Synergistic Antifungal Activity of Zinc Pyrithione and Nystatin against Multi-Drug-Resistant Candida ( Candidozyma ) auris : Evidence from In Vitro and In Vivo Models

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Authors: Larissa Rodrigues Pimentel, Fabíola Lucini, Ludmilla Cardoso Coferri, Yasmim Isabel Retore, Julia Pimentel Arantes, Cleison da Rocha Leite, Adriana Araújo de Almeida-Apolonio, Carlos Reinier García Cardoso, Alex Polatto Carvalho, Fabrício Fagundes Pereira, Simone Simionatto, Kelly Mari Pires de Oliveira
+1 more Luana Rossato
Cited by: 1
References: 45

Abstract

High Resolution Image Download MS PowerPoint Slide Candida ( Candidozyma ) auris is a multidrug-resistant fungal pathogen that presents a growing global health concern due to its resistance to conventional antifungals. This study evaluated the antifungal potential of zinc pyrithione (ZnPT) and nystatin (NYS), both individually and in combination, against C. auris . Minimum inhibitory and fungicidal concentrations were determined, alongside assays for biofilm inhibition and eradication, including tests on porcine skin. Mechanistic evaluations included assessments of cell membrane integrity, efflux pump inhibition, and sorbitol protection. Safety was analyzed through hemocompatibility, the Ames test, and acute toxicity in Tenebrio molitor larvae. ZnPT + NYS combination had a synergistic antifungal effect, effectively inhibiting biofilm formation and increasing membrane permeability, as evidenced by protein leakage. No nucleotide leakage or mutagenic effects were observed, indicating low genotoxic risk. While ZnPT alone exhibited toxicity in T. molitor, the combination remained within safe limits. Overall, the ZnPT + NYS combination demonstrated strong antifungal and antibiofilm activity against C. auris, with favorable safety outcomes. These findings support further investigation into its clinical potential as a treatment strategy against this emerging pathogen.

Fields of Study & Subjects

Protease and Inhibitor Mechanisms Antifungal resistance and susceptibility Peptidase Inhibition and Analysis

Publication details

Journal / source
ACS Infectious Diseases
Publisher
American Chemical Society (ACS)
Volume
12
Issue
3
Pages
1064–1074
Publication date
26 February 2026
Language
EN