Biozentrum, University of Basel, Basel, Switzerland.
Institute of Medical Microbiology, University of Zürich, Zürich, Switzerland.
PLoS Biol. 2021 Nov 16;19(11):e3001424. doi: 10.1371/journal.pbio.3001424. eCollection 2021 Nov.
Bacteriophages, the viruses infecting bacteria, hold great potential for the treatment of multidrug-resistant bacterial infections and other applications due to their unparalleled diversity and recent breakthroughs in their genetic engineering. However, fundamental knowledge of the molecular mechanisms underlying phage-host interactions is mostly confined to a few traditional model systems and did not keep pace with the recent massive expansion of the field. The true potential of molecular biology encoded by these viruses has therefore remained largely untapped, and phages for therapy or other applications are often still selected empirically. We therefore sought to promote a systematic exploration of phage-host interactions by composing a well-assorted library of 68 newly isolated phages infecting the model organism Escherichia coli that we share with the community as the BASEL (BActeriophage SElection for your Laboratory) collection. This collection is largely representative of natural E. coli phage diversity and was intensively characterized phenotypically and genomically alongside 10 well-studied traditional model phages. We experimentally determined essential host receptors of all phages, quantified their sensitivity to 11 defense systems across different layers of bacterial immunity, and matched these results to the phages' host range across a panel of pathogenic enterobacterial strains. Clear patterns in the distribution of phage phenotypes and genomic features highlighted systematic differences in the potency of different immunity systems and suggested the molecular basis of receptor specificity in several phage groups. Our results also indicate strong trade-offs between fitness traits like broad host recognition and resistance to bacterial immunity that might drive the divergent adaptation of different phage groups to specific ecological niches. We envision that the BASEL collection will inspire future work exploring the biology of bacteriophages and their hosts by facilitating the discovery of underlying molecular mechanisms as the basis for an effective translation into biotechnology or therapeutic applications.
噬菌体是感染细菌的病毒,由于其无与伦比的多样性和遗传工程方面的最新突破,它们在治疗多药耐药性细菌感染和其他应用方面具有巨大潜力。然而,噬菌体-宿主相互作用的分子机制的基本知识主要局限于少数传统的模式系统,并且没有跟上该领域的最近大规模扩张。因此,这些病毒所编码的分子生物学的真正潜力在很大程度上尚未被开发,用于治疗或其他应用的噬菌体通常仍然是经验性选择的。因此,我们试图通过组合一个由 68 种新分离的噬菌体组成的良好混合文库来促进噬菌体-宿主相互作用的系统探索,这些噬菌体感染模式生物大肠杆菌,我们与社区共享该文库作为 BASEL(BActeriophage SElection for your Laboratory)文库。该文库在很大程度上代表了天然大肠杆菌噬菌体的多样性,并与 10 种经过充分研究的传统模式噬菌体一起进行了表型和基因组的深入特征分析。我们实验确定了所有噬菌体的必需宿主受体,量化了它们对细菌免疫不同层次的 11 种防御系统的敏感性,并将这些结果与噬菌体在一组致病性肠杆菌菌株中的宿主范围相匹配。噬菌体表型和基因组特征的分布模式表明,不同免疫系统的效力存在系统差异,并暗示了几个噬菌体群体中受体特异性的分子基础。我们的结果还表明,在适应特定生态位方面,不同噬菌体群体之间的广泛宿主识别和抵抗细菌免疫等适应性特征之间存在强烈的权衡。我们设想,BASEL 文库将通过促进对基础分子机制的发现,为生物技术或治疗应用的有效转化提供依据,从而激发未来探索噬菌体及其宿主生物学的工作。