Evaluating the effects of SARS-CoV-2 Spike mutation D614G on transmissibility and pathogenicity

Erik Volz ORCID logo; Verity Hill ORCID logo; John T McCrone; Anna Price ORCID logo; David Jorgensen ORCID logo; Áine O’Toole ORCID logo; Joel Southgate; Robert Johnson; Ben Jackson; Fabricia F Nascimento; +21 more... Sara M Rey; Samuel M Nicholls ORCID logo; Rachel M Colquhoun; Ana da Silva Filipe; James Shepherd; David J Pascall; Rajiv Shah; Natasha Jesudason; Kathy Li; Ruth Jarrett; Nicole Pacchiarini; Matthew Bull; Lily Geidelberg; Igor Siveroni; Ian Goodfellow; Nicholas J Loman; Oliver G Pybus; David L Robertson; Emma C Thomson ORCID logo; Andrew Rambaut; Thomas R Connor ORCID logo; (2020) Evaluating the effects of SARS-CoV-2 Spike mutation D614G on transmissibility and pathogenicity. BMJ. DOI: 10.1101/2020.07.31.20166082
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<jats:title>Summary</jats:title><jats:p>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 data set, 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.</jats:p>


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