Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SA, UK.
Department of Paediatrics, Cambridge University Hospitals, Hills Road, Cambridge CB2 0QQ, UK.
Sci Adv. 2021 Feb 12;7(7). doi: 10.1126/sciadv.abe5054. Print 2021 Feb.
We present INSIGHT [isothermal NASBA (nucleic acid sequence-based amplification) sequencing-based high-throughput test], a two-stage coronavirus disease 2019 testing strategy, using a barcoded isothermal NASBA reaction. It combines point-of-care diagnosis with next-generation sequencing, aiming to achieve population-scale testing. Stage 1 allows a quick decentralized readout for early isolation of presymptomatic or asymptomatic patients. It gives results within 1 to 2 hours, using either fluorescence detection or a lateral flow readout, while simultaneously incorporating sample-specific barcodes. The same reaction products from potentially hundreds of thousands of samples can then be pooled and used in a highly multiplexed sequencing-based assay in stage 2. This second stage confirms the near-patient testing results and facilitates centralized data collection. The 95% limit of detection is <50 copies of viral RNA per reaction. INSIGHT is suitable for further development into a rapid home-based, point-of-care assay and is potentially scalable to the population level.
我们提出了 INSIGHT(等温 NASBA(基于核酸序列的扩增)测序高通量检测),这是一种两阶段的 2019 年冠状病毒病检测策略,使用带条形码的等温 NASBA 反应。它将即时护理诊断与下一代测序相结合,旨在实现大规模人群检测。第一阶段允许快速分散式读出,以便早期隔离有症状或无症状的患者。它使用荧光检测或侧流读数在 1 至 2 小时内提供结果,同时结合样本特异性条形码。然后,可以将来自可能数十万份样本的相同反应产物汇集在一起,并在第二阶段的基于测序的高度多重检测中使用。第二阶段确认了床边检测结果,并促进了集中数据收集。95%的检测下限为每个反应 <50 拷贝的病毒 RNA。INSIGHT 适合进一步开发为快速、基于家庭的即时护理检测,并且具有潜在的可扩展性,适用于人群水平。