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首个改良分子遗传学检测结核病及利福平、异烟肼耐药性的评估。

First evaluation of an improved assay for molecular genetic detection of tuberculosis as well as rifampin and isoniazid resistances.

机构信息

Microbiology & Morphology Laboratory Phthisiopneumology Institute, Chisinau, Moldova.

出版信息

J Clin Microbiol. 2012 Apr;50(4):1264-9. doi: 10.1128/JCM.05903-11. Epub 2012 Feb 1.

DOI:10.1128/JCM.05903-11
PMID:22301019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3318528/
Abstract

The commercially available line probe assay MTBDRplus 2.0 (Hain Lifescience, Nehren, Germany) was evaluated for its ability to detect Mycobacterium tuberculosis complex (MTBC) and mutations conferring resistance to rifampin (RMP) and isoniazid (INH) directly in smear-negative and smear-positive pulmonary clinical specimens under routine laboratory conditions. A total of 348 samples originating from Moldova, a high-incidence country for tuberculosis (TB), were investigated. Two hundred fifty-seven (73.9%) were smear negative, 12 samples were excluded, and 81 (23.3%) were smear positive. Two DNA extraction methods were applied. Compared to culture and clinical data as the reference standard (adapted from Vadwai V et al., J. Clin. Microbiol. 49:2540-2545, 2011), overall sensitivity and specificity were 87.6 and 99.2%, respectively. One hundred four of the 257 smear-negative samples turned out to be culture positive, and 20 were MTBC culture negative but were positive based on clinical symptoms. The combined sensitivity and specificity in the subgroup of smear-negative samples were calculated to be 79.8 and 99.2%, respectively. MTBDRplus 2.0 detected RMP and INH resistance with sensitivity and specificity of 94.3 and 96.0%, respectively. In conclusion, the MTBDRplus 2.0 assay is a rapid and highly sensitive test for the detection of M. tuberculosis strains from smear-positive and -negative clinical specimens and provides additional information on RMP and INH resistance status, which can easily be included in routine laboratory work flow.

摘要

市售的线探针检测 MTBDRplus 2.0(德国海恩生命科学公司,Nehren)在常规实验室条件下,用于直接检测涂阴和涂阳的肺临床标本中的结核分枝杆菌复合群(MTBC)和利福平(RMP)及异烟肼(INH)耐药突变的能力进行了评估。共检测了来自高结核发病率国家摩尔多瓦的 348 个样本。257 个(73.9%)为涂阴样本,12 个样本被排除,81 个(23.3%)为涂阳样本。应用了两种 DNA 提取方法。与培养和临床数据作为参考标准(改编自 Vadwai V 等人,J. Clin. Microbiol. 49:2540-2545, 2011)相比,总体敏感性和特异性分别为 87.6%和 99.2%。257 个涂阴样本中有 104 个培养阳性,20 个 MTBC 培养阴性,但基于临床症状呈阳性。在涂阴样本亚组中计算的联合敏感性和特异性分别为 79.8%和 99.2%。MTBDRplus 2.0 检测 RMP 和 INH 耐药的敏感性和特异性分别为 94.3%和 96.0%。总之,MTBDRplus 2.0 检测法是一种快速、高度敏感的检测方法,可用于检测涂阴和涂阳的临床标本中的结核分枝杆菌株,并提供有关 RMP 和 INH 耐药状态的额外信息,这很容易被纳入常规实验室工作流程。

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