铜绿假单胞菌
群体感应
绿脓素
生物膜
化学
粘菌素
妥布霉素
环丙沙星
多重耐药
微生物学
群体猝灭
抗生素
流出
抗菌剂
药理学
细菌
生物化学
庆大霉素
生物
遗传学
作者
Jun Liu,Jinsong Hou,Yiqun Chang,Lijun Peng,Xiaoyi Zhang,Zhiying Miao,Ping‐Hua Sun,Jing Lin,Wei‐Min Chen
标识
DOI:10.1021/acs.jmedchem.1c01781
摘要
Development of new bacterial biofilm inhibitors as antibacterial synergists is an effective strategy to solve the resistance of Pseudomonas aeruginosa. In this paper, a series of 3-hydroxy-pyridin-4(1H)-ones were synthesized and evaluated, and the hit compound (20p) was identified with the effects of inhibiting the production of pyocyanin (IC50 = 8.6 μM) and biofilm formation (IC50 = 4.5 μM). Mechanistic studies confirmed that 20p inhibits the formation of bacterial biofilm by inhibiting the expression of pqsA, blocking pqs quorum sensing system quinolone biosynthesis. Moreover, we systematically investigated the bactericidal effects of combining currently approved antibiotics for CF including tobramycin, ciprofloxacin, and colistin E with 20p, which showed obvious antibacterial synergy to overcome antibiotics resistance in multidrug-resistant P. aeruginosa biofilms. The result indicates that compound 20p may be used in the future as a potentially novel antibacterial synergist candidate for the treatment of P. aeruginosa infections.
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