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粪肠球菌V583双组分信号转导系统的系统性失活及表型特征分析

Systematic inactivation and phenotypic characterization of two-component signal transduction systems of Enterococcus faecalis V583.

作者信息

Hancock Lynn E, Perego Marta

机构信息

Division of Cellular Biology, Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA 92037, USA.

出版信息

J Bacteriol. 2004 Dec;186(23):7951-8. doi: 10.1128/JB.186.23.7951-7958.2004.

Abstract

The ability of enterococci to adapt and respond to different environmental stimuli, including the host environment, led us to investigate the role of two-component signal transduction in the regulation of Enterococcus faecalis physiology. Using a bioinformatic approach, we previously identified 17 two-component systems (TCS), consisting of a sensory histidine kinase and the cognate response regulator, as well as an additional orphan response regulator (L. E. Hancock and M. Perego, J. Bacteriol. 184:5819-5825, 2002). In an effort to identify the potential function of each TCS in the biology of E. faecalis clinical isolate strain V583, we constructed insertion mutations in each of the response regulators. We were able to inactivate 17 of 18 response regulators, the exception being an ortholog of YycF, previously shown to be essential for viability in a variety of gram-positive microorganisms. The biological effects of the remaining mutations were assessed by using a number of assays, including antibiotic resistance, biofilm formation, and environmental stress. We identified TCS related to antibiotic resistance and environmental stress and found one system which controls the initiation of biofilm development by E. faecalis.

摘要

肠球菌适应并响应包括宿主环境在内的不同环境刺激的能力,促使我们研究双组分信号转导在粪肠球菌生理学调节中的作用。我们之前采用生物信息学方法,鉴定出17个双组分系统(TCS),其中包括一个传感组氨酸激酶和同源反应调节因子,以及一个额外的孤儿反应调节因子(L.E.汉考克和M.佩雷戈,《细菌学杂志》184:5819 - 5825,2002年)。为了确定每个TCS在粪肠球菌临床分离株V583生物学中的潜在功能,我们在每个反应调节因子中构建了插入突变。我们能够使18个反应调节因子中的17个失活,唯一的例外是YycF的一个直系同源物,此前已证明它对多种革兰氏阳性微生物的生存能力至关重要。通过使用多种检测方法,包括抗生素抗性、生物膜形成和环境应激,评估了其余突变的生物学效应。我们鉴定出了与抗生素抗性和环境应激相关的TCS,并发现了一个控制粪肠球菌生物膜形成起始的系统。

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