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首页> 外文期刊>Journal of Clinical Microbiology >Specific identification of Mycobacterium tuberculosis with the luciferase reporter mycobacteriophage: use of p-nitro-alpha-acetylamino-beta-hydroxy propiophenone.
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Specific identification of Mycobacterium tuberculosis with the luciferase reporter mycobacteriophage: use of p-nitro-alpha-acetylamino-beta-hydroxy propiophenone.

机译:用萤光素酶报道分子分枝杆菌特异性鉴定结核分枝杆菌:使用对硝基-α-乙酰基氨基-β-羟基苯乙酮。

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摘要

We have previously described a luciferase reporter mycobacteriophage (LRP) assay that can detect Mycobacterium tuberculosis and characterize mycobacterial drug susceptibility patterns within 24 to 48 h in positive cultures. One drawback of this LRP protocol is the ability of the recombinant mycobacteriophage phAE40 to infect a variety of Mycobacterium species, thus limiting its specificity for the detection of M. tuberculosis. In this study, we have (i) explored the host range of phAE40, (ii) developed a modified LRP assay that exploits the selective inhibitory effect of the compound p-nitro-alpha-acetylamino-beta-hydroxy propiophenone (NAP) against members of the M. tuberculosis complex to differentiate between the tubercle bacillus and other mycobacterial species, and (iii) tested over 300 samples, including primary clinical isolates and drug-resistant strains of M. tuberculosis, demonstrating the ability of the NAP-modified LRP assay to identify M. tuberculosis complex organisms with high degrees of sensitivity and specificity.
机译:我们之前已经描述了一种萤光素酶记者分枝杆菌噬菌体(LRP)检测法,可以检测到结核分枝杆菌并鉴定阳性培养物中24至48小时内的分枝杆菌药物敏感性模式。该LRP方案的一个缺点是重组分枝杆菌噬菌体phAE40感染多种分枝杆菌种类的能力,因此限制了其对结核分枝杆菌检测的特异性。在这项研究中,我们(i)探索了phAE40的宿主范围,(ii)开发了改良的LRP测定方法,该方法利用了化合物对硝基-α-乙酰氨基-β-羟基苯乙酮(NAP)对成员的选择性抑制作用结核分枝杆菌复合物区分结核杆菌和其他分枝杆菌种类,并且(iii)测试了300多个样品,包括结核分枝杆菌的主要临床分离株和耐药菌株,证明了NAP修饰的LRP分析的能力以高度的敏感性和特异性鉴定结核分枝杆菌复杂生物。

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