Sherrington Sarah L, Sorsby Eleanor, Mahtey Nabeel, Kumwenda Pizga, Lenardon Megan D, Brown Ian, Ballou Elizabeth R, MacCallum Donna M, Hall Rebecca A
Institute of Microbiology and Infection, and School of Biosciences, University of Birmingham, Edgbaston, Birmingham, United Kingdom.
MRC Centre for Medical Mycology, Aberdeen Fungal Group, Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom.
PLoS Pathog. 2017 May 22;13(5):e1006403. doi: 10.1371/journal.ppat.1006403. eCollection 2017 May.
Candida albicans is able to proliferate in environments that vary dramatically in ambient pH, a trait required for colonising niches such as the stomach, vaginal mucosal and the GI tract. Here we show that growth in acidic environments involves cell wall remodelling which results in enhanced chitin and β-glucan exposure at the cell wall periphery. Unmasking of the underlying immuno-stimulatory β-glucan in acidic environments enhanced innate immune recognition of C. albicans by macrophages and neutrophils, and induced a stronger proinflammatory cytokine response, driven through the C-type lectin-like receptor, Dectin-1. This enhanced inflammatory response resulted in significant recruitment of neutrophils in an intraperitoneal model of infection, a hallmark of symptomatic vaginal colonisation. Enhanced chitin exposure resulted from reduced expression of the cell wall chitinase Cht2, via a Bcr1-Rim101 dependent signalling cascade, while increased β-glucan exposure was regulated via a non-canonical signalling pathway. We propose that this "unmasking" of the cell wall may induce non-protective hyper activation of the immune system during growth in acidic niches, and may attribute to symptomatic vaginal infection.
白色念珠菌能够在环境pH值差异极大的环境中增殖,这是其在胃部、阴道黏膜和胃肠道等生态位定殖所必需的特性。在此我们表明,在酸性环境中的生长涉及细胞壁重塑,这导致细胞壁周边的几丁质和β-葡聚糖暴露增加。在酸性环境中,潜在的免疫刺激β-葡聚糖的暴露增强了巨噬细胞和中性粒细胞对白色念珠菌的天然免疫识别,并通过C型凝集素样受体Dectin-1诱导了更强的促炎细胞因子反应。这种增强的炎症反应导致在腹腔感染模型中大量募集中性粒细胞,这是有症状的阴道定殖的一个标志。几丁质暴露增加是由于细胞壁几丁质酶Cht2的表达降低,通过Bcr1-Rim101依赖性信号级联反应实现,而β-葡聚糖暴露增加则通过非经典信号通路调节。我们提出,这种细胞壁的“暴露”可能在酸性生态位生长期间诱导免疫系统的非保护性过度激活,并可能导致有症状的阴道感染。