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Rapid and Flexible RT-qPCR Surveillance Platforms To Detect SARS-CoV-2 Mutations
Multiple mutations in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) increase transmission, disease severity, and immune evasion and facilitate zoonotic or anthropozoonotic infections. Four such mutations, ΔH69/V70, L452R, E484K, and N501Y, occurred in the SA...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927487/ https://www.ncbi.nlm.nih.gov/pubmed/36625603 http://dx.doi.org/10.1128/spectrum.03591-22 |
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author | Spiess, Katja Gunalan, Vithiagaran Marving, Ellinor Nielsen, Sofie Holdflod Jørgensen, Michelle G. P. Fomsgaard, Anna S. Nielsen, Line Alfaro-Núñez, Alonzo Karst, Søren M. Mortensen, Shila Rasmussen, Morten Lassaunière, Ria Rosenstierne, Maiken Worsøe Polacek, Charlotta Fonager, Jannik Cohen, Arieh S. Nielsen, Claus Fomsgaard, Anders |
author_facet | Spiess, Katja Gunalan, Vithiagaran Marving, Ellinor Nielsen, Sofie Holdflod Jørgensen, Michelle G. P. Fomsgaard, Anna S. Nielsen, Line Alfaro-Núñez, Alonzo Karst, Søren M. Mortensen, Shila Rasmussen, Morten Lassaunière, Ria Rosenstierne, Maiken Worsøe Polacek, Charlotta Fonager, Jannik Cohen, Arieh S. Nielsen, Claus Fomsgaard, Anders |
author_sort | Spiess, Katja |
collection | PubMed |
description | Multiple mutations in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) increase transmission, disease severity, and immune evasion and facilitate zoonotic or anthropozoonotic infections. Four such mutations, ΔH69/V70, L452R, E484K, and N501Y, occurred in the SARS-CoV-2 spike glycoprotein in combinations that allow the simultaneous detection of VOCs. Here, we present two flexible reverse transcription-quantitative PCR (RT-qPCR) platforms for small- and large-scale screening (also known as variant PCR) to detect these mutations and schemes for adapting the platforms to future mutations. The large-scale RT-qPCR platform was validated by pairwise matching of RT-qPCR results with whole-genome sequencing (WGS) consensus genomes, showing high specificity and sensitivity. Both platforms are valuable examples of complementing WGS to support the rapid detection of VOCs. Our mutational signature approach served as an important intervention measure for the Danish public health system to detect and delay the emergence of new VOCs. IMPORTANCE Denmark weathered the SARS-CoV-2 crisis with relatively low rates of infection and death. Intensive testing strategies with the aim of detecting SARS-CoV-2 in symptomatic and nonsymptomatic individuals were available by establishing a national test system called TestCenter Denmark. This testing regime included the detection of SARS-CoV-2 signature mutations, with referral to the national health system, thereby delaying outbreaks of variants of concern. Our study describes the design of the large-scale RT-qPCR platform established at TestCenter Denmark in conjunction with whole-genome sequencing to report mutations of concern to the national health system. Validation of the large-scale RT-qPCR platform using paired WGS consensus genomes showed high sensitivity and specificity. For smaller laboratories with limited infrastructure, we developed a flexible small-scale RT-qPCR platform to detect three signature mutations in a single run. The RT-qPCR platforms are important tools to support the control of the SARS-CoV-2 endemic in Denmark. |
format | Online Article Text |
id | pubmed-9927487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-99274872023-02-15 Rapid and Flexible RT-qPCR Surveillance Platforms To Detect SARS-CoV-2 Mutations Spiess, Katja Gunalan, Vithiagaran Marving, Ellinor Nielsen, Sofie Holdflod Jørgensen, Michelle G. P. Fomsgaard, Anna S. Nielsen, Line Alfaro-Núñez, Alonzo Karst, Søren M. Mortensen, Shila Rasmussen, Morten Lassaunière, Ria Rosenstierne, Maiken Worsøe Polacek, Charlotta Fonager, Jannik Cohen, Arieh S. Nielsen, Claus Fomsgaard, Anders Microbiol Spectr Research Article Multiple mutations in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) increase transmission, disease severity, and immune evasion and facilitate zoonotic or anthropozoonotic infections. Four such mutations, ΔH69/V70, L452R, E484K, and N501Y, occurred in the SARS-CoV-2 spike glycoprotein in combinations that allow the simultaneous detection of VOCs. Here, we present two flexible reverse transcription-quantitative PCR (RT-qPCR) platforms for small- and large-scale screening (also known as variant PCR) to detect these mutations and schemes for adapting the platforms to future mutations. The large-scale RT-qPCR platform was validated by pairwise matching of RT-qPCR results with whole-genome sequencing (WGS) consensus genomes, showing high specificity and sensitivity. Both platforms are valuable examples of complementing WGS to support the rapid detection of VOCs. Our mutational signature approach served as an important intervention measure for the Danish public health system to detect and delay the emergence of new VOCs. IMPORTANCE Denmark weathered the SARS-CoV-2 crisis with relatively low rates of infection and death. Intensive testing strategies with the aim of detecting SARS-CoV-2 in symptomatic and nonsymptomatic individuals were available by establishing a national test system called TestCenter Denmark. This testing regime included the detection of SARS-CoV-2 signature mutations, with referral to the national health system, thereby delaying outbreaks of variants of concern. Our study describes the design of the large-scale RT-qPCR platform established at TestCenter Denmark in conjunction with whole-genome sequencing to report mutations of concern to the national health system. Validation of the large-scale RT-qPCR platform using paired WGS consensus genomes showed high sensitivity and specificity. For smaller laboratories with limited infrastructure, we developed a flexible small-scale RT-qPCR platform to detect three signature mutations in a single run. The RT-qPCR platforms are important tools to support the control of the SARS-CoV-2 endemic in Denmark. American Society for Microbiology 2023-01-09 /pmc/articles/PMC9927487/ /pubmed/36625603 http://dx.doi.org/10.1128/spectrum.03591-22 Text en Copyright © 2023 Spiess et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Spiess, Katja Gunalan, Vithiagaran Marving, Ellinor Nielsen, Sofie Holdflod Jørgensen, Michelle G. P. Fomsgaard, Anna S. Nielsen, Line Alfaro-Núñez, Alonzo Karst, Søren M. Mortensen, Shila Rasmussen, Morten Lassaunière, Ria Rosenstierne, Maiken Worsøe Polacek, Charlotta Fonager, Jannik Cohen, Arieh S. Nielsen, Claus Fomsgaard, Anders Rapid and Flexible RT-qPCR Surveillance Platforms To Detect SARS-CoV-2 Mutations |
title | Rapid and Flexible RT-qPCR Surveillance Platforms To Detect SARS-CoV-2 Mutations |
title_full | Rapid and Flexible RT-qPCR Surveillance Platforms To Detect SARS-CoV-2 Mutations |
title_fullStr | Rapid and Flexible RT-qPCR Surveillance Platforms To Detect SARS-CoV-2 Mutations |
title_full_unstemmed | Rapid and Flexible RT-qPCR Surveillance Platforms To Detect SARS-CoV-2 Mutations |
title_short | Rapid and Flexible RT-qPCR Surveillance Platforms To Detect SARS-CoV-2 Mutations |
title_sort | rapid and flexible rt-qpcr surveillance platforms to detect sars-cov-2 mutations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927487/ https://www.ncbi.nlm.nih.gov/pubmed/36625603 http://dx.doi.org/10.1128/spectrum.03591-22 |
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