Department of Bioengineering, Stanford University, Stanford, CA 94305, USA; Allen Discovery Center for Systems Modeling of Infection, Stanford University, Stanford, CA 94305, USA.
Allen Discovery Center for Systems Modeling of Infection, Stanford University, Stanford, CA 94305, USA; Department of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Cell Syst. 2020 Mar 25;10(3):254-264.e9. doi: 10.1016/j.cels.2020.02.006. Epub 2020 Mar 18.
Half of the bacteria in the human gut microbiome are lysogens containing integrated prophages, which may activate in stressful immune environments. Although lysogens are likely to be phagocytosed by macrophages, whether prophage activation occurs or influences the outcome of bacterial infection remains unexplored. To study the dynamics of bacteria-phage interactions in living cells-in particular, the macrophage-triggered induction and lysis of dormant prophages in the phagosome-we adopted a tripartite system where murine macrophages engulf E. coli, which are lysogenic with an engineered bacteriophage λ, containing a fluorescent lysis reporter. Pre-induced prophages are capable of lysing the host bacterium and propagating infection to neighboring bacteria in the same phagosome. A non-canonical pathway, mediated by PhoP, is involved with the native λ phage induction inside phagocytosed E. coli. These findings suggest two possible mechanisms by which induced prophages may function to aid the bactericidal activity of macrophages.
人类肠道微生物组中的一半细菌是含有整合噬菌体的溶原菌,这些噬菌体可能在应激免疫环境中被激活。尽管溶原菌很可能被巨噬细胞吞噬,但噬菌体的激活是否发生以及是否会影响细菌感染的结果仍未被探索。为了研究活细胞中细菌-噬菌体相互作用的动态,特别是研究巨噬细胞触发潜伏噬菌体在吞噬体中的诱导和裂解,我们采用了一个三方系统,其中包含一个荧光裂解报告基因的工程噬菌体 λ,噬菌体会感染吞噬了 E. coli 的小鼠巨噬细胞。预先诱导的噬菌体能够裂解宿主细菌,并将感染传播到同一吞噬体中的邻近细菌。非经典途径由 PhoP 介导,参与了吞噬的 E. coli 内天然 λ 噬菌体的诱导。这些发现表明,诱导的噬菌体可能通过两种可能的机制来辅助巨噬细胞的杀菌活性。