Department of Microbiology, Harvard Medical School, Boston, MA 02115.
Institute of Infectiology, Center for Molecular Biology of Inflammation, University of Münster, 48149 Münster, Germany.
Proc Natl Acad Sci U S A. 2021 Jan 5;118(1). doi: 10.1073/pnas.2018365118. Epub 2020 Dec 21.
The type 6 secretion system (T6SS) is a dynamic organelle encoded by many gram-negative bacteria that can be used to kill competing bacterial prey species in densely occupied niches. Some predatory species, such as , use their T6SS in an untargeted fashion while in contrast, assembles and fires its T6SS apparatus only after detecting initial attacks by other bacterial prey cells; this targeted attack strategy has been termed the T6SS tit-for-tat response. Molecules that interact with the outer membrane such as polymyxin B can also trigger assembly of T6SS organelles via a signal transduction pathway that involves protein phosphorylation. Recent work suggests that a phospholipase T6SS effector (TseL) of can induce T6SS dynamic activity in when delivered to or expressed in the periplasmic space of this organism. Here, we report that inhibiting expression of essential genes involved in outer membrane biogenesis can also trigger T6SS activation in Specifically, we developed a CRISPR interference (CRISPRi) system to knock down expression of , , and and found that these knockdowns activated T6SS activity. This increase in T6SS activity was dependent on the same signal transduction pathway that was previously shown to be required for the tit-for-tat response. We conclude that outer membrane perturbation can be sensed by to activate the T6SS even when the disruption is generated by aberrant cell envelope biogenesis.
6 型分泌系统(T6SS)是许多革兰氏阴性菌编码的一种动态细胞器,可用于在密集栖息的小生境中杀死竞争的细菌猎物物种。一些捕食性物种,如 ,以非靶向的方式使用它们的 T6SS,而相比之下, 只有在检测到其他细菌猎物细胞的初始攻击后才组装和发射其 T6SS 装置;这种靶向攻击策略被称为 T6SS 以牙还牙反应。与 外膜相互作用的分子,如多粘菌素 B,也可以通过涉及蛋白磷酸化的信号转导途径触发 T6SS 器官的组装。最近的工作表明, 的一种磷脂酶 T6SS 效应物(TseL)可以在该生物的周质空间中或在该生物中表达时,诱导 中的 T6SS 动态活性。在这里,我们报告说,抑制参与外膜生物发生的必需基因的表达也可以触发 中的 T6SS 激活。具体来说,我们开发了一种 CRISPR 干扰(CRISPRi)系统来敲低 、 、 和 的表达,发现这些敲低激活了 T6SS 活性。这种 T6SS 活性的增加依赖于先前显示对于以牙还牙反应所必需的相同信号转导途径。我们得出结论,即使是由异常细胞包膜生物发生引起的破坏,外膜扰动也可以被 感知,从而激活 T6SS。