基于纳米孔的靶向测序测试,用于结核病的直接鉴定、基因分型和耐药性突变检测:靶向新一代测序技术的并行比较。

IF 6.1 2区 医学 Q1 MICROBIOLOGY Journal of Clinical Microbiology Pub Date : 2024-10-16 Epub Date: 2024-09-06 DOI:10.1128/jcm.00815-24
Andrea Maurizio Cabibbe, Kiarash Moghaddasi, Virginia Batignani, Godstime Stephen Kojo Morgan, Federico Di Marco, Daniela Maria Cirillo
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引用次数: 0

摘要

我们研究了基于靶向新一代测序(tNGS)的牛津纳米孔诊断公司(Oxford Nanopore Diagnostics)AmPORE TB 检测试剂盒的性能,该试剂盒最近被世界卫生组织(WHO)批准为肺结核(TB)诊断试剂盒,用于检测呼吸道标本的耐药性。共有 104 份 Xpert MTB/RIF 阳性肺结核痰标本的 DNA 样本使用 AmPORE TB 试剂盒进行了检测,GenoScreen Deeplex Myc-TB 作为对比 tNGS 检测。对于 AmPORE TB,DNA 样本在 MinION 设备上分为五次测序。数据分析使用专有软件进行。世界卫生组织的突变目录用于耐药性解释。与 Deeplex Myc-TB 相比,该检测方法的有效率高达 98%(102/104 个 DNA 样本),结核菌阳性标本的平均读数覆盖率相同,在检测与利福平、吡嗪酰胺、氟喹诺酮类、乙胺丁醇和辣椒霉素耐药性相关的突变时,阳性和阴性一致率均为 100%。其余药物的主要差异可归因于不同的检测板设计。对于每批 22 份 DNA 样品,从提取 DNA 到 tNGS 报告,AmPORE TB 的周转时间约为 5-6 小时。与 Deeplex Myc-TB.Importance 相比,AmPORE TB 检测方法将 tNGS 报告时间从数天大幅缩短至数小时,并在耐药 TB 图谱分析方面表现出良好的性能:结核分枝杆菌的靶向新一代测序(tNGS)提供了与新型耐多药/耐利福平结核病治疗方案相匹配的全面耐药性预测,并获得了世界卫生组织的批准,可在 2024 年用于呼吸道样本的临床检测。本研究首次评估了牛津纳米孔诊断公司 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。
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Nanopore-based targeted sequencing test for direct tuberculosis identification, genotyping, and detection of drug resistance mutations: a side-by-side comparison of targeted next-generation sequencing technologies.

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.

Importance: Targeted next-generation sequencing (tNGS) of Mycobacterium tuberculosis 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.

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来源期刊
Journal of Clinical Microbiology
Journal of Clinical Microbiology 医学-微生物学
CiteScore
17.10
自引率
4.30%
发文量
347
审稿时长
3 months
期刊介绍: The Journal of Clinical Microbiology® disseminates the latest research concerning the laboratory diagnosis of human and animal infections, along with the laboratory's role in epidemiology and the management of infectious diseases.
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