Experimental evolution identifies adaptive aneuploidy as a mechanism of fluconazole resistance in Candida auris.

Candida auris is a newly emerging fungal pathogen of humans and has attracted considerable attention from both the clinical and basic research communities. Clinical isolates of C. auris are often resistant to one or more antifungal agents. To explore how antifungal resistance develops, we performed experimental evolution assays in the current study using a fluconazole-susceptible isolate of C. auris (BJCA001). After a series of passages through medium containing increased concentrations of fluconazole, fungal cells acquired resistance. By sequencing and comparing the genomes of the parental fluconazole-susceptible strain and 26 experimentally evolved strains of C. auris, we found that a portion of fluconazole-resistant strains carried one extra copy of Chromosome V. In the absence of fluconazole, C. auris cells rapidly became susceptible and lost the extra copy of Chromosome V. Genomic and RNA-Seq analyses indicate that this chromosome carries a number of drug resistance-related genes, which were transcriptionally up-regulated in the resistant, aneuploid strains. Moreover, missense mutations were identified in genes TAC1B, RRP6, and SFT2 in all experimentally evolved strains. Our findings suggest that the gain of an extra copy of chromosome V is associated with the rapid acquisition of fluconazole-resistance and may represent an important evolutionary mechanism of antifungal resistance in C. auris.