Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73019, United States.
School of Medicine, Saint Louis University, St. Louis, Missouri 63110, United States.
ACS Infect Dis. 2024 Jun 14;10(6):2239-2249. doi: 10.1021/acsinfecdis.4c00190. Epub 2024 May 24.
Multidrug-resistant is a serious threat pathogen rapidly spreading in clinics and causing a range of complicated human infections. The major contributor to antibiotic resistance is the overproduction of AdeIJK and AdeABC multidrug efflux pumps of the resistance-nodulation-division (RND) superfamily of proteins. The dominant role of efflux in antibiotic resistance and the relatively high permeability of the outer membrane to amphiphilic compounds make this pathogen a promising target for the discovery of clinically relevant efflux pump inhibitors. In this study, we identified 4,6-diaminoquoniline analogs with inhibitory activities against AdeIJK efflux pump and followed up on these compounds with a focused synthetic program to improve the target specificity and to reduce cytotoxicity. We identified several candidates that potentiate antibacterial activities of antibiotics erythromycin, tetracycline, and novobiocin not only in the laboratory antibiotic susceptible strain ATCC17978 but also in multidrug-resistant clinical isolates AB5075 and AYE. The best analogs potentiated the activities of antibiotics in low micromolar concentrations, did not have antibacterial activities on their own, inhibited AdeIJK-mediated efflux of its fluorescent substrate ethidium ion, and had low cytotoxicity in A549 human lung epithelial cells.
多重耐药是一种严重的威胁病原体,在临床上迅速传播,并导致一系列复杂的人类感染。抗生素耐药性的主要原因是 AdeIJK 和 AdeABC 多药外排泵的过度产生,这些泵属于抗性 - 结节 - 分裂(RND)超家族的蛋白质。外排在外排抗生素耐药性和相对较高的亲脂性化合物对 外膜的通透性方面起着主导作用,使该病原体成为发现临床相关外排泵抑制剂的有希望的靶标。在这项研究中,我们鉴定了具有抑制 AdeIJK 外排泵活性的 4,6-二氨基喹啉类似物,并通过集中的合成计划跟进这些化合物,以提高目标特异性并降低细胞毒性。我们确定了几种候选药物,它们不仅在实验室抗生素敏感菌株 ATCC17978 中,而且在多药耐药临床分离株 AB5075 和 AYE 中,增强了抗生素红霉素、四环素和新生霉素的抗菌活性。最好的类似物以低微摩尔浓度增强抗生素的活性,本身没有抗菌活性,抑制 AdeIJK 介导的其荧光底物吖啶橙离子的外排,并且在 A549 人肺上皮细胞中具有低细胞毒性。