Droplet-Microarray: Miniaturized Platform for High-Throughput Screening of Antimicrobial Compounds

被引:27
|
作者
Lei, Wenxi [1 ]
Demir, Konstantin [1 ]
Overhage, Joerg [3 ]
Grunze, Michael [4 ]
Schwartz, Thomas [5 ]
Levkin, Pavel A. [1 ,2 ]
机构
[1] Karlsruhe Inst Technol, Inst Biol & Chem Syst Funct Mol Syst, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
[2] Karlsruhe Inst Technol, Inst Organ Chem, D-76131 Karlsruhe, Germany
[3] Carleton Univ, Dept Hlth Sci, Ottawa, ON K1S 5B6, Canada
[4] Max Planck Inst Med Res, Dept Cellular Biophys, Jahnstr 29, D-69120 Heidelberg, Germany
[5] Karlsruhe Inst Technol, Inst Funct Interfaces, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
关键词
antibiotic resistance screening; droplet-microarray; facultative pathogenicPseudomonas aeruginosa; PSEUDOMONAS-AERUGINOSA; RESISTANCE; IDENTIFICATION; MECHANISMS; INHIBITORS; BACTERIA; STRAINS; ARRAY; CHIP;
D O I
10.1002/adbi.202000073
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Currently, there are no time-saving and cost-effective high-throughput screening methods for the evaluation of bacterial drug-resistance. In this study, a droplet microarray (DMA) system is established as a miniaturized platform for high-throughput screening of antibacterial compounds using the emerging, opportunistic human pathogenPseudomonas aeruginosa(P. aeruginosa) as a target. Based on the differences in wettability of DMA slides, a rapid method for generating microarrays of nanoliter-sized droplets containing bacteria is developed. The bacterial growth in droplets is evaluated using fluorescence. The new method enables immediate screening with libraries of antibiotics. A novel simple colorimetric readout method compatible with the nanoliter size of the droplets is established. Furthermore, the drug-resistance ofP. aeruginosa49, a multi-resistant strain from an environmental isolate, is investigated. This study demonstrates the potential of the DMA platform for the rapid formation of microarrays of bacteria for high-throughput drug screening.
引用
收藏
页数:9
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