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首页> 外文期刊>BMC Infectious Diseases >PCR-reverse blot hybridization assay in respiratory specimens for rapid detection and differentiation of mycobacteria in HIV-negative population
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PCR-reverse blot hybridization assay in respiratory specimens for rapid detection and differentiation of mycobacteria in HIV-negative population

机译:PCR - 逆向印迹杂交测定呼吸试样中的艾滋病阴性群体的快速检测和分化分枝杆菌

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摘要

Rapid identification of pathogenic Mycobacterium species is critical for a successful treatment. However, traditional method is time-consuming and cannot discriminate isolated non-tuberculosis mycobacteria (NTM) at species level. In the retrospective study, we evaluated the clinical applicability of PCR-reverse blot hybridization assay (PCR-REBA Myco-ID) with clinical specimens for rapid detection and differentiation of mycobacterial species. A total of 334 sputum and 362 bronchial alveolar lavage fluids (BALF) from 696 patients with mycobacterium pulmonary disease (MPD) and 210 patients with non-mycobacterium pulmonary disease used as controls were analyzed. Sputum or BALF were obtained for MGIT 960-TBc ID test and PCR-REBA Myco-ID assay. High resolution melt analysis (HRM) was used to resolve inconsistent results of MGIT 960-TBc ID test and PCR-REBA Myco-ID assay. A total of 334 sputum and 362 BALF specimens from 696 MPD patients (292 MTB and 404 NTM) were eventually analyzed. In total, 292 MTBC and 436 NTM isolates (mixed infection of two species in 32 specimens) across 10 Mycobacterium species were identified. The most frequently isolated NTM species were M. intracellulare (n?=?236, 54.1%), followed by M. abscessus (n?=?106, 24.3%), M. kansasii (n?=?46, 10.6%), M. avium (n?=?36, 8.3%). Twenty-two cases had M. intracellulare and M. abscessus mixed infection and ten cases had M. avium and M. abscessus mixed infection. A high level of agreement (n?=?696; 94.5%) was found between MGIT 960-TBc ID and PCR-REBA Myco-ID (k?=?0.845, P?=?0.000). PCR-REBA Myco-ID assay had higher AUC for both MTBC and NTM than MGIT 960-TBc ID test. PCR-REBA Myco-ID has the advantages of rapid, comparatively easy to perform, relatively low cost and superior accuracy in mycobacterial species identification compared with MGIT 960-TBc ID. We recommend it into workflow of mycobacterial laboratories especially in source-limited countries.
机译:致病性分枝杆菌物种的快速鉴定对于成功治疗至关重要。然而,传统方法是耗时的,不能在物种水平下歧视分离的非结核分枝杆菌(NTM)。在回顾性研究中,我们评估了PCR反向污染杂交测定(PCR-REBA MYCO-ID)与临床试样的临床适用性,以快速检测和分解分枝杆菌物种。分析了334例痰和362条支气管肺泡灌洗液(BALF),可分析696名二分枝杆菌(MPD)和210例非分枝杆菌肺病患者用作对照的患者。为Mgit 960-TBC ID测试和PCR-REBA Myco-ID测定获得痰或BALF。高分辨率熔体分析(HRM)用于解决MgIT 960-TBC ID测试和PCR-REBA Myco-ID测定的不一致结果。最终分析了总共334例来自696 MPD患者(292MTB和404ntm)的332个痰和362个BALF标本。鉴定了总共292 MTBC和436个NTM分离物(32种样本中的两个物种的混合感染)。最常分离的NTM物种是M.细胞内(n?= 236,54.1%),然后是M.脓肿(n?= 106,24.3%),M. kansasii(n?= 46,10.6%) ,M. Avium(n?=?36,8.3%)。二十二个病例有M.细胞内和M.脓肿混合感染和10例疾病和M. Abscessus Mixcrection感染。在MGIT 960-TBC ID和PCR-REBA MYCO-ID(k = 0.845,P≤0.845,P?= 0.000)之间发现了高水平的协议(n?= 396; 94.5%)。 PCR-REBA Myco-ID测定对于MGIT 960-TBC ID测试,MTBC和NTM的AUC具有更高的AUC。 PCR-REBA Myco-ID具有快速,相对易于在分枝杆菌物种鉴定中进行快速,相对较低,成本相对较低,精度优越,与MGIT 960-TBC ID相比。我们建议它进入分枝杆菌实验室的工作流程,特别是在源码有限的国家。

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