Quorum sensing-dependent regulation and blockade of exoprotease production in Aeromonas hydrophila

被引:210
作者
Swift, S
Lynch, MJ
Fish, L
Kirke, DF
Tomás, JM
Stewart, GSAB
Williams, P
机构
[1] Univ Nottingham, Queens Med Ctr, Inst Infect & Immun, Nottingham NG7 2UH, England
[2] Univ Nottingham, Queens Med Ctr, Sch Clin Lab Sci, Nottingham NG7 2UH, England
[3] Univ Nottingham, Sch Pharmaceut Sci, Nottingham NG7 2RD, England
[4] Univ Barcelona, Fac Biol, Dept Microbiol, E-08071 Barcelona, Spain
基金
英国惠康基金;
关键词
D O I
10.1128/IAI.67.10.5192-5199.1999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In Aeromonas hydrophila, the ahyI gene encodes a protein responsible for the synthesis of the quorum sensing signal N-butanoyl-L-homoserine lactone (C4-HSL). Inactivation of the ahyI gene on the A. hydrophila chromosome abolishes C4-HSL production. The exoprotease activity of A. hydrophila consists of both serine protease and metalloprotease activities; in the ahyI-negative strain, both are substantially reduced but can be restored by the addition of exogenous C4-HSL. In contrast, mutation of the LuxR homolog AhyR results in the loss of both exoprotease activities, which cannot be restored by exogenous C4-HSL. Furthermore, a substantial reduction in the production of exoprotease by the ahyI(+) parent strain is obtained by the addition of N-acylhomoserine lactone analogs that have acyl side chains of 10, 12, or 14 carbons. The inclusion of N-(3-oxododecanoyl)-L-homoserine lactone or N-(3-oxotetradecanoyl)-L-homoserine lactone at 10 mu M in overnight cultures of A. hydrophila abolishes exoprotease production in azocasein assays and reduces the activity of all the exoprotease species seen in zymograms.
引用
收藏
页码:5192 / 5199
页数:8
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