Antifungal Drug Concentration Impacts the Spectrum of Adaptive Mutations in Candida albicans

Robert T Todd, Natthapon Soisangwan, Sam Peters, Bailey Kemp, Taylor Crooks, Aleeza Gerstein, Anna Selmecki

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Invasive fungal infections are a leading global cause of human mortality. Only three major classes of antifungal drugs are widely used, and resistance to all three classes can arise rapidly. The most widely prescribed antifungal drug, fluconazole, disseminates rapidly and reaches a wide range of concentrations throughout the body. The impact of drug concentration on the spectrum and effect of mutations acquired during adaptation is not known for any fungal pathogen, and how the specific level of a given stress influences the distribution of beneficial mutations has been poorly explored in general. We evolved 144 lineages from three genetically distinct clinical isolates of Candida albicans to four concentrations of fluconazole (0, 1, 8, and 64 μg/ml) and performed comprehensive phenotypic and genomic comparisons of ancestral and evolved populations. Adaptation to different fluconazole concentrations resulted in distinct adaptive trajectories. In general, lineages evolved to drug concentrations close to their MIC50 (the level of drug that reduces growth by 50% in the ancestor) tended to rapidly evolve an increased MIC50 and acquired distinct segmental aneuploidies and copy number variations. By contrast, lineages evolved to drug concentrations above their ancestral MIC50 tended to acquire a different suite of mutational changes and increased in drug tolerance (the ability of a subpopulation of cells to grow slowly above their MIC50). This is the first evidence that different concentrations of drug can select for different genotypic and phenotypic outcomes in vitro and may explain observed in vivo drug response variation.

Original languageEnglish (US)
Article numbermsad009
JournalMolecular biology and evolution
Volume40
Issue number1
DOIs
StatePublished - Jan 1 2023

Bibliographical note

Funding Information:
We are grateful to Selmecki lab members and colleagues, especially Laura Burrack, Xin Zhou, Petra Vande Zande, and Nancy Scott for helpful critiques of the manuscript. This work was supported by a University of Minnesota UMR Fellowship with the Bioinformatics and Computational Biology program (to N.S.); the National Institutes of Health R01AI143689; and the Burroughs Wellcome Fund Investigators in the Pathogenesis of Infectious Diseases (#1020388) to A.S.

Publisher Copyright:
© 2023 The Author(s). Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution.

Keywords

  • Candida albicans
  • aneuploidy
  • antifungal drug resistance
  • antifungal drug tolerance
  • copy number variation
  • polyploidy

PubMed: MeSH publication types

  • Journal Article
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

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