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Activation of Motility by Sensing Short-Chain Fatty Acids via Two Steps in a Flagellar Gene Regulatory Cascade in Enterohemorrhagic Escherichia coli▿ †

机译:通过肠出血性大肠杆菌鞭毛基因调控级联中的两个步骤检测短链脂肪酸来激活运动。

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摘要

The regulated expression of virulence genes is critical for successful infection by an intestinal pathogen. Bacteria rely on sensing environmental signals to find preferable niches and reach the infectious state. Orally ingested enterohemorrhagic Escherichia coli (EHEC) travels through the gastrointestinal tract and encounters a variety of environmental factors, some of which act as triggering signals for the induction of virulence genes. Butyrate, one of the main short-chain fatty acids (SCFAs), is such a signal, enhancing the expression of genes for intimate attachment and type III secretion. We further explored the role of SCFAs and found a positive effect of SCFAs on flagellar expression. Although EHEC did not produce flagella when grown in Dulbecco's modified Eagle's medium (DMEM), a tissue culture medium that enhances virulence gene expression, the addition of SCFAs to the medium induced the production of flagella, and the EHEC bacteria became motile. Among SCFAs, butyrate simultaneously activates both virulence and flagellar genes. Flagella did not affect initial adherence, and they were not expressed in adherent bacteria during microcolony formation. SCFAs activated flagellar genes via two regulatory steps. Butyrate activated the flhDC regulatory genes through leucine-responsive regulatory protein (Lrp), which is also a regulator of virulence genes. However, butyrate, acetate, and propionate also activated downstream genes independently of flhDC activation. Consequently, when encountering increased concentrations of SCFAs, which are abundant in acetate, in the intestine, EHEC first activates flagellar production and motility, followed by genes involved in adherence and type III secretion, which leads to efficient adherence in a preferable niche.
机译:毒力基因的调控表达对于肠道病原体的成功感染至关重要。细菌依靠感测环境信号来找到理想的生态位并达到传染状态。口服摄入的大肠埃希氏大肠杆菌(EHEC)穿过胃肠道并遇到各种环境因素,其中一些环境因素可作为诱导致病基因的触发信号。丁酸酯是主要的短链脂肪酸(SCFA)之一,它是一种信号,增强了紧密附着和III型分泌基因的表达。我们进一步探讨了SCFA的作用,并发现了SCFA对鞭毛表达的积极作用。尽管EHEC在Dulbecco改良的Eagle's培养基(DMEM)(一种增强毒力基因表达的组织培养基)中生长时不会产生鞭毛,但向培养基中添加SCFA会诱导鞭毛的产生,并且EHEC细菌能够运动。在SCFA中,丁酸酯同时激活毒力和鞭毛基因。鞭毛不影响初始粘附,并且在小菌落形成过程中它们不在粘附细菌中表达。 SCFA通过两个调节步骤激活鞭毛基因。丁酸通过亮氨酸反应性调节蛋白(Lrp)激活flhDC调节基因,该蛋白也是毒力基因的调节剂。但是,丁酸,乙酸和丙酸酯也独立于flhDC激活而激活下游基因。因此,当肠中遇到浓度较高的富含乙酸盐的SCFA时,EHEC首先激活鞭毛的产生和运动,然后激活参与粘附和III型分泌的基因,从而在优选的生态位中有效粘附。

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