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本文引用的文献

1
Iron and quorum sensing coordinately regulate the expression of vulnibactin biosynthesis in Vibrio vulnificus.铁和群体感应协同调节创伤弧菌毒力因子生物合成基因簇的表达。
J Biol Chem. 2012 Aug 3;287(32):26727-39. doi: 10.1074/jbc.M112.374165. Epub 2012 Jun 13.
2
Regulation of cytotoxicity by quorum-sensing signaling in Vibrio vulnificus is mediated by SmcR, a repressor of hlyU.群体感应信号调控创伤弧菌细胞毒性的机制是通过 SmcR 介导的,SmcR 是 hlyU 的阻遏蛋白。
J Bacteriol. 2011 May;193(10):2557-65. doi: 10.1128/JB.01259-10. Epub 2011 Mar 11.
3
Complete genome sequence of Vibrio vulnificus MO6-24/O.创伤弧菌 MO6-24/O 的全基因组序列
J Bacteriol. 2011 Apr;193(8):2062-3. doi: 10.1128/JB.00110-11. Epub 2011 Feb 11.
4
Vibrio vulnificus rtxA1 gene recombination generates toxin variants with altered potency during intestinal infection.创伤弧菌 rtxA1 基因重组在肠道感染过程中产生效力改变的毒素变异体。
Proc Natl Acad Sci U S A. 2011 Jan 25;108(4):1645-50. doi: 10.1073/pnas.1014339108. Epub 2011 Jan 10.
5
Bacterial quorum-sensing network architectures.细菌群体感应网络架构
Annu Rev Genet. 2009;43:197-222. doi: 10.1146/annurev-genet-102108-134304.
6
Vibrio vulnificus produces quorum sensing signals of the AHL-class.创伤弧菌产生AHL类群体感应信号。
FEMS Microbiol Ecol. 2009 Jul;69(1):16-26. doi: 10.1111/j.1574-6941.2009.00691.x. Epub 2009 Apr 25.
7
Vibrio vulnificus: disease and pathogenesis.创伤弧菌:疾病与发病机制
Infect Immun. 2009 May;77(5):1723-33. doi: 10.1128/IAI.01046-08. Epub 2009 Mar 2.
8
Proteomic analysis of Vibrio vulnificus M2799 grown under iron-repleted and iron-depleted conditions.在铁充足和铁缺乏条件下生长的创伤弧菌M2799的蛋白质组学分析。
Microb Pathog. 2009 Mar;46(3):171-7. doi: 10.1016/j.micpath.2008.12.004. Epub 2009 Jan 6.
9
Gene dosage compensation calibrates four regulatory RNAs to control Vibrio cholerae quorum sensing.基因剂量补偿校准四种调控RNA以控制霍乱弧菌群体感应。
EMBO J. 2009 Feb 18;28(4):429-39. doi: 10.1038/emboj.2008.300. Epub 2009 Jan 22.
10
A consensus sequence for binding of SmcR, a Vibrio vulnificus LuxR homologue, and genome-wide identification of the SmcR regulon.创伤弧菌LuxR同源物SmcR结合的共有序列以及SmcR调控子的全基因组鉴定。
J Biol Chem. 2008 Aug 29;283(35):23610-8. doi: 10.1074/jbc.M801480200. Epub 2008 Jun 25.

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.

DOI:10.1128/IAI.00375-13
PMID:23716618
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3719590/
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。