生物
免疫系统
核心
噬菌体
病毒学
免疫学
微生物学
细胞生物学
遗传学
基因
大肠杆菌
作者
Yuping Li,Linlin Guan,Isabelle Becher,Kira S. Makarova,Xueli Cao,Surabhi Hareendranath,Jingwen Guan,Frank Stein,Siqi Yang,Arne Boergel,Karine Lapouge,Kim Remans,David A. Agard,Mikhail M. Savitski,Athanasios Typas,Eugene V. Koonin,Yue Feng,Joseph Bondy‐Denomy
出处
期刊:Cell
[Cell Press]
日期:2025-03-01
标识
DOI:10.1016/j.cell.2025.02.016
摘要
Jumbo bacteriophages of the ϕKZ-like family assemble a lipid-based early phage infection (EPI) vesicle and a proteinaceous nucleus-like structure during infection. These structures protect the phage from nucleases and may create selective pressure for immunity mechanisms targeting this specific phage family. Here, we identify "jumbo phage killer" (Juk), a two-component immune system that terminates infection of ϕKZ-like phages, suppressing the expression of early phage genes and preventing phage DNA replication and phage nucleus assembly while saving the cell. JukA (formerly YaaW) rapidly senses the EPI vesicle by binding to an early-expressed phage protein, gp241, and then directly recruits JukB. The JukB effector structurally resembles a pore-forming toxin and destabilizes the EPI vesicle. Functional anti-ϕKZ JukA homologs are found across bacterial phyla, associated with diverse effectors. These findings reveal a widespread defense system that specifically targets early events executed by ϕKZ-like jumbo phages prior to phage nucleus assembly.
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