Center for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.
Center for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA
Antimicrob Agents Chemother. 2017 Dec 21;62(1). doi: 10.1128/AAC.01674-17. Print 2018 Jan.
is the primary causative agent of dental caries and contributes to the multispecies biofilm known as dental plaque. An adenylate kinase-based assay was optimized for to detect cell lysis when exposed to the Selleck library (Selleck Chemical, Houston, TX) of 853 FDA-approved drugs in, to our knowledge, the first high-throughput drug screen in We found 126 drugs with activity against planktonic cultures, and they were classified into six categories: antibacterials (61), antineoplastics (23), ion channel effectors (9), other antimicrobials (7), antifungals (6), and other (20). These drugs were also tested for activity against biofilm cultures, and 24 compounds were found to inhibit biofilm formation, 6 killed preexisting biofilms, 84 exhibited biofilm inhibition and killing activity, and 12 had no activity against biofilms. The activities of 9 selected compounds that exhibited antimicrobial activity were further characterized for their activity against planktonic and biofilm cultures. Together, our results suggest that exhibits a susceptibility profile to a diverse array of established and novel antibacterials.
是龋齿的主要病原体,并有助于形成被称为牙菌斑的多物种生物膜。我们优化了基于腺苷酸激酶的检测方法,以检测在我们所知的首次高通量药物筛选中暴露于 Selleck 文库(休斯顿,TX 的 Selleck Chemical)中 853 种 FDA 批准药物时的细胞裂解,用于检测 。我们发现了 126 种对抗浮游培养物的活性药物,它们分为六类:抗菌药物(61)、抗肿瘤药物(23)、离子通道效应物(9)、其他抗菌药物(7)、抗真菌药物(6)和其他(20)。这些药物也针对生物膜培养物进行了活性测试,发现 24 种化合物可抑制生物膜形成,6 种化合物可杀死已存在的生物膜,84 种化合物具有生物膜抑制和杀伤活性,12 种化合物对生物膜无活性。对表现出抗菌活性的 9 种选定化合物的活性进行了进一步表征,以研究它们对浮游和生物膜培养物的活性。总之,我们的结果表明,对各种已建立和新型抗菌药物具有敏感性。