Biozentrum, University of Basel, Basel, Switzerland.
Institute of Food, Nutrition and Health, D-HEST, ETH Zurich, Zurich, Switzerland.
Nat Commun. 2024 Jan 2;15(1):175. doi: 10.1038/s41467-023-44157-3.
Bacteriophages are ubiquitous viral predators that have primarily been studied using fast-growing laboratory cultures of their bacterial hosts. However, microbial life in nature is mostly in a slow- or non-growing, dormant state. Here, we show that diverse phages can infect deep-dormant bacteria and suspend their replication until the host resuscitates ("hibernation"). However, a newly isolated Pseudomonas aeruginosa phage, named Paride, can directly replicate and induce the lysis of deep-dormant hosts. While non-growing bacteria are notoriously tolerant to antibiotic drugs, the combination with Paride enables the carbapenem meropenem to eradicate deep-dormant cultures in vitro and to reduce a resilient bacterial infection of a tissue cage implant in mice. Our work might inspire new treatments for persistent bacterial infections and, more broadly, highlights two viral strategies to infect dormant bacteria (hibernation and direct replication) that will guide future studies on phage-host interactions.
噬菌体是无处不在的病毒捕食者,主要通过其细菌宿主的快速生长实验室培养来研究。然而,自然界中的微生物生命大多处于缓慢生长或非生长、休眠状态。在这里,我们表明,多种噬菌体可以感染深度休眠的细菌,并暂停其复制,直到宿主复苏(“冬眠”)。然而,一种新分离的铜绿假单胞菌噬菌体,命名为 Paride,可以直接复制并诱导深度休眠宿主的裂解。虽然非生长细菌对抗生素药物具有明显的耐受性,但与 Paride 结合可以使碳青霉烯类药物美罗培南在体外消灭深度休眠的培养物,并减少组织笼植入物中细菌感染的恢复。我们的工作可能会为持久性细菌感染提供新的治疗方法,更广泛地说,强调了两种感染休眠细菌的病毒策略(冬眠和直接复制),这将指导未来关于噬菌体-宿主相互作用的研究。