生物
溶解循环
微生物学
细菌
多药耐受
铜绿假单胞菌
细菌病毒
噬菌体疗法
病毒学
病毒复制
噬菌体
病毒
生物膜
大肠杆菌
遗传学
基因
作者
Enea Maffei,Anne-Kathrin Woischnig,Marco Burkolter,Yannik Heyer,Dorentina Humolli,Nicole Thürkauf,Thomas Bock,Alexander Schmidt,Pablo Manfredi,Adrian Egli,Nina Khanna,Urs Jenal,Alexander Harms
标识
DOI:10.1038/s41467-023-44157-3
摘要
Abstract 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.
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