Zhang Senfeng, Ma Shengsheng, Wang Feizuo, Hu Chunyi
Department of Biological Sciences, Faculty of Science, National University of Singapore, Singapore 117543, Singapore.
Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Singapore.
Eng Microbiol. 2024 Jun 4;4(3):100156. doi: 10.1016/j.engmic.2024.100156. eCollection 2024 Sep.
The adaptive survival mechanisms of bacterial pathogens under host-induced stress are crucial for understanding pathogenesis. Recently, Uppalapati et al. revealed a unique dual function of the Gifsy-1 prophage terminase in : it acts as a transfer ribonuclease (tRNase) under oxidative stress. The Gifsy-1 prophage terminase targets and fragments tRNA to halt translation and temporarily impairs bacterial growth when exposed to high levels of ROS generated by the host immune cells. This response not only preserves genomic integrity by facilitating DNA repair but also inhibits prophage mobilization, thereby aiding in bacterial survival within vertebrate hosts. This study highlights a novel intersection between phage biology and bacterial adaptive strategies.
细菌病原体在宿主诱导的应激下的适应性生存机制对于理解发病机制至关重要。最近,乌帕拉帕蒂等人揭示了Gifsy-1原噬菌体末端酶的一种独特双重功能:在氧化应激下它作为一种转移核糖核酸酶(tRNase)发挥作用。当暴露于宿主免疫细胞产生的高水平活性氧时,Gifsy-1原噬菌体末端酶靶向并切割tRNA以停止翻译,并暂时损害细菌生长。这种反应不仅通过促进DNA修复来维持基因组完整性,还抑制原噬菌体的移动,从而有助于细菌在脊椎动物宿主体内生存。这项研究突出了噬菌体生物学与细菌适应性策略之间的一个新交叉点。