Characterization of the emerging B.1.621 variant of interest of SARS-CoV-2
0301 basic medicine
Evolution
Short Communication
Genome, Viral
Colombia
Severity of Illness Index
Evolution, Molecular
03 medical and health sciences
Protein Domains
Humans
Phylogeny
0303 health sciences
SARS-CoV-2
Variants
COVID-19
High-Throughput Nucleotide Sequencing
Variantes
3. Good health
Evolución
Phylogeography
Amino Acid Substitution
Epidemiological Monitoring
Mutation
Spike Glycoprotein, Coronavirus
DOI:
10.1016/j.meegid.2021.105038
Publication Date:
2021-08-14T15:08:30Z
AUTHORS (21)
ABSTRACT
SummaryThe genetic diversity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has the potential to impact the virus transmissibility and the escape from natural infection- or vaccine-elicited neutralizing antibodies. Here, representative samples from circulating SARS-CoV-2 in Colombia between January and April 2021, were processed for genome sequencing and lineage determination following the nanopore amplicon ARTIC network protocol and PANGOLIN pipeline. This strategy allowed us to identify the emergence of the B.1.621 lineage, considered a variant of interest (VOI) with the accumulation of several substitutions affecting the Spike protein, including the amino acid changes T95I, Y144T, Y145S and the insertion 146N in the N-terminal domain, R346K, E484K and N501Y in the Receptor-binding Domain (RBD) and P681H1 in the S1/S2 cleavage site of the Spike protein. The rapid increase in frequency and fixation in a relatively short time in Magdalena, Atlántico, Bolivar, Bogotá D.C, and Santander that were near the theoretical herd immunity suggests an epidemiologic impact. Further studies will be required to assess the biological and epidemiologic roles of the substitution pattern found in the B.1.621 lineage.HighlightsMonitoring the emergence of new variants of SARS-CoV-2 in real time is a worldwide priority.Emerging variants of SARS-CoV-2 may have high impact biological implications for public healthThe SARS-CoV-2 B.1.621 variant of interest was characterized by several substitutions: T95I, Y144T, Y145S, ins146N, R346K, E484K, N501Y and P681H in spike protein.
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