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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
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.
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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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