铜绿假单胞菌
微生物学
抗菌剂
化学
抗生素
抗生素耐药性
环丙沙星
药品
抗药性
联合疗法
行动方式
细菌
生物
药理学
后天抵抗
假单胞菌
DNA
铁载体
多粘菌素
DNA损伤
作者
Jianwei Chen,Jiangwei Pan,Xingyue Lu,Lu Wang,Keli Tan,Yujie Yue,Liting Gu,Siqi Wang,Minghong Chen,Hong Jiang,Yu Pan,Yuanquan Yu,Jianwei Nai,Dahong Zhang,Hong Wang
标识
DOI:10.1016/j.xcrm.2026.102637
摘要
Antimicrobial resistance exacerbates the difficulty of clinical bacterial infection treatment, as single-target antibiotics rapidly lose efficacy shortly post-clinical use. Such resistance highlights an urgent need for multitargeted therapeutics. Metalloantibiotics, combining metal ions with antimicrobials to disrupt diverse bacterial pathways, represent a promising strategy to circumvent resistance. Here, we engineer a sideromycin-bismuth molecular nanoassembly for treating ciprofloxacin-resistant Pseudomonas aeruginosa. Using phylogenomics-driven methods, we identify four hydroxamate siderophores from Streptomyces fradiae and rationally design sideromycin 7 by a structure-based strategy. Sideromycin 7 forms a 7-Bi3+ coordination complex with bismuth citrate, exerting a three-pronged antibacterial mode of action: direct DNA binding to induce damage and arrest replication, suppression of KdpC synthesis to block KdpFABC-mediated potassium transport, and inhibition of ATP production. In murine models, this combination therapy exhibits potent efficacy against ciprofloxacin-resistant P. aeruginosa with a considerable safety index. Our findings highlight the potential of phylogenomics-guided metalloantibiotic engineering for overcoming drug resistance.
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