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Comparative Analysis of SARS-CoV-2 Variants of Concern, Including Omicron, Highlights Their Common and Distinctive Amino Acid Substitution Patterns, Especially at the Spike ORF

Thumbnail
Auteur
Nikolaidis M., Papakyriakou A., Chlichlia K., Markoulatos P., Oliver S.G., Amoutzias G.D.
Date
2022
Language
en
DOI
10.3390/v14040707
Sujet
arginine
asparagine
aspartic acid
coronavirus spike glycoprotein
cytosine
glutamic acid
glycine
histidine
lysine
proline
threonine
coronavirus spike glycoprotein
spike protein, SARS-CoV-2
amino acid sequence
amino acid substitution
amino terminal sequence
Article
bioinformatics
comparative study
controlled study
coronavirus disease 2019
gene and nucleic acid parameters
gene mutation
genetic recombination
mutation rate
nonhuman
nucleotide sequence
nucleotide substitution
open reading frame
phylogeny
point mutation
protein domain
protein motif
purifying selection
receptor binding domain
receptor binding motif
recurrent mutation
SARS-CoV-2 Lambda variant
SARS-CoV-2 lineage B.1.1.529
SARS-CoV-2 variant 20J/501Y.V3
SARS-CoV-2 variant 501Y.V2
Severe acute respiratory syndrome coronavirus 2
variant of concern
variant of interest
virus nucleocapsid
amino acid substitution
genetics
human
metabolism
Amino Acid Substitution
COVID-19
Humans
Phylogeny
SARS-CoV-2
Spike Glycoprotein, Coronavirus
MDPI
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Résumé
In order to gain a deeper understanding of the recently emerged and highly divergent Omicron variant of concern (VoC), a study of amino acid substitution (AAS) patterns was performed and compared with those of the other four successful variants of concern (Alpha, Beta, Gamma, Delta) and one closely related variant of interest (VoI—Lambda). The Spike ORF consistently emerges as an AAS hotspot in all six lineages, but in Omicron this enrichment is significantly higher. The progenitors of each of these VoC/VoI lineages underwent positive selection in the Spike ORF. However, once they were established, their Spike ORFs have been undergoing purifying selection, despite the application of global vaccination schemes from 2021 onwards. Our analyses reject the hypothesis that the heavily mutated receptor binding domain (RBD) of the Omicron Spike was introduced via recombination from another closely related Sarbecovirus. Thus, successive point mutations appear as the most parsimonious scenario. Intriguingly, in each of the six lineages, we observed a significant number of AAS wherein the new residue is not present at any homologous site among the other known Sarbecoviruses. Such AAS should be further investigated as potential adaptations to the human host. By studying the phylogenetic distribution of AAS shared between the six lineages, we observed that the Omicron (BA.1) lineage had the highest number (8/10) of recurrent mutations. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.
URI
http://hdl.handle.net/11615/77194
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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