Differential Regulation of Escherichia coli fim Genes following Binding to Mannose Receptors.

IF 1.1 Q4 MICROBIOLOGY Journal of Pathogens Pub Date : 2018-05-22 eCollection Date: 2018-01-01 DOI:10.1155/2018/2897581
William R Schwan, Michael T Beck, Chia S Hung, Scott J Hultgren
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引用次数: 12

Abstract

Regulation of the uropathogenic Escherichia coli (UPEC) fimB and fimE genes was examined following type 1 pili binding to mannose-coated Sepharose beads. Within 25 min after mannose attachment, fimE expression dropped eightfold, whereas fimB transcription increased about two- to fourfold. Because both fim genes encode site-specific recombinases that affect the position of the fimS element containing the fimA promoter, the positioning of fimS was also examined. The fimS element changed to slightly more Phase-OFF in bacteria mixed with plain beads, whereas UPEC cells interacting with mannose-coated beads had significantly less Phase-OFF orientation of fimS under pH 7 conditions. On the other hand, Phase-OFF oriented fimS increased fourfold when UPEC cells were mixed with plain beads in a pH 5.5 environment. Positioning of fimS was also affected by fimH mutations, demonstrating that the FimH ligand binding to its receptor facilitates the changes. Moreover, enzyme immunoassays showed that UPEC cells had greater type 1 pili expression when mixed with mannose-coated beads versus plain beads. These results indicate that, after type 1 pilus binding to tethered mannose receptors, the physiology of the E. coli cells changes to maintain the expression of type 1 pili even when awash in an acidic environment.

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大肠杆菌膜基因与甘露糖受体结合后的差异调控。
研究了1型菌毛与甘露糖包被的Sepharose beads结合后尿路致病性大肠杆菌(UPEC) fimB和time基因的调控。甘露糖附着后25分钟内,time表达量下降了8倍,而fimB转录量增加了约2至4倍。由于这两个膜基因编码的位点特异性重组酶会影响含有fimA启动子的fimS元件的位置,因此也对fimS的定位进行了研究。在pH为7的条件下,与甘露糖包被微球相互作用的UPEC细胞中,fimS的相脱取向明显减少。另一方面,当UPEC细胞与普通珠混合在pH为5.5的环境中时,Phase-OFF取向的薄膜增加了四倍。fimS的定位也受到fimH突变的影响,这表明fimH配体与其受体的结合促进了这种变化。此外,酶免疫分析显示,与普通珠粒相比,混合甘露糖包被珠粒的UPEC细胞具有更高的1型菌毛表达。这些结果表明,当1型菌毛与拴系甘露糖受体结合后,大肠杆菌细胞的生理机能发生变化,即使在酸性环境中也能维持1型菌毛的表达。
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来源期刊
Journal of Pathogens
Journal of Pathogens MICROBIOLOGY-
自引率
0.00%
发文量
4
审稿时长
15 weeks
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