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An Automated Miniaturized Method to Perform and Analyze Antimicrobial Drug Synergy Assays

机译:一种执行和分析抗菌药物协同作用分析的自动化小型方法

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摘要

In the light of emerging antibiotic resistance mechanisms found in bacteria throughout the world, discovery of drugs that potentiate the effect of currently available antibiotics remains an important aspect of pharmaceutical research in the 21st century. Well-established clinical tests exist to determine synergy in vitro, but these are only optimal for low-throughput experimentation while leaving analysis of results and interpretation of high-throughput microscale assays poorly standardized. Here, we describe a miniaturized broth microdilution checkerboard assay and data analysis method in 384-well plate format that conforms to the Clinical Laboratory and Standards Institute (CLSI) methods. This method has been automated and developed to rapidly determine the synergism of current antibiotics with various beta-lactamase inhibitors emerging from our antimicrobial research efforts. This technique increases test throughput and integrity of results, and saves test compound and labor. We facilitated the interpretation of results with an automated analysis tool allowing us to rapidly qualify inter- and intraplate robustness, determine efficacy of multiple antibiotics at the same time, and standardize the results of synergy interpretation. This procedure should enhance high-throughput antimicrobial drug discovery and supersedes former techniques.
机译:鉴于全世界细菌中出现的新出现的抗生素抗性机制,发现可增强当前可用抗生素作用的药物仍然是21世纪药物研究的重要方面。存在完善的临床测试来确定体外协同作用,但这些测试仅适用于低通量实验,而对结果的分析和对高通量微量分析的解释却标准化程度较低。在这里,我们以384孔板形式描述符合临床实验室和标准协会(CLSI)方法的小型肉汤微稀释棋盘法和数据分析方法。该方法已经自动化并开发出来,可以快速确定当前抗生素与各种抗菌素研究产生的β-内酰胺酶抑制剂的协同作用。该技术可提高测试通量和结果的完整性,并节省测试化合物和人工。我们使用自动化分析工具促进了结果的解释,使我们能够快速确定板间和板内的稳健性,同时确定多种抗生素的疗效,并标准化协同解释的结果。此过程应增强高通量抗菌药物的发现,并取代以前的技术。

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