Division of Biological Sciences, University of Montana, Missoula, MT 59812.
Department of Microbiology and Cell Biology, Montana State University, Bozeman, MT 59717.
Proc Natl Acad Sci U S A. 2023 Feb 28;120(9):e2216430120. doi: 10.1073/pnas.2216430120. Epub 2023 Feb 21.
Monitoring the extracellular environment for danger signals is a critical aspect of cellular survival. However, the danger signals released by dying bacteria and the mechanisms bacteria use for threat assessment remain largely unexplored. Here we show that lysis of cells releases polyamines that are subsequently taken up by surviving cells via a mechanism that relies on Gac/Rsm signaling. While intracellular polyamines spike in surviving cells, the duration of this spike varies according to the infection status of the cell. In bacteriophage-infected cells, intracellular polyamines are maintained at high levels, which inhibits replication of the bacteriophage genome. Many bacteriophages package linear DNA genomes and linear DNA is sufficient to trigger intracellular polyamine accumulation, suggesting that linear DNA is sensed as a second danger signal. Collectively, these results demonstrate how polyamines released by dying cells together with linear DNA allow to make threat assessments of cellular injury.
监测细胞外环境中的危险信号是细胞存活的关键方面。然而,死亡细菌释放的危险信号以及细菌用于威胁评估的机制在很大程度上仍未得到探索。在这里,我们表明,细胞的裂解会释放多胺,随后这些多胺会通过依赖 Gac/Rsm 信号的机制被存活细胞吸收。虽然存活细胞中的细胞内多胺会激增,但这种激增的持续时间取决于细胞的感染状态。在噬菌体感染的细胞中,细胞内多胺保持在高水平,这抑制了噬菌体基因组的复制。许多噬菌体包装线性 DNA 基因组,而线性 DNA 足以触发细胞内多胺的积累,这表明线性 DNA 被视为第二个危险信号。总的来说,这些结果表明,死亡细胞释放的多胺与线性 DNA 一起,使能够对细胞损伤做出威胁评估。