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Accommodating individual travel history and unsampled diversity in Bayesian phylogeographic inference of SARS-CoV-2.
Lemey, Philippe; Hong, Samuel L; Hill, Verity; Baele, Guy; Poletto, Chiara; Colizza, Vittoria; O'Toole, Áine; McCrone, John T; Andersen, Kristian G; Worobey, Michael; Nelson, Martha I; Rambaut, Andrew; Suchard, Marc A.
  • Lemey P; Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Laboratory of Clinical and Evolutionary Virology, Leuven, Belgium. philippe.lemey@kuleuven.be.
  • Hong SL; Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Laboratory of Clinical and Evolutionary Virology, Leuven, Belgium.
  • Hill V; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, EH9 3FL, UK.
  • Baele G; Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Laboratory of Clinical and Evolutionary Virology, Leuven, Belgium.
  • Poletto C; INSERM, Sorbonne Université, Institut Pierre Louis d'Epidémiologie et de Santé Publique IPLESP, F75012, Paris, France.
  • Colizza V; INSERM, Sorbonne Université, Institut Pierre Louis d'Epidémiologie et de Santé Publique IPLESP, F75012, Paris, France.
  • O'Toole Á; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, EH9 3FL, UK.
  • McCrone JT; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, EH9 3FL, UK.
  • Andersen KG; Department of Immunology and Microbiology, Scripps Research, La Jolla, CA, 92037, USA.
  • Worobey M; Department of Ecology and Evolutionary Biology, University of Arizona, Tucson, AZ, 85721, USA.
  • Nelson MI; Division of International Epidemiology and Population Studies, Fogarty International Center, National Institutes of Health, Bethesda, MD, 20892, USA.
  • Rambaut A; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, EH9 3FL, UK.
  • Suchard MA; Department of Biomathematics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, 90095, USA. msuchard@ucla.edu.
Nat Commun ; 11(1): 5110, 2020 10 09.
Article in English | MEDLINE | ID: covidwho-841957
ABSTRACT
Spatiotemporal bias in genome sampling can severely confound discrete trait phylogeographic inference. This has impeded our ability to accurately track the spread of SARS-CoV-2, the virus responsible for the COVID-19 pandemic, despite the availability of unprecedented numbers of SARS-CoV-2 genomes. Here, we present an approach to integrate individual travel history data in Bayesian phylogeographic inference and apply it to the early spread of SARS-CoV-2. We demonstrate that including travel history data yields i) more realistic hypotheses of virus spread and ii) higher posterior predictive accuracy compared to including only sampling location. We further explore methods to ameliorate the impact of sampling bias by augmenting the phylogeographic analysis with lineages from undersampled locations. Our reconstructions reinforce specific transmission hypotheses suggested by the inclusion of travel history data, but also suggest alternative routes of virus migration that are plausible within the epidemiological context but are not apparent with current sampling efforts.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Travel / Coronavirus Infections / Betacoronavirus Type of study: Observational study / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2020 Document Type: Article Affiliation country: S41467-020-18877-9

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Travel / Coronavirus Infections / Betacoronavirus Type of study: Observational study / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2020 Document Type: Article Affiliation country: S41467-020-18877-9