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The Microevolution of Antifungal Drug Resistance in Pathogenic Fungi

The mortality rates of invasive fungal infections remain high because of the limited number of antifungal drugs available and antifungal drug resistance, which can rapidly evolve during treatment. Mutations in key resistance genes such as ERG11 were postulated to be the predominant cause of antifung...

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Autor principal: Boyce, Kylie J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673521/
https://www.ncbi.nlm.nih.gov/pubmed/38004768
http://dx.doi.org/10.3390/microorganisms11112757
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author Boyce, Kylie J.
author_facet Boyce, Kylie J.
author_sort Boyce, Kylie J.
collection PubMed
description The mortality rates of invasive fungal infections remain high because of the limited number of antifungal drugs available and antifungal drug resistance, which can rapidly evolve during treatment. Mutations in key resistance genes such as ERG11 were postulated to be the predominant cause of antifungal drug resistance in the clinic. However, recent advances in whole genome sequencing have revealed that there are multiple mechanisms leading to the microevolution of resistance. In many fungal species, resistance can emerge through ERG11-independent mechanisms and through the accumulation of mutations in many genes to generate a polygenic resistance phenotype. In addition, genome sequencing has revealed that full or partial aneuploidy commonly occurs in clinical or microevolved in vitro isolates to confer antifungal resistance. This review will provide an overview of the mutations known to be selected during the adaptive microevolution of antifungal drug resistance and focus on how recent advances in genome sequencing technology have enhanced our understanding of this process.
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spelling pubmed-106735212023-11-13 The Microevolution of Antifungal Drug Resistance in Pathogenic Fungi Boyce, Kylie J. Microorganisms Review The mortality rates of invasive fungal infections remain high because of the limited number of antifungal drugs available and antifungal drug resistance, which can rapidly evolve during treatment. Mutations in key resistance genes such as ERG11 were postulated to be the predominant cause of antifungal drug resistance in the clinic. However, recent advances in whole genome sequencing have revealed that there are multiple mechanisms leading to the microevolution of resistance. In many fungal species, resistance can emerge through ERG11-independent mechanisms and through the accumulation of mutations in many genes to generate a polygenic resistance phenotype. In addition, genome sequencing has revealed that full or partial aneuploidy commonly occurs in clinical or microevolved in vitro isolates to confer antifungal resistance. This review will provide an overview of the mutations known to be selected during the adaptive microevolution of antifungal drug resistance and focus on how recent advances in genome sequencing technology have enhanced our understanding of this process. MDPI 2023-11-13 /pmc/articles/PMC10673521/ /pubmed/38004768 http://dx.doi.org/10.3390/microorganisms11112757 Text en © 2023 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Boyce, Kylie J.
The Microevolution of Antifungal Drug Resistance in Pathogenic Fungi
title The Microevolution of Antifungal Drug Resistance in Pathogenic Fungi
title_full The Microevolution of Antifungal Drug Resistance in Pathogenic Fungi
title_fullStr The Microevolution of Antifungal Drug Resistance in Pathogenic Fungi
title_full_unstemmed The Microevolution of Antifungal Drug Resistance in Pathogenic Fungi
title_short The Microevolution of Antifungal Drug Resistance in Pathogenic Fungi
title_sort microevolution of antifungal drug resistance in pathogenic fungi
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673521/
https://www.ncbi.nlm.nih.gov/pubmed/38004768
http://dx.doi.org/10.3390/microorganisms11112757
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