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FliZ是一种鞭毛调节因子,在昆虫病原细菌嗜线虫致病杆菌的运动性、溶血素表达和毒力之间起关键作用。

FliZ, a flagellar regulator, is at the crossroads between motility, haemolysin expression and virulence in the insect pathogenic bacterium Xenorhabdus.

作者信息

Lanois Anne, Jubelin Grégory, Givaudan Alain

机构信息

INRA, UMR 1133 Laboratoire EMIP, F-34000 Montpellier, France.

出版信息

Mol Microbiol. 2008 Apr;68(2):516-33. doi: 10.1111/j.1365-2958.2008.06168.x.

Abstract

There is a complex interplay between the regulation of flagellar motility and the expression of virulence factors in many bacterial pathogens. We investigated the role of FliZ in the regulation of flagellar and virulence genes in Xenorhabdus nematophila, an insect pathogen. The fliZ gene is the second gene in the fliAZ operon in X. nematophila. In vivo transcription analysis revealed a positive feedback loop of fliAZ transcription in which FliZ activates flhDC, the master operon of flagellar regulon in X. nematophila, leading to an increased transcription of the FlhDC-dependent promoter of fliAZ. We also showed that fliAZ and flhDC mutants lacked motility, had no haemolysin or Tween lipase activity and displayed an attenuated virulence phenotype in insects. Lipase activity is controlled by FliA, whereas haemolysin production and full virulence phenotype have been reported to be FliZ-dependent. Transcriptional analysis revealed that FliZ directly controlled expression of the xhlBA and xaxAB operons, which encode haemolysins from the two-partner secretion system and the binary XaxAB toxin family respectively. We suggest that this regulatory pathway may also occur in other pathogenic enterobacteria with genes encoding members of these two growing families of haemolysins.

摘要

在许多细菌病原体中,鞭毛运动的调控与毒力因子的表达之间存在复杂的相互作用。我们研究了FliZ在嗜线虫致病杆菌(一种昆虫病原体)中对鞭毛和毒力基因调控的作用。fliZ基因是嗜线虫致病杆菌中fliAZ操纵子的第二个基因。体内转录分析揭示了fliAZ转录的正反馈回路,其中FliZ激活flhDC(嗜线虫致病杆菌鞭毛调节子的主操纵子),导致fliAZ的FlhDC依赖性启动子转录增加。我们还表明,fliAZ和flhDC突变体缺乏运动性,没有溶血素或吐温脂肪酶活性,并且在昆虫中表现出毒力减弱的表型。脂肪酶活性受FliA控制,而溶血素的产生和完整的毒力表型据报道依赖于FliZ。转录分析表明,FliZ直接控制xhlBA和xaxAB操纵子的表达,这两个操纵子分别编码来自双组分分泌系统的溶血素和二元XaxAB毒素家族。我们认为,这种调控途径也可能发生在其他致病肠杆菌中,这些肠杆菌具有编码这两个不断增加的溶血素家族成员的基因。

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