赖氨酸
抗生素耐药性
抗生素
生物
金黄色葡萄球菌
计算生物学
抗菌剂
微生物学
噬菌体
细菌
遗传学
大肠杆菌
基因
作者
Yue Zhang,Runze Li,Geng Zou,Yating Guo,Renwei Wu,Yang Zhou,Huanchun Chen,Rui Zhou,Rob Lavigne,Phillip J. Bergen,Jian Li,Jinquan Li
标识
DOI:10.1002/advs.202404049
摘要
Abstract The rapid rise of antibiotic resistance and slow discovery of new antibiotics have threatened global health. While novel phage lysins have emerged as potential antibacterial agents, experimental screening methods for novel lysins pose significant challenges due to the enormous workload. Here, the first unified software package, namely DeepLysin, is developed to employ artificial intelligence for mining the vast genome reservoirs (“dark matter”) for novel antibacterial phage lysins. Putative lysins are computationally screened from uncharacterized Staphylococcus aureus phages and 17 novel lysins are randomly selected for experimental validation. Seven candidates exhibit excellent in vitro antibacterial activity, with LLysSA9 exceeding that of the best‐in‐class alternative. The efficacy of LLysSA9 is further demonstrated in mouse bloodstream and wound infection models. Therefore, this study demonstrates the potential of integrating computational and experimental approaches to expedite the discovery of new antibacterial proteins for combating increasing antimicrobial resistance.
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