Laboratory of Fungal Pathogenesis, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India; Graduate Studies, Regional Centre for Biotechnology, Faridabad, Haryana, India.
Laboratory of Fungal Pathogenesis, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India.
J Biol Chem. 2022 Feb;298(2):101593. doi: 10.1016/j.jbc.2022.101593. Epub 2022 Jan 17.
Invasive candidiasis poses a major healthcare threat. The human opportunistic fungal pathogen Candida glabrata, which causes mucosal and deep-seated infections, is armed with distinct virulence attributes, including a family of 11 glycosylphosphatidylinositol-linked aspartyl proteases, CgYapsins. Here, we have profiled total membrane proteomes of the C. glabrata wildtype and 11 proteases-deficient strain, Cgyps1-11Δ, by mass spectrometry analysis and uncovered a novel role for fungal yapsins in glucose sensing and homeostasis. Furthermore, through label-free quantitative membrane proteome analysis, we showed differential abundance of 42% of identified membrane proteins, with electron transport chain and glycolysis proteins displaying lower and higher abundance in Cgyps1-11Δ cells, compared with wildtype cells, respectively. We also demonstrated elevated glucose uptake and upregulation of genes that code for the low-glucose sensor CgSnf3, transcriptional regulators CgMig1 and CgRgt1, and hexose transporter CgHxt2/10 in the Cgyps1-11Δ mutant. We further elucidated a potential underlying mechanism through genetic and transcript measurement analysis under low- and high-glucose conditions and found CgSNF3 deletion to rescue high glucose uptake and attenuated growth of the Cgyps1-11Δ mutant in YPD medium, thereby linking CgYapsins with regulation of the CgSnf3-dependent low-glucose sensing pathway. Last, high ethanol production, diminished mitochondrial membrane potential, and elevated susceptibility to oxidative phosphorylation inhibitors point toward increased fermentative and decreased respiratory metabolism in the Cgyps1-11Δ mutant. Altogether, our findings revealed new possible glucose metabolism-regulatory roles for putative cell surface-associated CgYapsins and advanced our understanding of fungal carbohydrate homeostasis mechanisms.
侵袭性念珠菌病构成了重大的医疗保健威胁。人体机会性真菌病原体光滑念珠菌会导致黏膜和深部感染,它具有独特的毒力特性,包括一个由 11 种糖基磷脂酰肌醇连接的天冬氨酸蛋白酶家族,即 CgYapsins。在这里,我们通过质谱分析对光滑念珠菌野生型和 11 种蛋白酶缺陷型菌株 Cgyps1-11Δ 的总膜蛋白质组进行了分析,并揭示了真菌 Yapsins 在葡萄糖感应和稳态中的新作用。此外,通过无标记定量膜蛋白质组分析,我们发现鉴定出的膜蛋白中有 42%的蛋白丰度存在差异,与野生型细胞相比,Cgyps1-11Δ 细胞中的电子传递链和糖酵解蛋白丰度较低,而 Cgyps1-11Δ 细胞中的电子传递链和糖酵解蛋白丰度较高。我们还证明了在 Cgyps1-11Δ 突变体中葡萄糖摄取增加,以及编码低葡萄糖传感器 CgSnf3、转录调节剂 CgMig1 和 CgRgt1 和己糖转运蛋白 CgHxt2/10 的基因上调。我们进一步通过在低葡萄糖和高葡萄糖条件下进行遗传和转录测量分析,阐明了潜在的潜在机制,并发现 CgSNF3 缺失可挽救 Cgyps1-11Δ 突变体在 YPD 培养基中的高葡萄糖摄取和生长减弱,从而将 CgYapsins 与 CgSnf3 依赖的低葡萄糖感应途径的调节联系起来。最后,高乙醇产量、线粒体膜电位降低和对氧化磷酸化抑制剂的敏感性增加表明 Cgyps1-11Δ 突变体中发酵代谢增加和呼吸代谢减少。总之,我们的研究结果揭示了潜在的细胞表面相关 CgYapsins 在葡萄糖代谢调节中的新作用,并提高了我们对真菌碳水化合物稳态机制的理解。