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Evaluation of Mycobacterium tuberculosis drugsusceptibility in clinical specimens from Nigeria using genotype MTBDRplus andMTBDRsl assays

机译:结核分枝杆菌药物的评价使用基因型MTBDRplus和PCR检测来自尼日利亚的临床标本的敏感性MTBDRsl分析

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摘要

The incidence of tuberculosis (TB) and especially multidrug-resistant TB (MDR) continues to increase alarmingly worldwide, and reliable and fast diagnosis of MDR is essential for the adequate treatment of patients. In contrast to the standard culture methods, nucleid acid amplification tests (NAATs) provide information about presence of Mycobacterium tuberculosis complex (MTBC) DNA and a potential resistance pattern within hours. We analyzed specimens of 110 patients from Nigeria comparing culture-based drug susceptibility testing (DST) to NAAT assays detecting isoniazid (INH), rifampicin (RMP) (GenoType MTBDRplus), and ethambutol (EMB) (GenoType MTBDRsl) resistance. Compared to DST, the GenoType MTBDRplus and MTBDRsl showed a specificity of 100% (86.3–100) and a sensitivity of 86% (42.1–99.6%) for detection of INH and a specificity of 100% (86.3–100) and a sensitivity of 83% (35.9–99.6%) for detection of RMP, and a sensitivity 100% (47.8–100%) for EMB resistance. However, in two strains, the NAAT assays provided false susceptible results as the mutations causing resistance were in genomic regions not covered by the probes of the GenoType MTBDRplus assay. We show that, in combination to DST, application of the GenoType MTBDRplus and GenoType MTBDRsl assays might bea useful additional tool to allow a rapid and safe diagnosis of MDR andextensively drug-resistant (XDR) MTBC.
机译:结核病(TB),尤其是耐多药结核病(MDR)的发生率在世界范围内持续增长,令人震惊,可靠,快速的MDR诊断对于适当治疗患者至关重要。与标准培养方法相比,核酸扩增测试(NAAT)可在数小时内提供有关结核分枝杆菌复合物(MTBC)DNA的存在和潜在耐药性模式的信息。我们分析了来自尼日利亚的110位患者的标本,将其基于文化的药敏测试(DST)与NAAT检测进行了比较,检测了异烟肼(INH),利福平(RMP)(GenoType MTBDRplus)和乙胺丁醇(EMB)(GenoType MTBDRsl)耐药性。与DST相比,GenoType MTBDRplus和MTBDRsl显示100%(86.3–100)的特异性,对INH的检测灵敏度为86%(42.1–99.6%),特异性为100%(86.3–100)和灵敏度。 RMP的检测率为83%(35.9–99.6%),EMB耐药性的灵敏度为100%(47.8–100%)。然而,在两种菌株中,NAAT分析提供了错误的易感结果,因为引起抗性的突变发生在基因型MTBDRplus分析探针未涵盖的基因组区域。我们表明,结合DST,GenoType MTBDRplus和GenoType MTBDRsl检测的应用可能是一个有用的附加工具,可以快速安全地诊断MDR和广泛耐药(XDR)MTBC。

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