Nanopore Targeted Sequencing for the Accurate and Comprehensive Detection of SARS-CoV-2 and Other Respiratory Viruses.
Ming WangAisi FuBen HuYongqing TongRan LiuZhen LiuJiashuang GuBin XiangJianghao LiuWen JiangGaigai ShenWanxu ZhaoDong MenZixin DengLilei YuWu WeiYan LiTian-Gang LiuPublished in: Small (Weinheim an der Bergstrasse, Germany) (2020)
The ongoing global novel coronavirus pneumonia COVID-19 outbreak has engendered numerous cases of infection and death. COVID-19 diagnosis relies upon nucleic acid detection; however, currently recommended methods exhibit high false-negative rates and are unable to identify other respiratory virus infections, thereby resulting in patient misdiagnosis and impeding epidemic containment. Combining the advantages of targeted amplification and long-read, real-time nanopore sequencing, herein, nanopore targeted sequencing (NTS) is developed to detect SARS-CoV-2 and other respiratory viruses simultaneously within 6-10 h, with a limit of detection of ten standard plasmid copies per reaction. Compared with its specificity for five common respiratory viruses, the specificity of NTS for SARS-CoV-2 reaches 100%. Parallel testing with approved real-time reverse transcription-polymerase chain reaction kits for SARS-CoV-2 and NTS using 61 nucleic acid samples from suspected COVID-19 cases show that NTS identifies more infected patients (22/61) as positive, while also effectively monitoring for mutated nucleic acid sequences, categorizing types of SARS-CoV-2, and detecting other respiratory viruses in the test sample. NTS is thus suitable for COVID-19 diagnosis; moreover, this platform can be further extended for diagnosing other viruses and pathogens.
Keyphrases
- sars cov
- nucleic acid
- respiratory syndrome coronavirus
- single molecule
- cancer therapy
- single cell
- respiratory tract
- loop mediated isothermal amplification
- genetic diversity
- coronavirus disease
- real time pcr
- escherichia coli
- label free
- high throughput
- crispr cas
- high resolution
- drug delivery
- intensive care unit
- gene expression
- pulmonary embolism
- mass spectrometry
- structural basis
- respiratory failure