Cellular and Molecular Immunology Research Centre, School of Human Sciences, London Metropolitan University, London, United Kingdom.
School of Biological and Chemical Sciences, Queen Mary University of London, London, United Kingdom.
Front Cell Infect Microbiol. 2019 Jun 27;9:227. doi: 10.3389/fcimb.2019.00227. eCollection 2019.
Outer membrane and membrane vesicles (OMV/MV) are released from bacteria and participate in cell communication, biofilm formation and host-pathogen interactions. Peptidylarginine deiminases (PADs) are phylogenetically conserved enzymes that catalyze post-translational deimination/citrullination of proteins, causing structural and functional changes in target proteins. PADs also play major roles in the regulation of eukaryotic extracellular vesicle release. Here we show phylogenetically conserved pathways of PAD-mediated OMV/MV release in bacteria and describe deiminated/citrullinated proteins in and their derived OMV/MVs. Furthermore, we show that PAD inhibitors can be used to effectively reduce OMV/MV release, both in Gram-negative and Gram-positive bacteria. Importantly, this resulted in enhanced antibiotic sensitivity of both and to a range of antibiotics tested. Our findings reveal novel strategies for applying pharmacological OMV/MV-inhibition to reduce antibiotic resistance.
外膜和膜泡(OMV/MV)从细菌中释放出来,并参与细胞通讯、生物膜形成和宿主-病原体相互作用。肽基精氨酸脱亚氨酶(PADs)是进化上保守的酶,可催化蛋白质的翻译后脱亚胺/瓜氨酸化,导致靶蛋白的结构和功能发生变化。PADs 还在真核细胞外囊泡释放的调控中发挥主要作用。在这里,我们展示了细菌中 PAD 介导的 OMV/MV 释放的进化保守途径,并描述了 和它们衍生的 OMV/MVs 中的脱亚胺/瓜氨酸化蛋白。此外,我们还表明,PAD 抑制剂可有效减少革兰氏阴性和革兰氏阳性细菌的 OMV/MV 释放。重要的是,这导致 和 对测试的一系列抗生素的敏感性增强。我们的发现揭示了应用药理学 OMV/MV 抑制来减少抗生素耐药性的新策略。