Tuberculosis Omics Research Consortium, Family Medicine and Population Health, Institute of Global Health, Faculty of Medicine and Health Sciences, University of Antwerpgrid.5284.b, Antwerp, Belgium.
Unit of Mycobacteriology, Institute of Tropical Medicine, Antwerp, Belgium.
J Clin Microbiol. 2022 Jan 19;60(1):e0064621. doi: 10.1128/JCM.00646-21. Epub 2021 Jun 16.
The next-generation, short-read sequencing technologies that generate comprehensive, whole-genome data with single nucleotide resolution have already advanced tuberculosis diagnosis, treatment, surveillance, and source investigation. Their high costs, tedious and lengthy processes, and large equipment remain major hurdles for research use in high tuberculosis burden countries and implementation into routine care. The portable next-generation sequencing devices developed by Oxford Nanopore Technologies (ONT) are attractive alternatives due to their long-read sequence capability, compact low-cost hardware, and continued improvements in accuracy and throughput. A systematic review of the published literature demonstrated limited uptake of ONT sequencing in tuberculosis research and clinical care. Of the 12 eligible articles presenting ONT sequencing data on at least one Mycobacterium tuberculosis sample, four addressed software development for long-read ONT sequencing data with potential applications for M. tuberculosis. Only eight studies presented results of ONT sequencing of M. tuberculosis, of which five performed whole-genome and three did targeted sequencing. Based on these findings, we summarize the standard processes, reflect on the current limitations of ONT sequencing technology, and the research needed to overcome the main hurdles. The low capital cost, portable nature and continued improvement in the performance of ONT sequencing make it an attractive option for sequencing for research and clinical care, but limited data are available on its application in the tuberculosis field. Important research investment is needed to unleash the full potential of ONT sequencing for tuberculosis research and care.
下一代短读测序技术以单核苷酸分辨率生成全面的全基因组数据,已经推动了结核病的诊断、治疗、监测和传染源调查。然而,其高昂的成本、繁琐冗长的流程以及大型设备仍然是高结核病负担国家开展研究和将其纳入常规护理的主要障碍。牛津纳米孔技术(ONT)开发的便携式下一代测序设备由于其长读长测序能力、紧凑且低成本的硬件以及在准确性和通量方面的持续改进,具有很大吸引力。对已发表文献的系统评价表明,ONT 测序在结核病研究和临床护理中的应用有限。在 12 篇符合条件的文章中,有 4 篇文章介绍了针对长读 ONT 测序数据的软件开发,这些开发具有应用于结核分枝杆菌的潜力。只有 8 项研究报告了结核分枝杆菌的 ONT 测序结果,其中 5 项进行了全基因组测序,3 项进行了靶向测序。基于这些发现,我们总结了标准流程,反思了 ONT 测序技术目前的局限性以及克服主要障碍所需的研究。ONT 测序的低资本成本、便携性以及性能的持续改进使其成为研究和临床护理测序的一个有吸引力的选择,但在结核病领域,其应用的数据有限。需要重要的研究投资来充分发挥 ONT 测序在结核病研究和护理中的潜力。