Back to Search Start Over

Aneuploidy enables cross-tolerance to unrelated antifungal drugs in Candida parapsilosis .

Authors :
Sun LL
Li H
Yan TH
Cao YB
Jiang YY
Yang F
Source :
Frontiers in microbiology [Front Microbiol] 2023 Apr 11; Vol. 14, pp. 1137083. Date of Electronic Publication: 2023 Apr 11 (Print Publication: 2023).
Publication Year :
2023

Abstract

Candida parapsilosis is an emerging major human fungal pathogen. Echinocandins are first-line antifungal drugs for the treatment of invasive Candida infections. In clinical isolates, tolerance to echinocandins in Candida species is mostly due to point mutations of FKS genes, which encode the target protein of echinocandins. However, here, we found chromosome 5 trisomy was the major mechanism of adaptation to the echinocandin drug caspofungin, and FKS mutations were rare events. Chromosome 5 trisomy conferred tolerance to echinocandin drugs caspofungin and micafungin and cross-tolerance to 5-flucytosine, another class of antifungal drugs. The inherent instability of aneuploidy caused unstable drug tolerance. Tolerance to echinocandins might be due to increased copy number and expression of CHS7 , which encodes chitin synthase. Although copy number of chitinase genes CHT3 and CHT4 was also increased to the trisomic level, the expression was buffered to the disomic level. Tolerance to 5-flucytosine might be due to the decreased expression of FUR1 . Therefore, the pleiotropic effect of aneuploidy on antifungal tolerance was due to the simultaneous regulation of genes on the aneuploid chromosome and genes on euploid chromosomes. In summary, aneuploidy provides a rapid and reversible mechanism of drug tolerance and cross-tolerance in C. parapsilosis .<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2023 Sun, Li, Yan, Cao, Jiang and Yang.)

Details

Language :
English
ISSN :
1664-302X
Volume :
14
Database :
MEDLINE
Journal :
Frontiers in microbiology
Publication Type :
Academic Journal
Accession number :
37113223
Full Text :
https://doi.org/10.3389/fmicb.2023.1137083