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Rapid and sensitive amplicon-based genome sequencing of SARS-CoV-2

As SARS-CoV-2 variants of concern emerged, the genome sequencing of SARS-CoV-2 strains became more important. In this study, SARS-CoV-2 was sequenced using amplicon-based genome sequencing with MinION. The primer panel used in this study consisted of only 11 primer panels and the size of the amplico...

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Autores principales: Park, Changwoo, Kim, Kwan Woo, Park, Dongju, Hassan, Zohaib ul, Park, Edmond Changkyun, Lee, Chang-Seop, Rahman, MD Tazikur, Yi, Hana, Kim, Seil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428490/
https://www.ncbi.nlm.nih.gov/pubmed/36060750
http://dx.doi.org/10.3389/fmicb.2022.876085
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author Park, Changwoo
Kim, Kwan Woo
Park, Dongju
Hassan, Zohaib ul
Park, Edmond Changkyun
Lee, Chang-Seop
Rahman, MD Tazikur
Yi, Hana
Kim, Seil
author_facet Park, Changwoo
Kim, Kwan Woo
Park, Dongju
Hassan, Zohaib ul
Park, Edmond Changkyun
Lee, Chang-Seop
Rahman, MD Tazikur
Yi, Hana
Kim, Seil
author_sort Park, Changwoo
collection PubMed
description As SARS-CoV-2 variants of concern emerged, the genome sequencing of SARS-CoV-2 strains became more important. In this study, SARS-CoV-2 was sequenced using amplicon-based genome sequencing with MinION. The primer panel used in this study consisted of only 11 primer panels and the size of the amplicons was approximately 3 kb. Full genome sequences were obtained with a hundred copies of the SARS-CoV-2 genome, and 92.33% and 75.39% of the genome sequences were obtained with 10 copies of the SARS-CoV-2 genome. The few differences in nucleotide sequences originated from mutations in laboratory cultures and/or mixed nucleotide sequences. The quantification of the SARS-CoV-2 genomic RNA was done using RT-ddPCR methods, and the level of LoD indicated that this sequencing method can be used for any RT-qPCR positive clinical sample. The sequencing results of the SARS-CoV-2 variants and clinical samples showed that our methods were very reliable. The genome sequences of five individual clinical samples were almost identical, and the analysis of the sequence variance showed that most of these nucleotide substitutions were observed in the genome sequences of the other clinical samples, indicating this amplicon-based whole-genome sequencing method can be used in various clinical fields.
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spelling pubmed-94284902022-09-01 Rapid and sensitive amplicon-based genome sequencing of SARS-CoV-2 Park, Changwoo Kim, Kwan Woo Park, Dongju Hassan, Zohaib ul Park, Edmond Changkyun Lee, Chang-Seop Rahman, MD Tazikur Yi, Hana Kim, Seil Front Microbiol Microbiology As SARS-CoV-2 variants of concern emerged, the genome sequencing of SARS-CoV-2 strains became more important. In this study, SARS-CoV-2 was sequenced using amplicon-based genome sequencing with MinION. The primer panel used in this study consisted of only 11 primer panels and the size of the amplicons was approximately 3 kb. Full genome sequences were obtained with a hundred copies of the SARS-CoV-2 genome, and 92.33% and 75.39% of the genome sequences were obtained with 10 copies of the SARS-CoV-2 genome. The few differences in nucleotide sequences originated from mutations in laboratory cultures and/or mixed nucleotide sequences. The quantification of the SARS-CoV-2 genomic RNA was done using RT-ddPCR methods, and the level of LoD indicated that this sequencing method can be used for any RT-qPCR positive clinical sample. The sequencing results of the SARS-CoV-2 variants and clinical samples showed that our methods were very reliable. The genome sequences of five individual clinical samples were almost identical, and the analysis of the sequence variance showed that most of these nucleotide substitutions were observed in the genome sequences of the other clinical samples, indicating this amplicon-based whole-genome sequencing method can be used in various clinical fields. Frontiers Media S.A. 2022-08-17 /pmc/articles/PMC9428490/ /pubmed/36060750 http://dx.doi.org/10.3389/fmicb.2022.876085 Text en Copyright © 2022 Park, Kim, Park, Hassan, Park, Lee, Rahman, Yi and Kim. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Park, Changwoo
Kim, Kwan Woo
Park, Dongju
Hassan, Zohaib ul
Park, Edmond Changkyun
Lee, Chang-Seop
Rahman, MD Tazikur
Yi, Hana
Kim, Seil
Rapid and sensitive amplicon-based genome sequencing of SARS-CoV-2
title Rapid and sensitive amplicon-based genome sequencing of SARS-CoV-2
title_full Rapid and sensitive amplicon-based genome sequencing of SARS-CoV-2
title_fullStr Rapid and sensitive amplicon-based genome sequencing of SARS-CoV-2
title_full_unstemmed Rapid and sensitive amplicon-based genome sequencing of SARS-CoV-2
title_short Rapid and sensitive amplicon-based genome sequencing of SARS-CoV-2
title_sort rapid and sensitive amplicon-based genome sequencing of sars-cov-2
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428490/
https://www.ncbi.nlm.nih.gov/pubmed/36060750
http://dx.doi.org/10.3389/fmicb.2022.876085
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