University of Guelph, Department of Molecular and Cellular Biology, Guelph, ON N1G 2W1, Canada.
Queen's University, Department of Community Health and Epidemiology, Kingston, ON K7L 3N6, Canada.
Cell Host Microbe. 2024 May 8;32(5):768-778.e9. doi: 10.1016/j.chom.2024.04.001. Epub 2024 Apr 22.
Microbiomes feature complex interactions between diverse bacteria and bacteriophages. Synthetic microbiomes offer a powerful way to study these interactions; however, a major challenge is obtaining a representative bacteriophage population during the bacterial isolation process. We demonstrate that colony isolation reliably excludes virulent viruses from sample sources with low virion-to-bacteria ratios such as feces, creating "virulent virus-free" controls. When the virulent dsDNA virome is reintroduced to a 73-strain synthetic gut microbiome in a bioreactor model of the human colon, virulent viruses target susceptible strains without significantly altering community structure or metabolism. In addition, we detected signals of prophage induction that associate with virulent predation. Overall, our findings indicate that dilution-based isolation methods generate synthetic gut microbiomes that are heavily depleted, if not devoid, of virulent viruses and that such viruses, if reintroduced, have a targeted effect on community assembly, metabolism, and prophage replication.
微生物组具有多种细菌和噬菌体之间复杂的相互作用。合成微生物组提供了一种研究这些相互作用的强大方法;然而,主要的挑战是在细菌分离过程中获得有代表性的噬菌体群体。我们证明,在粪便等病毒与细菌比值低的样本来源中,菌落分离可靠地排除了毒性病毒,从而产生了“无毒性病毒”对照。当毒性 dsDNA 病毒组被重新引入到一个 73 株合成肠道微生物组中,在人类结肠的生物反应器模型中,毒性病毒会针对易感菌株,而不会显著改变群落结构或代谢。此外,我们还检测到与毒性捕食相关的原噬菌体诱导信号。总的来说,我们的研究结果表明,基于稀释的分离方法产生的合成肠道微生物组严重缺乏(如果不是完全缺乏)毒性病毒,而如果重新引入此类病毒,它们会对群落组装、代谢和原噬菌体复制产生靶向效应。