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Rapid High-Throughput Whole-Genome Sequencing of SARS-CoV-2 by Using One-Step Reverse Transcription-PCR Amplification with an Integrated Microfluidic System and Next-Generation Sequencing
The long-lasting global COVID-19 pandemic demands timely genomic investigation of SARS-CoV-2 viruses. Here, we report a simple and efficient workflow for whole-genome sequencing utilizing one-step reverse transcription-PCR (RT-PCR) amplification on a microfluidic platform, followed by MiSeq amplicon...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8091833/ https://www.ncbi.nlm.nih.gov/pubmed/33653700 http://dx.doi.org/10.1128/JCM.02784-20 |
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author | Li, Tao Chung, Hye Kyung Pireku, Papa K. Beitzel, Brett F. Sanborn, Mark A. Tang, Cynthia Y. Hammer, Richard D. Ritter, Detlef Wan, Xiu-Feng Maljkovic Berry, Irina Hang, Jun |
author_facet | Li, Tao Chung, Hye Kyung Pireku, Papa K. Beitzel, Brett F. Sanborn, Mark A. Tang, Cynthia Y. Hammer, Richard D. Ritter, Detlef Wan, Xiu-Feng Maljkovic Berry, Irina Hang, Jun |
author_sort | Li, Tao |
collection | PubMed |
description | The long-lasting global COVID-19 pandemic demands timely genomic investigation of SARS-CoV-2 viruses. Here, we report a simple and efficient workflow for whole-genome sequencing utilizing one-step reverse transcription-PCR (RT-PCR) amplification on a microfluidic platform, followed by MiSeq amplicon sequencing. The method uses Fluidigm integrated fluidic circuit (IFC) and instruments to amplify 48 samples with 39 pairs of primers, including 35 custom-designed primer pairs and four additional primer pairs from the ARTIC network protocol v3. Application of this method on RNA samples from both viral isolates and clinical specimens demonstrates robustness and efficiency in obtaining the full genome sequence of SARS-CoV-2. |
format | Online Article Text |
id | pubmed-8091833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-80918332021-05-18 Rapid High-Throughput Whole-Genome Sequencing of SARS-CoV-2 by Using One-Step Reverse Transcription-PCR Amplification with an Integrated Microfluidic System and Next-Generation Sequencing Li, Tao Chung, Hye Kyung Pireku, Papa K. Beitzel, Brett F. Sanborn, Mark A. Tang, Cynthia Y. Hammer, Richard D. Ritter, Detlef Wan, Xiu-Feng Maljkovic Berry, Irina Hang, Jun J Clin Microbiol Virology The long-lasting global COVID-19 pandemic demands timely genomic investigation of SARS-CoV-2 viruses. Here, we report a simple and efficient workflow for whole-genome sequencing utilizing one-step reverse transcription-PCR (RT-PCR) amplification on a microfluidic platform, followed by MiSeq amplicon sequencing. The method uses Fluidigm integrated fluidic circuit (IFC) and instruments to amplify 48 samples with 39 pairs of primers, including 35 custom-designed primer pairs and four additional primer pairs from the ARTIC network protocol v3. Application of this method on RNA samples from both viral isolates and clinical specimens demonstrates robustness and efficiency in obtaining the full genome sequence of SARS-CoV-2. American Society for Microbiology 2021-04-20 /pmc/articles/PMC8091833/ /pubmed/33653700 http://dx.doi.org/10.1128/JCM.02784-20 Text en This is a work of the U.S. Government and is not subject to copyright protection in the United States. Foreign copyrights may apply. https://doi.org/10.1128/ASMCopyrightv2This article is made available via the PMC Open Access Subset for unrestricted noncommercial re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Virology Li, Tao Chung, Hye Kyung Pireku, Papa K. Beitzel, Brett F. Sanborn, Mark A. Tang, Cynthia Y. Hammer, Richard D. Ritter, Detlef Wan, Xiu-Feng Maljkovic Berry, Irina Hang, Jun Rapid High-Throughput Whole-Genome Sequencing of SARS-CoV-2 by Using One-Step Reverse Transcription-PCR Amplification with an Integrated Microfluidic System and Next-Generation Sequencing |
title | Rapid High-Throughput Whole-Genome Sequencing of SARS-CoV-2 by Using One-Step Reverse Transcription-PCR Amplification with an Integrated Microfluidic System and Next-Generation Sequencing |
title_full | Rapid High-Throughput Whole-Genome Sequencing of SARS-CoV-2 by Using One-Step Reverse Transcription-PCR Amplification with an Integrated Microfluidic System and Next-Generation Sequencing |
title_fullStr | Rapid High-Throughput Whole-Genome Sequencing of SARS-CoV-2 by Using One-Step Reverse Transcription-PCR Amplification with an Integrated Microfluidic System and Next-Generation Sequencing |
title_full_unstemmed | Rapid High-Throughput Whole-Genome Sequencing of SARS-CoV-2 by Using One-Step Reverse Transcription-PCR Amplification with an Integrated Microfluidic System and Next-Generation Sequencing |
title_short | Rapid High-Throughput Whole-Genome Sequencing of SARS-CoV-2 by Using One-Step Reverse Transcription-PCR Amplification with an Integrated Microfluidic System and Next-Generation Sequencing |
title_sort | rapid high-throughput whole-genome sequencing of sars-cov-2 by using one-step reverse transcription-pcr amplification with an integrated microfluidic system and next-generation sequencing |
topic | Virology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8091833/ https://www.ncbi.nlm.nih.gov/pubmed/33653700 http://dx.doi.org/10.1128/JCM.02784-20 |
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