Department of Microbiology, E.P.H. Costa del Sol, Marbella (Málaga), Spain.
Diagn Microbiol Infect Dis. 2010 Oct;68(2):123-31. doi: 10.1016/j.diagmicrobio.2010.06.006.
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.
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。