Jakobsen Tim Holm, Alhede Maria, Hultqvist Louise Dahl, Bjarnsholt Thomas, Givskov Michael
Costerton Biofilm Centre, Department of Immunology and Microbiology, Faculty of Health Sciences, University of Copenhagen, Blegdamsvej 3B, 2200, Copenhagen, Denmark.
Department of Clinical Microbiology, Rigshospitalet, 2100, Copenhagen, Denmark.
Methods Mol Biol. 2018;1673:275-285. doi: 10.1007/978-1-4939-7309-5_21.
The formation of biofilms in conjunction with quorum sensing (QS) regulated expression of virulence by opportunistic pathogens contributes significantly to immune evasion and tolerance to a variety of antimicrobial treatments. The present protocol describes methods to determine the in vitro efficacy of potential QS inhibitors (QSIs). Work on Pseudomonas aeruginosa has shown that chemical blockage of QS is a promising new antimicrobial strategy. Several live bacterial reporter systems have been developed to screen extracts and pure compounds for QSI activity. Here we describe the usage of reporter strains consisting of a lasB-gfp or rhlA-gfp fusion in P. aeruginosa for qualitative and quantitative evaluation of the inhibition of two of the major QS pathways, monitored as reduced expression of green fluorescence. By the use of an in vitro flow cell system it is possible to study the QSI activity by monitoring its ability to interfere with the protective functions of bacterial biofilm. For evaluation of the global effects of QSI compounds, we present a protocol for the DNA microarray based transcriptomics. Using these in vitro methods it is possible to evaluate the potential of various QSI compounds.
由机会致病菌形成的生物膜与群体感应(QS)调节的毒力表达相结合,对免疫逃避和对多种抗菌治疗的耐受性有显著贡献。本方案描述了确定潜在群体感应抑制剂(QSIs)体外疗效的方法。对铜绿假单胞菌的研究表明,化学阻断群体感应是一种有前景的新型抗菌策略。已经开发了几种活细菌报告系统来筛选提取物和纯化合物的群体感应抑制活性。在这里,我们描述了在铜绿假单胞菌中使用由lasB - gfp或rhlA - gfp融合组成的报告菌株,对两条主要群体感应途径的抑制进行定性和定量评估,通过绿色荧光表达降低来监测。利用体外流动细胞系统,可以通过监测其干扰细菌生物膜保护功能的能力来研究群体感应抑制剂活性。为了评估群体感应抑制剂化合物的整体效应,我们提出了基于DNA微阵列的转录组学方案。使用这些体外方法可以评估各种群体感应抑制剂化合物的潜力。