College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China.
Vet Microbiol. 2013 Aug 30;165(3-4):378-83. doi: 10.1016/j.vetmic.2013.04.020. Epub 2013 Apr 30.
To investigate the effect of the Quorum Sensing (QS)-I system on the expression of virulence factors in Shiga toxin producing and verotoxin-producing Escherichia coli (STEC and VTEC), the yenI gene from Yersinia enterocolitica was cloned into E. coli F18ab 107/86. Recombinant E. coli transformed with yenI produced acyl-homoserine lactone synthase (AHL), as measured using cross-streaking assays with the reporter biosensor strain Chromobacterium violaceum CV026. The AI-1 positive recombinant F18ab E. coli exhibited impaired expression of flagella, decreased motility, reduced biofilm formation and AI-2 production, as well as attenuated adherence and invasion on IPEC-J2 cells. This study provides new insights to the crucial function of AI-1 in regulating STEC virulence.
为了研究群体感应(QS)-I 系统对产志贺毒素和产 verotoxin 的大肠杆菌(STEC 和 VTEC)毒力因子表达的影响,本研究从肠侵袭性大肠杆菌(Yersinia enterocolitica)中克隆 yenI 基因至大肠杆菌 F18ab 107/86。采用带有报告生物传感器菌株 Chromobacterium violaceum CV026 的交叉划线实验,证实携带 yenI 的重组大肠杆菌能够产生酰基高丝氨酸内酯合酶(AHL)。AI-1 阳性的重组 F18ab 大肠杆菌 flagella 表达受损,运动能力下降,生物膜形成和 AI-2 产生减少,对 IPEC-J2 细胞的黏附和侵袭能力减弱。本研究为 AI-1 在调节 STEC 毒力方面的关键功能提供了新的见解。