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鉴定和差异基因表达在光滑念珠菌生物膜中的黏附素样壁蛋白。

Identification and differential gene expression of adhesin-like wall proteins in Candida glabrata biofilms.

机构信息

Department of Preventive Dentistry, Academic Centre for Dentistry Amsterdam (ACTA), University of Amsterdam and VU University Amsterdam, Amsterdam, The Netherlands.

出版信息

Mycopathologia. 2011 Dec;172(6):415-27. doi: 10.1007/s11046-011-9446-2. Epub 2011 Jul 17.

DOI:10.1007/s11046-011-9446-2
PMID:21769633
Abstract

An important initial step in biofilm development and subsequent establishment of fungal infections by the human pathogen Candida glabrata is adherence to a surface. Adherence is mediated through a large number of differentially regulated cell wall-bound adhesins. The fungus can modify the incorporation of adhesins in the cell wall allowing crucial adaptations to new environments. In this study, expression and cell wall incorporation of C. glabrata adhesins were evaluated in biofilms cultured in two different media: YPD and a semi-defined medium SdmYg. Tandem mass spectrometry of isolated C. glabrata cell walls identified 22 proteins including six adhesins: the novel adhesins Awp5 and Awp6, Epa3 and the previously identified adhesins Epa6, Awp2 and Awp4. Regulation of expression of these and other relevant adhesin genes was investigated using real-time qPCR analysis. For most adhesin genes, significant up-regulation was observed in biofilms in at least one of the culturing media. However, this was not the case for EPA6 and AWP2, which is consistent with their gene products already being abundantly present in planktonic cultures grown in YPD medium. Furthermore, most of the adhesin genes tested also show medium-dependent differential regulation. These results underline the idea that many adhesins in C. glabrata are involved in biofilm formation and that their expression is tightly regulated and dependent on environmental conditions and growth phase. This may contribute to its potential to form resilient biofilms and cause infection in various host tissues.

摘要

在人类病原体光滑念珠菌发展生物膜并随后建立真菌感染的初始重要步骤中,黏附在表面上是关键的一步。黏附是通过大量差异调控的细胞壁结合黏附素介导的。真菌可以修饰细胞壁中黏附素的整合,从而使其适应新的环境。在这项研究中,我们评估了光滑念珠菌黏附素在两种不同培养基(YPD 和半定义培养基 SdmYg)中培养的生物膜中的表达和细胞壁整合。通过对分离的光滑念珠菌细胞壁进行串联质谱分析,鉴定出 22 种蛋白质,其中包括 6 种黏附素:新型黏附素 Awp5 和 Awp6、Epa3 和之前鉴定的黏附素 Epa6、Awp2 和 Awp4。使用实时 qPCR 分析研究了这些和其他相关黏附素基因的表达调控。对于大多数黏附素基因,在至少一种培养介质的生物膜中观察到显著的上调。然而,这并不是 EPA6 和 AWP2 的情况,这与它们的基因产物已经在 YPD 培养基中生长的浮游培养物中大量存在是一致的。此外,测试的大多数黏附素基因也表现出与介质相关的差异调控。这些结果强调了这样一个观点,即光滑念珠菌中的许多黏附素参与生物膜的形成,其表达受到严格调控,并取决于环境条件和生长阶段。这可能有助于其形成有弹性的生物膜并在各种宿主组织中引起感染的潜力。

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