The trend of phylogenetic and epitope variations of SARS-CoV-2 Omicron sub-lineages in Iran

IntroductionSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been a significant public health issue worldwide in recent years. The most recently circulating variant of SARS-CoV-2, Omicron, and its rapid evolution into various sub-lineages have raised concerns regarding the effects of...

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Main Authors: Mehdi Shabani, Ahmad Nejati, Jila Yavarian, Kaveh Sadeghi, Sevrin Zadheidar, Akram Sadat Ahmadi, Monire Ghadirali, Arghavan Zebardast, Adel Abedi, Mohammad Hossein Najmi, Nazanin-Zahra Shafiei-Jandaghi, Talat Mokhtari-Azad
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Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Microbiology
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Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2024.1531712/full
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author Mehdi Shabani
Ahmad Nejati
Jila Yavarian
Jila Yavarian
Kaveh Sadeghi
Sevrin Zadheidar
Akram Sadat Ahmadi
Monire Ghadirali
Arghavan Zebardast
Adel Abedi
Mohammad Hossein Najmi
Nazanin-Zahra Shafiei-Jandaghi
Talat Mokhtari-Azad
author_facet Mehdi Shabani
Ahmad Nejati
Jila Yavarian
Jila Yavarian
Kaveh Sadeghi
Sevrin Zadheidar
Akram Sadat Ahmadi
Monire Ghadirali
Arghavan Zebardast
Adel Abedi
Mohammad Hossein Najmi
Nazanin-Zahra Shafiei-Jandaghi
Talat Mokhtari-Azad
author_sort Mehdi Shabani
collection DOAJ
description IntroductionSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been a significant public health issue worldwide in recent years. The most recently circulating variant of SARS-CoV-2, Omicron, and its rapid evolution into various sub-lineages have raised concerns regarding the effects of the immunity on the virus epitopes, in the human population. The present study evaluated and compared these important variations among different Omicron sub-lineages in Iran.MethodologyFrom October 2023 to August 2024, high coverage whole genome sequences of 49 SARS-CoV-2 strains were subjected to phylogenetic analysis and evaluation of B cell, CD4+, and CD8+ T cell epitopes in Iran National Influenza Centre.ResultsThe phylogenetic tree exhibited eight Nextstrain clades (21L, 22F, 23B, 23H, 23D, 24A, 24B, and 24C) in 48 studied strains, and one recombinant strain (XDK.1). The evaluation of B cell, CD4+, and CD8+ T cell epitopes in all studied strains revealed 31, 65, and 78%, of conservation, respectively. The low B cell epitopes conservation rate among Omicron sub-lineages underscored the escaping from neutralizing humoral immunity. T cell epitopes of the SARS-CoV-2 were considerably preserved across major Omicron sub-lineages. Conservation levels varied based on the epitope class (higher for CD8+ vs. CD4+), protein (higher for non-spike vs. spike), and clades (higher for 21L, 22F, 23B, 23H, 23D, and 24B vs. 24A and 24C).ConclusionHerein, the increased conservation of CD8+ epitopes compared to CD4+ and B cell epitopes is probably attributable to the shorter length of the peptides associated with CD8+ epitopes. The high rate of T-cell epitopes conservation in non-spike proteins among different sub-lineages of the Omicron in this study highlighted the importance of cell-mediated immunity and suggested that non-spike proteins might be more attractive targets for future SARS-CoV-2 vaccines.
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spelling doaj-art-583db5217a274ebf8f2e09f99b292c8e2025-01-29T13:19:31ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2025-01-011510.3389/fmicb.2024.15317121531712The trend of phylogenetic and epitope variations of SARS-CoV-2 Omicron sub-lineages in IranMehdi Shabani0Ahmad Nejati1Jila Yavarian2Jila Yavarian3Kaveh Sadeghi4Sevrin Zadheidar5Akram Sadat Ahmadi6Monire Ghadirali7Arghavan Zebardast8Adel Abedi9Mohammad Hossein Najmi10Nazanin-Zahra Shafiei-Jandaghi11Talat Mokhtari-Azad12Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, IranDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, IranDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, IranResearch Center for Antibiotic Stewardship and Antimicrobial Resistance, Tehran University of Medical Sciences, Tehran, IranDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, IranDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, IranDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, IranDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, IranDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, IranDepartment of Mathematics, Shahid Beheshti University, Tehran, IranDepartment of Bioinformatics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, IranDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, IranDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, IranIntroductionSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been a significant public health issue worldwide in recent years. The most recently circulating variant of SARS-CoV-2, Omicron, and its rapid evolution into various sub-lineages have raised concerns regarding the effects of the immunity on the virus epitopes, in the human population. The present study evaluated and compared these important variations among different Omicron sub-lineages in Iran.MethodologyFrom October 2023 to August 2024, high coverage whole genome sequences of 49 SARS-CoV-2 strains were subjected to phylogenetic analysis and evaluation of B cell, CD4+, and CD8+ T cell epitopes in Iran National Influenza Centre.ResultsThe phylogenetic tree exhibited eight Nextstrain clades (21L, 22F, 23B, 23H, 23D, 24A, 24B, and 24C) in 48 studied strains, and one recombinant strain (XDK.1). The evaluation of B cell, CD4+, and CD8+ T cell epitopes in all studied strains revealed 31, 65, and 78%, of conservation, respectively. The low B cell epitopes conservation rate among Omicron sub-lineages underscored the escaping from neutralizing humoral immunity. T cell epitopes of the SARS-CoV-2 were considerably preserved across major Omicron sub-lineages. Conservation levels varied based on the epitope class (higher for CD8+ vs. CD4+), protein (higher for non-spike vs. spike), and clades (higher for 21L, 22F, 23B, 23H, 23D, and 24B vs. 24A and 24C).ConclusionHerein, the increased conservation of CD8+ epitopes compared to CD4+ and B cell epitopes is probably attributable to the shorter length of the peptides associated with CD8+ epitopes. The high rate of T-cell epitopes conservation in non-spike proteins among different sub-lineages of the Omicron in this study highlighted the importance of cell-mediated immunity and suggested that non-spike proteins might be more attractive targets for future SARS-CoV-2 vaccines.https://www.frontiersin.org/articles/10.3389/fmicb.2024.1531712/fullSARS-CoV-2Omicron sub-lineagesphylogeneticepitope variationsimmunity
spellingShingle Mehdi Shabani
Ahmad Nejati
Jila Yavarian
Jila Yavarian
Kaveh Sadeghi
Sevrin Zadheidar
Akram Sadat Ahmadi
Monire Ghadirali
Arghavan Zebardast
Adel Abedi
Mohammad Hossein Najmi
Nazanin-Zahra Shafiei-Jandaghi
Talat Mokhtari-Azad
The trend of phylogenetic and epitope variations of SARS-CoV-2 Omicron sub-lineages in Iran
Frontiers in Microbiology
SARS-CoV-2
Omicron sub-lineages
phylogenetic
epitope variations
immunity
title The trend of phylogenetic and epitope variations of SARS-CoV-2 Omicron sub-lineages in Iran
title_full The trend of phylogenetic and epitope variations of SARS-CoV-2 Omicron sub-lineages in Iran
title_fullStr The trend of phylogenetic and epitope variations of SARS-CoV-2 Omicron sub-lineages in Iran
title_full_unstemmed The trend of phylogenetic and epitope variations of SARS-CoV-2 Omicron sub-lineages in Iran
title_short The trend of phylogenetic and epitope variations of SARS-CoV-2 Omicron sub-lineages in Iran
title_sort trend of phylogenetic and epitope variations of sars cov 2 omicron sub lineages in iran
topic SARS-CoV-2
Omicron sub-lineages
phylogenetic
epitope variations
immunity
url https://www.frontiersin.org/articles/10.3389/fmicb.2024.1531712/full
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