Quorum sensing orchestrates parallel cell death pathways in Vibrio cholerae via Type 6 secretion-dependent and -independent mechanisms.

IF 9.4 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Proceedings of the National Academy of Sciences of the United States of America Pub Date : 2024-11-12 Epub Date: 2024-11-05 DOI:10.1073/pnas.2412642121
Ameya A Mashruwala, Bonnie L Bassler
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Abstract

Quorum sensing (QS) is a cell-to-cell communication process that enables bacteria to coordinate group behaviors. In Vibrio cholerae colonies, a program of spatial-temporal cell death is among the QS-controlled traits. Cell death occurs in two phases, first along the colony rim, and subsequently, at the colony center. Both cell death phases are driven by the type 6 secretion system (T6SS). Here, we show that HapR, the master QS regulator, does not control t6ss gene expression nor T6SS-mediated killing activity. Nonetheless, a ΔhapR strain displays no cell death at the colony rim. RNA-Sequencing (RNA-Seq) analyses reveal that HapR activates expression of an operon containing four genes of unknown function, vca0646-0649. Epistasis and overexpression studies show that two of the genes, vca0646 and vca0647, are required to drive cell death in both a ΔhapR and a ΔhapR Δt6ss strain. Thus, vca0646-0649 are regulated by HapR but act independently of the T6SS machinery to cause cell death, suggesting that a second, parallel pathway to cell death exists in V. cholerae.

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法定量感知通过 6 型分泌依赖性和非依赖性机制协调霍乱弧菌的平行细胞死亡途径。
法定量感应(QS)是一种细胞间通信过程,能使细菌协调群体行为。在霍乱弧菌菌落中,由 QS 控制的特征之一是空间-时间细胞死亡程序。细胞死亡分为两个阶段,首先是沿着菌落边缘,然后是在菌落中心。这两个细胞死亡阶段都由 6 型分泌系统(T6SS)驱动。在这里,我们发现主 QS 调节器 HapR 既不控制 t6ss 基因的表达,也不控制 T6SS 介导的杀伤活性。然而,ΔhapR 菌株在菌落边缘不会出现细胞死亡。RNA 序列(RNA-Seq)分析显示,HapR 激活了一个包含四个功能未知基因 vca0646-0649 的操作子的表达。外显和过表达研究表明,其中两个基因 vca0646 和 vca0647 是驱动 ΔhapR 和 ΔhapR Δt6ss 菌株细胞死亡所必需的。因此,vca0646-0649受HapR调控,但其作用独立于T6SS机制而导致细胞死亡,这表明霍乱弧菌中存在第二种平行的细胞死亡途径。
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来源期刊
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
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