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首页> 外文期刊>Journal of Clinical Microbiology >Diagnostic Performance of the New Version (v2.0) of GenoType MTBDRsl Assay for Detection of Resistance to Fluoroquinolones and Second-Line Injectable Drugs: a Multicenter Study
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Diagnostic Performance of the New Version (v2.0) of GenoType MTBDRsl Assay for Detection of Resistance to Fluoroquinolones and Second-Line Injectable Drugs: a Multicenter Study

机译:GenoType MTBDRsl检测新版本(v2.0)对氟喹诺酮和二线可注射药物耐药性检测的诊断性能:多中心研究

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摘要

Resistance to fluoroquinolones (FLQ) and second-line injectable drugs (SLID) is steadily increasing, especially in eastern European countries, posing a serious threat to effective tuberculosis (TB) infection control and adequate patient management. The availability of rapid molecular tests for the detection of extensively drug-resistant TB (XDR-TB) is critical in areas with high rates of multidrug-resistant TB (MDR-TB) and XDR-TB and limited conventional drug susceptibility testing (DST) capacity. We conducted a multicenter study to evaluate the performance of the new version (v2.0) of the Genotype MTBDRsl assay compared to phenotypic DST and sequencing on a panel of 228 Mycobacterium tuberculosis isolates and 231 smear-positive clinical specimens. The inclusion of probes for the detection of mutations in the eis promoter region in the MTBDRsl v2.0 test resulted in a higher sensitivity for detection of kanamycin resistance for both direct and indirect testing (96% and 95.4%, respectively) than that seen with the original version of the assay, whereas the test sensitivities for detection of FLQ resistance remained unchanged (93% and 83.6% for direct and indirect testing, respectively). Moreover, MTBDRsl v2.0 showed better performance characteristics than v1.0 for the detection of XDR-TB, with high specificity and sensitivities of 81.8% and 80.4% for direct and indirect testing, respectively. MTBDRsl v2.0 thus represents a reliable test for the rapid detection of resistance to second-line drugs and a useful screening tool to guide the initiation of appropriate MDR-TB treatment.
机译:对氟喹诺酮类药物(FLQ)和二线注射药物(SLID)的耐药性正在稳步提高,尤其是在东欧国家,这对有效的结核病(TB)感染控制和适当的患者管理构成了严重威胁。快速的分子检测可用于检测广泛耐药的结核病(XDR-TB),这在多重耐药结核病(MDR-TB)和XDR-TB发病率高且常规药物敏感性试验(DST)受限的地区至关重要容量。我们进行了一项多中心研究,以评估新版(v2.0)基因型MTBDR sl 与表型DST相比的性能,并在228株结核分枝杆菌分离株和231涂片阳性的面板上进行测序临床标本。在MTBDR sl v2.0测试中包含用于检测e is 启动子区域突变的探针可提高检测卡那霉素对两种直接耐药的敏感性间接检测法和间接检测法(分别为96%和95.4%),比原始检测法要高,而检测FLQ耐药性的检测灵敏度保持不变(直接和间接检测法分别为93%和83.6%)。而且,MTBDR sl v2.0在检测XDR-TB方面表现出比v1.0更好的性能特征,直接和间接检测的特异性和灵敏度分别为81.8%和80.4%。因此,MTBDR sl v2.0代表了一种快速检测对二线药物耐药性的可靠测试,并且是指导适当MDR-TB治疗开始的有用筛选工具。

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