Design, Synthesis, and Biological Evaluation of N-Acyl-Homoserine Lactone Analogs of Quorum Sensing in Pseudomonas aeruginosa

被引:7
|
作者
Wei, Zhenyu [1 ]
Li, Ting [1 ]
Gu, Yan [2 ]
Zhang, Qian [1 ]
Wang, Enhui [1 ]
Li, Wenbo [1 ]
Wang, Xin [2 ]
Li, Yang [2 ]
Li, Hongyu [1 ,2 ]
机构
[1] Lanzhou Univ, Inst Microbiol, Sch Life Sci, Int Sci & Technol Cooperat Base Biopharmaceut, Lanzhou, Peoples R China
[2] Lanzhou Univ, Gansu High Throughput Screening & Creat Ctr Hlth P, Sch Pharm, Lanzhou, Peoples R China
来源
FRONTIERS IN CHEMISTRY | 2022年 / 10卷
基金
中国国家自然科学基金;
关键词
AHL analogs; quorum sensing; Pseudomonas aeruginosa; anti-virulence; antibiofilm; BIOFILM FORMATION; VIRULENCE; NETWORK; INHIBITION; REGULATOR; PATHOGEN; GENE; LASR;
D O I
10.3389/fchem.2022.948687
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Quorum sensing plays a necessary role in the production of virulence factors and the formation of biofilm on Pseudomonas aeruginosa. Thus, the development of inhibition of quorum sensing is one of the most promising methods to control bacterial infection and antibiotic resistance. In this work, nine novel AHL analogs were designed, synthesized, and evaluated as potential quorum sensing inhibitors. The results depicted that structural modifications have significant effects on quorum sensing inhibition activity of AHL molecules. Without inhibiting the growth of P. aeruginosa, 2-(4-bromophenyl)-N-(2-oxotetrapyridinefuran-3-yl) butanamide (compound no.10) showed the excellent performance in inhibiting biofilm formation and virulence factor production among all the compounds through robustly suppressing the expression of QS related genes. In a molecular docking study, compound no.10 exhibited a higher affinity toward LasR than other AHL analogs. In addition, compound no.10 also exhibits the best inhibition effect on virulence production in the Caenorhabditis elegans infection model.
引用
收藏
页数:11
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