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Generation and transmission of interlineage recombinants in the SARS-CoV-2 pandemic
We present evidence for multiple independent origins of recombinant SARS-CoV-2 viruses sampled from late 2020 and early 2021 in the United Kingdom. Their genomes carry single-nucleotide polymorphisms and deletions that are characteristic of the B.1.1.7 variant of concern but lack the full complement...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367733/ https://www.ncbi.nlm.nih.gov/pubmed/34499854 http://dx.doi.org/10.1016/j.cell.2021.08.014 |
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author | Jackson, Ben Boni, Maciej F. Bull, Matthew J. Colleran, Amy Colquhoun, Rachel M. Darby, Alistair C. Haldenby, Sam Hill, Verity Lucaci, Anita McCrone, John T. Nicholls, Samuel M. O’Toole, Áine Pacchiarini, Nicole Poplawski, Radoslaw Scher, Emily Todd, Flora Webster, Hermione J. Whitehead, Mark Wierzbicki, Claudia Loman, Nicholas J. Connor, Thomas R. Robertson, David L. Pybus, Oliver G. Rambaut, Andrew |
author_facet | Jackson, Ben Boni, Maciej F. Bull, Matthew J. Colleran, Amy Colquhoun, Rachel M. Darby, Alistair C. Haldenby, Sam Hill, Verity Lucaci, Anita McCrone, John T. Nicholls, Samuel M. O’Toole, Áine Pacchiarini, Nicole Poplawski, Radoslaw Scher, Emily Todd, Flora Webster, Hermione J. Whitehead, Mark Wierzbicki, Claudia Loman, Nicholas J. Connor, Thomas R. Robertson, David L. Pybus, Oliver G. Rambaut, Andrew |
author_sort | Jackson, Ben |
collection | PubMed |
description | We present evidence for multiple independent origins of recombinant SARS-CoV-2 viruses sampled from late 2020 and early 2021 in the United Kingdom. Their genomes carry single-nucleotide polymorphisms and deletions that are characteristic of the B.1.1.7 variant of concern but lack the full complement of lineage-defining mutations. Instead, the remainder of their genomes share contiguous genetic variation with non-B.1.1.7 viruses circulating in the same geographic area at the same time as the recombinants. In four instances, there was evidence for onward transmission of a recombinant-origin virus, including one transmission cluster of 45 sequenced cases over the course of 2 months. The inferred genomic locations of recombination breakpoints suggest that every community-transmitted recombinant virus inherited its spike region from a B.1.1.7 parental virus, consistent with a transmission advantage for B.1.1.7’s set of mutations. |
format | Online Article Text |
id | pubmed-8367733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83677332021-08-17 Generation and transmission of interlineage recombinants in the SARS-CoV-2 pandemic Jackson, Ben Boni, Maciej F. Bull, Matthew J. Colleran, Amy Colquhoun, Rachel M. Darby, Alistair C. Haldenby, Sam Hill, Verity Lucaci, Anita McCrone, John T. Nicholls, Samuel M. O’Toole, Áine Pacchiarini, Nicole Poplawski, Radoslaw Scher, Emily Todd, Flora Webster, Hermione J. Whitehead, Mark Wierzbicki, Claudia Loman, Nicholas J. Connor, Thomas R. Robertson, David L. Pybus, Oliver G. Rambaut, Andrew Cell Article We present evidence for multiple independent origins of recombinant SARS-CoV-2 viruses sampled from late 2020 and early 2021 in the United Kingdom. Their genomes carry single-nucleotide polymorphisms and deletions that are characteristic of the B.1.1.7 variant of concern but lack the full complement of lineage-defining mutations. Instead, the remainder of their genomes share contiguous genetic variation with non-B.1.1.7 viruses circulating in the same geographic area at the same time as the recombinants. In four instances, there was evidence for onward transmission of a recombinant-origin virus, including one transmission cluster of 45 sequenced cases over the course of 2 months. The inferred genomic locations of recombination breakpoints suggest that every community-transmitted recombinant virus inherited its spike region from a B.1.1.7 parental virus, consistent with a transmission advantage for B.1.1.7’s set of mutations. Cell Press 2021-09-30 /pmc/articles/PMC8367733/ /pubmed/34499854 http://dx.doi.org/10.1016/j.cell.2021.08.014 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jackson, Ben Boni, Maciej F. Bull, Matthew J. Colleran, Amy Colquhoun, Rachel M. Darby, Alistair C. Haldenby, Sam Hill, Verity Lucaci, Anita McCrone, John T. Nicholls, Samuel M. O’Toole, Áine Pacchiarini, Nicole Poplawski, Radoslaw Scher, Emily Todd, Flora Webster, Hermione J. Whitehead, Mark Wierzbicki, Claudia Loman, Nicholas J. Connor, Thomas R. Robertson, David L. Pybus, Oliver G. Rambaut, Andrew Generation and transmission of interlineage recombinants in the SARS-CoV-2 pandemic |
title | Generation and transmission of interlineage recombinants in the SARS-CoV-2 pandemic |
title_full | Generation and transmission of interlineage recombinants in the SARS-CoV-2 pandemic |
title_fullStr | Generation and transmission of interlineage recombinants in the SARS-CoV-2 pandemic |
title_full_unstemmed | Generation and transmission of interlineage recombinants in the SARS-CoV-2 pandemic |
title_short | Generation and transmission of interlineage recombinants in the SARS-CoV-2 pandemic |
title_sort | generation and transmission of interlineage recombinants in the sars-cov-2 pandemic |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367733/ https://www.ncbi.nlm.nih.gov/pubmed/34499854 http://dx.doi.org/10.1016/j.cell.2021.08.014 |
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