SARS-CoV-2 Spike Protein Mutations in Different Variants: A Comparison Between Vaccinated and Unvaccinated Population in Western Amazonia

The increased transmissibility of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has generated variants of concern (VOCs) throughout the pandemic, responsible for waves of cases worldwide. To monitor mutations in the S gene of SARS-CoV-2 in different variants, we evaluated 1497 individ...

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Main Authors: Gabriella Sgorlon, Tárcio Peixoto Roca, Ana Maisa Passos-Silva, Márlon Grégori Flores Custódio, Jackson Alves da Silva Queiroz, André Luiz Ferreira da Silva, Karolaine Santos Teixeira, Flávia Serrano Batista, Juan Miguel Villalobos Salcedo, Rita de Cassia P. Rampazzo, Felipe Gomes Naveca, Deusilene Vieira
Format: Article
Language:English
Published: SAGE Publishing 2023-07-01
Series:Bioinformatics and Biology Insights
Online Access:https://doi.org/10.1177/11779322231186477
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author Gabriella Sgorlon
Tárcio Peixoto Roca
Ana Maisa Passos-Silva
Márlon Grégori Flores Custódio
Jackson Alves da Silva Queiroz
André Luiz Ferreira da Silva
Karolaine Santos Teixeira
Flávia Serrano Batista
Juan Miguel Villalobos Salcedo
Rita de Cassia P. Rampazzo
Felipe Gomes Naveca
Deusilene Vieira
author_facet Gabriella Sgorlon
Tárcio Peixoto Roca
Ana Maisa Passos-Silva
Márlon Grégori Flores Custódio
Jackson Alves da Silva Queiroz
André Luiz Ferreira da Silva
Karolaine Santos Teixeira
Flávia Serrano Batista
Juan Miguel Villalobos Salcedo
Rita de Cassia P. Rampazzo
Felipe Gomes Naveca
Deusilene Vieira
author_sort Gabriella Sgorlon
collection DOAJ
description The increased transmissibility of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has generated variants of concern (VOCs) throughout the pandemic, responsible for waves of cases worldwide. To monitor mutations in the S gene of SARS-CoV-2 in different variants, we evaluated 1497 individuals with COVID-19 in western Amazonia in the period April 2021 to July 2022. The epidemiological and clinical data of the individuals were collected; subsequently, the samples were extracted using a commercial kit, the viral load was assessed, and viral genomes were sequenced. We analyzed the quality and mutations of the genomes and maximum likelihood phylogenetic inference. However, 3 main clusters were observed, referring to Gamma (52.91%), Delta (24.38%), and Omicron (20.38%) VOCs with wide distribution in all health regions of the Rondônia state. Regarding the vaccination profile, there was a higher percentage of unvaccinated and partially vaccinated individuals, with more representatives by the Gamma variant. A total of 1412 sequences were suitable for mutation analysis in the S gene region. The Omicron VOC showed 38 mutations, with the Delta and Gamma variants with 16 and 17, respectively. The VOC Omicron and Gamma shared 4 mutations E484K, H655Y, N501Y, and N679K with high frequency, and Delta and Omicron 2 mutations (T478K and T95I). Regarding the comparison between the frequency of mutations for each variant concerning the vaccination groups, there were no changes in mutations for each group. In conclusion, the study showed a temporal increase in mutations and subvariants for characterized strains. Furthermore, the vaccination profile did not impact significant changes in the mutational profile yet remains a determining factor for severe disease.
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spelling doaj.art-cfc9b7cbf3504365841f93e655fe44342023-07-15T06:03:25ZengSAGE PublishingBioinformatics and Biology Insights1177-93222023-07-011710.1177/11779322231186477SARS-CoV-2 Spike Protein Mutations in Different Variants: A Comparison Between Vaccinated and Unvaccinated Population in Western AmazoniaGabriella Sgorlon0Tárcio Peixoto Roca1Ana Maisa Passos-Silva2Márlon Grégori Flores Custódio3Jackson Alves da Silva Queiroz4André Luiz Ferreira da Silva5Karolaine Santos Teixeira6Flávia Serrano Batista7Juan Miguel Villalobos Salcedo8Rita de Cassia P. Rampazzo9Felipe Gomes Naveca10Deusilene Vieira11Centro de Pesquisa em Medicina Tropical de Rondônia (CEPEM/RO), Porto Velho, BrazilLaboratório de Hepatites Virais, Instituto Oswaldo Cruz (IOC), FIOCRUZ, Rio de Janeiro, BrazilCentro de Pesquisa em Medicina Tropical de Rondônia (CEPEM/RO), Porto Velho, BrazilLaboratório de Virologia Molecular, Fundação Oswaldo Cruz Rondônia (FIOCRUZ/RO), Porto Velho, BrazilCentro de Pesquisa em Medicina Tropical de Rondônia (CEPEM/RO), Porto Velho, BrazilCentro de Pesquisa em Medicina Tropical de Rondônia (CEPEM/RO), Porto Velho, BrazilCentro de Pesquisa em Medicina Tropical de Rondônia (CEPEM/RO), Porto Velho, BrazilCoordenação Estadual do Covid-19, AGEVISA/RO, Porto Velho, BrazilCentro de Pesquisa em Medicina Tropical de Rondônia (CEPEM/RO), Porto Velho, BrazilInstituto de Biologia Molecular do Paraná (IBMP), Curitiba, BrazilLaboratório de Virologia do Instituto Leônidas e Maria Deane, FIOCRUZ/AM, Manaus, BrazilCentro de Pesquisa em Medicina Tropical de Rondônia (CEPEM/RO), Porto Velho, BrazilThe increased transmissibility of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has generated variants of concern (VOCs) throughout the pandemic, responsible for waves of cases worldwide. To monitor mutations in the S gene of SARS-CoV-2 in different variants, we evaluated 1497 individuals with COVID-19 in western Amazonia in the period April 2021 to July 2022. The epidemiological and clinical data of the individuals were collected; subsequently, the samples were extracted using a commercial kit, the viral load was assessed, and viral genomes were sequenced. We analyzed the quality and mutations of the genomes and maximum likelihood phylogenetic inference. However, 3 main clusters were observed, referring to Gamma (52.91%), Delta (24.38%), and Omicron (20.38%) VOCs with wide distribution in all health regions of the Rondônia state. Regarding the vaccination profile, there was a higher percentage of unvaccinated and partially vaccinated individuals, with more representatives by the Gamma variant. A total of 1412 sequences were suitable for mutation analysis in the S gene region. The Omicron VOC showed 38 mutations, with the Delta and Gamma variants with 16 and 17, respectively. The VOC Omicron and Gamma shared 4 mutations E484K, H655Y, N501Y, and N679K with high frequency, and Delta and Omicron 2 mutations (T478K and T95I). Regarding the comparison between the frequency of mutations for each variant concerning the vaccination groups, there were no changes in mutations for each group. In conclusion, the study showed a temporal increase in mutations and subvariants for characterized strains. Furthermore, the vaccination profile did not impact significant changes in the mutational profile yet remains a determining factor for severe disease.https://doi.org/10.1177/11779322231186477
spellingShingle Gabriella Sgorlon
Tárcio Peixoto Roca
Ana Maisa Passos-Silva
Márlon Grégori Flores Custódio
Jackson Alves da Silva Queiroz
André Luiz Ferreira da Silva
Karolaine Santos Teixeira
Flávia Serrano Batista
Juan Miguel Villalobos Salcedo
Rita de Cassia P. Rampazzo
Felipe Gomes Naveca
Deusilene Vieira
SARS-CoV-2 Spike Protein Mutations in Different Variants: A Comparison Between Vaccinated and Unvaccinated Population in Western Amazonia
Bioinformatics and Biology Insights
title SARS-CoV-2 Spike Protein Mutations in Different Variants: A Comparison Between Vaccinated and Unvaccinated Population in Western Amazonia
title_full SARS-CoV-2 Spike Protein Mutations in Different Variants: A Comparison Between Vaccinated and Unvaccinated Population in Western Amazonia
title_fullStr SARS-CoV-2 Spike Protein Mutations in Different Variants: A Comparison Between Vaccinated and Unvaccinated Population in Western Amazonia
title_full_unstemmed SARS-CoV-2 Spike Protein Mutations in Different Variants: A Comparison Between Vaccinated and Unvaccinated Population in Western Amazonia
title_short SARS-CoV-2 Spike Protein Mutations in Different Variants: A Comparison Between Vaccinated and Unvaccinated Population in Western Amazonia
title_sort sars cov 2 spike protein mutations in different variants a comparison between vaccinated and unvaccinated population in western amazonia
url https://doi.org/10.1177/11779322231186477
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