Zeise Karen D, Erb-Downward John R, Huffnagle Gary B
Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA.
Mary H. Weiser Food Allergy Center, University of Michigan, Ann Arbor, Michigan, USA.
Microbiol Spectr. 2025 Jul;13(7):e0302424. doi: 10.1128/spectrum.03024-24. Epub 2025 May 22.
is a clinically significant fungal pathogen capable of adapting to diverse host environments, including steep oxygen gradients ranging from ~21% oxygen to anaerobic. The ability to withstand varied oxygen levels is paramount to establishing colonization and persisting in host niches, and oxygen deprivation can also augment antifungal resistance. In this study, we used RNA sequencing to compare the global transcriptomic profiles of two strains of (SC5314 and CHN1) grown purely anaerobically to those grown aerobically. In SC5314, we observed a strong induction of the alternative oxidase and several genes encoding subunits of mitochondrial enzyme complexes I, II, and V, signifying a shift to alternative respiration. Consistent with the diminished ATP production from this process, there was a significant downregulation of genes associated with growth and metabolism, including histones and ribosomal proteins, as well as chitinases and other genes involved in cell wall remodeling. Interestingly, the anaerobic cultures had decreased expression of candidalysin () and other virulence factors, contrasting with other studies reporting enhanced pathogenicity under oxygen deprivation. There were a greater number of significantly upregulated genes in CHN1 compared to SC5314; however, most of the top 50 upregulated genes under anaerobic conditions were consistent between the two strains. The predominant difference in down-regulated genes between the two strains could be mapped to differences in hyphal transformation under aerobic conditions. Overall, our study provides a window into the molecular mechanisms of adaptation between aerobic to anaerobic environments.IMPORTANCE is a leading cause of fungal infections in humans, posing significant clinical challenges due to its remarkable adaptability and increasing antifungal resistance. Anaerobic environments can promote antifungal resistance, necessitating a deeper understanding of how adapts to anoxia. While much research has been done to identify mechanisms underlying adaptation to hypoxia (i.e., low oxygen), this is the first study evaluating the global transcriptomic response of to anoxia (no oxygen). Here, we uncover key transcriptomic changes that enable to survive in the absence of oxygen, which are distinct from those identified under hypoxic conditions. Our research addresses a gap in current knowledge that may be exploited for combatting antifungal resistance.
是一种具有临床意义的真菌病原体,能够适应多种宿主环境,包括从约21%氧气到无氧的陡峭氧梯度。耐受不同氧水平的能力对于在宿主生态位中建立定植和持续存在至关重要,并且缺氧也可增强抗真菌耐药性。在本研究中,我们使用RNA测序比较了两株(SC5314和CHN1)在纯厌氧条件下生长与在需氧条件下生长的全局转录组图谱。在SC5314中,我们观察到交替氧化酶以及几个编码线粒体酶复合物I、II和V亚基的基因强烈诱导,这表明向交替呼吸转变。与此过程中ATP产生减少一致,与生长和代谢相关的基因,包括组蛋白和核糖体蛋白,以及几丁质酶和其他参与细胞壁重塑的基因显著下调。有趣的是,厌氧培养物中念珠菌溶素()和其他毒力因子的表达降低,这与其他报道缺氧条件下致病性增强的研究形成对比。与SC5314相比,CHN1中有更多显著上调的基因;然而,在厌氧条件下上调的前50个基因中,大多数在两株之间是一致的。两株下调基因的主要差异可归因于需氧条件下菌丝转化的差异。总体而言,我们的研究为了解从需氧环境到厌氧环境的适应分子机制提供了一个窗口。重要性是人类真菌感染的主要原因,由于其显著的适应性和不断增加的抗真菌耐药性,带来了重大的临床挑战。厌氧环境可促进抗真菌耐药性,因此有必要更深入地了解如何适应缺氧。虽然已经进行了许多研究来确定适应低氧(即低氧)的潜在机制,但这是第一项评估对缺氧(无氧)的全局转录组反应的研究。在这里,我们发现了使能够在无氧条件下存活的关键转录组变化,这些变化与在低氧条件下确定的变化不同。我们的研究填补了当前知识的空白,这可能被用于对抗真菌耐药性。