The azole-resistance phenotype of a <i>Nakaseomyces glabratus</i> clinical strain encoding a wild-type <i>PDR1</i> allele involves the efflux pumps Aus1 and Pdh1 and Cyb5, an alternative reductase required for ergosterol biosynthesis

The emergence of resistance to azoles among strains of <i>Nakaseomyces glabratus</i> is a major cause of concern, considering the importance of this yeast in causing human infections. In this work, we disclose a set of genes that mediate the azole-resistance phenotype of a resistant clinical strain, with one of these players (Cyb5) being also implicated in biosynthesis of ergosterol for the first time. With this, we increase a set of possible therapeutic targets that can be used in future studies to develop new antifungals.

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Publication Details

Journal
Microbiology Spectrum
Published
2026-03-27
DOI
https://doi.org/10.1128/spectrum.03344-25
Primary Topic
Antifungal resistance and susceptibility
Type
article
Field-Weighted Citation Impact
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article

The azole-resistance phenotype of a Nakaseomyces glabratus clinical strain encoding a wild-type PDR1 allele involves the efflux pumps Aus1 and Pdh1 and Cyb5, an alternative reductase required for ergosterol biosynthesis

Josie E. Parker, M. Joana F. Pinheiro, Nuno Pereira Mira, Fábio Fernandes et al.
Microbiology Spectrum
Antifungal resistance and susceptibility
article

The azole-resistance phenotype of a Nakaseomyces glabratus clinical strain encoding a wild-type PDR1 allele involves the efflux pumps Aus1 and Pdh1 and Cyb5, an alternative reductase required for ergosterol biosynthesis

Josie E. Parker, M. Joana F. Pinheiro, Nuno Pereira Mira, Fábio Fernandes, Maria T. Ferreira
article en

Abstract

The emergence of resistance to azoles among strains of <i>Nakaseomyces glabratus</i> is a major cause of concern, considering the importance of this yeast in causing human infections. In this work, we disclose a set of genes that mediate the azole-resistance phenotype of a resistant clinical strain, with one of these players (Cyb5) being also implicated in biosynthesis of ergosterol for the first time. With this, we increase a set of possible therapeutic targets that can be used in future studies to develop new antifungals.

Microbiology Spectrum
Institute for Biotechnology and Bioengineering (PT), Cardiff University (GB)
Openalex Percentile: Top 6%
Antifungal resistance and susceptibility
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