抗生素
褪黑素
微生物学
生物
病菌
多杀性巴氏杆菌
革兰氏阴性菌
重新调整用途
人类病原体
细菌
生物化学
生态学
遗传学
大肠杆菌
神经科学
基因
作者
Fang He,Yuan Liu,Li Pan,Xiaoyan Wu,Yaoyao Xia,Dong Zhang,Nengzhang Li,Yuanyi Peng,Guoqiang Zhu,Rüdiger Hardeland,Rüssel J. Reiter,Wenkai Ren
标识
DOI:10.1007/s11427-021-2032-9
摘要
Bacterial infections caused by Gram-negative pathogens represent a growing burden for public health worldwide. Despite the urgent need for new antibiotics that effectively fight against pathogenic bacteria, very few compounds are currently under development or approved in the clinical setting. Repurposing compounds for other uses offers a productive strategy for the development of new antibiotics. Here we report that the multifaceted melatonin effectively improves survival rates of mice and decreases bacterial loads in the lung during infection. Mechanistically, melatonin specifically inhibits the activity of citrate synthase of Gram-negative pathogens through directly binding to the R300, D363, and H265 sites, particularly for the notorious Pasteurella multocida. These findings highlight that usage of melatonin is a feasible and alternative therapy to tackle the increasing threat of Gram-negative pathogen infections via disrupting metabolic flux of bacteria.
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