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PCR assay to enhance global surveillance for SARS-CoV-2 variants of concern

With the emergence of SARS-CoV-2 variants that may increase transmissibility and/or cause escape from immune responses(1–3), there is an urgent need for the targeted surveillance of circulating lineages. It was found that the B.1.1.7 (also 501Y.V1) variant first detected in the UK(4,5) could be sere...

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Autores principales: Vogels, Chantal B.F., Breban, Mallery I., Alpert, Tara, Petrone, Mary E., Watkins, Anne E., Ott, Isabel M., de Jesus, Jaqueline Goes, Claro, Ingra Morales, Ferreira, Giulia Magalhães, Crispim, Myuki A.E., Singh, Lavanya, Tegally, Houriiyah, Anyaneji, Ugochukwu J., Hodcroft, Emma B., Mason, Christopher E., Khullar, Gaurav, Metti, Jessica, Dudley, Joel T., MacKay, Matthew J., Nash, Megan, Wang, Jianhui, Liu, Chen, Hui, Pei, Murphy, Steven, Neal, Caleb, Laszlo, Eva, Landry, Marie L., Muyombwe, Anthony, Downing, Randy, Razeq, Jafar, de Oliveira, Tulio, Faria, Nuno R., Sabino, Ester C., Neher, Richard A., Fauver, Joseph R., Grubaugh, Nathan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987060/
https://www.ncbi.nlm.nih.gov/pubmed/33758901
http://dx.doi.org/10.1101/2021.01.28.21250486
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author Vogels, Chantal B.F.
Breban, Mallery I.
Alpert, Tara
Petrone, Mary E.
Watkins, Anne E.
Ott, Isabel M.
de Jesus, Jaqueline Goes
Claro, Ingra Morales
Ferreira, Giulia Magalhães
Crispim, Myuki A.E.
Singh, Lavanya
Tegally, Houriiyah
Anyaneji, Ugochukwu J.
Hodcroft, Emma B.
Mason, Christopher E.
Khullar, Gaurav
Metti, Jessica
Dudley, Joel T.
MacKay, Matthew J.
Nash, Megan
Wang, Jianhui
Liu, Chen
Hui, Pei
Murphy, Steven
Neal, Caleb
Laszlo, Eva
Landry, Marie L.
Muyombwe, Anthony
Downing, Randy
Razeq, Jafar
de Oliveira, Tulio
Faria, Nuno R.
Sabino, Ester C.
Neher, Richard A.
Fauver, Joseph R.
Grubaugh, Nathan D.
author_facet Vogels, Chantal B.F.
Breban, Mallery I.
Alpert, Tara
Petrone, Mary E.
Watkins, Anne E.
Ott, Isabel M.
de Jesus, Jaqueline Goes
Claro, Ingra Morales
Ferreira, Giulia Magalhães
Crispim, Myuki A.E.
Singh, Lavanya
Tegally, Houriiyah
Anyaneji, Ugochukwu J.
Hodcroft, Emma B.
Mason, Christopher E.
Khullar, Gaurav
Metti, Jessica
Dudley, Joel T.
MacKay, Matthew J.
Nash, Megan
Wang, Jianhui
Liu, Chen
Hui, Pei
Murphy, Steven
Neal, Caleb
Laszlo, Eva
Landry, Marie L.
Muyombwe, Anthony
Downing, Randy
Razeq, Jafar
de Oliveira, Tulio
Faria, Nuno R.
Sabino, Ester C.
Neher, Richard A.
Fauver, Joseph R.
Grubaugh, Nathan D.
author_sort Vogels, Chantal B.F.
collection PubMed
description With the emergence of SARS-CoV-2 variants that may increase transmissibility and/or cause escape from immune responses(1–3), there is an urgent need for the targeted surveillance of circulating lineages. It was found that the B.1.1.7 (also 501Y.V1) variant first detected in the UK(4,5) could be serendipitously detected by the ThermoFisher TaqPath COVID-19 PCR assay because a key deletion in these viruses, spike Δ69-70, would cause a “spike gene target failure” (SGTF) result. However, a SGTF result is not definitive for B.1.1.7, and this assay cannot detect other variants of concern that lack spike Δ69-70, such as B.1.351 (also 501Y.V2) detected in South Africa(6) and P.1 (also 501Y.V3) recently detected in Brazil(7). We identified a deletion in the ORF1a gene (ORF1a Δ3675-3677) in all three variants, which has not yet been widely detected in other SARS-CoV-2 lineages. Using ORF1a Δ3675-3677 as the primary target and spike Δ69-70 to differentiate, we designed and validated an open source PCR assay to detect SARS-CoV-2 variants of concern(8). Our assay can be rapidly deployed in laboratories around the world to enhance surveillance for the local emergence spread of B.1.1.7, B.1.351, and P.1.
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spelling pubmed-79870602021-03-24 PCR assay to enhance global surveillance for SARS-CoV-2 variants of concern Vogels, Chantal B.F. Breban, Mallery I. Alpert, Tara Petrone, Mary E. Watkins, Anne E. Ott, Isabel M. de Jesus, Jaqueline Goes Claro, Ingra Morales Ferreira, Giulia Magalhães Crispim, Myuki A.E. Singh, Lavanya Tegally, Houriiyah Anyaneji, Ugochukwu J. Hodcroft, Emma B. Mason, Christopher E. Khullar, Gaurav Metti, Jessica Dudley, Joel T. MacKay, Matthew J. Nash, Megan Wang, Jianhui Liu, Chen Hui, Pei Murphy, Steven Neal, Caleb Laszlo, Eva Landry, Marie L. Muyombwe, Anthony Downing, Randy Razeq, Jafar de Oliveira, Tulio Faria, Nuno R. Sabino, Ester C. Neher, Richard A. Fauver, Joseph R. Grubaugh, Nathan D. medRxiv Article With the emergence of SARS-CoV-2 variants that may increase transmissibility and/or cause escape from immune responses(1–3), there is an urgent need for the targeted surveillance of circulating lineages. It was found that the B.1.1.7 (also 501Y.V1) variant first detected in the UK(4,5) could be serendipitously detected by the ThermoFisher TaqPath COVID-19 PCR assay because a key deletion in these viruses, spike Δ69-70, would cause a “spike gene target failure” (SGTF) result. However, a SGTF result is not definitive for B.1.1.7, and this assay cannot detect other variants of concern that lack spike Δ69-70, such as B.1.351 (also 501Y.V2) detected in South Africa(6) and P.1 (also 501Y.V3) recently detected in Brazil(7). We identified a deletion in the ORF1a gene (ORF1a Δ3675-3677) in all three variants, which has not yet been widely detected in other SARS-CoV-2 lineages. Using ORF1a Δ3675-3677 as the primary target and spike Δ69-70 to differentiate, we designed and validated an open source PCR assay to detect SARS-CoV-2 variants of concern(8). Our assay can be rapidly deployed in laboratories around the world to enhance surveillance for the local emergence spread of B.1.1.7, B.1.351, and P.1. Cold Spring Harbor Laboratory 2021-03-12 /pmc/articles/PMC7987060/ /pubmed/33758901 http://dx.doi.org/10.1101/2021.01.28.21250486 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Vogels, Chantal B.F.
Breban, Mallery I.
Alpert, Tara
Petrone, Mary E.
Watkins, Anne E.
Ott, Isabel M.
de Jesus, Jaqueline Goes
Claro, Ingra Morales
Ferreira, Giulia Magalhães
Crispim, Myuki A.E.
Singh, Lavanya
Tegally, Houriiyah
Anyaneji, Ugochukwu J.
Hodcroft, Emma B.
Mason, Christopher E.
Khullar, Gaurav
Metti, Jessica
Dudley, Joel T.
MacKay, Matthew J.
Nash, Megan
Wang, Jianhui
Liu, Chen
Hui, Pei
Murphy, Steven
Neal, Caleb
Laszlo, Eva
Landry, Marie L.
Muyombwe, Anthony
Downing, Randy
Razeq, Jafar
de Oliveira, Tulio
Faria, Nuno R.
Sabino, Ester C.
Neher, Richard A.
Fauver, Joseph R.
Grubaugh, Nathan D.
PCR assay to enhance global surveillance for SARS-CoV-2 variants of concern
title PCR assay to enhance global surveillance for SARS-CoV-2 variants of concern
title_full PCR assay to enhance global surveillance for SARS-CoV-2 variants of concern
title_fullStr PCR assay to enhance global surveillance for SARS-CoV-2 variants of concern
title_full_unstemmed PCR assay to enhance global surveillance for SARS-CoV-2 variants of concern
title_short PCR assay to enhance global surveillance for SARS-CoV-2 variants of concern
title_sort pcr assay to enhance global surveillance for sars-cov-2 variants of concern
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987060/
https://www.ncbi.nlm.nih.gov/pubmed/33758901
http://dx.doi.org/10.1101/2021.01.28.21250486
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