relies on fungal culture and microscopic examination, methods that are often time-consuming and lack sensitivity. This study aimed to develop and compare real-time PCR assays for the simultaneous detection and differentiation of three major dermatophytes in dogs: Microsporum canis, Nannizzia gypsea, and Trichophyton mentagrophytes. Three qPCR platforms targeting the chitin synthase 1 (CHS1) gene—SYBR Green, EvaGreen, and dual-emission fluorescence resonance energy transfer (FRET)—were evaluated. The FRET assay demonstrated the highest performance, achieving a detection limit of a single gene copy per reaction and producing distinct melting profiles that enabled accurate species discrimination (M. canis ~56.1 °C, N. gypsea ~53.0 °C, T. mentagrophytes ~51.8 °C). In contrast, SYBR Green and EvaGreen assays showed reduced sensitivity and cross-reactivity with non-target fungi. All assays were validated using three ATCC reference strains, ten clinical isolates of the target dermatophytes, and nine additional fungal species, including Nocardia, Aspergillus, Fusarium, Sporothrix, and Candida. Overall, FRET-qPCR exhibited a 100% specificity and a detection limit of one copy of target gene per reaction, offering a rapid, reliable tool for accurate diagnosis and molecular surveillance of dermatophytosis in companion animals.

## Linked entities

- **Genes:** LYST (lysosomal trafficking regulator) [NCBI Gene 1130]
- **Diseases:** dermatophytosis (MONDO:0004678)
- **Species:** Microsporum canis (taxon 63405), Nannizzia gypsea (taxon 63402), Trichophyton mentagrophytes (taxon 523103), Nocardia (taxon 1817), Aspergillus (taxon 5052), Fusarium (taxon 5506), Sporothrix (taxon 29907), Candida (taxon 5475)

## Full-text entities

- **Diseases:** Canine Dermatophytes (MESH:D003881), fungal (MESH:D009181), dermatophytosis (MESH:D014005)
- **Chemicals:** SYBR (-)
- **Species:** Nocardia (genus) [taxon 1817], Trichophyton mentagrophytes (species) [taxon 523103], Candida [taxon 1535326], Canis lupus familiaris (dog, subspecies) [taxon 9615], Sporothrix (genus) [taxon 29907], Aspergillus (genus) [taxon 5052], Nannizzia gypsea (species) [taxon 63402], Microsporum canis (species) [taxon 63405]

## Full text

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## Figures

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## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12565227/full.md

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Source: https://tomesphere.com/paper/PMC12565227