Lehman Kelly M, Grabowicz Marcin
Microbiology and Molecular Genetics Program, Graduate Division of Biological and Biomedical Sciences, Laney Graduate School, Emory University, Atlanta, GA 30322, USA.
Emory Antibiotic Resistance Center, Emory University School of Medicine, Atlanta, GA 30322, USA.
Antibiotics (Basel). 2019 Sep 24;8(4):163. doi: 10.3390/antibiotics8040163.
Gram-negative bacteria shield themselves from antibiotics by producing an outer membrane (OM) that forms a formidable permeability barrier. Multidrug resistance among these organisms is a particularly acute problem that is exacerbated by the OM. The poor penetrance of many available antibiotics prevents their clinical use, and efforts to discover novel classes of antibiotics against Gram-negative bacteria have been unsuccessful for almost 50 years. Recent insights into how the OM is built offer new hope. Several essential multiprotein molecular machines (Bam, Lpt, and Lol) work in concert to assemble the barrier and offer a swathe of new targets for novel therapeutic development. Murepavadin has been at the vanguard of these efforts, but its recently reported phase III clinical trial toxicity has tempered the anticipation of imminent new clinical options. Nonetheless, the many concerted efforts aimed at breaking down the OM barrier provide a source of ongoing optimism for what may soon come through the development pipeline. We will review the current state of drug development against the OM assembly targets, highlighting insightful new discovery approaches and strategies.
革兰氏阴性菌通过产生外膜来保护自身免受抗生素侵害,外膜形成了一道强大的渗透屏障。这些微生物中的多重耐药性是一个特别严重的问题,外膜使其更加恶化。许多现有抗生素的低渗透性阻碍了它们的临床应用,近50年来,研发针对革兰氏阴性菌的新型抗生素的努力一直没有成功。最近对如何构建外膜的深入了解带来了新的希望。几种重要的多蛋白分子机器(Bam、Lpt和Lol)协同工作来组装这道屏障,并为新型治疗药物的开发提供了一系列新靶点。莫雷帕拉丁一直处于这些努力的前沿,但最近报道的其III期临床试验毒性降低了人们对即将出现新临床选择的预期。尽管如此,旨在突破外膜屏障的诸多协同努力为即将通过研发流程的药物带来了持续的乐观情绪。我们将回顾针对外膜组装靶点的药物研发现状,重点介绍有见地的新发现方法和策略。