Division of Infectious Diseases, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI 02903, USA.
State Key Laboratory of Animal Nutrition, College of Animal Science & Technology, China Agricultural University, Beijing 100193, PR China.
Future Med Chem. 2018 Feb;10(3):283-296. doi: 10.4155/fmc-2017-0159. Epub 2018 Jan 15.
Staphylococcus aureus is a major cause of severe hospital-acquired infections, and biofilm formation is an important part of staphylococcal pathogenesis. Therefore, developing new antimicrobial agents against both planktonic cells and biofilm of S. aureus is a major challenge.
Three 1,3,4-oxadiazole derivatives exhibited antimicrobial activity against seven S. aureus strains in vitro, with minimum inhibitory concentrations ranging from 4 to 32 μg/ml. At 4 × minimum inhibitory concentration, all compounds killed cells within 24 h, demonstrating bactericidal activity. In addition to their effects against planktonic cells, these compounds prevented biofilm formation in a dose-dependent manner, with inhibitory concentrations for biofilm formation ranging from 8 to 32 μg/ml. Interestingly, higher concentrations of these compounds were effective against mature biofilms and all compounds downregulated the transcription of the biofilm-related gene spa.
We report three new 1,3,4-oxadiazole derivatives that have bactericidal activity and could provide as alternatives to combat S. aureus.
金黄色葡萄球菌是严重医院获得性感染的主要原因,生物膜形成是葡萄球菌发病机制的重要组成部分。因此,开发针对金黄色葡萄球菌浮游细胞和生物膜的新型抗菌剂是一项重大挑战。
三种 1,3,4-噁二唑衍生物在体外对 7 株金黄色葡萄球菌表现出抗菌活性,最小抑菌浓度范围为 4 至 32μg/ml。在 4×最小抑菌浓度下,所有化合物在 24 小时内杀死细胞,表现出杀菌活性。除了对浮游细胞的作用外,这些化合物还以剂量依赖的方式抑制生物膜形成,生物膜形成的抑制浓度范围为 8 至 32μg/ml。有趣的是,这些化合物的较高浓度对成熟生物膜有效,并且所有化合物均下调与生物膜相关的 spa 基因的转录。
我们报告了三种具有杀菌活性的新型 1,3,4-噁二唑衍生物,它们可能是对抗金黄色葡萄球菌的替代药物。