Genomic Analyses of Major SARS-CoV-2 Variants Predicting Multiple Regions of Pathogenic and Transmissive Importance

The rapid evolution of SARS-CoV-2 has fueled its global proliferation since its discovery in 2019, with several notable variants having been responsible for increases in cases of coronavirus disease 2019 (COVID-19). Analyses of codon bias and usage in these variants between phylogenetic clades or li...

Full description

Bibliographic Details
Main Authors: Steven W. Brugger, Julianne H. Grose, Craig H. Decker, Brett E. Pickett, Mary F. Davis
Format: Article
Language:English
Published: MDPI AG 2024-02-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/16/2/276
_version_ 1797296809470590976
author Steven W. Brugger
Julianne H. Grose
Craig H. Decker
Brett E. Pickett
Mary F. Davis
author_facet Steven W. Brugger
Julianne H. Grose
Craig H. Decker
Brett E. Pickett
Mary F. Davis
author_sort Steven W. Brugger
collection DOAJ
description The rapid evolution of SARS-CoV-2 has fueled its global proliferation since its discovery in 2019, with several notable variants having been responsible for increases in cases of coronavirus disease 2019 (COVID-19). Analyses of codon bias and usage in these variants between phylogenetic clades or lineages may grant insights into the evolution of SARS-CoV-2 and identify target codons indicative of evolutionary or mutative trends that may prove useful in tracking or defending oneself against emerging strains. We processed a cohort of 120 SARS-CoV-2 genome sequences through a statistical and bioinformatic pipeline to identify codons presenting evidence of selective pressure as well as codon coevolution. We report the identification of two codon sites in the <i>orf8</i> and <i>N</i> genes demonstrating such evidence with real-world impacts on pathogenicity and transmissivity.
first_indexed 2024-03-07T22:10:13Z
format Article
id doaj.art-73bd2d7930f94926bca570ba886d1117
institution Directory Open Access Journal
issn 1999-4915
language English
last_indexed 2024-03-07T22:10:13Z
publishDate 2024-02-01
publisher MDPI AG
record_format Article
series Viruses
spelling doaj.art-73bd2d7930f94926bca570ba886d11172024-02-23T15:37:41ZengMDPI AGViruses1999-49152024-02-0116227610.3390/v16020276Genomic Analyses of Major SARS-CoV-2 Variants Predicting Multiple Regions of Pathogenic and Transmissive ImportanceSteven W. Brugger0Julianne H. Grose1Craig H. Decker2Brett E. Pickett3Mary F. Davis4Department of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602, USADepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602, USADepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602, USADepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602, USADepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602, USAThe rapid evolution of SARS-CoV-2 has fueled its global proliferation since its discovery in 2019, with several notable variants having been responsible for increases in cases of coronavirus disease 2019 (COVID-19). Analyses of codon bias and usage in these variants between phylogenetic clades or lineages may grant insights into the evolution of SARS-CoV-2 and identify target codons indicative of evolutionary or mutative trends that may prove useful in tracking or defending oneself against emerging strains. We processed a cohort of 120 SARS-CoV-2 genome sequences through a statistical and bioinformatic pipeline to identify codons presenting evidence of selective pressure as well as codon coevolution. We report the identification of two codon sites in the <i>orf8</i> and <i>N</i> genes demonstrating such evidence with real-world impacts on pathogenicity and transmissivity.https://www.mdpi.com/1999-4915/16/2/276SARS-CoV-2genomicsbioinformaticscoevolutioncodon bias
spellingShingle Steven W. Brugger
Julianne H. Grose
Craig H. Decker
Brett E. Pickett
Mary F. Davis
Genomic Analyses of Major SARS-CoV-2 Variants Predicting Multiple Regions of Pathogenic and Transmissive Importance
Viruses
SARS-CoV-2
genomics
bioinformatics
coevolution
codon bias
title Genomic Analyses of Major SARS-CoV-2 Variants Predicting Multiple Regions of Pathogenic and Transmissive Importance
title_full Genomic Analyses of Major SARS-CoV-2 Variants Predicting Multiple Regions of Pathogenic and Transmissive Importance
title_fullStr Genomic Analyses of Major SARS-CoV-2 Variants Predicting Multiple Regions of Pathogenic and Transmissive Importance
title_full_unstemmed Genomic Analyses of Major SARS-CoV-2 Variants Predicting Multiple Regions of Pathogenic and Transmissive Importance
title_short Genomic Analyses of Major SARS-CoV-2 Variants Predicting Multiple Regions of Pathogenic and Transmissive Importance
title_sort genomic analyses of major sars cov 2 variants predicting multiple regions of pathogenic and transmissive importance
topic SARS-CoV-2
genomics
bioinformatics
coevolution
codon bias
url https://www.mdpi.com/1999-4915/16/2/276
work_keys_str_mv AT stevenwbrugger genomicanalysesofmajorsarscov2variantspredictingmultipleregionsofpathogenicandtransmissiveimportance
AT juliannehgrose genomicanalysesofmajorsarscov2variantspredictingmultipleregionsofpathogenicandtransmissiveimportance
AT craighdecker genomicanalysesofmajorsarscov2variantspredictingmultipleregionsofpathogenicandtransmissiveimportance
AT brettepickett genomicanalysesofmajorsarscov2variantspredictingmultipleregionsofpathogenicandtransmissiveimportance
AT maryfdavis genomicanalysesofmajorsarscov2variantspredictingmultipleregionsofpathogenicandtransmissiveimportance