Tandem gene duplications contributed to high-level azole resistance in a rapidly expanding Candida tropicalis population
Invasive diseases caused by the globally distributed commensal yeast Candida tropicalis are associated with mortality rates of greater than 50%. Notable increases of azole resistance have been observed in this species, particularly within Asia-Pacific regions. Here, we carried out a genetic populati...
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Veröffentlicht in: | Nature communications 2023-12, Vol.14 (1), p.8369-8369, Article 8369 |
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Zusammenfassung: | Invasive diseases caused by the globally distributed commensal yeast
Candida tropicalis
are associated with mortality rates of greater than 50%. Notable increases of azole resistance have been observed in this species, particularly within Asia-Pacific regions. Here, we carried out a genetic population study on 1571 global
C. tropicalis
isolates using multilocus sequence typing (MLST). In addition, whole-genome sequencing (WGS) analysis was conducted on 629 of these strains, comprising 448 clinical invasive strains obtained in this study and 181 genomes sourced from public databases. We found that MLST clade 4 is the predominant azole-resistant clone. WGS analyses demonstrated that dramatically increasing rates of azole resistance are associated with a rapid expansion of cluster AZR, a sublineage of clade 4. Cluster AZR isolates exhibited a distinct high-level azole resistance, which was induced by tandem duplications of the
ERG11
A395T
gene allele.
Ty3/gypsy
-like retrotransposons were found to be highly enriched in this population. The alarming expansion of
C. tropicalis
cluster AZR population underscores the urgent need for strategies against growing threats of antifungal resistance.
Candida tropicalis
is a cause of invasive candidiasis infection in humans that has been increasingly associated with azole drug resistance. In this study, the authors investigate the genetic basis for azole resistance through analysis of whole-genome sequencing and multilocus sequence typing data. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-023-43380-2 |