Suppr超能文献

艰难梭菌孢子形成起始途径的特征及其在毒素产生中的作用。

Characterization of the sporulation initiation pathway of Clostridium difficile and its role in toxin production.

作者信息

Underwood Sarah, Guan Shuang, Vijayasubhash Vinod, Baines Simon D, Graham Luke, Lewis Richard J, Wilcox Mark H, Stephenson Keith

机构信息

Institute of Molecular and Cellular Biology, Faculty of Biological Sciences, Leeds University, Leeds, United Kingdom.

出版信息

J Bacteriol. 2009 Dec;191(23):7296-305. doi: 10.1128/JB.00882-09. Epub 2009 Sep 25.

Abstract

Clostridium difficile is responsible for significant mortality and morbidity in the hospitalized elderly. C. difficile spores are infectious and are a major factor contributing to nosocomial transmission. The Spo0A response regulator is the master regulator for sporulation initiation and can influence many other cellular processes. Using the ClosTron gene knockout system, we inactivated genes encoding Spo0A and a putative sporulation-associated sensor histidine kinase in C. difficile. Inactivation of spo0A resulted in an asporogeneous phenotype, whereas inactivation of the kinase reduced C. difficile sporulation capacity by 3.5-fold, suggesting that this kinase also has a role in sporulation initiation. Furthermore, inactivation of either spo0A or the kinase resulted in a marked defect in C. difficile toxin production. Therefore, Spo0A and the signaling pathway that modulates its activity appear to be involved in regulation of toxin synthesis in C. difficile. In addition, Spo0A was directly phosphorylated by a putative sporulation-associated kinase, supporting the hypothesis that sporulation initiation in C. difficile is controlled by a two-component signal transduction system rather than a multicomponent phosphorelay. The implications of these findings for C. difficile sporulation, virulence, and transmission are discussed.

摘要

艰难梭菌可导致住院老年人出现严重的死亡率和发病率。艰难梭菌孢子具有传染性,是导致医院内传播的主要因素。Spo0A应答调节因子是孢子形成起始的主要调节因子,可影响许多其他细胞过程。利用ClosTron基因敲除系统,我们在艰难梭菌中使编码Spo0A和一种假定的与孢子形成相关的传感组氨酸激酶的基因失活。spo0A失活导致无孢子形成表型,而该激酶失活使艰难梭菌的孢子形成能力降低3.5倍,这表明该激酶在孢子形成起始中也发挥作用。此外,spo0A或该激酶失活均导致艰难梭菌毒素产生出现明显缺陷。因此,Spo0A及其调节活性的信号通路似乎参与了艰难梭菌毒素合成的调控。此外,Spo0A被一种假定的与孢子形成相关的激酶直接磷酸化,支持了艰难梭菌孢子形成起始由双组分信号转导系统而非多组分磷酸传递系统控制的假说。本文讨论了这些发现对艰难梭菌孢子形成、毒力和传播的影响。

相似文献

引用本文的文献

本文引用的文献

5
The ClosTron: a universal gene knock-out system for the genus Clostridium.ClosTron:一种用于梭菌属的通用基因敲除系统。
J Microbiol Methods. 2007 Sep;70(3):452-64. doi: 10.1016/j.mimet.2007.05.021. Epub 2007 Jun 18.
6
Clostridium difficile-associated diarrhoea.艰难梭菌相关性腹泻
Intern Med J. 2007 Aug;37(8):561-8. doi: 10.1111/j.1445-5994.2007.01403.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验