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Evaluating the Effects of SARS-CoV-2 Spike Mutation D614G on Transmissibility and Pathogenicity.
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; Goodfellow, Ian; Loman, Nicholas J; Pybus, Oliver G; Robertson, David L; Thomson, Emma C; Rambaut, Andrew; Connor, Thomas R.
  • Volz E; MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK. Electronic address: e.volz@imperial.ac.uk.
  • Hill V; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK.
  • McCrone JT; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK.
  • Price A; School of Biosciences, Cardiff University, Cardiff, UK.
  • Jorgensen D; MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
  • O'Toole Á; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK.
  • Southgate J; School of Biosciences, Cardiff University, Cardiff, UK; Pathogen Genomics Unit, Public Health Wales NHS Trust, Cardiff, UK.
  • Johnson R; MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
  • Jackson B; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK.
  • Nascimento FF; MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
  • Rey SM; Pathogen Genomics Unit, Public Health Wales NHS Trust, Cardiff, UK.
  • Nicholls SM; Institute of Microbiology and Infection, University of Birmingham, Birmingham, UK.
  • Colquhoun RM; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK.
  • da Silva Filipe A; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Shepherd J; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Pascall DJ; Institute of Biodiversity, Animal Health and Comparative Medicine, Boyd Orr Centre for Population and Ecosystem Health, University of Glasgow, Glasgow, UK.
  • Shah R; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Jesudason N; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Li K; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Jarrett R; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Pacchiarini N; Pathogen Genomics Unit, Public Health Wales NHS Trust, Cardiff, UK.
  • Bull M; Pathogen Genomics Unit, Public Health Wales NHS Trust, Cardiff, UK.
  • Geidelberg L; MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
  • Siveroni I; MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
  • Goodfellow I; Department of Pathology, University of Cambridge, Cambridge, UK.
  • Loman NJ; Institute of Microbiology and Infection, University of Birmingham, Birmingham, UK.
  • Pybus OG; Department of Zoology, University of Oxford, Oxford, UK; Department of Pathobiology and Population Sciences, The Royal Veterinary College, London, UK.
  • Robertson DL; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Thomson EC; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Rambaut A; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK. Electronic address: a.rambaut@ed.ac.uk.
  • Connor TR; School of Biosciences, Cardiff University, Cardiff, UK; Pathogen Genomics Unit, Public Health Wales NHS Trust, Cardiff, UK; Quadram Institute Bioscience, Norwich, UK. Electronic address: connortr@cardiff.ac.uk.
Cell ; 184(1): 64-75.e11, 2021 01 07.
Article in English | MEDLINE | ID: covidwho-1064909
Preprint
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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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Amino Acid Substitution / Spike Glycoprotein, Coronavirus / SARS-CoV-2 / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Variants Limits: Humans Country/Region as subject: Europa Language: English Journal: Cell Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Amino Acid Substitution / Spike Glycoprotein, Coronavirus / SARS-CoV-2 / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Variants Limits: Humans Country/Region as subject: Europa Language: English Journal: Cell Year: 2021 Document Type: Article