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SirA直系同源物影响运动性和毒力。

SirA orthologs affect both motility and virulence.

作者信息

Goodier R I, Ahmer B M

机构信息

Department of Microbiology, The Ohio State University, Columbus, Ohio 43210, USA.

出版信息

J Bacteriol. 2001 Apr;183(7):2249-58. doi: 10.1128/JB.183.7.2249-2258.2001.

Abstract

The sirA gene of Salmonella enterica serovar Typhimurium encodes a two-component response regulator of the FixJ family that has a positive regulatory influence on the expression of type III secretion genes involved with epithelial cell invasion and the elicitation of bovine gastroenteritis. SirA orthologs in Pseudomonas, Vibrio, and Erwinia control the expression of distinct virulence genes in these genera, but an evolutionarily conserved target of SirA regulation has never been identified. In this study we tested the hypothesis that sirA may be an ancient member of the flagellar regulon. We examined the effect of a sirA mutation on transcriptional fusions to flagellar promoters (flhD, fliE, fliF, flgA, flgB, fliC, fliD, motA, and fliA) while using fusions to the virulence gene sopB as a positive control. SirA had only small regulatory effects on all fusions in liquid medium (less than fivefold). However, in various types of motility agar plates, sirA was able to activate a sopB fusion by up to 63-fold while repressing flagellar fusions by values exceeding 100-fold. Mutations in the sirA orthologs of Escherichia coli, Vibrio cholerae, Pseudomonas fluorescens, and Pseudomonas aeruginosa result in defects in either motility or motility gene regulation, suggesting that control of flagellar regulons may be an evolutionarily conserved function of sirA orthologs. The implications for our understanding of virulence gene regulation in the gamma Proteobacteria are discussed.

摘要

鼠伤寒沙门氏菌肠炎血清型的sirA基因编码FixJ家族的双组分应答调节因子,对参与上皮细胞侵袭和引发牛肠胃炎的III型分泌基因的表达具有正向调节作用。假单胞菌属、弧菌属和欧文氏菌属中的SirA直系同源物控制这些属中不同毒力基因的表达,但尚未确定SirA调节的进化保守靶点。在本研究中,我们测试了sirA可能是鞭毛调节子古老成员的假设。我们在使用毒力基因sopB的融合作为阳性对照的同时,研究了sirA突变对鞭毛启动子(flhD、fliE、fliF、flgA、flgB、fliC、fliD、motA和fliA)转录融合的影响。SirA对液体培养基中的所有融合只有很小的调节作用(小于五倍)。然而,在各种类型的运动性琼脂平板上,sirA能够激活sopB融合高达63倍,同时抑制鞭毛融合超过100倍。大肠杆菌、霍乱弧菌、荧光假单胞菌和铜绿假单胞菌的sirA直系同源物中的突变导致运动性或运动性基因调节缺陷,这表明鞭毛调节子的控制可能是sirA直系同源物的进化保守功能。我们讨论了对理解γ-变形菌中毒力基因调节的意义。

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