Department of Biochemistry and Biomedical Sciences, McMaster University, 1200 Main Street West, Hamilton, Ontario, L8N 3Z5, Canada; Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, 1200 Main Street West, Hamilton, Ontario, L8N 3Z5, Canada.
Curr Opin Chem Biol. 2022 Feb;66:102099. doi: 10.1016/j.cbpa.2021.102099. Epub 2021 Nov 19.
Because of the rise in antibiotic resistance and the dwindling pipeline of effective antibiotics, it is imperative to explore avenues that breathe new life into existing drugs. This is particularly important for intrinsically resistant Gram-negative bacteria, which are exceedingly difficult to treat. The Gram-negative outer membrane (OM) prevents the entry of a plethora of antibiotics that are effective against Gram-positive bacteria, despite the presence of the targets of these drugs. Uncovering molecules that increase the permeability of the OM to sensitize Gram-negative bacteria to otherwise ineffective antibiotics is an approach that has recently garnered increased attention in the field. In this review, we survey chemical matter which has been shown to potentiate antibiotics against Gram-negative bacteria by perturbing the OM. These include peptides, nanoparticles, macromolecules, antibiotic conjugates, and small molecules.
由于抗生素耐药性的上升和有效抗生素数量的减少,探索为现有药物注入新活力的途径势在必行。这对于固有耐药的革兰氏阴性菌尤其重要,因为这些细菌极难治疗。革兰氏阴性外膜 (OM) 阻止了许多针对革兰氏阳性菌有效的抗生素的进入,尽管这些药物的靶标存在。揭示能够增加 OM 通透性的分子,使革兰氏阴性菌对其他无效的抗生素敏感,这是最近该领域越来越受到关注的一种方法。在这篇综述中,我们调查了已经显示通过扰乱 OM 来增强抗生素对革兰氏阴性菌作用的化学物质。这些包括肽、纳米颗粒、大分子、抗生素缀合物和小分子。