首页> 外文期刊>International Journal of Mycobacteriology >Rapid drug-susceptibility testing of Mycobacterium tuberculosis clinical isolates to first-line antitubercular drugs by nitrate reductase assay: A comparison with proportion method
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Rapid drug-susceptibility testing of Mycobacterium tuberculosis clinical isolates to first-line antitubercular drugs by nitrate reductase assay: A comparison with proportion method

机译:硝酸还原酶法快速检测结核分枝杆菌临床分离株对一线抗结核药物的药敏性:与比例法的比较

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Objectiue/background: Early initiation of therapy in patients with tuberculosis is imperative for its control. Conventional methods of susceptibility testing such as the proportion method (PM) require visual detection and counting of colonies that takes up to 6 weeks. Rapid and simple phenotypic methods that have been endorsed by the World Health Organization can serve as alternatives.Methods: In this study, we evaluated the colorimetric nitrate reductase assay, which utilizes the detection of nitrate reduction as an indicator of growth much earlier compared with PM (within 7-14 days). The susceptibility of 75 clinical isolates of Mycobacterium tuberculosis to four first-line antitubercular drugs was tested by nitrate reductase assay and compared with the standard PM. In this assay, inoculation was done on both drug-free and drug-containing Lowenstein-Jensen medium containing sodiumnitrate. After incubation for 7-14 days, reduction to nitrite was taken as an indicator of growth, which was detected by color change on addition of Griess reagent.Results: Agreement between nitrate reductase assay and PM was 100% for rifampicin, 97.30% for isoniazid, 93.30% for streptomycin, and 98.60% for ethambutol. Cost/isolate with this assay was found to be approximately two times lesser than that of PM. Allresults were obtained in 7-14 days by nitrate reductase assay, which was significantly rapid compared with 42 days taken for obtaining results by PM.Conclusion: Nitrate reductase assay can be used as a rapid and inexpensive method for drug-susceptibility testing of M. tuberculosis for first-line antitubercular drugs without compromising accuracy of standard methods.
机译:目的/背景:结核病患者尽早开始治疗对于控制其势在必行。常规的药敏测试方法,例如比例法(PM),需要目视检测和计数菌落,最多需要6周。方法:在这项研究中,我们评估了比色硝酸盐还原酶测定法,该方法利用硝酸盐还原度检测作为比PM提早得多的生长指标,可以替代世界卫生组织认可的快速和简单的表型方法。 (7-14天内)。通过硝酸还原酶测定法测试了75种结核分枝杆菌临床分离株对四种一线抗结核药物的敏感性,并与标准PM进行了比较。在该测定中,在无药和含药的含有硝酸钠的Lowenstein-Jensen培养基上均进行了接种。孵育7-14天后,以亚硝酸盐的还原为生长指标,通过添加Griess试剂的颜色变化来检测。结果:利福平的硝酸还原酶测定与PM的一致性为100%,异烟肼为97.30% ,链霉素为93.30%,乙胺丁醇为98.60%。发现该测定的成本/隔离度比PM低约两倍。硝酸还原酶测定法在7-14天内获得所有结果,与用PM获得结果的42天相比,该结果显着快。结论:硝酸还原酶测定法可作为一种快速,廉价的方法对M进行药敏试验。一线抗结核药物治疗结核病,但不影响标准方法的准确性。

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