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体积虽小作用重大:新型小分子热休克蛋白 Hsp21 介导白念珠菌的应激适应和毒力。

Small but crucial: the novel small heat shock protein Hsp21 mediates stress adaptation and virulence in Candida albicans.

机构信息

Department of Microbial Pathogenicity Mechanisms, Hans-Knoell-Institute, Jena, Germany.

出版信息

PLoS One. 2012;7(6):e38584. doi: 10.1371/journal.pone.0038584. Epub 2012 Jun 7.

Abstract

Small heat shock proteins (sHsps) have multiple cellular functions. However, the biological function of sHsps in pathogenic microorganisms is largely unknown. In the present study we identified and characterized the novel sHsp Hsp21 of the human fungal pathogen Candida albicans. Using a reverse genetics approach we demonstrate the importance of Hsp21 for resistance of C. albicans to specific stresses, including thermal and oxidative stress. Furthermore, a hsp21Δ/Δ mutant was defective in invasive growth and formed significantly shorter filaments compared to the wild type under various filament-inducing conditions. Although adhesion to and invasion into human-derived endothelial and oral epithelial cells was unaltered, the hsp21Δ/Δ mutant exhibited a strongly reduced capacity to damage both cell lines. Furthermore, Hsp21 was required for resisting killing by human neutrophils. Measurements of intracellular levels of stress protective molecules demonstrated that Hsp21 is involved in both glycerol and glycogen regulation and plays a major role in trehalose homeostasis in response to elevated temperatures. Mutants defective in trehalose and, to a lesser extent, glycerol synthesis phenocopied HSP21 deletion in terms of increased susceptibility to environmental stress, strongly impaired capacity to damage epithelial cells and increased sensitivity to the killing activities of human primary neutrophils. Via systematic analysis of the three main C. albicans stress-responsive kinases (Mkc1, Cek1, Hog1) under a range of stressors, we demonstrate Hsp21-dependent phosphorylation of Cek1 in response to elevated temperatures. Finally, the hsp21Δ/Δ mutant displayed strongly attenuated virulence in two in vivo infection models. Taken together, Hsp21 mediates adaptation to specific stresses via fine-tuning homeostasis of compatible solutes and activation of the Cek1 pathway, and is crucial for multiple stages of C. albicans pathogenicity. Hsp21 therefore represents the first reported example of a small heat shock protein functioning as a virulence factor in a eukaryotic pathogen.

摘要

小分子热休克蛋白(sHsps)具有多种细胞功能。然而,致病性微生物中小分子热休克蛋白的生物学功能在很大程度上是未知的。在本研究中,我们鉴定并表征了人类真菌病原体白色念珠菌的新型小分子热休克蛋白 Hsp21。通过反向遗传学方法,我们证明了 Hsp21 对于白色念珠菌抵抗特定应激的重要性,包括热应激和氧化应激。此外,与野生型相比,hsp21Δ/Δ 突变体在各种诱导丝状生长的条件下,丝状生长缺陷,形成的菌丝明显较短。尽管对人源性内皮细胞和口腔上皮细胞的黏附和侵袭没有改变,但 hsp21Δ/Δ 突变体对这两种细胞系的损伤能力明显降低。此外,Hsp21 对于抵抗人中性粒细胞的杀伤作用是必需的。应激保护分子的细胞内水平的测量表明,Hsp21 参与甘油和糖原的调节,并在响应高温时在海藻糖稳态中起主要作用。在海藻糖和(在较小程度上)甘油合成中缺陷的突变体在对环境应激的敏感性增加、对上皮细胞损伤能力的严重损害以及对人原代中性粒细胞杀伤活性的敏感性增加方面,与 HSP21 缺失表型相似。通过在一系列应激原下对三种主要的白色念珠菌应激响应激酶(Mkc1、Cek1、Hog1)进行系统分析,我们证明了 Hsp21 依赖性的 Cek1 在响应高温时的磷酸化。最后,hsp21Δ/Δ 突变体在两种体内感染模型中表现出明显减弱的毒力。总之,Hsp21 通过微调相容溶质的稳态和激活 Cek1 途径来介导对特定应激的适应,并且对于白色念珠菌的多个致病阶段至关重要。因此,Hsp21 代表了第一个报道的作为真核病原体毒力因子的小分子热休克蛋白的例子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de15/3369842/052a06cac0a2/pone.0038584.g001.jpg

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