Aneuploidy Formation in the Filamentous Fungus Aspergillus flavus in Response to Azole Stress

Omer Barda1, Sudharsan Sadhasivam1, Di Gong1

  • 1Department of Food Sciences, Institute of Postharvest and Food Sciences, Agricultural Research Organization, Volcani Center, Rishon LeZion, Israel.

Microbiology Spectrum
|June 26, 2023
PubMed

Insights

Aspergillus flavus develops resistance to the antifungal drug voriconazole through aneuploidy, specifically chromosome duplication. This mechanism, previously observed only in yeasts, allows the fungus to adapt to drug exposure and can revert to susceptibility.

Area of Science:

  • Mycology
  • Antifungal Resistance
  • Genetics

Background:

  • Aspergillus flavus is a significant agricultural contaminant producing aflatoxins and a cause of invasive aspergillosis in immunocompromised individuals.
  • Azole drugs, like voriconazole, are crucial for treating Aspergillus infections, but resistance is an emerging threat.
  • Known azole resistance mechanisms in Aspergillus spp. primarily involve mutations in the *cyp51* gene.

Purpose of the Study:

  • To investigate alternative molecular mechanisms of azole resistance in Aspergillus flavus beyond point mutations.
  • To understand how Aspergillus flavus adapts to high concentrations of the antifungal drug voriconazole.

Main Methods:

  • Exposure of an aflatoxin-producing Aspergillus flavus strain to increasing concentrations of voriconazole.
  • Whole-genome sequencing of voriconazole-resistant isolates.
  • Analysis of chromosomal changes, including aneuploidy (whole or segmental chromosome duplications).

Main Results:

  • Voriconazole-resistant Aspergillus flavus strains were generated through aneuploidy, specifically duplication of chromosome 8 or segmental duplication of chromosome 3.
  • The observed aneuploidy-mediated resistance was plastic, with resistant clones reverting to azole susceptibility upon drug withdrawal.
  • This study demonstrates aneuploidy as a novel mechanism for azole resistance in filamentous fungi.

Conclusions:

  • Aspergillus flavus can acquire voriconazole resistance through aneuploidy, a mechanism previously thought to be limited to yeasts.
  • This finding expands our understanding of antifungal resistance in filamentous fungi and highlights the need for monitoring such mechanisms.
  • The plasticity of this resistance suggests potential evolutionary strategies for fungal pathogens.