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大肠杆菌CFT073中P菌毛相变异频率的调控

Regulation of P-fimbrial phase variation frequencies in Escherichia coli CFT073.

作者信息

Holden Nicola, Totsika Makrina, Dixon Lynn, Catherwood Kirsteen, Gally David L

机构信息

Centre for Infectious Diseases, Royal (Dick) School of Veterinary Studies, Chancellor's Building, University of Edinburgh, 49 Little France Crescent, Edinburgh EH16 4SB, United Kingdom.

出版信息

Infect Immun. 2007 Jul;75(7):3325-34. doi: 10.1128/IAI.01989-06. Epub 2007 Apr 23.

Abstract

Adherence of uropathogenic Escherichia coli to host tissue is required for infection and is mediated by fimbriae, such as pyelonephritis-associated pili (Pap). Expression of P fimbriae is regulated by phase variation, and to date, phase transition frequencies have been measured only for pap regulatory region constructs integrated into the E. coli K-12 chromosome. The aim of this work was to measure P phase transition frequencies in clinical isolates for the first time, including frequencies for the sequenced strain E. coli CFT073. P fimbriation and associated phase transition frequencies were measured for two E. coli clinical isolates and compared with levels for homologous pap constructs in E. coli K-12. Fimbriation and off-to-on transition frequencies were always higher in the clinical isolate. It was concluded that the regulatory inputs controlling papI expression are likely to be different in E. coli CFT073 and E. coli K-12 as (i) phase variation could be stimulated in E. coli K-12 by induction of papI and (ii) the level of expression of a papI::gfp(+) fusion was higher in E. coli CFT073 than in E. coli K-12. Furthermore, phase transition frequencies for the two E. coli CFT073 pap clusters were shown to be different depending on the culture conditions, indicating that there is a hierarchy of expression depending on signal inputs.

摘要

尿路致病性大肠杆菌对宿主组织的黏附是感染所必需的,且由菌毛介导,如肾盂肾炎相关菌毛(Pap)。P菌毛的表达受相变调控,迄今为止,仅对整合到大肠杆菌K-12染色体中的pap调控区构建体测量了相变频率。这项工作的目的是首次测量临床分离株中的P相变频率,包括测序菌株大肠杆菌CFT073的频率。对两株大肠杆菌临床分离株测量了P菌毛形成及相关的相变频率,并与大肠杆菌K-12中同源pap构建体的水平进行比较。临床分离株中的菌毛形成和从关闭到开启的相变频率总是更高。得出的结论是,控制papI表达的调控输入在大肠杆菌CFT073和大肠杆菌K-12中可能不同,原因如下:(i)在大肠杆菌K-12中诱导papI可刺激相变;(ii)papI::gfp(+)融合蛋白在大肠杆菌CFT073中的表达水平高于大肠杆菌K-12。此外,已表明两株大肠杆菌CFT073的pap簇的相变频率因培养条件而异,这表明根据信号输入存在表达层次结构。

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