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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2021
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.
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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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