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Title: | Tracking down the origin and subsequent spread of SARS-CoV-2 lineage B.1.619 | Authors: | Bollen , Nena Hong, Samuel L. Potter, Barney, I Lienhard, Reto Tritten, Marie-Lise Sierro, Nicolas Guedj, Emmanuel Dulize, Remi Bornand, David Auberson, Mehdi Berthouzoz, Maxime Duvoisin, Pauline Ivanov, Nikolai, V Peitsch, Manuel C. Hill, Verity Matheeussen, Veerle Bontems, Sebastien Verhasselt, Bruno Degosserie, Jonathan WAUMANS, Luc Bayon-Vicente, Guillaume Reynders , Marijke Cattoir, Lien Coste, Valentin Valgaeren, Hanne Van Weyenbergh, Johan Cuypers, Lize Andre, Emmanuel Durkin, Keith Maes, Piet Khan , Kamran Huber, Carmen Suchard, Marc A. Maidadi Foudi, Martin Godwe, Celestin Moumbeket Yifomnjou, Moise Henri Landry, Messanga Njouom, Richard Mbala Kingebeni, Placide Oluniyi, Paul Olawoye, Idowu B. Happi, Christian Ayouba, Ahidjo Peeters , Martine Behillil, Sylvie Simon-Loriere, Etienne Holzer, Martin Dellicour, Simon Dudas, Gytis Baele, Guy |
Issue Date: | 2025 | Publisher: | OXFORD UNIV PRESS | Source: | Virus evolution, 11 (1) (Art N° veaf017) | Abstract: | Since late 2020, the emergence of variants of concern (VOCs) of SARS-CoV-2 has been of concern to public health, researchers and policymakers. Mutations in the SARS-CoV-2 genome-for which clear evidence is available indicating a significant impact on transmissibility, severity and/or immunity-illustrate the importance of genomic surveillance and monitoring the evolution and geographic spread of novel lineages. Lineage B.1.619 was first detected in Switzerland in January 2021, in international travellers returning from Cameroon. This lineage was subsequently also detected in Rwanda, Belgium, Cameroon, France, and many other countries and is characterised by spike protein amino acid mutations N440K and E484K in the receptor binding domain, which are associated with immune escape and higher infectiousness. In this study, we perform a phylogeographic analysis to track the geographic origin and subsequent dispersal of SARS-CoV-2 lineage B.1.619. We employ a recently developed travel history-aware phylogeographic model, enabling us to incorporate genomic sequences with associated travel information. We estimate that B.1.619 most likely originated in Cameroon, in November 2020. We estimate the influence of the number of air-traffic passengers on the dispersal of B.1.619 but find no significant effect, illustrative of the complex dispersal patterns of SARS-CoV-2 lineages. Finally, we examine the metadata associated with infected Belgian patients and report a wide range of symptoms and medical interventions. | Notes: | Bollen, N (corresponding author), Herestr 49,Box 1030B, B-3000 Leuven, Belgium. nena.bollen@kuleuven.be |
Keywords: | SARS-CoV-2;COVID-19;B.1.619;phylogenetics;phylogeography;GLMair traffic;Bayesian inference;Markov chain Monte Carlo | Document URI: | http://hdl.handle.net/1942/47534 | e-ISSN: | 2057-1577 | DOI: | 10.1093/ve/veaf017 | ISI #: | 001582837600001 | Rights: | The Author(s) 2025. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/ licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com. | Category: | A1 | Type: | Journal Contribution |
Appears in Collections: | Research publications |
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