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Tracking the evolution of the SARS-CoV-2 Delta variant of concern: analysis of genetic diversity and selection across the whole viral genome

BACKGROUND: Since 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has diversified extensively, producing five highly virulent lineages designated as variants of concern (VOCs). The Delta VOC emerged in India with increased transmission, immune evasion, and mortality, causing a mas...

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Autores principales: Li, Katherine, Melnychuk, Stephanie, Sandstrom, Paul, Ji, Hezhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443222/
https://www.ncbi.nlm.nih.gov/pubmed/37614597
http://dx.doi.org/10.3389/fmicb.2023.1222301
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author Li, Katherine
Melnychuk, Stephanie
Sandstrom, Paul
Ji, Hezhao
author_facet Li, Katherine
Melnychuk, Stephanie
Sandstrom, Paul
Ji, Hezhao
author_sort Li, Katherine
collection PubMed
description BACKGROUND: Since 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has diversified extensively, producing five highly virulent lineages designated as variants of concern (VOCs). The Delta VOC emerged in India with increased transmission, immune evasion, and mortality, causing a massive global case surge in 2021. This study aims to understand how the Delta VOC evolved by characterizing mutation patterns in the viral population before and after its emergence. Furthermore, we aim to identify the influence of positive and negative selection on VOC evolution and understand the prevalence of different mutation types in the viral genome. METHODS: Three groups of whole viral genomes were retrieved from GISAID, sourced from India, with collection periods as follows: Group A—during the initial appearance of SARS-CoV-2; Group B—just before the emergence of the Delta variant; Group C—after the establishment of the Delta variant in India. Mutations in >1% of each group were identified with BioEdit to reveal differences in mutation quantity and type. Sites under positive or negative selection were identified with FUBAR. The results were compared to determine how mutations correspond with selective pressures and how viral mutation profiles changed to reflect genetic diversity before and after VOC emergence. RESULTS: The number of mutations increased progressively in Groups A–C, with Group C reporting a 2.2- and 1.9-fold increase from Groups A and B, respectively. Among all the observed mutations, Group C had the highest percentage of deletions (22.7%; vs. 4.2% and 2.6% in Groups A and B, respectively), and most mutations altered the final amino acid code, such as non-synonymous substitutions and deletions. Conversely, Group B had the most synonymous substitutions that are effectively silent. The number of sites experiencing positive selection increased in Groups A–C, but Group B had 2.4- and 2.6 times more sites under negative selection compared to Groups A and C, respectively. CONCLUSION: Our findings demonstrated that viral genetic diversity continuously increased during and after the emergence of the Delta VOC. Despite this, Group B reports heightened negative selection, which potentially preserves important gene regions during evolution. Group C contains an unprecedented quantity of mutations and positively selected sites, providing strong evidence of active viral adaptation in the population.
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spelling pubmed-104432222023-08-23 Tracking the evolution of the SARS-CoV-2 Delta variant of concern: analysis of genetic diversity and selection across the whole viral genome Li, Katherine Melnychuk, Stephanie Sandstrom, Paul Ji, Hezhao Front Microbiol Microbiology BACKGROUND: Since 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has diversified extensively, producing five highly virulent lineages designated as variants of concern (VOCs). The Delta VOC emerged in India with increased transmission, immune evasion, and mortality, causing a massive global case surge in 2021. This study aims to understand how the Delta VOC evolved by characterizing mutation patterns in the viral population before and after its emergence. Furthermore, we aim to identify the influence of positive and negative selection on VOC evolution and understand the prevalence of different mutation types in the viral genome. METHODS: Three groups of whole viral genomes were retrieved from GISAID, sourced from India, with collection periods as follows: Group A—during the initial appearance of SARS-CoV-2; Group B—just before the emergence of the Delta variant; Group C—after the establishment of the Delta variant in India. Mutations in >1% of each group were identified with BioEdit to reveal differences in mutation quantity and type. Sites under positive or negative selection were identified with FUBAR. The results were compared to determine how mutations correspond with selective pressures and how viral mutation profiles changed to reflect genetic diversity before and after VOC emergence. RESULTS: The number of mutations increased progressively in Groups A–C, with Group C reporting a 2.2- and 1.9-fold increase from Groups A and B, respectively. Among all the observed mutations, Group C had the highest percentage of deletions (22.7%; vs. 4.2% and 2.6% in Groups A and B, respectively), and most mutations altered the final amino acid code, such as non-synonymous substitutions and deletions. Conversely, Group B had the most synonymous substitutions that are effectively silent. The number of sites experiencing positive selection increased in Groups A–C, but Group B had 2.4- and 2.6 times more sites under negative selection compared to Groups A and C, respectively. CONCLUSION: Our findings demonstrated that viral genetic diversity continuously increased during and after the emergence of the Delta VOC. Despite this, Group B reports heightened negative selection, which potentially preserves important gene regions during evolution. Group C contains an unprecedented quantity of mutations and positively selected sites, providing strong evidence of active viral adaptation in the population. Frontiers Media S.A. 2023-08-08 /pmc/articles/PMC10443222/ /pubmed/37614597 http://dx.doi.org/10.3389/fmicb.2023.1222301 Text en Copyright © 2023 Li, Melnychuk, Sandstrom and Ji. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Li, Katherine
Melnychuk, Stephanie
Sandstrom, Paul
Ji, Hezhao
Tracking the evolution of the SARS-CoV-2 Delta variant of concern: analysis of genetic diversity and selection across the whole viral genome
title Tracking the evolution of the SARS-CoV-2 Delta variant of concern: analysis of genetic diversity and selection across the whole viral genome
title_full Tracking the evolution of the SARS-CoV-2 Delta variant of concern: analysis of genetic diversity and selection across the whole viral genome
title_fullStr Tracking the evolution of the SARS-CoV-2 Delta variant of concern: analysis of genetic diversity and selection across the whole viral genome
title_full_unstemmed Tracking the evolution of the SARS-CoV-2 Delta variant of concern: analysis of genetic diversity and selection across the whole viral genome
title_short Tracking the evolution of the SARS-CoV-2 Delta variant of concern: analysis of genetic diversity and selection across the whole viral genome
title_sort tracking the evolution of the sars-cov-2 delta variant of concern: analysis of genetic diversity and selection across the whole viral genome
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443222/
https://www.ncbi.nlm.nih.gov/pubmed/37614597
http://dx.doi.org/10.3389/fmicb.2023.1222301
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