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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.
Abstract:
Aspergillus flavus is a mycotoxigenic fungus that contaminates many important agricultural crops with aflatoxin B1, the most toxic and carcinogenic natural compound. This fungus is also the second leading cause of human invasive aspergillosis, after Aspergillus fumigatus, a disease that is particularly prevalent in immunocompromised individuals. Azole drugs are considered the most effective compounds in controlling Aspergillus infections both in clinical and agricultural settings. Emergence of azole resistance in Aspergillus spp. is typically associated with point mutations in cyp51 orthologs that encode lanosterol 14α-demethylase, a component of the ergosterol biosynthesis pathway that is also the target of azoles. We hypothesized that alternative molecular mechanisms are also responsible for acquisition of azole resistance in filamentous fungi. We found that an aflatoxin-producing A. flavus strain adapted to voriconazole exposure at levels above the MIC through whole or segmental aneuploidy of specific chromosomes. We confirm a complete duplication of chromosome 8 in two sequentially isolated clones and a segmental duplication of chromosome 3 in another clone, emphasizing the potential diversity of aneuploidy-mediated resistance mechanisms. The plasticity of aneuploidy-mediated resistance was evidenced by the ability of voriconazole-resistant clones to revert to their original level of azole susceptibility following repeated transfers on drug-free media. This study provides new insights into mechanisms of azole resistance in a filamentous fungus. IMPORTANCE Fungal pathogens cause human disease and threaten global food security by contaminating crops with toxins (mycotoxins). Aspergillus flavus is an opportunistic mycotoxigenic fungus that causes invasive and noninvasive aspergillosis, diseases with high rates of mortality in immunocompromised individuals. Additionally, this fungus contaminates most major crops with the notorious carcinogen, aflatoxin. Voriconazole is the drug of choice to treat infections caused by Aspergillus spp. Although azole resistance mechanisms have been well characterized in clinical isolates of Aspergillus fumigatus, the molecular basis of azole resistance in A. flavus remains unclear. Whole-genome sequencing of eight voriconazole-resistant isolates revealed that, among other factors, A. flavus adapts to high concentrations of voriconazole by duplication of specific chromosomes (i.e., aneuploidy). Our discovery of aneuploidy-mediated resistance in a filamentous fungus represents a paradigm shift, as this type of resistance was previously thought to occur only in yeasts. This observation provides the first experimental evidence of aneuploidy-mediated azole resistance in the filamentous fungus A. flavus.
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.
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Fungal Phylum Ascomycota
Fungal Group Zygomycota