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The bile salt glycocholate induces global changes in gene and protein expression and activates virulence in enterotoxigenic Escherichia coli

机译:胆汁盐甘胆酸盐可诱导基因和蛋白质表达的整体变化并激活肠毒素性大肠杆菌中的毒力

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摘要

Pathogenic bacteria use specific host factors to modulate virulence and stress responses during infection. We found previously that the host factor bile and the bile component glyco-conjugated cholate (NaGCH, sodium glycocholate) upregulate the colonization factor CS5 in enterotoxigenic Escherichia coli (ETEC). To further understand the global regulatory effects of bile and NaGCH, we performed Illumina RNA-Seq and found that crude bile and NaGCH altered the expression of 61 genes in CS5 + CS6 ETEC isolates. The most striking finding was high induction of the CS5 operon (csfA-F), its putative transcription factor csvR, and the putative ETEC virulence factor cexE. iTRAQ-coupled LC-MS/MS proteomic analyses verified induction of the plasmid-borne virulence proteins CS5 and CexE and also showed that NaGCH affected the expression of bacterial membrane proteins. Furthermore, NaGCH induced bacteria to aggregate, increased their adherence to epithelial cells, and reduced their motility. Our results indicate that CS5 + CS6 ETEC use NaGCH present in the small intestine as a signal to initiate colonization of the epithelium.
机译:病原细菌使用特定的宿主因子来调节感染过程中的毒力和应激反应。我们先前发现宿主因子胆汁和胆汁成分的糖结合胆酸盐(NaGCH,甘胆酸钠)上调了肠毒素性大肠杆菌(ETEC)中的定居因子CS5。为了进一步了解胆汁和NaGCH的全球调节作用,我们进行了Illumina RNA-Seq实验,发现粗胆汁和NaGCH改变了CS5 ++ CS6 ETEC分离物中61个基因的表达。最惊人的发现是CS5操纵子(csfA-F),其假定的转录因子csvR和假定的ETEC毒力因子cexE的高诱导。 iTRAQ偶联的LC-MS / MS蛋白质组学分析证实了质粒携带的毒力蛋白CS5和CexE的诱导,还显示NaGCH影响细菌膜蛋白的表达。此外,NaGCH诱导细菌聚集,增加其对上皮细胞的粘附性并降低其运动性。我们的结果表明,CS5 ++ CS6 ETEC使用小肠中存在的NaGCH作为启动上皮定植的信号。

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