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通过细胞间通讯诱导自溶在……中产生膜泡

Membrane vesicle production via cell-to-cell communication-induced autolysis in .

作者信息

Nagasawa Ryo, Ito Tamami, Yamamoto Chika, Unoki Mio, Obana Nozomu, Nomura Nobuhiko, Toyofuku Masanori

机构信息

Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan.

Graduate School of Science and Technology, University of Tsukuba, Tsukuba, Ibaraki, Japan.

出版信息

Microbiol Spectr. 2025 Jul;13(7):e0033425. doi: 10.1128/spectrum.00334-25. Epub 2025 May 23.

Abstract

Membrane vesicles (MVs) released from bacteria into the extracellular environment play various roles in bacterial and bacterial-host interactions. In Gram-positive bacteria, cell wall degradation or damage is crucial for cytoplasmic MV (CMV) release because the cytoplasmic membrane must pass through the thick cell wall to the extracellular space. Although , a major causative agent of dental caries, is known to release CMVs that are involved in pathogenicity and biofilm formation, the mechanism by which CMV production is triggered is unknown. In this study, we demonstrate that induces CMV release via the Com system, a cell-to-cell communication system mediated by peptide signals. CMV release is primarily dependent on autolysin encoded by , which is regulated by the Com system. Electron microscopy observations indicated that CMV release was accompanied by cell death in a subpopulation of cells. We compared the protein profiles of CMVs, showing that CMVs induced via the Com system contained not only secreted proteins but also cytoplasmic proteins specifically expressed during Com system activation. We further demonstrate that the functionality of CMVs in biofilm formation differed depending on how they were induced.IMPORTANCEBacteria release membrane vesicles (MVs) that are involved in diverse biological processes such as cell-to-cell communication and also affect the bacterial host through their immunomodulatory activity. Recent studies have focused on elucidating the mechanisms underlying MV formation. In Gram-positive bacteria, it has been shown that cell death represents a major pathway for MV formation. Since cell death would not benefit the dying cell, but may provide benefit to the remaining cells, it is essential to understand the regulatory mechanisms governing the formation of MVs at the population level. Here, we show that MV formation in is regulated by cell-to-cell communication. A subpopulation of cells triggers cell death-meditated MV formation, from which the remaining cells derive benefits. This is the first report showing cell-to-cell communication regulates MV formation in Gram-positive bacteria that would provide insights into the regulatory mechanisms governing cell death-mediated MV formation at the population level.

摘要

从细菌释放到细胞外环境中的膜泡(MVs)在细菌间以及细菌与宿主的相互作用中发挥着多种作用。在革兰氏阳性菌中,细胞壁的降解或损伤对于细胞质膜泡(CMV)的释放至关重要,因为细胞质膜必须穿过厚厚的细胞壁才能到达细胞外空间。虽然变形链球菌作为龋齿的主要致病菌,已知其会释放参与致病性和生物膜形成的CMVs,但其触发CMV产生的机制尚不清楚。在本研究中,我们证明变形链球菌通过Com系统诱导CMV释放,Com系统是一种由肽信号介导的细胞间通讯系统。CMV的释放主要依赖于变形链球菌编码的自溶素,而自溶素受Com系统调控。电子显微镜观察表明,CMV的释放在一部分细胞中伴随着细胞死亡。我们比较了CMVs的蛋白质谱,结果显示通过Com系统诱导产生的CMVs不仅含有分泌蛋白,还含有在Com系统激活过程中特异性表达的细胞质蛋白。我们进一步证明,CMVs在生物膜形成中的功能因其诱导方式的不同而有所差异。

重要性

细菌释放的膜泡(MVs)参与多种生物学过程,如细胞间通讯,并且通过其免疫调节活性影响细菌宿主。最近的研究集中在阐明MV形成的潜在机制。在革兰氏阳性菌中,已表明细胞死亡是MV形成的主要途径。由于细胞死亡对垂死细胞没有益处,但可能对其余细胞有益,因此了解在群体水平上控制MV形成的调控机制至关重要。在这里,我们表明变形链球菌中MV的形成受细胞间通讯调控。一部分细胞触发细胞死亡介导的MV形成,其余细胞从中获益。这是第一份显示细胞间通讯调节革兰氏阳性菌中MV形成的报告,这将为在群体水平上控制细胞死亡介导的MV形成的调控机制提供见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50fc/12211075/7ac58c0ba483/spectrum.00334-25.f001.jpg

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