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首页> 外文期刊>Journal of Clinical Microbiology >Validation of the FluoroType MTBDR Assay for Detection of Rifampin and Isoniazid Resistance in Mycobacterium tuberculosis Complex Isolates
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Validation of the FluoroType MTBDR Assay for Detection of Rifampin and Isoniazid Resistance in Mycobacterium tuberculosis Complex Isolates

机译:用于检测结核分枝杆菌复杂分离物中的利福平和异烟肼耐药性的Fluorotype MTBDR检测方法的验证

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摘要

ABSTRACT For Mycobacterium tuberculosis complex (MTBC), the rapid and accurate diagnosis of drug resistance is crucial to ensure early initiation of appropriate therapy. Recently, a new molecular diagnostic test, the FluoroType MTBDR, aimed at detecting rifampin and isoniazid resistance has become available. This study aimed to evaluate the FluoroType MTBDR in comparison to phenotypic drug susceptibility testing (DST) using M. tuberculosis complex isolates. MTBC isolates underwent phenotypic DST and were tested using the FluoroType MTBDR and Genotype MTBDRplus. Sanger sequencing of the key regions of rpoB , katG , inhA , and aphC was performed for isolates with discordant phenotypic and molecular results. Furthermore, isolates with specific wild-type bands missing in the Genotype MTBDRplus, indicating the presence of a mutation, were investigated by Sanger sequencing. Specificity and sensitivity, defined as the proportions of isolates correctly determined as susceptible and resistant by the FluoroType MTBDR compared to phenotypic DST, were calculated. A total of 180 culture isolates were included; phenotypic DST showed 85 isolates susceptible to isoniazid and rifampin, 7 with isoniazid monoresistance, 7 with rifampin monoresistance, and 81 with multidrug resistance. The specificity of the FluoroType MTBDR was 100% (95% confidence interval [CI], 96.0 to 100%) for both rifampin and isoniazid. The sensitivity was 91.7% (95% CI, 83.6 to 96.6%) for isoniazid and 98.9% (95% CI, 93.8 to 100.0%) for rifampin. The FluoroType MTBDR has a high sensitivity and specificity for the detection of rifampin and isoniazid resistance when using culture isolates.
机译:摘要对于结核分枝杆菌复合物(MTBC),对耐药性的快速准确诊断对于确保及早开始适当治疗至关重要。最近,一种旨在检测利福平和异烟肼耐药性的新型分子诊断测试,即FluoroType MTBDR。这项研究旨在评估与使用结核分枝杆菌复杂分离物的表型药物敏感性测试(DST)相比,FluoroType MTBDR。 MTBC分离株进行了表型DST,并使用FluoroType MTBDR和Genotype MTBDRplus进行了测试。对具有不一致的表型和分子结果的分离株进行了rpoB,katG,inhA和aphC关键区域的Sanger测序。此外,通过Sanger测序研究了在基因型MTBDRplus中缺失特定野生型条带的分离株,表明存在突变。计算特异性和敏感性,定义为与表型DST相比,由FluoroType MTBDR正确确定为易感和耐药的分离物比例。总共包括180个培养分离株;表型DST显示85株对异烟肼和利福平敏感的分离株,7株对异烟肼单抗,7株对利福平单抗,81株对多药耐药。对于利福平和异烟肼,FluoroType MTBDR的特异性均为100%(95%置信区间[CI]为96.0至100%)。异烟肼的敏感性为91.7%(95%CI,83.6至96.6%),利福平的敏感性为98.9%(95%CI,93.8至100.0%)。当使用培养分离物时,FluoroType MTBDR对检测利福平和异烟肼的耐药性具有很高的灵敏度和特异性。

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