# Rapid Detection of Fungi in Nail Specimens Using Multi‐Tube Recombinase Polymerase Amplification Assay

**Authors:** Rong Wu, Meirong Li, Weian Du, Zetao Chen, Songchao Yin, Ling Hu, Liyan Xi, Jing Zhang, Huaiqiu Huang

PMC · DOI: 10.1111/myc.70162 · Mycoses · 2026-02-14

## TL;DR

A new rapid molecular test detects fungi in nail samples faster and more accurately than traditional methods.

## Contribution

A multi-tube RPA assay was developed for rapid, sensitive, and specific detection of multiple fungal pathogens in nail specimens.

## Key findings

- The RPA assay detected 1 pg of genomic DNA with a turnaround time of less than 70 minutes.
- The assay showed 86.0% sensitivity and 85.0% specificity in clinical nail specimens.
- RPA outperformed fungal culture and microscopy in sensitivity while maintaining good specificity.

## Abstract

Conventional diagnostic methods for onychomycosis possess disadvantages related to limited sensitivity, extended turnaround times and strong reliance on operator expertise.

To develop a molecular assay with high sensitivity and specificity for rapid detection of multiple fungal pathogens in nail specimens.

A multi‐tube recombinase polymerase amplification (RPA) assay with fluorescent signal detection was developed, targeting pan‐fungal, Trichophyton rubrum, T. interdigitale, pan‐Candida, 
Candida albicans
, pan‐Trichosporon and pan‐Aspergillus. The analytical sensitivity and specificity of the assay were evaluated using fungal strains, and its performance was assessed in 81 clinical nail specimens in parallel with calcofluor white fluorescence microscopy and fungal culture.

The multi‐tube RPA assay demonstrated a detection limit of 1 pg of genomic DNA for all targets, with a turnaround time of < 70 min. In the evaluation of 81 clinical nail specimens, Bayesian latent class analysis estimated sensitivities of 86.0% for multi‐tube RPA, 67.0% for fungal culture and 77.0% for microscopy, with corresponding specificities of 85.0%, 89.0% and 87.0%. The positive and negative predictive values were 92.0% and 72.0% for multi‐tube RPA, 93.0% and 55.0% for fungal culture, and 93.0% and 66.0% for microscopy.

Compared with fungal culture and microscopy, the multi‐tube RPA assay demonstrated superior sensitivity while maintaining good specificity, facilitating the identification of fungal pathogens at the species level in nail specimens. Its operational simplicity, enhanced diagnostic performance and reduced processing times make it a promising alternative for the mycological diagnosis of onychomycosis.

## Linked entities

- **Diseases:** onychomycosis (MONDO:0001628)
- **Species:** Trichophyton rubrum (taxon 5551), Candida albicans (taxon 5476), Trichosporon (taxon 5552), Aspergillus (taxon 5052)

## Full-text entities

- **Diseases:** onychomycosis (MESH:D014009), fungal (MESH:D009181)
- **Chemicals:** calcofluor (-)
- **Species:** Trichophyton interdigitale (species) [taxon 101480], Trichosporon (genus) [taxon 5552], Trichophyton rubrum (species) [taxon 5551], Aspergillus (genus) [taxon 5052], Candida albicans (species) [taxon 5476]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12905661/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12905661/full.md

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Source: https://tomesphere.com/paper/PMC12905661