Murphy Erin R, Payne Shelley M
University of Texas at Austin, Section of Molecular Genetics and Microbiology, 1 University Station A5000, Austin, TX 78712, USA.
Infect Immun. 2007 Jul;75(7):3470-7. doi: 10.1128/IAI.00112-07. Epub 2007 Apr 16.
Regulation of bacterial gene expression by small RNA (sRNA) molecules is an increasingly recognized phenomenon but one that is not yet fully understood. We show that the sRNA RyhB suppresses several virulence-associated phenotypes of Shigella dysenteriae, a causative agent of bacillary dysentery in humans. The virulence genes repressed by S. dysenteriae RyhB include those encoding the type III secretion apparatus, its secreted effectors, and specific chaperones. Suppression of Shigella virulence occurs via RyhB-dependent repression of the transcriptional activator VirB, leading to reduced expression of genes within the VirB regulon. Efficient repression of virB is mediated by a single-stranded region of RyhB that is distinct from the region required for repression of Shigella sodB. Regulation of virB by RyhB implicates iron as an environmental factor contributing to the complex regulation of Shigella virulence determinants.
小RNA(sRNA)分子对细菌基因表达的调控是一种日益受到认可的现象,但尚未完全被理解。我们发现sRNA RyhB可抑制痢疾志贺氏菌(人类细菌性痢疾的病原体)的几种与毒力相关的表型。被痢疾志贺氏菌RyhB抑制的毒力基因包括那些编码III型分泌装置、其分泌效应物和特定伴侣蛋白的基因。痢疾志贺氏菌毒力的抑制是通过RyhB依赖的转录激活因子VirB的抑制实现的,导致VirB调控子内基因的表达减少。virB的有效抑制由RyhB的一个单链区域介导,该区域与抑制痢疾志贺氏菌sodB所需的区域不同。RyhB对virB的调控表明铁是一个环境因素,有助于痢疾志贺氏菌毒力决定因素的复杂调控。