首页> 外文OA文献 >Surface stress induces a conserved cell wall stress response in the pathogenic fungus Candida albicans
【2h】

Surface stress induces a conserved cell wall stress response in the pathogenic fungus Candida albicans

机译:表面应力在致病真菌白色念珠菌中诱导了保守的细胞壁应力反应

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The human fungal pathogen Candida albicans can grow at temperatures of up to 45°C. Here, we show that at 42°C substantially less biomass was formed than at 37°C. The cells also became more sensitive to wall-perturbing compounds, and the wall chitin levels increased, changes that are indicative of wall stress. Quantitative mass spectrometry of the wall proteome using 15N metabolically labeled wall proteins as internal standards revealed that at 42°C the levels of the β-glucan transglycosylases Phr1 and Phr2, the predicted chitin transglycosylases Crh11 and Utr2, and the wall maintenance protein Ecm33 increased. Consistent with our previous results for fluconazole stress, this suggests that a wall-remodeling response is mounted to relieve wall stress. Thermal stress as well as different wall and membrane stressors led to an increased phosphorylation of the mitogen-activated protein (MAP) kinase Mkc1, suggesting activation of the cell wall integrity (CWI) pathway. Furthermore, all wall and membrane stresses tested resulted in diminished cell separation. This was accompanied by decreased secretion of the major chitinase Cht3 and the endoglucanase Eng1 into the medium. Consistent with this, cht3 cells showed a similar phenotype. When treated with exogenous chitinase, cell clusters both from stressed cells and mutant strains were dispersed, underlining the importance of Cht3 for cell separation. We propose that surface stresses lead to a conserved cell wall remodeling response that is mainly governed by Mkc1 and is characterized by chitin reinforcement of the wall and the expression of remedial wall remodeling enzymes.
机译:人类真菌病原体白色念珠菌可以在高达45°C的温度下生长。在这里,我们表明在42°C时形成的生物量比在37°C时少得多。这些细胞对壁扰动化合物也变得更加敏感,壁几丁质水平增加,这种变化指示壁应力。使用15N代谢标记的壁蛋白作为内标物对壁蛋白质组进行的定量质谱分析显示,在42°C下,β-葡聚糖转糖基化酶Phr1和Phr2的水平,预测的几丁质转糖基化酶Crh11和Utr2以及壁维持蛋白Ecm33均增加。与我们先前对氟康唑应力的结果一致,这表明壁重塑反应可减轻壁应力。热应激以及不同的壁和膜应激源导致有丝分裂原激活的蛋白(MAP)激酶Mkc1的磷酸化增加,表明细胞壁完整性(CWI)通路的激活。此外,测试的所有壁和膜应力导致细胞分离减少。这伴随着主要几丁质酶Cht3和内切葡聚糖酶Eng1向培养基的分泌减少。与此一致,cht3细胞表现出相似的表型。当用外源几丁质酶处理时,来自应激细胞和突变菌株的细胞簇均被分散,从而强调了Cht3对细胞分离的重要性。我们建议表面应力导致保守的细胞壁重塑反应,主要由Mkc1支配,其特征是几丁质增强壁和表达补救壁重塑酶。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号