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本文引用的文献

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Membrane vesicles in sea water: heterogeneous DNA content and implications for viral abundance estimates.海水中的膜泡:DNA含量的异质性及其对病毒丰度估计的影响
ISME J. 2017 Feb;11(2):394-404. doi: 10.1038/ismej.2016.134. Epub 2016 Nov 8.
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A Two-Component Regulatory System Impacts Extracellular Membrane-Derived Vesicle Production in Group A Streptococcus.一种双组分调控系统影响A群链球菌细胞外膜衍生囊泡的产生。
mBio. 2016 Nov 1;7(6):e00207-16. doi: 10.1128/mBio.00207-16.
3
Explosive cell lysis as a mechanism for the biogenesis of bacterial membrane vesicles and biofilms.作为细菌膜泡和生物膜生物发生机制的爆炸性细胞裂解
Nat Commun. 2016 Apr 14;7:11220. doi: 10.1038/ncomms11220.
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A novel mechanism for the biogenesis of outer membrane vesicles in Gram-negative bacteria.革兰氏阴性菌外膜囊泡生物发生的一种新机制。
Nat Commun. 2016 Jan 25;7:10515. doi: 10.1038/ncomms10515.
5
Through the wall: extracellular vesicles in Gram-positive bacteria, mycobacteria and fungi.穿越细胞壁:革兰氏阳性菌、分枝杆菌和真菌中的细胞外囊泡
Nat Rev Microbiol. 2015 Oct;13(10):620-30. doi: 10.1038/nrmicro3480. Epub 2015 Sep 1.
6
Immune modulation by bacterial outer membrane vesicles.细菌外膜囊泡的免疫调节作用。
Nat Rev Immunol. 2015 Jun;15(6):375-87. doi: 10.1038/nri3837. Epub 2015 May 15.
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The CpAL quorum sensing system regulates production of hemolysins CPA and PFO to build Clostridium perfringens biofilms.CpAL群体感应系统调节溶血素CPA和PFO的产生,以形成产气荚膜梭菌生物膜。
Infect Immun. 2015 Jun;83(6):2430-42. doi: 10.1128/IAI.00240-15. Epub 2015 Mar 30.
8
Diverse mechanisms regulate sporulation sigma factor activity in the Firmicutes.多种机制调节厚壁菌门中的芽孢形成σ因子活性。
Curr Opin Microbiol. 2015 Apr;24:88-95. doi: 10.1016/j.mib.2015.01.006. Epub 2015 Feb 1.
9
The Clostridium sporulation programs: diversity and preservation of endospore differentiation.梭菌芽孢形成程序:芽孢分化的多样性与保守性
Microbiol Mol Biol Rev. 2015 Mar;79(1):19-37. doi: 10.1128/MMBR.00025-14.
10
Inflammatory responses to a Clostridium perfringens type A strain and α-toxin in primary intestinal epithelial cells of chicken embryos.鸡胚原代肠上皮细胞对A型产气荚膜梭菌菌株及α毒素的炎症反应。
Avian Pathol. 2015;44(2):81-91. doi: 10.1080/03079457.2015.1005573.

免疫活性梭菌膜泡的产生受芽孢形成因子调控。

Immunoactive Clostridial Membrane Vesicle Production Is Regulated by a Sporulation Factor.

作者信息

Obana Nozomu, Nakao Ryoma, Nagayama Kyoko, Nakamura Kouji, Senpuku Hidenobu, Nomura Nobuhiko

机构信息

Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Japan.

Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo, Japan.

出版信息

Infect Immun. 2017 Apr 21;85(5). doi: 10.1128/IAI.00096-17. Print 2017 May.

DOI:10.1128/IAI.00096-17
PMID:28223348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5400848/
Abstract

Recently, many Gram-positive bacteria as well as Gram-negative bacteria have been reported to produce membrane vesicles (MVs), but little is known regarding the regulators involved in MV formation. We found that a Gram-positive anaerobic pathogen, , produces MVs predominantly containing membrane proteins and cell wall components. These MVs stimulated proinflammatory cytokine production in mouse macrophage-like cells. We suggested that MVs induced interleukin-6 production through the Toll-like receptor 2 (TLR2) signaling pathway. Thus, the MV could have a role in the bacterium-host interaction and bacterial infection pathogenesis. Moreover, we found that the sporulation master regulator gene was required for vesiculogenesis. A conserved, phosphorylated aspartate residue of Spo0A was indispensable for MV production, suggesting that the phosphorylation of Spo0A triggers MV production. Multiple orphan sensor kinases necessary for sporulation were also required to maximize MV production. These findings imply that actively produces immunoactive MVs in response to the environment changing, as recognized by membrane-spanning sensor kinases and by modulating the phosphorylation level of Spo0A.

摘要

最近,据报道许多革兰氏阳性菌和革兰氏阴性菌都会产生膜泡(MVs),但对于参与MV形成的调节因子却知之甚少。我们发现一种革兰氏阳性厌氧病原体,主要产生含有膜蛋白和细胞壁成分的MVs。这些MVs刺激小鼠巨噬细胞样细胞中促炎细胞因子的产生。我们认为MVs通过Toll样受体2(TLR2)信号通路诱导白细胞介素-6的产生。因此,MVs可能在细菌与宿主的相互作用及细菌感染发病机制中发挥作用。此外,我们发现芽孢形成主调节基因对于膜泡形成是必需的。Spo0A一个保守的磷酸化天冬氨酸残基对于MVs的产生不可或缺,这表明Spo0A的磷酸化触发了MVs的产生。芽孢形成所需的多种孤儿传感激酶对于使MVs产量最大化也是必需的。这些发现意味着会根据环境变化,如通过跨膜传感激酶识别以及调节Spo0A的磷酸化水平,积极产生具有免疫活性的MVs。