Targeting Biofilm Associated Staphylococcus aureus Using Resazurin Based Drug-susceptibility Assay

被引:14
作者
Dalecki, Alex G. [1 ]
Crawford, Cameron L. [1 ]
Wolschendorf, Frank [1 ]
机构
[1] Univ Alabama Birmingham, Div Infect Dis, Dept Med, Birmingham, AL 35233 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2016年 / 111期
关键词
Infection; Issue; 111; Staphylococcus aureus; biofilm; resazurin; minimal biofilm eradication concentration; drug discovery; Neocuproine; Neocuproine copper complex;
D O I
10.3791/53925
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Most pathogenic bacteria are able to form biofilms during infection, but due to the difficulty of manipulating and assessing biofilms, the vast majority of laboratory work is conducted with planktonic cells. Here, we describe a peg plate biofilm assay as performed with Staphylococcus aureus. Bacterial biofilms are grown on pegs attached to a 96-well microtiter plate lid, washed through gentle submersion in buffer, and placed in a drug challenge plate. After subsequent incubation they are again washed and moved to a final recovery plate, in which the fluorescent dye resazurin serves as a viability indicator. This assay offers greatly increased ease-of-use, reliability, and reproducibility, as well as a wealth of data when conducted as a kinetic read. Moreover, this assay can be adapted to a medium-throughput drug screening approach by which an endpoint fluorescent readout is taken instead, offering a path for drug discovery efforts.
引用
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页数:6
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