Design, synthesis and evaluation of halogenated furanone derivatives as quorum sensing inhibitors in Pseudomonas aeruginosa.

Design, synthesis and evaluation of halogenated furanone derivatives as quorum sensing inhibitors in Pseudomonas aeruginosa.

Chang, Yiqun;Wang, Peng-Cheng;Ma, Hong-Ming;Chen, Si-Yu;Fu, Yu-Hang;Liu, Yuan-Yuan;Wang, Xuan;Yu, Guang-Chao;Huang, Tao;Hibbs, David E;Zhou, Hai-Bo;Chen, Wei-Min;Lin, Jing;Wang, Chao;Zheng, Jun-Xia;Sun, Ping-Hua;
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences 2019 pp. 105058
311
chang2019designeuropean

Abstract

The biofilm formation of Pseudomonas aeruginosa (P. aeruginosa) is regulated by a phenomenon of quorum sensing (QS). With 5-hydroxyl-3,4-halogenated-5H-furan-2-ones as beginning, analogs bearing alkyl chains, vinyl bromide, or aromatic rings were designed and synthesized. The minimum inhibitory concentration (MIC) of the compounds against P. aeruginosa was assayed and the biofilm inhibition ratio was determined at different concentrations lower than the MIC. C-5 aromatic substituted furanones showed remarkable biofilm formation as well as inhibition of virulence factor production in P. aeruginosa. Fluorescence report analysis identified the QS regulatory mechanism of the most active compound 29. This study provides us a novel candidate for combating drug resistant bacteria strains by merely inhibiting biofilm formation. Without suppressing the regular life cycle of the bacteria, bacterial resistance mechanisms may not be activated.

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ID: 29690
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