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A systems biology approach sheds new light on Escherichia coli acid resistance

机译:系统生物学方法为大肠杆菌抗酸性提供了新思路

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摘要

In order to develop an infection, diarrhogenic Escherichia coli has to pass through the stomach, where the pH can be as low as 1. Mechanisms that enable E. coli to survive in low pH are thus potentially relevant for pathogenicity. Four acid response systems involved in reducing the concentration of intracellular protons have been identified so far. However, it is still unclear to what extent the regulation of other important cellular functions may be required for survival in acid conditions. Here, we have combined molecular and phenotypic analysis of wild-type and mutant strains with computational network inference to identify molecular pathways underlying E. coli response to mild and strong acid conditions. The interpretative model we have developed led to the hypothesis that a complex transcriptional programme, dependent on the two-component system regulator OmpR and involving a switch between aerobic and anaerobic metabolism, may be key for survival. Experimental validation has shown that the OmpR is responsible for controlling a sizeable component of the transcriptional programme to acid exposure. Moreover, we found that a ΔompR strain was unable to mount any transcriptional response to acid exposure and had one of the strongest acid sensitive phenotype observed.
机译:为了发展感染,腹泻性大肠埃希氏菌必须通过pH值可低至1的胃。因此,使大肠杆菌能够在低pH中生存的机制可能与致病性有关。迄今为止,已经发现了四个涉及降低细胞内质子浓度的酸反应系统。然而,尚不清楚在酸性条件下存活可能需要在何种程度上调节其他重要细胞功能。在这里,我们将野生型和突变菌株的分子和表型分析与计算网络推论相结合,以鉴定出大肠杆菌对轻度和强酸条件响应的分子途径。我们开发的解释模型导致了这样一个假说,即依赖于两组分系统调节剂OmpR的复杂转录程序,可能涉及有氧代谢和无氧代谢之间的转换,可能是生存的关键。实验验证表明,OmpR负责控制转录程序的较大组成部分对酸的暴露。此外,我们发现ΔompR菌株无法对酸暴露产生任何转录反应,并具有观察到的最强的酸敏感性表型之一。

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