Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/47534
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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