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本文引用的文献

1
Interplay between cyclic AMP-cyclic AMP receptor protein and cyclic di-GMP signaling in Vibrio cholerae biofilm formation.霍乱弧菌生物膜形成过程中,环磷酸腺苷-环磷酸腺苷受体蛋白与环二鸟苷酸信号之间的相互作用。
J Bacteriol. 2008 Oct;190(20):6646-59. doi: 10.1128/JB.00466-08. Epub 2008 Aug 15.
2
The Salmonellae PhoQ sensor: mechanisms of detection of phagosome signals.沙门氏菌PhoQ传感器:吞噬体信号的检测机制
Cell Microbiol. 2008 Mar;10(3):576-82. doi: 10.1111/j.1462-5822.2007.01111.x. Epub 2008 Jan 3.
3
Genomic SELEX search for target promoters under the control of the PhoQP-RstBA signal relay cascade.在PhoQP-RstBA信号转导级联控制下,通过基因组SELEX筛选靶标启动子。
J Bacteriol. 2007 Jul;189(13):4791-9. doi: 10.1128/JB.00319-07. Epub 2007 Apr 27.
4
Biofilm acts as a microenvironment for plankton-associated Vibrio cholerae in the aquatic environment of Bangladesh.在孟加拉国的水生环境中,生物膜作为与浮游霍乱弧菌相关的微环境。
Microbiol Immunol. 2007;51(4):369-79. doi: 10.1111/j.1348-0421.2007.tb03924.x.
5
The rbmBCDEF gene cluster modulates development of rugose colony morphology and biofilm formation in Vibrio cholerae.rbmBCDEF基因簇调节霍乱弧菌中粗糙菌落形态的发育和生物膜形成。
J Bacteriol. 2007 Mar;189(6):2319-30. doi: 10.1128/JB.01569-06. Epub 2007 Jan 12.
6
Regulation of rugosity and biofilm formation in Vibrio cholerae: comparison of VpsT and VpsR regulons and epistasis analysis of vpsT, vpsR, and hapR.霍乱弧菌中粗糙度和生物膜形成的调控:VpsT和VpsR调控子的比较以及vpsT、vpsR和hapR的上位性分析
J Bacteriol. 2007 Jan;189(2):388-402. doi: 10.1128/JB.00981-06. Epub 2006 Oct 27.
7
Transcriptome and phenotypic responses of Vibrio cholerae to increased cyclic di-GMP level.霍乱弧菌对环二鸟苷水平升高的转录组和表型反应。
J Bacteriol. 2006 May;188(10):3600-13. doi: 10.1128/JB.188.10.3600-3613.2006.
8
Cyclic-diGMP signal transduction systems in Vibrio cholerae: modulation of rugosity and biofilm formation.霍乱弧菌中的环二鸟苷酸信号转导系统:对粗糙度和生物膜形成的调节
Mol Microbiol. 2006 Apr;60(2):331-48. doi: 10.1111/j.1365-2958.2006.05106.x.
9
Identification and characterization of RbmA, a novel protein required for the development of rugose colony morphology and biofilm structure in Vibrio cholerae.霍乱弧菌中形成皱纹菌落形态和生物膜结构所需的一种新型蛋白质RbmA的鉴定与特性分析
J Bacteriol. 2006 Feb;188(3):1049-59. doi: 10.1128/JB.188.3.1049-1059.2006.
10
Calcium influences cellular and extracellular product formation during biofilm-associated growth of a marine Pseudoalteromonas sp.钙在海洋假交替单胞菌生物膜相关生长过程中影响细胞内和细胞外产物的形成。
Microbiology (Reading). 2005 Sep;151(Pt 9):2885-2897. doi: 10.1099/mic.0.28041-0.

鉴定一种影响霍乱弧菌生物膜形成的钙调控负调控系统。

Identification of a calcium-controlled negative regulatory system affecting Vibrio cholerae biofilm formation.

作者信息

Bilecen Kivanc, Yildiz Fitnat H

机构信息

Department of Microbiology and Environmental Toxicology, University of California, Santa Cruz, CA 95064, USA.

出版信息

Environ Microbiol. 2009 Aug;11(8):2015-29. doi: 10.1111/j.1462-2920.2009.01923.x. Epub 2009 Apr 9.

DOI:10.1111/j.1462-2920.2009.01923.x
PMID:19397680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2756528/
Abstract

Vibrio cholerae's capacity to cause outbreaks of cholera is linked to its survival and adaptability to changes in aquatic environments. One of the environmental conditions that can vary in V. cholerae's natural aquatic habitats is calcium (Ca(+2)). In this study, we investigated the response of V. cholerae to changes in extracellular Ca(2+) levels. Whole-genome expression profiling revealed that Ca(2+) decreased the expression of genes required for biofilm matrix production. Luria-Bertani (LB) medium supplemented with Ca(2+) (LBCa(2+)) caused V. cholerae to form biofilms with decreased thickness and increased roughness, as compared with biofilms formed in LB. Furthermore, addition of Ca(2+) led to dissolution in biofilms. Transcription of two genes encoding a two-component regulatory system pair, now termed calcium-regulated sensor (carS) and regulator (carR), was decreased in cells grown in LBCa(2+). Analysis of null and overexpression alleles of carS and carR revealed that expression of vps (Vibriopolysaccharide) genes and biofilm formation are negatively regulated by the CarRS two-component regulatory system. Through epistasis analysis we determined that CarR acts in parallel with HapR, the negative regulator of vps gene expression.

摘要

霍乱弧菌引发霍乱疫情的能力与其在水生环境中的生存及适应变化的能力相关。在霍乱弧菌的天然水生栖息地中,钙(Ca(+2))是一种会发生变化的环境条件。在本研究中,我们调查了霍乱弧菌对细胞外Ca(2+)水平变化的反应。全基因组表达谱分析显示,Ca(2+)降低了生物膜基质产生所需基因的表达。与在LB培养基中形成的生物膜相比,添加了Ca(2+)的Luria-Bertani(LB)培养基(LBCa(2+))使霍乱弧菌形成的生物膜厚度减小且粗糙度增加。此外,添加Ca(2+)导致生物膜溶解。在LBCa(2+)中生长的细胞中,编码一个双组分调节系统对(现称为钙调节传感器(carS)和调节子(carR))的两个基因的转录减少。对carS和carR的缺失和过表达等位基因的分析表明,vps(霍乱弧菌多糖)基因的表达和生物膜形成受到CarRS双组分调节系统的负调控。通过上位性分析,我们确定CarR与vps基因表达的负调节子HapR平行发挥作用。