细菌
多重耐药
预酸化
粘菌素
抗生素
微生物学
革兰氏阴性菌
生物
化学
天然产物
大肠杆菌
生物化学
遗传学
基因
酶
作者
Meirong Song,Ying Liu,Tingting Li,Xiaojia Liu,Zhihui Hao,Shuangyang Ding,Pharkphoom Panichayupakaranant,Kui Zhu,Jianzhong Shen
标识
DOI:10.1002/advs.202100749
摘要
The increasing emergence and dissemination of multidrug resistant (MDR) bacterial pathogens accelerate the desires for new antibiotics. Natural products dominate the preferred chemical scaffolds for the discovery of antibacterial agents. Here, the potential of natural flavonoids from plants against MDR bacteria, is demonstrated. Structure-activity relationship analysis shows the prenylation modulates the activity of flavonoids and obtains two compounds, α-mangostin (AMG) and isobavachalcone (IBC). AMG and IBC not only display rapid bactericidal activity against Gram-positive bacteria, but also restore the susceptibility of colistin against Gram-negative pathogens. Mechanistic studies generally show such compounds bind to the phospholipids of bacterial membrane, and result in the dissipation of proton motive force and metabolic perturbations, through distinctive modes of action. The efficacy of AMG and IBC in four models associated with infection or contamination, is demonstrated. These results suggest that natural products of plants may be a promising and underappreciated reservoir to circumvent the existing antibiotic resistance.
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