Journal article
bioRxiv, 2020
APA
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Lythgoe, K., Hall, M., Ferretti, L., de Cesare, M., Macintyre-Cockett, G., Trebes, A., … Golubchik, T. (2020). Shared SARS-CoV-2 diversity suggests localised transmission of minority variants. BioRxiv.
Chicago/Turabian
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Lythgoe, K., M. Hall, L. Ferretti, M. de Cesare, G. Macintyre-Cockett, A. Trebes, M. Andersson, et al. “Shared SARS-CoV-2 Diversity Suggests Localised Transmission of Minority Variants.” bioRxiv (2020).
MLA
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Lythgoe, K., et al. “Shared SARS-CoV-2 Diversity Suggests Localised Transmission of Minority Variants.” BioRxiv, 2020.
BibTeX Click to copy
@article{k2020a,
title = {Shared SARS-CoV-2 diversity suggests localised transmission of minority variants},
year = {2020},
journal = {bioRxiv},
author = {Lythgoe, K. and Hall, M. and Ferretti, L. and de Cesare, M. and Macintyre-Cockett, G. and Trebes, A. and Andersson, M. and Otecko, N. and Wise, E. and Moore, N. and Lynch, J. and Kidd, S. and Cortes, N. and Mori, M. and Justice, A. and Green, A. and Ansari, M. and Abeler-Dörner, Lucie and Moore, C. and Peto, T. and Shaw, R. and Simmonds, P. and Buck, D. and Todd, J. and Bonsall, D. and Fraser, C. and Golubchik, T.}
}
SARS-CoV-2, the causative agent of COVID-19, emerged in late 2019 causing a global pandemic, with the United Kingdom (UK) one of the hardest hit countries. Rapid sequencing and publication of consensus genomes have enabled phylogenetic analysis of the virus, demonstrating SARS-CoV-2 evolves relatively slowly1, but with multiple sites in the genome that appear inconsistent with the overall consensus phylogeny2. To understand these discrepancies, we used veSEQ3, a targeted RNA-seq approach, to quantify minor allele frequencies in 413 clinical samples from two UK locations. We show that SARS-CoV-2 infections are characterised by extensive within-host diversity, which is frequently shared among infected individuals with patterns consistent with geographical structure. These results were reproducible in data from other sequencing locations around the UK, where we find evidence of mixed infection by major circulating lineages with patterns that cannot readily be explained by artefacts in the data. We conclude that SARS-CoV-2 diversity is transmissible, and propose that geographic patterns are generated by co-circulation of distinct viral populations. Co-transmission of mixed populations could open opportunities for resolving clusters of transmission and understanding pathogenesis.