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Rapid susceptibility testing for nontuberculosis mycobacteria using flow cytometry.

机译:使用流式细胞仪对非结核分枝杆菌进行快速药敏试验。

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We demonstrated previously that susceptibility testing of Mycobacterium tuberculosis could be accomplished within 24 h after the organisms were incubated with antituberculosis agents by using fluorescein diacetate (FDA) staining and flow cytometry. Continued studies have now shown that assay suspensions containing M. avium, M. fortuitum, M. gordonae, or M. marinum incubated with various concentrations of ciprofloxacin, clarithromycin, erythromycin, kanamycin, rifampin, tobramycin hydrolyzed less FDA than drug-free controls. Suspensions of treated and nontreated mycobacteria could be easily differentiated at 6 and 24 h after the initiation of the susceptibility assays by using FDA staining and flow cytometry. In addition, multiplication of the mycobacteria was not required to discern differences between drug-free suspensions of mycobacteria and those treated with antimycobacterial agents. The flow cytometric assay is simple, reproducible, and rapid.
机译:我们先前证明,可以通过使用双乙酸荧光素(FDA)染色和流式细胞术在将微生物与抗结核药一起孵育后24小时内完成结核分枝杆菌的药敏试验。现在继续进行的研究表明,与不同浓度的环丙沙星,克拉霉素,红霉素,卡那霉素,利福平,妥布霉素相比,与不同浓度药物相比,含有鸟莫尔分枝杆菌,福特分枝杆菌,戈登分枝杆菌或海藻分枝杆菌的分析悬浮液对FDA的水解较少。通过使用FDA染色和流式细胞术,在药敏试验开始后的6和24 h内,可以轻松地区分已处理和未处理的分枝杆菌的悬浮液。另外,不需要分枝杆菌的繁殖来辨别无药物的分枝杆菌悬浮液和用抗分枝杆菌药物治疗的悬浮液之间的差异。流式细胞仪测定法简单,可重复且快速。

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