Naamidine A reveals a promising zinc-binding strategy for topical antifungal therapy

Fungal disease affects over a billion people worldwide. Naamidine A inhibits the growth of diverse fungal pathogens through an unknown mechanism. Here, we show that the supplementation of medium with excess zinc abolishes the antifungal activity of naamidine A. Furthermore, we highlight that naamidine A has <i>in vitro</i> activity against terbinafine-resistant <i>Trichophyton spp</i>. and <i>in vivo</i> efficacy in a mouse model of dermatomycosis caused by <i>T. mentagrophytes,</i> highlighting its therapeutic potential as a topical treatment.

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Publication Details

Journal
Antimicrobial Agents and Chemotherapy
Published
2024-09-26
DOI
https://doi.org/10.1128/aac.01194-24
Citations
2
Primary Topic
Antifungal resistance and susceptibility
Type
article
Field-Weighted Citation Impact
0.78

Funders

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article

Naamidine A reveals a promising zinc-binding strategy for topical antifungal therapy

Emily Puumala, Priya Uppuluri, Luke J. Whitesell, Leah E. Cowen et al.
2 citations
Antimicrobial Agents and Chemotherapy
Antifungal resistance and susceptibility
0.78
article

Naamidine A reveals a promising zinc-binding strategy for topical antifungal therapy

Emily Puumala, Priya Uppuluri, Luke J. Whitesell, Leah E. Cowen, Tanja Grkovic, Barry R. O’Keefe, Christopher C. Thornburg, Sunna Nabeela, Nicole Robbins
article en
2 citations

Abstract

Fungal disease affects over a billion people worldwide. Naamidine A inhibits the growth of diverse fungal pathogens through an unknown mechanism. Here, we show that the supplementation of medium with excess zinc abolishes the antifungal activity of naamidine A. Furthermore, we highlight that naamidine A has <i>in vitro</i> activity against terbinafine-resistant <i>Trichophyton spp</i>. and <i>in vivo</i> efficacy in a mouse model of dermatomycosis caused by <i>T. mentagrophytes,</i> highlighting its therapeutic potential as a topical treatment.

Antimicrobial Agents and ChemotherapyVol. 68(11)
Leidos (United States) (US), Target (United States) (US), University of California, Los Angeles (US), University of Toronto (CA), Los Angeles Medical Center (US), Frederick National Laboratory for Cancer Research (US), National Cancer Institute (US), Center for Cancer Research (US)
U.S. Department of Health and Human Services, Canadian Institute for Advanced Research, National Institutes of Health, Canadian Institutes of Health Research, National Cancer Institute, National Institute of Allergy and Infectious Diseases, Moonshot Research and Development Program, Cancer Moonshot
Good health and well-being
Openalex Percentile: Top 27%
Antifungal resistance and susceptibility
0.78
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