Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Jul 24;10(8):515.
doi: 10.3390/jof10080515.

New Diagnostic Strategy for Onychomycosis: First-Line Utilization of DermaGenius® PCR and Calcofluor Microscopy Combined with Selective Culturing

Affiliations

New Diagnostic Strategy for Onychomycosis: First-Line Utilization of DermaGenius® PCR and Calcofluor Microscopy Combined with Selective Culturing

Séverine Evrard et al. J Fungi (Basel). .

Abstract

Onychomycosis (OM) is a widespread infection requiring prolonged treatment with potential side effects. Diagnostic certainty is therefore essential before initiating antifungal therapy. Molecular biology has already shown benefits in reducing the time to diagnosis, providing technical ease, and increasing sensitivity for the respective species that molecular tests can detect. Nevertheless, causative agents are numerous, and culture remains essential, particularly for detecting non-dermatophytes mold infections. This study compared the performance of three different diagnostic strategies: conventional culture technique, the multiplex DermaGenius® 2.0 PCR (DG), and a mixed PCR/culture algorithm guided by the result of direct examination with calcofluor (DEC). The mixed algorithm (MA) prioritizes DG PCR and DEC as the primary diagnostic tools, supplemented by selective sample inoculation when mycelial elements are visualized in DEC and when DG PCR fails to detect any fungus or identifies a fungus with morphology differing from that observed in DEC (filamentous fungi versus yeasts). With only 13% of samples requiring inoculation, MA emerged as the most effective strategy, demonstrating significantly higher sensitivity (98.18%; p < 0.001) compared to single-method approaches (78.18% for DG PCR alone and 74.55% for culture alone) while maintaining a specificity comparable to DG PCR (100%). This new approach saves time in result delivery, requires fewer human resources, and increases diagnostic accuracy to better meet the needs of clinicians.

Keywords: calcofluor; culture; dermatophytes; diagnostic strategy; hyphae; mold; multiplex PCR; onychomycosis; yeast.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Distribution of fungus type according to the patient’s age.

References

    1. Moreno G., Arenas R. Other fungi causing onychomycosis. Clin. Dermatol. 2010;28:160–163. doi: 10.1016/j.clindermatol.2009.12.009. - DOI - PubMed
    1. Piraccini B.M., Alessandrini A. Onychomycosis: A review. J. Fungi. 2015;1:30–43. doi: 10.3390/jof1010030. - DOI - PMC - PubMed
    1. Nouripour-Sisakht S., Mirhendi H., Shidfar M., Ahmadi B., Rezaei-Matehkolaei A., Geramishoar M., Zarei F., Jalalizand N. Aspergillus species as emerging causative agents of onychomycosis. J. Med. Mycol. 2015;25:101–107. doi: 10.1016/j.mycmed.2014.12.001. - DOI - PubMed
    1. Kuvandik G., Çetin M., Genctoy G., Horoz M., Duru M., Akcali C., Satar S., Kiykim A., Kaya H. The prevalance, epidemiology and risk factors for onychomycosis in hemodialysis patients. BMC Infect. Dis. 2007;7:102. doi: 10.1186/1471-2334-7-102. - DOI - PMC - PubMed
    1. Eenglish M.P. Nails and fungi. Br. J. Dermatol. 1976;94:697–701. doi: 10.1111/j.1365-2133.1976.tb05171.x. - DOI - PubMed

LinkOut - more resources