Department of Microbiology, Tumor and Cell biology, Karolinska Institutet, Stockholm, Box 280, S-17177, Stockholm, Sweden.
Institute of Biomedicine, Department of Microbiology and Immunology, University of Gothenburg, Box 435, S-405 30, Göteborg, Sweden.
Sci Rep. 2019 Jan 14;9(1):108. doi: 10.1038/s41598-018-36414-z.
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.
病原菌利用特定的宿主因子在感染过程中调节毒力和应激反应。我们之前发现,宿主因子胆汁和胆汁成分糖结合胆酸盐(NaGCH,sodium glycocholate)上调肠产毒性大肠杆菌(ETEC)的定植因子 CS5。为了进一步了解胆汁和 NaGCH 的全局调控作用,我们进行了 Illumina RNA-Seq 分析,发现粗胆汁和 NaGCH 改变了 CS5+CS6 ETEC 分离株中 61 个基因的表达。最显著的发现是 CS5 操纵子(csfA-F)、其假定转录因子 csvR 和假定 ETEC 毒力因子 cexE 的高诱导。iTRAQ 耦联 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,还表明 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黏附,并降低其运动性。我们的结果表明,CS5+CS6 ETEC 将小肠中存在的 NaGCH 用作启动上皮定植的信号。