Laboratory of Bacteriology, The Rockefeller University, New York, NY, USA.
Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, USA.
Nature. 2024 May;629(8011):410-416. doi: 10.1038/s41586-024-07329-9. Epub 2024 Apr 17.
Bacteria have adapted to phage predation by evolving a vast assortment of defence systems. Although anti-phage immunity genes can be identified using bioinformatic tools, the discovery of novel systems is restricted to the available prokaryotic sequence data. Here, to overcome this limitation, we infected Escherichia coli carrying a soil metagenomic DNA library with the lytic coliphage T4 to isolate clones carrying protective genes. Following this approach, we identified Brig1, a DNA glycosylase that excises α-glucosyl-hydroxymethylcytosine nucleobases from the bacteriophage T4 genome to generate abasic sites and inhibit viral replication. Brig1 homologues that provide immunity against T-even phages are present in multiple phage defence loci across distinct clades of bacteria. Our study highlights the benefits of screening unsequenced DNA and reveals prokaryotic DNA glycosylases as important players in the bacteria-phage arms race.
细菌通过进化出各种各样的防御系统来适应噬菌体的捕食。虽然可以使用生物信息学工具来识别抗噬菌体免疫基因,但新系统的发现仅限于现有的原核序列数据。在这里,为了克服这一限制,我们用裂解性大肠杆菌噬菌体 T4 感染携带土壤宏基因组 DNA 文库的大肠杆菌,以分离携带保护性基因的克隆。通过这种方法,我们鉴定出 Brig1,一种 DNA 糖基化酶,它从噬菌体 T4 基因组中切除α-葡萄糖基-羟甲基胞嘧啶核苷碱基,产生无碱基位点并抑制病毒复制。在不同细菌分类群的多个噬菌体防御基因座中都存在针对 T 偶数噬菌体的 Brig1 同源物。我们的研究强调了筛选未测序 DNA 的好处,并揭示了原核 DNA 糖基化酶是细菌-噬菌体军备竞赛中的重要参与者。