Humolli Dorentina, Piel Damien, Maffei Enea, Heyer Yannik, Agustoni Elia, Shaidullina Aisylu, Willi Luc, Imwinkelried Patrick, Estermann Fabienne, Cuénod Aline, Buser Dominik P, Alampi Carola, Chami Mohamed, Egli Adrian, Hiller Sebastian, Dunne Matthew, Harms Alexander
Institute of Food, Nutrition, and Health (IFNH), ETH Zürich, Zürich, Switzerland.
Biozentrum, University of Basel, Basel, Switzerland.
PLoS Biol. 2025 Apr 7;23(4):e3003063. doi: 10.1371/journal.pbio.3003063. eCollection 2025 Apr.
Research on bacteriophages, the viruses infecting bacteria, has fueled the development of modern molecular biology and inspired their therapeutic application to combat bacterial multidrug resistance. However, most work has so far focused on a few model phages which impedes direct applications of these findings in clinics and suggests that a vast potential of powerful molecular biology has remained untapped. We have therefore recently composed the BASEL collection of Escherichia coli phages (BActeriophage SElection for your Laboratory), which made a relevant diversity of phages infecting the E. coli K-12 laboratory strain accessible to the community. These phages are widely used, but their assorted diversity has remained limited by the E. coli K-12 host. We have therefore now genetically overcome the two major limitations of E. coli K-12, its lack of O-antigen glycans and the presence of resident bacterial immunity. Restoring O-antigen expression resulted in the isolation of diverse additional viral groups like Kagunavirus, Nonanavirus, Gordonclarkvirinae, and Gamaleyavirus, while eliminating all known antiviral defenses of E. coli K-12 additionally enabled us to isolate phages of Wifcevirus genus. Even though some of these viral groups appear to be common in nature, no phages from any of them had previously been isolated using E. coli laboratory strains, and they had thus remained largely understudied. Overall, 37 new phage isolates have been added to complete the BASEL collection. These phages were deeply characterized genomically and phenotypically with regard to host receptors, sensitivity to antiviral defense systems, and host range. Our results highlighted dominant roles of the O-antigen barrier for viral host recognition and of restriction-modification systems in bacterial immunity. We anticipate that the completed BASEL collection will propel research on phage-host interactions and their molecular mechanisms, deepening our understanding of viral ecology and fostering innovations in biotechnology and antimicrobial therapy.
对噬菌体(即感染细菌的病毒)的研究推动了现代分子生物学的发展,并激发了其在对抗细菌多重耐药性方面的治疗应用。然而,迄今为止,大多数工作都集中在少数几种模式噬菌体上,这阻碍了这些研究结果在临床上的直接应用,也表明强大的分子生物学的巨大潜力尚未得到开发。因此,我们最近组建了大肠杆菌噬菌体的BASEL文库(用于您实验室的细菌噬菌体选择),使科学界能够获得感染大肠杆菌K-12实验室菌株的多种相关噬菌体。这些噬菌体被广泛使用,但其种类多样性一直受到大肠杆菌K-12宿主的限制。因此,我们现在已经通过基因手段克服了大肠杆菌K-12的两个主要局限性,即其缺乏O抗原聚糖以及存在常驻细菌免疫。恢复O抗原表达导致分离出了多种其他病毒组,如卡古纳病毒、诺纳病毒、戈登克拉克病毒亚科和加马列病毒,而消除大肠杆菌K-12所有已知的抗病毒防御机制还使我们能够分离出威夫病毒属的噬菌体。尽管其中一些病毒组在自然界中似乎很常见,但以前从未使用大肠杆菌实验室菌株分离出其中任何一种噬菌体,因此它们在很大程度上仍未得到充分研究。总体而言,已添加37种新的噬菌体分离株以完善BASEL文库。这些噬菌体在宿主受体、对抗病毒防御系统的敏感性和宿主范围方面进行了深入的基因组和表型特征分析。我们的结果突出了O抗原屏障在病毒宿主识别中的主导作用以及限制修饰系统在细菌免疫中的作用。我们预计,完整的BASEL文库将推动噬菌体-宿主相互作用及其分子机制的研究,加深我们对病毒生态学的理解,并促进生物技术和抗菌治疗方面的创新。