粘菌素
肺炎克雷伯菌
微生物学
流出
多重耐药
生物
药理学
铜绿假单胞菌
细菌
抗药性
抗生素
大肠杆菌
生物化学
基因
遗传学
作者
Qiushuang Sheng,Xiaoning Hou,Yang Wang,Nan Wang,Xuming Deng,Zhongmei Wen,Dan Li,Li Li,Yonglin Zhou,Jianfeng Wang
标识
DOI:10.1021/acs.jafc.2c06615
摘要
The efficacy of colistin, the last option against multidrug-resistant (MDR) Gram-negative bacteria, is severely threatened by the prevalence of plasmid- or chromosome-mediated colistin resistance genes. Herein, naringenin has dramatically restored colistin sensitivity against colistin-resistant Klebsiella pneumoniae infection without affecting bacterial viability, inducing resistance and causing obvious cell toxicity. Mechanism analysis reveals that naringenin potentiates colistin activity by multiple strategies including inhibition of mobilized colistin resistance gene activity, repression of two-component system regulation, and acceleration of reactive oxygen species-mediated oxidative damage. A lung-targeted delivery system of naringenin microspheres has been designed to facilitate naringenin bioavailability, accompanied by an effective potentiation of colistin for Klebsiella pneumoniae infection. Consequently, a new recognition of naringenin microspheres has been elucidated to restore colistin efficacy against colistin-resistant Gram-negative pathogens, which may be an effective strategy of developing potential candidates for MDR Gram-negative bacteria infection.
科研通智能强力驱动
Strongly Powered by AbleSci AI