Mycobacterial phage TM4 requires a eukaryotic-like Ser/Thr protein kinase to silence and escape anti-phage immunity

被引:3
|
作者
Li, Xiaohui [1 ]
Long, Xiating [1 ]
Chen, Liu [1 ]
Guo, Xiao [1 ]
Lu, Lining [1 ]
Hu, Lihua [1 ]
He, Zheng-Guo [1 ]
机构
[1] Guangxi Univ, Coll Life Sci & Technol, Guangxi Res Ctr Microbial & Enzyme Engn Technol, State Key Lab Conservat & Utilizat Subtrop Agrobio, Nanning 530004, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
ABORTIVE INFECTION SYSTEM; SERINE/THREONINE KINASES; TIR DOMAINS; TUBERCULOSIS; RESISTANCE; BACTERIA; GENES; WIDESPREAD; SUBSTRATE; SMEGMATIS;
D O I
10.1016/j.chom.2023.07.005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In eukaryotic cells, serine/threonine protein kinases (StpKs) play important roles in limiting viral infections. StpKs are commonly activated upon infections, inhibiting the expression of genes central for viral replication. Here, we report that a eukaryotic-like StpK7 encoded by MSMEG_1200 in M. smegmatis is required for mycobacteriophage TM4 to escape bacterial defense. stpK7 is located within a gene island, MSMEG_1191-MSMEG_1200, containing multiple anti-phage genes resembling the BREX (bacteriophage exclusion) phage-resistance system. StpK7 negatively regulates the expression of this gene island. Following phage TM4 infec-tion, StpK7 is induced, directly phosphorylating the transcriptional regulator MSMEG_1198 and inhibiting its positive regulatory activity, thus reducing the expression of multiple downstream genes in the BREX-like gene island. Further analysis showed that genes within this anti-phage island critically regulate mycobacterial lipid hemostasis and phage adsorption. Collectively, this work characterizes a regulatory network driven by StpK7, which is utilized by phage TM4 to escape from the host defense against mycobacteria.
引用
收藏
页码:1469 / +
页数:17
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