生物膜
多药耐受
微生物学
达托霉素
细菌
抗生素
结核分枝杆菌
金黄色葡萄球菌
耐甲氧西林金黄色葡萄球菌
万古霉素
生物
肺结核
医学
遗传学
病理
作者
Aaron T. Garrison,Yasmeen Abouelhassan,Dimitris Kallifidas,Fang Bai,Maria Ukhanova,Volker Mai,Shouguang Jin,Hendrik Luesch,Robert W. Huigens
标识
DOI:10.1002/anie.201508155
摘要
Conventional antibiotics are ineffective against non-replicating bacteria (for example, bacteria within biofilms). We report a series of halogenated phenazines (HP), inspired by marine antibiotic 1, that targets persistent bacteria. HP 14 demonstrated the most potent biofilm eradication activities to date against MRSA, MRSE, and VRE biofilms (MBEC = 0.2-12.5 μM), as well as the effective killing of MRSA persister cells in non-biofilm cultures. Frontline MRSA treatments, vancomycin and daptomycin, were unable to eradicate MRSA biofilms or non-biofilm persisters alongside 14. HP 13 displayed potent antibacterial activity against slow-growing M. tuberculosis (MIC = 3.13 μM), the leading cause of death by bacterial infection around the world. HP analogues effectively target persistent bacteria through a mechanism that is non-toxic to mammalian cells and could have a significant impact on treatments for chronic bacterial infections.
科研通智能强力驱动
Strongly Powered by AbleSci AI