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Iron Regulates Expression of Bacillus cereus Hemolysin II via Global Regulator Fur

机译:铁通过全球调节皮毛调节蜡状芽孢杆菌溶血素II的表达

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摘要

The capacity of pathogens to respond to environmental signals, such as iron concentration, is key to bacterial survival and establishment of a successful infection. Bacillus cereus is a widely distributed bacterium with distinct pathogenic properties. Hemolysin II (HlyII) is one of its pore-forming cytotoxins and has been shown to be involved in bacterial pathogenicity in a number of cell and animal models. Unlike many other B. cereus pathogenicity factors, HlyII is not regulated by pleiotropic transcriptional regulator PlcR but is controlled by its own regulator, HlyIIR. Using a combination of in vivo and in vitro techniques, we show that hlyII expression is also negatively regulated by iron by the global regulator Fur via direct interaction with the hlyII promoter. DNase I footprinting and in vitro transcription experiments indicate that Fur prevents RNA polymerase binding to the hlyII promoter. HlyII expression profiles demonstrate that both HlyIIR and Fur regulate HlyII expression in a concerted fashion, with the effect of Fur being maximal in the early stages of bacterial growth. In sum, these results show that Fur serves as a transcriptional repressor for hlyII expression.
机译:病原体对环境信号(例如铁浓度)作出反应的能力是细菌存活和成功感染的关键。蜡状芽孢杆菌是一种广泛分布的细菌,具有独特的致病特性。溶血素II(HlyII)是其成孔性细胞毒素之一,并且已在许多细胞和动物模型中证明与细菌致病性有关。与许多其他蜡状芽孢杆菌的致病性因子不同,HlyII不受多效转录调节因子PlcR的调控,但受其自身的调控因子HlyIIR的调控。使用体内和体外技术的组合,我们表明,hlyII表达也受到铁的负调节,由全局调节剂Fur通过与hlyII启动子直接相互作用而被铁负调节。 DNase I足迹和体外转录实验表明,Fur阻止RNA聚合酶与hlyII启动子结合。 HlyII表达谱表明,HlyIIR和Fur都以一致的方式调节HlyII表达,在细菌生长的早期,Fur的作用最大。总之,这些结果表明,Fur充当hlyII表达的转录阻遏物。

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