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Magnesium Sensing Regulates Intestinal Colonization of Enterohemorrhagic Escherichia coli O157:H7

机译:镁感测调节Enterohemorlagic <命名含量含量的肠道定子<命名含量=“属型”>大肠杆菌 O157:H7

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Sensing specific gut metabolites is an important strategy for inducing crucial virulence programs by enterohemorrhagic Escherichia coli (EHEC) O157:H7 during colonization and infection. Here, we identified a virulence-regulating pathway wherein the PhoQ/PhoP two-component regulatory system signals to the O island 119-encoded low magnesium-induced regulator A (LmiA), which, in turn, activates locus of enterocyte effacement (LEE) genes to promote EHEC O157:H7 adherence in the low-magnesium conditions of the large intestine. This regulatory pathway is widely present in a range of EHEC and enteropathogenic E. coli (EPEC) serotypes. Disruption of this pathway significantly decreased EHEC O157:H7 adherence in the mouse intestinal tract. Moreover, mice fed a magnesium-rich diet showed significantly reduced EHEC O157:H7 adherence in vivo , indicating that magnesium may help in preventing EHEC and EPEC infection in humans. ABSTRACT The large intestinal pathogen enterohemorrhagic Escherichia coli (EHEC) O157:H7 detects host cues to regulate virulence gene expression during colonization and infection. However, virulence regulatory mechanisms of EHEC O157:H7 in the human large intestine are not fully understood. Herein, we identified a virulence-regulating pathway where the PhoQ/PhoP two-component regulatory system senses low magnesium levels and signals to the O island 119-encoded Z4267 (LmiA; low magnesium-induced regulator A), directly activating loci of enterocyte effacement genes to promote EHEC O157:H7 adherence in the large intestine. Disruption of this pathway significantly decreased EHEC O157:H7 adherence in the mouse intestinal tract. Moreover, feeding mice a magnesium-rich diet significantly reduced EHEC O157:H7 adherence in vivo . This LmiA-mediated virulence regulatory pathway is also conserved among several EHEC and enteropathogenic E. coli serotypes; therefore, our findings support the use of magnesium as a dietary supplement and provide greater insights into the dietary cues that can prevent enteric infections.
机译:感测特异性肠道代谢物是在定殖和感染期间诱导肠杆菌大肠杆菌(EHEC)O157:H7诱导至关重要的毒力计划的重要策略。在此,我们鉴定了一种毒力调节途径,其中Phoq / Phop双组分调节系统信号向O岛119编码的低镁诱导的调节剂A(LMIA),反过来,这反过来激活肠溶效应(LEE)的基因座基因以促进EHEC O157:H7粘附在大肠的低镁条件下。该调节途径广泛存在于一系列eHEC和肠致病大肠杆菌(EPEC)血清型中。这种途径的破坏显着降低了小鼠肠道中的EHEC O157:H7粘附。此外,喂养富含镁的饮食的小鼠显着降低了体内的EHEC O157:H7粘附性,表明镁可能有助于预防人类的EHEC和EPEC感染。摘要大肠病病原体肠杆菌大肠杆菌(EHEC)O157:H7检测到宿主提示,以调节定子和感染期间的毒力基因表达。然而,人类大肠中EHEC O157:H7的毒力调节机制尚未完全理解。在此,我们鉴定了一种毒力调节途径,其中phoq / phop双组分调节系统对O岛119编码的Z4267(LMIa;低镁诱导的调节剂A)感测低镁水平和信号,直接激活肠细胞效应的基因座基因以促进EHEC O157:H7粘附在大肠中。这种途径的破坏显着降低了小鼠肠道中的EHEC O157:H7粘附。此外,富含镁饮食的小鼠显着降低了EHEC O157:H7粘附在体内。这种LMIa介导的毒力调节途径也在几种EHEC和肠道致病大肠杆菌血清型中保存;因此,我们的研究结果支持使用镁作为膳食补充剂,并对可以预防肠道感染的膳食提示提供更大的见解。

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