Emerging Bacterial Pathogens Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
J Clin Microbiol. 2024 Oct 16;62(10):e0081524. doi: 10.1128/jcm.00815-24. Epub 2024 Sep 6.
We investigated the performance of the targeted next-generation sequencing (tNGS)-based Oxford Nanopore Diagnostics AmPORE TB assay, recently approved by the World Health Organization (WHO) as tuberculosis (TB) diagnostic test for the detection of drug resistance on respiratory specimens. A total of 104 DNA samples from Xpert MTB/RIF-positive TB sputum specimens were tested using the AmPORE TB kit, with the GenoScreen Deeplex Myc-TB as a comparative tNGS assay. For AmPORE TB, DNA samples were divided into five sequencing runs on the MinION device. Data analysis was performed using proprietary software. The WHO catalog of mutations was used for drug resistance interpretation. The assay achieved a high validity rate of 98% (102/104 DNA samples), homogeneous mean reads coverage across TB-positive specimens, and 100% positive and negative agreements for detecting mutations associated with resistance to rifampicin, pyrazinamide, fluoroquinolones, ethambutol, and capreomycin compared with Deeplex Myc-TB. The main discrepancies for the remaining drugs were attributable to the different assay panel designs. The AmPORE TB turnaround time was approximately 5-6 hours from extracted DNA to tNGS reporting for batches of 22 DNA samples. The AmPORE TB assay drastically reduced the time to tNGS reporting from days to hours and showed good performance for drug-resistant TB profiling compared with Deeplex Myc-TB.
Targeted next-generation sequencing (tNGS) of provides comprehensive resistance predictions matched to new multidrug-resistant/rifampicin-resistant tuberculosis regimens and received World Health Organization approval for clinical use in respiratory samples in 2024. The advanced version of the Oxford Nanopore Diagnostics AmPORE TB tNGS kit was evaluated in this study for the first time and demonstrated good performance, flexibility, and faster turnaround time compared with the existing solutions.
我们研究了靶向下一代测序(tNGS)的牛津纳米孔诊断 AmPORE TB 检测的性能,该检测最近被世界卫生组织(WHO)批准为用于检测呼吸道标本中耐药性的结核病(TB)诊断检测。总共对 104 份来自 Xpert MTB/RIF 阳性的 TB 痰标本的 DNA 样本使用 AmPORE TB 试剂盒进行了检测,将 GenoScreen Deeplex Myc-TB 作为比较性 tNGS 检测。对于 AmPORE TB,将 DNA 样本在 MinION 设备上分为五个测序运行。使用专有软件进行数据分析。使用 WHO 突变目录进行耐药性解释。该检测的有效性率达到 98%(104 份 DNA 样本中的 102 份),TB 阳性标本的平均平均读覆盖度均匀,与 Deeplex Myc-TB 相比,对利福平、吡嗪酰胺、氟喹诺酮类、乙胺丁醇和卷曲霉素耐药相关的突变的阳性和阴性一致性均为 100%。对于其余药物,主要差异归因于不同的检测面板设计。从提取的 DNA 到 AmPORE TB 的 tNGS 报告,每个批次 22 个 DNA 样本的 AmPORE TB 周转时间约为 5-6 小时。与 Deeplex Myc-TB 相比,AmPORE TB 检测大大缩短了 tNGS 报告的时间,从几天缩短到几个小时,并显示出良好的性能,用于耐药性结核病分析。
靶向下一代测序(tNGS)为新的多药耐药/利福平耐药结核病方案提供了全面的耐药预测,并于 2024 年获得世界卫生组织批准用于呼吸道样本的临床使用。在这项研究中,首次评估了牛津纳米孔诊断 AmPORE TB tNGS 试剂盒的高级版本,与现有解决方案相比,该试剂盒表现出良好的性能、灵活性和更快的周转时间。