TY - JOUR
T1 - SARS-CoV-2 in Transit
T2 - Characterization of SARS-CoV-2 genomes from Venezuelan migrants in Colombia
AU - Patiño, Luz H.
AU - Ballesteros, Nathalia
AU - Muñoz, Marina
AU - Castañeda, Sergio
AU - Hernández, Carolina
AU - Gomez, Sergio
AU - Florez, Carolina
AU - Rico, Angelica
AU - Pardo, Liseth
AU - Hernandez-Pereira, Carlos E.
AU - Delgado-Noguera, Lourdes
AU - Grillet, Maria E.
AU - Hernandez, Matthew M.
AU - Khan, Zenab
AU - van de Guchte, Adriana
AU - Dutta, Jayeeta
AU - Gonzalez-Reiche, Ana S.
AU - Simon, Viviana
AU - van Bakel, Harm
AU - Sordillo, Emilia Mia
AU - Ramírez, Juan David
AU - Paniz-Mondolfi, Alberto E.
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2021/9
Y1 - 2021/9
N2 - Objectives: To evaluate the genomic epidemiology of SARS-CoV-2 from Venezuelan migrants living in Colombia. Methods: This study sequenced SARS-CoV-2 from 30 clinical specimens collected from Venezuelan migrants. Genomes were compared with the Wuhan reference genome to identify polymorphisms, reconstruct phylogenetic relationships and perform comparative genomic analyses. Geographic, sociodemographic and clinical data were also studied across genotypes. Results: This study demonstrated the presence of six distinct SARS-CoV-2 lineages circulating among Venezuelan migrants, as well as a close relationship between SARS-CoV-2 genomic sequences obtained from individuals living in the Venezuelan-Colombian border regions of La Guajira (Colombia) and Zulia (Venezuela). Three clusters (C-1, C-2 and C-3) were well supported by phylogenomic inference, supporting the hypothesis of three potential transmission routes across the Colombian-Venezuelan border. These genomes included point mutations previously associated with increased infectivity. A mutation (L18F) in the N-terminal domain of the spike protein that has been associated with compromised binding of neutralizing antibodies was found in 2 of 30 (6.6%) genomes. A statistically significant association was identified with symptomatology for cluster C2. Conclusion: The close phylogenetic relationships between SARS-CoV-2 genomes from Venezuelan migrants and from people living at the Venezuela-Colombian border support the importance of human movements for the spread of COVID-19 and for emerging virus variants.
AB - Objectives: To evaluate the genomic epidemiology of SARS-CoV-2 from Venezuelan migrants living in Colombia. Methods: This study sequenced SARS-CoV-2 from 30 clinical specimens collected from Venezuelan migrants. Genomes were compared with the Wuhan reference genome to identify polymorphisms, reconstruct phylogenetic relationships and perform comparative genomic analyses. Geographic, sociodemographic and clinical data were also studied across genotypes. Results: This study demonstrated the presence of six distinct SARS-CoV-2 lineages circulating among Venezuelan migrants, as well as a close relationship between SARS-CoV-2 genomic sequences obtained from individuals living in the Venezuelan-Colombian border regions of La Guajira (Colombia) and Zulia (Venezuela). Three clusters (C-1, C-2 and C-3) were well supported by phylogenomic inference, supporting the hypothesis of three potential transmission routes across the Colombian-Venezuelan border. These genomes included point mutations previously associated with increased infectivity. A mutation (L18F) in the N-terminal domain of the spike protein that has been associated with compromised binding of neutralizing antibodies was found in 2 of 30 (6.6%) genomes. A statistically significant association was identified with symptomatology for cluster C2. Conclusion: The close phylogenetic relationships between SARS-CoV-2 genomes from Venezuelan migrants and from people living at the Venezuela-Colombian border support the importance of human movements for the spread of COVID-19 and for emerging virus variants.
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U2 - 10.1016/j.ijid.2021.07.069
DO - 10.1016/j.ijid.2021.07.069
M3 - Article
C2 - 34333122
AN - SCOPUS:85113679834
SN - 1201-9712
VL - 110
SP - 410
EP - 416
JO - International Journal of Infectious Diseases
JF - International Journal of Infectious Diseases
ER -
