Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/122945
Title: Evaluating the Effects of SARS-CoV-2 Spike Mutation D614G on Transmissibility and Pathogenicity
Authors: Volz, Erik
Hill, Verity
McCrone, John T.
Price, Anna
Jorgensen, David
O'Toole, Áine
Southgate, Joel
Johnson, Robert
Jackson, Ben
Nascimento, Fabricia F.
Rey, Sara M.
Nicholls, Samuel M.
Colquhoun, Rachel M.
da Silva Filipe, Ana
Shepherd, James
Pascall, David J.
Shah, Rajiv
Jesudason, Natasha
Li, Kathy
Jarrett, Ruth
Pacchiarini, Nicole
Bull, Matthew
Geidelberg, Lily
Siveroni, Igor
Koshy, Cherian
Wise, Emma
Cortes, Nick
Lynch, Jessica
Kidd, Stephen
Mori, Matilde
Fairley, Derek J.
Curran, Tanya
McKenna, James P.
Adams, Helen
Fraser, Christophe
Golubchik, Tanya
Bonsall, David
Moore, Catrin
Caddy, Sarah L.
Khokhar, Fahad A.
Wantoch, Michelle
Reynolds, Nicola
Warne, Ben
Maksimovic, Joshua
Spellman, Karla
McCluggage, Kathryn
John, Michaela
Beer, Robert
Afifi, Safiah
Morgan, Sian
Marchbank, Angela
Kitchen, Christine
Gulliver, Huw
Merrick, Ian
Guest, Martyn
Munn, Robert
Workman, Trudy
Connor, Thomas R.
Fuller, William
Bresner, Catherine
Snell, Luke B.
Charalampous, Themoula
Nebbia, Gaia
Batra, Rahul
Edgeworth, Jonathan
Robson, Samuel C.
Beckett, Angela
Loveson, Katie F.
Aanensen, David M.
Underwood, Anthony P.
Yeats, Corin A.
Abudahab, Khalil
Taylor, Ben E.W.
Menegazzo, Mirko
Clark, Gemma
Smith, Wendy
Khakh, Manjinder
Fleming, Vicki M.
Lister, Michelle M.
Howson-Wells, Hannah C.
Berry, Louise
Boswell, Tim
Joseph, Amelia
Willingham, Iona
Bird, Paul
Helmer, Thomas
Fallon, Karlie
Holmes, Christopher
Tang, Julian
Raviprakash, Veena
Campbell, Sharon
Sheriff, Nicola
Loose, Matthew W.
Holmes, Nadine
Moore, Christopher
Carlile, Matthew
Wright, Victoria
Sang, Fei
Debebe, Johnny
Coll, Francesc
Betancor Quintana, Gilberto Jose 
UNESCO Clasification: 32 Ciencias médicas
320505 Enfermedades infecciosas
Keywords: COVID-19
Epidemiology
Evolution
Founder effect
SARS-CoV-2, et al
Issue Date: 2021
Journal: Cell 
Abstract: Global dispersal and increasing frequency of the SARS-CoV-2 spike protein variant D614G are suggestive of a selective advantage but may also be due to a random founder effect. We investigate the hypothesis for positive selection of spike D614G in the United Kingdom using more than 25,000 whole genome SARS-CoV-2 sequences. Despite the availability of a large dataset, well represented by both spike 614 variants, not all approaches showed a conclusive signal of positive selection. Population genetic analysis indicates that 614G increases in frequency relative to 614D in a manner consistent with a selective advantage. We do not find any indication that patients infected with the spike 614G variant have higher COVID-19 mortality or clinical severity, but 614G is associated with higher viral load and younger age of patients. Significant differences in growth and size of 614G phylogenetic clusters indicate a need for continued study of this variant.
URI: http://hdl.handle.net/10553/122945
ISSN: 0092-8674
DOI: 10.1016/j.cell.2020.11.020
Source: Cell [ISSN 0092-8674] , v. 184 (1), p. 64-75 e11 (Enero 2021)
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