SARS-CoV-2 Omicron subvariant genomic variation associations with immune evasion in Northern California: A retrospective cohort study.

<h4>Background</h4>The possibility of association between SARS-CoV-2 genomic variation and immune evasion is not known among persons with Omicron variant SARS-CoV-2 infection.<h4>Methods</h4>In a retrospective cohort, using Poisson regression adjusting for sociodemographic va...

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Main Authors: Joshua R Nugent, Mariah S Wood, Liyan Liu, Teal Bullick, Jeffrey M Schapiro, Phacharee Arunleung, Gautham Gautham, Shiffen Getabecha, Christina Morales, Laura B Amsden, Crystal A Hsiao, Debra A Wadford, Stacia K Wyman, Jacek Skarbinski
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2025-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0319218
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author Joshua R Nugent
Mariah S Wood
Liyan Liu
Teal Bullick
Jeffrey M Schapiro
Phacharee Arunleung
Gautham Gautham
Shiffen Getabecha
Christina Morales
Laura B Amsden
Crystal A Hsiao
Debra A Wadford
Stacia K Wyman
Jacek Skarbinski
author_facet Joshua R Nugent
Mariah S Wood
Liyan Liu
Teal Bullick
Jeffrey M Schapiro
Phacharee Arunleung
Gautham Gautham
Shiffen Getabecha
Christina Morales
Laura B Amsden
Crystal A Hsiao
Debra A Wadford
Stacia K Wyman
Jacek Skarbinski
author_sort Joshua R Nugent
collection DOAJ
description <h4>Background</h4>The possibility of association between SARS-CoV-2 genomic variation and immune evasion is not known among persons with Omicron variant SARS-CoV-2 infection.<h4>Methods</h4>In a retrospective cohort, using Poisson regression adjusting for sociodemographic variables and month of infection, we examined associations between individual non-lineage defining mutations and SARS-CoV-2 immunity status, defined as a) no prior recorded infection, b) not vaccinated but with at least one prior recorded infection, c) complete primary series vaccination, and/or d) primary series vaccination and ≥1 booster. We identified all non-synonymous single nucleotide polymorphisms (SNPs), insertions and deletions in SARS-CoV-2 genomes with ≥5% allelic frequency and population frequency of ≥5% and ≤95%. We also examined correlations between the presence of SNPs with each other, with subvariants, and over time.<h4>Results</h4>Seventy-nine mutations met inclusion criteria. Among 15,566 persons infected with Omicron SARS-CoV-2, 1,825 (12%) were unvaccinated with no prior recorded infection, 360 (2%) were unvaccinated with a recorded prior infection, 13,381 (86%) had a complete primary series vaccination, and 9,172 (58%) had at least one booster. After examining correlation between SNPs, 79 individual non-lineage defining mutations were organized into 38 groups. After correction for multiple testing, no individual SNPs or SNP groups were significantly associated with immunity status levels.<h4>Conclusions</h4>Genomic variation identified within SARS-CoV-2 Omicron specimens was not significantly associated with immunity status, suggesting that contribution of non-lineage defining SNPs to immune evasion is minimal. Larger-scale surveillance of SARS-CoV-2 genomes linked with clinical data can help provide information to inform future vaccine development.
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spelling doaj-art-52b2385eca374d2ab3e2a42c9f05c9572025-08-20T03:52:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032025-01-01202e031921810.1371/journal.pone.0319218SARS-CoV-2 Omicron subvariant genomic variation associations with immune evasion in Northern California: A retrospective cohort study.Joshua R NugentMariah S WoodLiyan LiuTeal BullickJeffrey M SchapiroPhacharee ArunleungGautham GauthamShiffen GetabechaChristina MoralesLaura B AmsdenCrystal A HsiaoDebra A WadfordStacia K WymanJacek Skarbinski<h4>Background</h4>The possibility of association between SARS-CoV-2 genomic variation and immune evasion is not known among persons with Omicron variant SARS-CoV-2 infection.<h4>Methods</h4>In a retrospective cohort, using Poisson regression adjusting for sociodemographic variables and month of infection, we examined associations between individual non-lineage defining mutations and SARS-CoV-2 immunity status, defined as a) no prior recorded infection, b) not vaccinated but with at least one prior recorded infection, c) complete primary series vaccination, and/or d) primary series vaccination and ≥1 booster. We identified all non-synonymous single nucleotide polymorphisms (SNPs), insertions and deletions in SARS-CoV-2 genomes with ≥5% allelic frequency and population frequency of ≥5% and ≤95%. We also examined correlations between the presence of SNPs with each other, with subvariants, and over time.<h4>Results</h4>Seventy-nine mutations met inclusion criteria. Among 15,566 persons infected with Omicron SARS-CoV-2, 1,825 (12%) were unvaccinated with no prior recorded infection, 360 (2%) were unvaccinated with a recorded prior infection, 13,381 (86%) had a complete primary series vaccination, and 9,172 (58%) had at least one booster. After examining correlation between SNPs, 79 individual non-lineage defining mutations were organized into 38 groups. After correction for multiple testing, no individual SNPs or SNP groups were significantly associated with immunity status levels.<h4>Conclusions</h4>Genomic variation identified within SARS-CoV-2 Omicron specimens was not significantly associated with immunity status, suggesting that contribution of non-lineage defining SNPs to immune evasion is minimal. Larger-scale surveillance of SARS-CoV-2 genomes linked with clinical data can help provide information to inform future vaccine development.https://doi.org/10.1371/journal.pone.0319218
spellingShingle Joshua R Nugent
Mariah S Wood
Liyan Liu
Teal Bullick
Jeffrey M Schapiro
Phacharee Arunleung
Gautham Gautham
Shiffen Getabecha
Christina Morales
Laura B Amsden
Crystal A Hsiao
Debra A Wadford
Stacia K Wyman
Jacek Skarbinski
SARS-CoV-2 Omicron subvariant genomic variation associations with immune evasion in Northern California: A retrospective cohort study.
PLoS ONE
title SARS-CoV-2 Omicron subvariant genomic variation associations with immune evasion in Northern California: A retrospective cohort study.
title_full SARS-CoV-2 Omicron subvariant genomic variation associations with immune evasion in Northern California: A retrospective cohort study.
title_fullStr SARS-CoV-2 Omicron subvariant genomic variation associations with immune evasion in Northern California: A retrospective cohort study.
title_full_unstemmed SARS-CoV-2 Omicron subvariant genomic variation associations with immune evasion in Northern California: A retrospective cohort study.
title_short SARS-CoV-2 Omicron subvariant genomic variation associations with immune evasion in Northern California: A retrospective cohort study.
title_sort sars cov 2 omicron subvariant genomic variation associations with immune evasion in northern california a retrospective cohort study
url https://doi.org/10.1371/journal.pone.0319218
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