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溶血曼氏杆菌A1及其他巴氏杆菌科细菌群体感应信号分子产生的研究

Studies on the production of quorum-sensing signal molecules in Mannheimia haemolytica A1 and other Pasteurellaceae species.

作者信息

Malott Rebecca J, Lo Reggie Y C

机构信息

Department of Microbiology, University of Guelph, N1G 2W1, Guelph, ON, Canada.

出版信息

FEMS Microbiol Lett. 2002 Jan 2;206(1):25-30. doi: 10.1111/j.1574-6968.2002.tb10981.x.

Abstract

The bioluminescence assay system using Vibrio harveyi reporter strains were used to examine quorum-sensing autoinducer (AI) activity from Mannheimia haemolytica A1 cell-free culture supernatant. We showed that M. haemolytica A1 cell-free culture supernatant contains molecules that can stimulate the quorum-sensing system that regulates the expression of the luciferase operon in V. harveyi. Specifically, M. haemolytica A1 can stimulate only the quorum system 2 but not system 1, suggesting that the culture supernatant only contains molecules similar to AI-2 of V. harveyi. The bioluminescence assay was also used to show that culture supernatants from related Pasteurellaceae organisms, Pasteurella multocida, Pasteurella trehalosi, Actinobacillus suis and Actinobacillus pleuropneumoniae, also contain AI-2-like molecules. This is consistent with the presence of a luxS homolog in the genomes of P. multocida and A. pleuropneumoniae. A luxS homolog was cloned by PCR from M. haemolytica A1 using sequencing data from the ongoing genome sequencing project. The cloned luxS(M.h.) was able to complement AI-2 production in the Escherichia coli DH5alpha luxS mutant. This is the first report of a quorum-sensing activity in M. haemolytica A1 and suggests that this bacterium utilizes this mechanism to regulate expression of genes under specific conditions.

摘要

使用哈维氏弧菌报告菌株的生物发光检测系统,用于检测溶血曼氏杆菌A1无细胞培养上清液中的群体感应自诱导物(AI)活性。我们发现,溶血曼氏杆菌A1无细胞培养上清液中含有能够刺激群体感应系统的分子,该系统可调节哈维氏弧菌中荧光素酶操纵子的表达。具体而言,溶血曼氏杆菌A1仅能刺激群体感应系统2,而不能刺激系统1,这表明培养上清液中仅含有与哈维氏弧菌AI-2相似的分子。生物发光检测还表明,相关巴斯德氏菌科生物多杀巴斯德氏菌、海藻糖巴斯德氏菌、猪放线杆菌和胸膜肺炎放线杆菌的培养上清液中也含有AI-2样分子。这与多杀巴斯德氏菌和胸膜肺炎放线杆菌基因组中存在luxS同源物一致。利用正在进行的基因组测序项目的测序数据,通过PCR从溶血曼氏杆菌A1中克隆出luxS同源物。克隆的luxS(M.h.)能够补充大肠杆菌DH5α luxS突变体中的AI-2产生。这是关于溶血曼氏杆菌A1群体感应活性的首次报道,表明该细菌利用这种机制在特定条件下调节基因表达。

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