Εμφάνιση απλής εγγραφής

dc.creatorNikolaidis M., Papakyriakou A., Chlichlia K., Markoulatos P., Oliver S.G., Amoutzias G.D.en
dc.date.accessioned2023-01-31T09:40:15Z
dc.date.available2023-01-31T09:40:15Z
dc.date.issued2022
dc.identifier10.3390/v14040707
dc.identifier.issn19994915
dc.identifier.urihttp://hdl.handle.net/11615/77194
dc.description.abstractIn 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.en
dc.language.isoenen
dc.sourceVirusesen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85128318712&doi=10.3390%2fv14040707&partnerID=40&md5=306ce329985bf9b4d7253d9815072f27
dc.subjectarginineen
dc.subjectasparagineen
dc.subjectaspartic aciden
dc.subjectcoronavirus spike glycoproteinen
dc.subjectcytosineen
dc.subjectglutamic aciden
dc.subjectglycineen
dc.subjecthistidineen
dc.subjectlysineen
dc.subjectprolineen
dc.subjectthreonineen
dc.subjectcoronavirus spike glycoproteinen
dc.subjectspike protein, SARS-CoV-2en
dc.subjectamino acid sequenceen
dc.subjectamino acid substitutionen
dc.subjectamino terminal sequenceen
dc.subjectArticleen
dc.subjectbioinformaticsen
dc.subjectcomparative studyen
dc.subjectcontrolled studyen
dc.subjectcoronavirus disease 2019en
dc.subjectgene and nucleic acid parametersen
dc.subjectgene mutationen
dc.subjectgenetic recombinationen
dc.subjectmutation rateen
dc.subjectnonhumanen
dc.subjectnucleotide sequenceen
dc.subjectnucleotide substitutionen
dc.subjectopen reading frameen
dc.subjectphylogenyen
dc.subjectpoint mutationen
dc.subjectprotein domainen
dc.subjectprotein motifen
dc.subjectpurifying selectionen
dc.subjectreceptor binding domainen
dc.subjectreceptor binding motifen
dc.subjectrecurrent mutationen
dc.subjectSARS-CoV-2 Lambda varianten
dc.subjectSARS-CoV-2 lineage B.1.1.529en
dc.subjectSARS-CoV-2 variant 20J/501Y.V3en
dc.subjectSARS-CoV-2 variant 501Y.V2en
dc.subjectSevere acute respiratory syndrome coronavirus 2en
dc.subjectvariant of concernen
dc.subjectvariant of interesten
dc.subjectvirus nucleocapsiden
dc.subjectamino acid substitutionen
dc.subjectgeneticsen
dc.subjecthumanen
dc.subjectmetabolismen
dc.subjectAmino Acid Substitutionen
dc.subjectCOVID-19en
dc.subjectHumansen
dc.subjectPhylogenyen
dc.subjectSARS-CoV-2en
dc.subjectSpike Glycoprotein, Coronavirusen
dc.subjectMDPIen
dc.titleComparative Analysis of SARS-CoV-2 Variants of Concern, Including Omicron, Highlights Their Common and Distinctive Amino Acid Substitution Patterns, Especially at the Spike ORFen
dc.typejournalArticleen


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