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评价 Speed-oligo® 分枝杆菌检测试剂盒在鉴定人临床新鲜液体和固体培养物中的分枝杆菌属的应用。

Evaluation of the Speed-oligo® Mycobacteria assay for identification of Mycobacterium spp. from fresh liquid and solid cultures of human clinical samples.

机构信息

Department of Microbiology, E.P.H. Costa del Sol, Marbella (Málaga), Spain.

出版信息

Diagn Microbiol Infect Dis. 2010 Oct;68(2):123-31. doi: 10.1016/j.diagmicrobio.2010.06.006.

Abstract

We evaluated the ability of a novel DNA strip assay (Speed-oligo® Mycobacteria) to differentiate mycobacterial species. It is based on polymerase chain reaction targeting 16S rRNA and 16S-23S rRNA regions and double-reverse hybridization on a dipstick using probes bound to colloidal gold and to the membrane. We blindly tested its capacity to identify 182 acid-fast bacilli grown on fresh liquid (BacT/Alert, MGIT) and solid (Lowenstein-Jensen) cultures (from Spanish mycobacteriology laboratories), previously identified by means of Genotype(®) Mycob.CM/AS or Gen-Probe(®) AccuprobeMTC, and 11 collection strains of mycobacteria-related organisms. Discrepancies were resolved by 16S rRNA sequencing. Results were interpreted by identification of 7 specific bands for the following: Mycobacterium sp., M. fortuitum, Mycobacterium avium-intracellulare complex, Mycobacterium tuberculosis complex, Mycobacterium kansasii, M. gordonae, and M. abscessus-chelonae complex. No cross-reactivity was observed with any mycobacteria-related organism. Concordant results were obtained for 177/182 bacilli (97.2%). There was only 1 major discrepancy, misidentification of Mycobacterium marinum as M. kansasii, verified by sequencing.

摘要

我们评估了一种新型 DNA 条带检测法(Speed-oligo® 分枝杆菌)区分分枝杆菌种的能力。它基于聚合酶链反应,针对 16S rRNA 和 16S-23S rRNA 区域,并在试纸上使用结合胶体金和膜的探针进行双反向杂交。我们对其在盲测条件下识别 182 株在新鲜液体(BacT/Alert、MGIT)和固体(Lowenstein-Jensen)培养物中生长的抗酸杆菌的能力进行了测试(来自西班牙分枝杆菌学实验室),这些细菌之前已通过 Genotype(®) Mycob.CM/AS 或 Gen-Probe(®) AccuprobeMTC 进行了鉴定,并且测试了 11 株分枝杆菌相关生物的收集株。通过 16S rRNA 测序解决了差异。通过识别以下 7 种特定条带来解释结果:分枝杆菌属、偶然分枝杆菌、鸟分枝杆菌复合群、结核分枝杆菌复合群、堪萨斯分枝杆菌、戈登分枝杆菌和脓肿分枝杆菌-龟分枝杆菌复合群。未观察到与任何分枝杆菌相关生物的交叉反应。182 株菌中有 177 株(97.2%)得到了一致的结果。只有 1 个主要差异,即通过测序验证的海洋分枝杆菌被误鉴定为堪萨斯分枝杆菌。

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