首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative Medium-throughput Enumeration of Mycobacteria
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Visualization of the Charcoal Agar Resazurin Assay for Semi-quantitative Medium-throughput Enumeration of Mycobacteria

机译:半定量中等通量分枝杆菌计数的木炭琼脂刃天青测定法的可视化

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摘要

There is an urgent need to discover and progress anti-infectives that shorten the duration of tuberculosis (TB) treatment. Mycobacterium tuberculosis, the etiological agent of TB, is refractory to rapid and lasting chemotherapy due to the presence of bacilli exhibiting phenotypic drug resistance. The >charcoal >agar >resazurin >assay (CARA) was developed as a tool to characterize active molecules discovered by high-throughput screening campaigns against replicating and non-replicating M. tuberculosis. Inclusion of activated charcoal in bacteriologic agar medium helps mitigate the impact of compound carry-over, and eliminates the requirement to pre-dilute cells prior to spotting on CARA microplates. After a 7-10 day incubation period at 37 °C, the reduction of resazurin by mycobacterial microcolonies growing on the surface of CARA microplate wells permits semi-quantitative assessment of bacterial numbers via fluorometry. The CARA detects approximately a 2-3 log10 difference in bacterial numbers and predicts a minimal bactericidal concentration leading to ≥99% bacterial kill (MBC≥99). The CARA helps determine whether a molecule is active on bacilli that are replicating, non-replicating, or both. Pilot experiments using the CARA facilitate the identification of which concentration of test agent and time of compound exposure require further evaluation by colony forming unit (CFU) assays. In addition, the CARA can predict if replicating actives are bactericidal or bacteriostatic.
机译:迫切需要发现并开发可缩短结核病(TB)治疗时间的抗感染药。结核分枝杆菌是结核病的病因,由于存在表现出表型耐药性的细菌,因此对快速而持久的化学治疗是难治的。 > c harcoal > a gar > r esazurin > asay(CARA)被开发为表征发现的活性分子的工具通过针对复制和非复制结核分枝杆菌的高通量筛选活动。在细菌琼脂培养基中加入活性炭有助于减轻化合物残留的影响,并消除了在点样到CARA微孔板上之前对细胞进行预稀释的要求。在37°C下孵育7-10天后,CARA微孔板表面生长的分枝杆菌微菌落减少了刃天青的含量,可通过荧光法半定量评估细菌数量。 CARA检测出细菌数量大约有2-3 log10的差异,并预测最小杀菌浓度,导致≥99%的细菌杀死(MBC≥99)。 CARA有助于确定分子是否对正在复制,未复制或二者兼有的细菌具有活性。使用CARA进行的试点实验有助于确定需要通过菌落形成单位(CFU)分析进行进一步评估的测试剂浓度和化合物暴露时间。此外,CARA可以预测复制活性物质是否具有杀菌作用。

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