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Human Alphacoronavirus Universal Primers for Genome Amplification and Sequencing

Rapid and accurate sequencing covering the entire genome is essential to identify genetic variations of viral pathogens. However, due to the low viral titers in clinical samples, certain amplification steps are required for viral genome sequencing. At present, there are no universal primers availabl...

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Autores principales: Choi, Sungmi, Kim, Kwan Woo, Ku, Keun Bon, Kim, Seong-Jun, Park, Changwoo, Park, Dongju, Kim, Seil, Yi, Hana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8990890/
https://www.ncbi.nlm.nih.gov/pubmed/35401489
http://dx.doi.org/10.3389/fmicb.2022.789665
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author Choi, Sungmi
Kim, Kwan Woo
Ku, Keun Bon
Kim, Seong-Jun
Park, Changwoo
Park, Dongju
Kim, Seil
Yi, Hana
author_facet Choi, Sungmi
Kim, Kwan Woo
Ku, Keun Bon
Kim, Seong-Jun
Park, Changwoo
Park, Dongju
Kim, Seil
Yi, Hana
author_sort Choi, Sungmi
collection PubMed
description Rapid and accurate sequencing covering the entire genome is essential to identify genetic variations of viral pathogens. However, due to the low viral titers in clinical samples, certain amplification steps are required for viral genome sequencing. At present, there are no universal primers available for alphacoronaviruses and that, since these viruses have diverse strains, new primers specific to the target strain must be continuously developed for sequencing. Thus, in this study, we aimed to develop a universal primer set valid for all human alphacoronaviruses and applicable to samples containing trace amounts of the virus. To this aim, we designed overlapping primer pairs capable of amplifying the entire genome of all known human alphacoronaviruses. The selected primers, named the AC primer set, were composed of 10 primer pairs stretching over the entire genome of alphacoronaviruses, and produced PCR products of the expected size (3–5 kb) from both the HCoV-229E and HCoV-NL63 strains. After genome amplification, an evaluation using various sequencing platforms was carried out. The amplicon library sequencing data were assembled into complete genome sequences in all sequencing strategies examined in this study. The sequencing accuracy varied depending on the sequencing technology, but all sequencing methods showed a sequencing error of less than 0.01%. In the mock clinical specimen, the detection limit was 10(−3) PFU/ml (10(2) copies/ml). The AC primer set and experimental procedure optimized in this study may enable the fast diagnosis of mutant alphacoronaviruses in future epidemics.
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spelling pubmed-89908902022-04-09 Human Alphacoronavirus Universal Primers for Genome Amplification and Sequencing Choi, Sungmi Kim, Kwan Woo Ku, Keun Bon Kim, Seong-Jun Park, Changwoo Park, Dongju Kim, Seil Yi, Hana Front Microbiol Microbiology Rapid and accurate sequencing covering the entire genome is essential to identify genetic variations of viral pathogens. However, due to the low viral titers in clinical samples, certain amplification steps are required for viral genome sequencing. At present, there are no universal primers available for alphacoronaviruses and that, since these viruses have diverse strains, new primers specific to the target strain must be continuously developed for sequencing. Thus, in this study, we aimed to develop a universal primer set valid for all human alphacoronaviruses and applicable to samples containing trace amounts of the virus. To this aim, we designed overlapping primer pairs capable of amplifying the entire genome of all known human alphacoronaviruses. The selected primers, named the AC primer set, were composed of 10 primer pairs stretching over the entire genome of alphacoronaviruses, and produced PCR products of the expected size (3–5 kb) from both the HCoV-229E and HCoV-NL63 strains. After genome amplification, an evaluation using various sequencing platforms was carried out. The amplicon library sequencing data were assembled into complete genome sequences in all sequencing strategies examined in this study. The sequencing accuracy varied depending on the sequencing technology, but all sequencing methods showed a sequencing error of less than 0.01%. In the mock clinical specimen, the detection limit was 10(−3) PFU/ml (10(2) copies/ml). The AC primer set and experimental procedure optimized in this study may enable the fast diagnosis of mutant alphacoronaviruses in future epidemics. Frontiers Media S.A. 2022-03-25 /pmc/articles/PMC8990890/ /pubmed/35401489 http://dx.doi.org/10.3389/fmicb.2022.789665 Text en Copyright © 2022 Choi, Kim, Ku, Kim, Park, Park, Kim and Yi. 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
Choi, Sungmi
Kim, Kwan Woo
Ku, Keun Bon
Kim, Seong-Jun
Park, Changwoo
Park, Dongju
Kim, Seil
Yi, Hana
Human Alphacoronavirus Universal Primers for Genome Amplification and Sequencing
title Human Alphacoronavirus Universal Primers for Genome Amplification and Sequencing
title_full Human Alphacoronavirus Universal Primers for Genome Amplification and Sequencing
title_fullStr Human Alphacoronavirus Universal Primers for Genome Amplification and Sequencing
title_full_unstemmed Human Alphacoronavirus Universal Primers for Genome Amplification and Sequencing
title_short Human Alphacoronavirus Universal Primers for Genome Amplification and Sequencing
title_sort human alphacoronavirus universal primers for genome amplification and sequencing
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8990890/
https://www.ncbi.nlm.nih.gov/pubmed/35401489
http://dx.doi.org/10.3389/fmicb.2022.789665
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