Department of Food Sciences, Institute of Postharvest and Food Sciences, Agricultural Research Organization, Volcani Center, Rishon LeZion, Israel.
Department of Vegetable and Field Crops, Institute of Plant Sciences, Agricultural Research Organization, Volcani Center, Rishon LeZion, Israel.
Microbiol Spectr. 2023 Aug 17;11(4):e0433922. doi: 10.1128/spectrum.04339-22. Epub 2023 Jun 26.
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 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. 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.
黄曲霉是一种产毒真菌,可污染包括玉米在内的多种重要农作物,产生黄曲霉毒素 B1,这是最具毒性和致癌性的天然化合物。这种真菌也是继烟曲霉之后导致人类侵袭性曲霉病的第二大主要原因,烟曲霉是一种在免疫功能低下人群中尤为普遍的疾病。唑类药物被认为是控制临床和农业环境中曲霉菌感染最有效的化合物。曲霉菌属中唑类药物耐药性的出现通常与编码角鲨烯 14α-去甲基酶的同源物中的点突变有关,角鲨烯 14α-去甲基酶是麦角固醇生物合成途径的一个组成部分,也是唑类药物的靶标。我们假设,丝状真菌获得唑类药物耐药性的机制也可能存在其他分子机制。我们发现,黄曲霉产毒素菌株通过特定染色体的全或部分非整倍体适应了高于 MIC 的伏立康唑暴露水平。我们在两个连续分离的克隆中证实了 8 号染色体的完全重复,在另一个克隆中证实了 3 号染色体的部分重复,这强调了非整倍体介导的耐药机制的潜在多样性。非整倍体介导的耐药性的可塑性通过伏立康唑耐药克隆在无药物培养基上反复传代后能够恢复到原来的唑类药物敏感性水平得到证明。这项研究为丝状真菌中的唑类药物耐药机制提供了新的见解。真菌病原体通过污染作物产生毒素(霉菌毒素)而导致人类疾病并威胁全球粮食安全。黄曲霉是一种机会性产毒真菌,可引起侵袭性和非侵袭性曲霉病,在免疫功能低下人群中死亡率很高。此外,这种真菌还会使大多数主要农作物受到臭名昭著的致癌物黄曲霉毒素的污染。伏立康唑是治疗曲霉菌属感染的首选药物。虽然临床分离株中已对唑类药物耐药机制进行了很好的描述,但黄曲霉对唑类药物耐药的分子基础仍不清楚。对 8 株伏立康唑耐药株的全基因组测序显示,除其他因素外,黄曲霉通过特定染色体的重复(即非整倍体)适应了高浓度的伏立康唑。我们在丝状真菌中发现的非整倍体介导的耐药性代表了一种范式转变,因为这种类型的耐药性以前被认为仅存在于酵母中。这一观察结果提供了丝状真菌黄曲霉中非整倍体介导的唑类药物耐药性的首个实验证据。