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SARS-CoV-2 within-host diversity and transmission.

Lythgoe, KA; Hall, M; Ferretti, L; de Cesare, M; MacIntyre-Cockett, G; Trebes, A; Andersson, M; Otecko, N; Wise, EL; Moore, N; et al. Lythgoe, KA; Hall, M; Ferretti, L; de Cesare, M; MacIntyre-Cockett, G; Trebes, A; Andersson, M; Otecko, N; Wise, EL; Moore, N; Lynch, J; Kidd, S; Cortes, N; Mori, M; Williams, R; Vernet, G; Justice, A; Green, A; Nicholls, SM; Ansari, MA; Abeler-Dörner, L; Moore, CE; Peto, TEA; Eyre, DW; Shaw, R; Simmonds, P; Buck, D; Todd, JA; Oxford Virus Sequencing Analysis Group (OVSG); Connor, TR; Ashraf, S; da Silva Filipe, A; Shepherd, J; Thomson, EC; COVID-19 Genomics UK (COG-UK) Consortium; Bonsall, D; Fraser, C; Golubchik, T (2021) SARS-CoV-2 within-host diversity and transmission. Science, 372 (6539). ISSN 1095-9203 https://doi.org/10.1126/science.abg0821
SGUL Authors: Moore, Catrin Elisabeth

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Abstract

Extensive global sampling and sequencing of the pandemic virus severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have enabled researchers to monitor its spread and to identify concerning new variants. Two important determinants of variant spread are how frequently they arise within individuals and how likely they are to be transmitted. To characterize within-host diversity and transmission, we deep-sequenced 1313 clinical samples from the United Kingdom. SARS-CoV-2 infections are characterized by low levels of within-host diversity when viral loads are high and by a narrow bottleneck at transmission. Most variants are either lost or occasionally fixed at the point of transmission, with minimal persistence of shared diversity, patterns that are readily observable on the phylogenetic tree. Our results suggest that transmission-enhancing and/or immune-escape SARS-CoV-2 variants are likely to arise infrequently but could spread rapidly if successfully transmitted.

Item Type: Article
Additional Information: Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: COVID-19, Coinfection, Coronavirus Infections, Coronavirus OC43, Human, Family Characteristics, Genetic Variation, Genome, Viral, Humans, Immune Evasion, Mutation, Phylogeny, RNA, Viral, RNA-Seq, SARS-CoV-2, Selection, Genetic, Spike Glycoprotein, Coronavirus, United Kingdom, Viral Load, Oxford Virus Sequencing Analysis Group (OVSG), COVID-19 Genomics UK (COG-UK) Consortium, Humans, Coronavirus OC43, Human, Coronavirus Infections, RNA, Viral, Viral Load, Family Characteristics, Phylogeny, Mutation, Genome, Viral, Genetic Variation, Selection, Genetic, Immune Evasion, Coinfection, Spike Glycoprotein, Coronavirus, United Kingdom, RNA-Seq, COVID-19, SARS-CoV-2, General Science & Technology
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Science
ISSN: 1095-9203
Language: eng
Dates:
DateEvent
16 April 2021Published
9 March 2021Published Online
3 March 2021Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
203141/Z/16/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
MC_PC_19027Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
107652/Z/15/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
220171/Z/20/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
WT103767MAWellcome Trusthttp://dx.doi.org/10.13039/100004440
209142/Z/17/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
OPP1176062Bill and Melinda Gates Foundationhttp://dx.doi.org/10.13039/100000865
PubMed ID: 33688063
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/114449
Publisher's version: https://doi.org/10.1126/science.abg0821

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