TY - JOUR
T1 - Emergence and widespread circulation of a recombinant SARS-CoV-2 lineage in North America
AU - Gutierrez, Bernardo
AU - Castelán Sánchez, Hugo G.
AU - Candido, Darlan da Silva
AU - Jackson, Ben
AU - Fleishon, Shay
AU - Houzet, Renaud
AU - Ruis, Christopher
AU - Delaye, Luis
AU - Faria, Nuno R.
AU - Rambaut, Andrew
AU - Pybus, Oliver G.
AU - Escalera-Zamudio, Marina
N1 - Publisher Copyright:
© 2022 The Author(s)
PY - 2022/8/10
Y1 - 2022/8/10
N2 - Although recombination is a feature of coronavirus evolution, previously detected recombinant lineages of SARS-CoV-2 have shown limited circulation thus far. Here, we present a detailed phylogenetic analysis of four SARS-CoV-2 lineages to investigate the possibility of virus recombination among them. Our analyses reveal well-supported phylogenetic differences between the Orf1ab region encoding viral non-structural proteins and the rest of the genome, including Spike (S) protein and remaining reading frames. By accounting for several deletions in NSP6, Orf3a, and S, we conclude that the B.1.628 major cluster, now designated as lineage XB, originated from a recombination event between viruses of B.1.631 and B.1.634 lineages. This scenario is supported by the spatiotemporal distribution of these lineages across the USA and Mexico during 2021, suggesting that the recombination event originated in this geographical region. This event raises important questions regarding the role and potential effects of recombination on SARS-CoV-2 evolution.
AB - Although recombination is a feature of coronavirus evolution, previously detected recombinant lineages of SARS-CoV-2 have shown limited circulation thus far. Here, we present a detailed phylogenetic analysis of four SARS-CoV-2 lineages to investigate the possibility of virus recombination among them. Our analyses reveal well-supported phylogenetic differences between the Orf1ab region encoding viral non-structural proteins and the rest of the genome, including Spike (S) protein and remaining reading frames. By accounting for several deletions in NSP6, Orf3a, and S, we conclude that the B.1.628 major cluster, now designated as lineage XB, originated from a recombination event between viruses of B.1.631 and B.1.634 lineages. This scenario is supported by the spatiotemporal distribution of these lineages across the USA and Mexico during 2021, suggesting that the recombination event originated in this geographical region. This event raises important questions regarding the role and potential effects of recombination on SARS-CoV-2 evolution.
KW - SARS-CoV-2
KW - molecular epidemiology
KW - phylogenetics
KW - recombination
UR - http://www.scopus.com/inward/record.url?scp=85134786953&partnerID=8YFLogxK
U2 - 10.1016/j.chom.2022.06.010
DO - 10.1016/j.chom.2022.06.010
M3 - Artículo
C2 - 35853454
AN - SCOPUS:85134786953
SN - 1931-3128
VL - 30
SP - 1112-1123.e3
JO - Cell Host and Microbe
JF - Cell Host and Microbe
IS - 8
ER -