Borselli Diane, Blanchet Marine, Bolla Jean-Michel, Muth Aaron, Skruber Kristen, Phanstiel Otto, Brunel Jean Michel
Aix-Marseille Université, IRBA, TMCD2 UMR-MD1, Faculté de Médecine, 27 Boulevard Jean Moulin, 13385, Marseille Cedex 05, France.
Centre de Recherche en Cancérologie de Marseille (CRCM), CNRS, UMR7258, Institut Paoli Calmettes, Aix-Marseille Université, UM 105, Inserm, U1068, 27 Boulevard Jean Moulin, 13385, Marseille Cedex 05, France.
Chembiochem. 2017 Feb 1;18(3):276-283. doi: 10.1002/cbic.201600532. Epub 2017 Jan 18.
Dihydromotuporamine C and its derivatives were evaluated for their in vitro antimicrobial activities and antibiotic enhancement properties against Gram-negative bacteria and clinical isolates. The mechanism of action of one of these derivatives, MOTU-N44, was investigated against Enterobacter aerogenes by using fluorescent dyes to evaluate outer-membrane depolarization and permeabilization. Its efficiency correlated with inhibition of dye transport, thus suggesting that these molecules inhibit drug transporters by de-energization of the efflux pump rather than by direct interaction of the molecule with the pump. This suggests that depowering the efflux pump provides another strategy to address antibiotic resistance.
对二氢莫土波胺C及其衍生物针对革兰氏阴性菌和临床分离株的体外抗菌活性及抗生素增强特性进行了评估。利用荧光染料评估外膜去极化和通透性,研究了其中一种衍生物MOTU-N44对产气肠杆菌的作用机制。其效果与染料转运抑制相关,因此表明这些分子通过使外排泵失能而非分子与泵的直接相互作用来抑制药物转运蛋白。这表明使外排泵失能为解决抗生素耐药性提供了另一种策略。