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本文引用的文献

1
A widespread family of polymorphic contact-dependent toxin delivery systems in bacteria.细菌中广泛存在的一类多态接触依赖性毒素输送系统家族。
Nature. 2010 Nov 18;468(7322):439-42. doi: 10.1038/nature09490.
2
Bacterial contact-dependent delivery systems.细菌接触依赖型分泌系统。
Annu Rev Genet. 2010;44:71-90. doi: 10.1146/annurev.genet.42.110807.091449.
3
The Vibrio cholerae type VI secretion system displays antimicrobial properties.霍乱弧菌的 VI 型分泌系统具有抗菌特性。
Proc Natl Acad Sci U S A. 2010 Nov 9;107(45):19520-4. doi: 10.1073/pnas.1012931107. Epub 2010 Oct 25.
4
Burkholderia type VI secretion systems have distinct roles in eukaryotic and bacterial cell interactions.伯克霍尔德菌 VI 型分泌系统在真核生物和细菌细胞相互作用中具有不同的作用。
PLoS Pathog. 2010 Aug 26;6(8):e1001068. doi: 10.1371/journal.ppat.1001068.
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Signals of growth regulation in bacteria.细菌生长调控信号。
Curr Opin Microbiol. 2009 Dec;12(6):667-73. doi: 10.1016/j.mib.2009.09.006. Epub 2009 Oct 23.
6
Contact-dependent growth inhibition causes reversible metabolic downregulation in Escherichia coli.接触依赖性生长抑制导致大肠杆菌中可逆的代谢下调。
J Bacteriol. 2009 Mar;191(6):1777-86. doi: 10.1128/JB.01437-08. Epub 2009 Jan 5.
7
Contact-dependent growth inhibition requires the essential outer membrane protein BamA (YaeT) as the receptor and the inner membrane transport protein AcrB.接触依赖性生长抑制需要必需的外膜蛋白BamA(YaeT)作为受体以及内膜转运蛋白AcrB。
Mol Microbiol. 2008 Oct;70(2):323-40. doi: 10.1111/j.1365-2958.2008.06404.x. Epub 2008 Aug 22.
8
New insight into the molecular mechanisms of two-partner secretion.对双组分分泌分子机制的新见解。
Trends Microbiol. 2007 Nov;15(11):508-15. doi: 10.1016/j.tim.2007.10.005. Epub 2007 Nov 7.
9
Structure and function of an essential component of the outer membrane protein assembly machine.外膜蛋白组装机器一个关键组分的结构与功能
Science. 2007 Aug 17;317(5840):961-4. doi: 10.1126/science.1143993.
10
Contact-dependent inhibition of growth in Escherichia coli.大肠杆菌生长的接触依赖性抑制
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棍状毒素:模块化细胞分裂素自传递系统在细菌竞争中发挥作用。

Toxin on a stick: modular CDI toxin delivery systems play roles in bacterial competition.

机构信息

Molecular Cellular and Developmental Biology, University of California, Santa Barbara, CA, USA.

出版信息

Virulence. 2011 Jul-Aug;2(4):356-9. doi: 10.4161/viru.2.4.16463. Epub 2011 Jul 1.

DOI:10.4161/viru.2.4.16463
PMID:21705856
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3173679/
Abstract

Contact-dependent growth inhibition (CDI) is the first contact-dependent competition system identified in bacteria. CDI is mediated by the CdiA/CdiB two-partner secretion system, and the BamA outer membrane protein serves as the CDI receptor on target cells. A small immunity protein, CdiI, is required to protect inhibitor cells from their own CDI system. Recent results from our group show that CDI systems are present in a number of important gram-negative plant and animal pathogens. The C-terminal region of CdiA (CdiA-CT) is polymorphic and contains growth inhibitory activity. The CdiA-CT from uropathogenic Esherichia coli 536 is a tRNase whereas a CdiA-CT from Dickeya dadantii 3937 has DNase activity. Accordingly, these bacteria contain distinct CdiI proteins, which specifically bind and inactivate cognate CdiA-CT. Remarkably, CdiA-CTs are modular: one CdiA "stick" can deliver different CdiA-CT toxins. We discuss these findings as well as results showing that CDI plays an important role in intra-strain bacterial competition in the natural world. A detailed mechanistic understanding of CDI could facilitate development of probiotics and antimicrobials that target specific pathogens.

摘要

接触依赖性生长抑制(CDI)是细菌中鉴定的第一个接触依赖性竞争系统。CDI 是由 CdiA/CdiB 双组分分泌系统介导的,BamA 外膜蛋白作为靶细胞上的 CDI 受体。一种小的免疫蛋白 CdiI 被需要来保护抑制剂细胞免受自身 CDI 系统的影响。我们小组的最新结果表明,CDI 系统存在于许多重要的革兰氏阴性植物和动物病原体中。CdiA 的 C 末端区域(CdiA-CT)是多态的,含有生长抑制活性。来自尿路致病性大肠杆菌 536 的 CdiA-CT 是一种 tRNase,而来自迪基氏菌 3937 的 CdiA-CT 具有 DNA 酶活性。因此,这些细菌含有不同的 CdiI 蛋白,这些蛋白特异性结合并失活同源的 CdiA-CT。值得注意的是,CdiA-CT 是模块化的:一个 CdiA“棒”可以传递不同的 CdiA-CT 毒素。我们讨论了这些发现以及表明 CDI 在自然界中菌株内细菌竞争中发挥重要作用的结果。对 CDI 的详细机制理解可以促进针对特定病原体的益生菌和抗菌药物的开发。