Pasqua Martina, Zennaro Alessandro, Trirocco Rita, Fanelli Giulia, Micheli Gioacchino, Grossi Milena, Colonna Bianca, Prosseda Gianni
Istituto Pasteur Italia, Dipartimento di Biologia e Biotecnologie "C. Darwin", Sapienza Università di Roma, Via dei Sardi 70, 00185 Rome, Italy.
Istituto di Biologia e Patologia Molecolari, Consiglio Nazionale delle Ricerche (CNR), P. le Aldo Moro 5, 00185 Roma, Italy.
Microorganisms. 2021 Feb 12;9(2):369. doi: 10.3390/microorganisms9020369.
Outer membrane vesicles (OMVs) are nanostructures mostly produced by blebbing of the outer membrane in Gram negative bacteria. They contain biologically active proteins and perform a variety of processes. OMV production is also a typical response to events inducing stress in the bacterial envelope. In these cases, hypervesiculation is regarded as a strategy to avoid the dangerous accumulation of undesired products within the periplasm. Several housekeeping genes influence the biogenesis of OMVs, including those correlated with peptidoglycan and cell wall dynamics. In this work, we have investigated the relationship between OMV production and the lysis module of the DLP12 cryptic prophage. This module is an operon encoding a holin, an endolysin and two spannins, and is known to be involved in cell wall maintenance. We find that deleting the lysis module increases OMV production, suggesting that during evolution this operon has been domesticated to regulate vesiculation, likely through the elimination of non-recyclable peptidoglycan fragments. We also show that the expression of the lysis module is negatively regulated by environmental stress stimuli as high osmolarity, low pH and low temperature. Our data further highlight how defective prophages finely contribute to bacterial host fitness.
外膜囊泡(OMVs)是纳米结构,主要由革兰氏阴性菌外膜的起泡产生。它们含有生物活性蛋白并执行多种过程。OMV的产生也是细菌包膜受到应激事件时的典型反应。在这些情况下,过度囊泡化被视为一种避免周质内不期望产物危险积累的策略。几个管家基因影响OMV的生物发生,包括那些与肽聚糖和细胞壁动态相关的基因。在这项工作中,我们研究了OMV产生与DLP12隐匿性原噬菌体的裂解模块之间的关系。该模块是一个操纵子,编码一种溶菌蛋白、一种内溶素和两种跨膜蛋白,已知其参与细胞壁维持。我们发现删除裂解模块会增加OMV的产生,这表明在进化过程中,这个操纵子已被驯化来调节囊泡化,可能是通过消除不可再循环的肽聚糖片段。我们还表明,裂解模块的表达受到高渗透压、低pH值和低温等环境应激刺激的负调控。我们的数据进一步突出了缺陷原噬菌体如何精细地促进细菌宿主的适应性。