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该毛铁复合物调节群体感应主调控因子 SmcR 的表达,以控制创伤弧菌毒力因子的表达。

The fur-iron complex modulates expression of the quorum-sensing master regulator, SmcR, to control expression of virulence factors in Vibrio vulnificus.

机构信息

Department of Life Science, Sogang University, Seoul, South Korea.

出版信息

Infect Immun. 2013 Aug;81(8):2888-98. doi: 10.1128/IAI.00375-13. Epub 2013 May 28.

Abstract

The gene vvpE, encoding the virulence factor elastase, is a member of the quorum-sensing regulon in Vibrio vulnificus and displays enhanced expression at high cell density. We observed that this gene was repressed under iron-rich conditions and that the repression was due to a Fur (ferric uptake regulator)-dependent repression of smcR, a gene encoding a quorum-sensing master regulator with similarity to luxR in Vibrio harveyi. A gel mobility shift assay and a footprinting experiment demonstrated that the Fur-iron complex binds directly to two regions upstream of smcR (-82 to -36 and -2 to +27, with respect to the transcription start site) with differing affinities. However, binding of the Fur-iron complex is reversible enough to allow expression of smcR to be induced by quorum sensing at high cell density under iron-rich conditions. Under iron-limiting conditions, Fur fails to bind either region and the expression of smcR is regulated solely by quorum sensing. These results suggest that two biologically important environmental signals, iron and quorum sensing, converge to direct the expression of smcR, which then coordinates the expression of virulence factors.

摘要

基因 vvpE 编码了弹性蛋白酶这种毒力因子,是创伤弧菌群体感应调控子的一个成员,在高细胞密度时表达增强。我们发现该基因在富含铁的条件下受到抑制,这种抑制是由于 Fur(铁摄取调节因子)依赖性抑制 smcR 所致,smcR 编码一个群体感应主调控因子,与 Harveyi 弧菌中的 luxR 具有相似性。凝胶迁移率变动分析和足迹实验表明 Fur-铁复合物以不同亲和力直接结合到 smcR 上游的两个区域(-82 到-36 和-2 到+27,相对于转录起始位点)。然而, Fur-铁复合物的结合是足够可逆的,允许在富含铁的条件下,高细胞密度时通过群体感应诱导 smcR 的表达。在缺铁条件下, Fur 无法结合任何一个区域,smcR 的表达仅受群体感应调控。这些结果表明,两种重要的生物环境信号,铁和群体感应,共同作用来指导 smcR 的表达,然后协调毒力因子的表达。

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