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φ(2)GFP10,一种高强度噬菌粒,可直接从痰样中检测和快速药敏试验结核分枝杆菌。

φ(2)GFP10, a high-intensity fluorophage, enables detection and rapid drug susceptibility testing of Mycobacterium tuberculosis directly from sputum samples.

机构信息

Department of Microbiology and Immunology, Albert Einstein College of Medicine, New York, New York, USA.

出版信息

J Clin Microbiol. 2012 Apr;50(4):1362-9. doi: 10.1128/JCM.06192-11. Epub 2012 Jan 25.

Abstract

The difficulty of diagnosing active tuberculosis (TB) and lack of rapid drug susceptibility testing (DST) at the point of care remain critical obstacles to TB control. This report describes a high-intensity mycobacterium-specific-fluorophage (φ(2)GFP10) that for the first time allows direct visualization of Mycobacterium tuberculosis in clinical sputum samples. Engineered features distinguishing φ(2)GFP10 from previous reporter phages include an improved vector backbone with increased cloning capacity and superior expression of fluorescent reporter genes through use of an efficient phage promoter. φ(2)GFP10 produces a 100-fold increase in fluorescence per cell compared to existing reporter phages. DST for isoniazid and oxofloxacin, carried out in cultured samples, was complete within 36 h. Use of φ(2)GFP10 detected M. tuberculosis in clinical sputum samples collected from TB patients. DST for rifampin and kanamycin from sputum samples yielded results after 12 h of incubation with φ(2)GFP10. Fluorophage φ(2)GFP10 has potential for clinical development as a rapid, sensitive, and inexpensive point-of-care diagnostic tool for M. tuberculosis infection and for rapid DST.

摘要

诊断活动性肺结核 (TB) 的困难以及缺乏现场快速药物敏感性检测 (DST),仍然是结核病控制的关键障碍。本报告描述了一种高强度的分枝杆菌特异性噬菌体能(φ(2)GFP10),它首次允许直接观察临床痰样本中的结核分枝杆菌。与以前的报告噬菌体相比,φ(2)GFP10 的工程设计特征包括改进的载体骨架,增加了克隆能力,并通过使用高效噬菌体启动子提高了荧光报告基因的表达。与现有的报告噬菌体相比,φ(2)GFP10 使每个细胞的荧光强度增加了 100 倍。在培养样本中进行的异烟肼和氧氟沙星 DST 在 36 小时内完成。φ(2)GFP10 可用于检测从结核病患者采集的临床痰样本中的结核分枝杆菌。用 φ(2)GFP10 孵育 12 小时后,从痰样中获得利福平利福平和卡那霉素 DST 的结果。噬菌体能 φ(2)GFP10 具有作为一种快速、敏感和廉价的 M. tuberculosis 感染和快速 DST 的现场即时诊断工具的临床开发潜力。

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