SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da FIOCRUZ (ARCA) |
Texto Completo: | https://www.arca.fiocruz.br/handle/icict/56559 |
Resumo: | Brazil ranks as third in terms of total number of reported SARS-CoV-2 cases globally. The COVID- 19 epidemic in Brazil was characterised by the co-circulation of multiple variants as a consequence of multiple independent introduction events occurring through time. Here, we describe the SARS-CoV-2 variants that are currently circulating and co-circulating in the country, with the aim to highlight which variants have driven the different epidemic waves. For this purpose, we retrieved metadata information of Coronavirus sequences collected in Brazil and available at the GISAID database. SARS-CoV-2 lineages have been identified along with eleven variants, labelled as VOCs (Alpha, Gamma, Beta, Delta and Omicron) VOIs (Lambda and Mu) VUMs (B.1.1.318) and FMVs (Zeta, Eta and B.1.1.519). Here we show that, in the Brazilian context, after 24 months of sustained transmission and evolution of SARS-CoV-2, local variants (among them the B.1.1.28 and B.1.1.33) were displaced by recently introduced VOCs firstly with the Gamma, followed by Delta and more recently Omicron. The rapid spread of some of those VOCs (such as Gamma and Omicron) was also mirror by a large increase in the number of cases and deaths in the country. This in turn reinforces that, due to the emergence of variants that appear to induce a substantial evasion against neutralizing antibody response, it is important to strengthen genomic effort within the country and how vaccination still remains a critical process to protect the vulnerable population, still at risk of infection and death. |
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Alcantara, Luiz Carlos JuniorNogueira, ElissonShuab, GabrielTosta, StephaneFristch, HeggerPimentel, VictorSouza-Neto, Jayme A.Coutinho, Luiz LehmannFukumasu, HeidgeSampaio, Sandra CoccuzzoElias, Maria CarolinaKashima, SimoneSlavov, Svetoslav NanevCiccozzi, MassimoCella, EleonoraLourenco, JoséFonseca, VagnerGiovanetti, Marta2023-01-23T17:34:08Z2023-01-23T17:34:08Z2022ALCANTARA, Luiz Carlos Junior et al. SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves. Journal Pre-proof, p. 1 - 11, Apr. 2022.https://www.arca.fiocruz.br/handle/icict/56559Brazil ranks as third in terms of total number of reported SARS-CoV-2 cases globally. The COVID- 19 epidemic in Brazil was characterised by the co-circulation of multiple variants as a consequence of multiple independent introduction events occurring through time. Here, we describe the SARS-CoV-2 variants that are currently circulating and co-circulating in the country, with the aim to highlight which variants have driven the different epidemic waves. For this purpose, we retrieved metadata information of Coronavirus sequences collected in Brazil and available at the GISAID database. SARS-CoV-2 lineages have been identified along with eleven variants, labelled as VOCs (Alpha, Gamma, Beta, Delta and Omicron) VOIs (Lambda and Mu) VUMs (B.1.1.318) and FMVs (Zeta, Eta and B.1.1.519). Here we show that, in the Brazilian context, after 24 months of sustained transmission and evolution of SARS-CoV-2, local variants (among them the B.1.1.28 and B.1.1.33) were displaced by recently introduced VOCs firstly with the Gamma, followed by Delta and more recently Omicron. The rapid spread of some of those VOCs (such as Gamma and Omicron) was also mirror by a large increase in the number of cases and deaths in the country. This in turn reinforces that, due to the emergence of variants that appear to induce a substantial evasion against neutralizing antibody response, it is important to strengthen genomic effort within the country and how vaccination still remains a critical process to protect the vulnerable population, still at risk of infection and death.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Flavivírus. Rio de Janeiro, RJ, Brasil / Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Laboratório de Genética Celular e Molecular. Belo Horizonte, MG, Brasil.Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Laboratório de Genética Celular e Molecular. Belo Horizonte, MG, Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Flavivírus. Rio de Janeiro, RJ, Brasil.Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Laboratório de Genética Celular e Molecular. Belo Horizonte, MG, Brasil.Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Laboratório de Genética Celular e Molecular. Belo Horizonte, MG, Brasil.Global Health and Tropical Medicine (GHTM), Instituto de Higiene e Medicina Tropical/Universidade Nova de Lisboa (IHMT/UNL), Lisbon, Portugal.Universidade de São Paulo. Escola de Ciências Agrícolas. Botucatu, SP, Brasil.Universidade de São Paulo, Centro de Genômica Funcional da ESALQ, Piracicaba, SP, Brasil.Universidade de São Paulo, Escola de Zootecnia e Engenharia de Alimentos. Departamento de Medicina Veterinária. Pirassunuga, SP, Brasil.Instituto Butantan, São Paulo, SP, Brasil.Instituto Butantan, São Paulo, SP, Brasil.Universidade de São Paulo. Escola de Medicina de Ribeirão Preto. Hemocentro de Ribeirão Preto. Ribeirão Preto, SP, Brasil.Universidade de São Paulo. Escola de Medicina de Ribeirão Preto. Hemocentro de Ribeirão Preto. Ribeirão Preto, SP, Brasil.Medical Statistic and Molecular Epidemiology Unit, University of Biomedical Campus, Rome, Italy.Department of Zoology, Peter Medawar Building, University of Oxford, Oxford, UK / Biosystems and Integrative Sciences Institute (BioISI), Universidade de Lisboa, Portugal.Organização Pan-Americana da Saúde/Organização Mundial da Saúde, Brasília, Distrito Federal, Brasil / KwaZulu-Natal Research Innovation and Sequencing Platform (KRISP), School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Flavivírus. Rio de Janeiro, RJ, Brasil / Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Laboratório de Genética Celular e Molecular. Belo Horizonte, MG, Brasil / Department of Science and Technology for Humans and the Environment, University of Campus Bio-Medico di Roma, Rome, Italy.engElsevier B.V.Epidemia de SARS-CoV-2; Deslocamento de variantes; Brasil; Ondas epidêmicas distintas impulsionadasSARS-CoV-2Epidemic in BrazilVariants displacementHave drivenDistinct epidemic wavesSARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic wavesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZLICENSElicense.txtlicense.txttext/plain; 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dc.title.en_US.fl_str_mv |
SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves |
title |
SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves |
spellingShingle |
SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves Alcantara, Luiz Carlos Junior Epidemia de SARS-CoV-2; Deslocamento de variantes; Brasil; Ondas epidêmicas distintas impulsionadas SARS-CoV-2 Epidemic in Brazil Variants displacement Have driven Distinct epidemic waves |
title_short |
SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves |
title_full |
SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves |
title_fullStr |
SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves |
title_full_unstemmed |
SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves |
title_sort |
SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves |
author |
Alcantara, Luiz Carlos Junior |
author_facet |
Alcantara, Luiz Carlos Junior Nogueira, Elisson Shuab, Gabriel Tosta, Stephane Fristch, Hegger Pimentel, Victor Souza-Neto, Jayme A. Coutinho, Luiz Lehmann Fukumasu, Heidge Sampaio, Sandra Coccuzzo Elias, Maria Carolina Kashima, Simone Slavov, Svetoslav Nanev Ciccozzi, Massimo Cella, Eleonora Lourenco, José Fonseca, Vagner Giovanetti, Marta |
author_role |
author |
author2 |
Nogueira, Elisson Shuab, Gabriel Tosta, Stephane Fristch, Hegger Pimentel, Victor Souza-Neto, Jayme A. Coutinho, Luiz Lehmann Fukumasu, Heidge Sampaio, Sandra Coccuzzo Elias, Maria Carolina Kashima, Simone Slavov, Svetoslav Nanev Ciccozzi, Massimo Cella, Eleonora Lourenco, José Fonseca, Vagner Giovanetti, Marta |
author2_role |
author author author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Alcantara, Luiz Carlos Junior Nogueira, Elisson Shuab, Gabriel Tosta, Stephane Fristch, Hegger Pimentel, Victor Souza-Neto, Jayme A. Coutinho, Luiz Lehmann Fukumasu, Heidge Sampaio, Sandra Coccuzzo Elias, Maria Carolina Kashima, Simone Slavov, Svetoslav Nanev Ciccozzi, Massimo Cella, Eleonora Lourenco, José Fonseca, Vagner Giovanetti, Marta |
dc.subject.other.en_US.fl_str_mv |
Epidemia de SARS-CoV-2; Deslocamento de variantes; Brasil; Ondas epidêmicas distintas impulsionadas |
topic |
Epidemia de SARS-CoV-2; Deslocamento de variantes; Brasil; Ondas epidêmicas distintas impulsionadas SARS-CoV-2 Epidemic in Brazil Variants displacement Have driven Distinct epidemic waves |
dc.subject.en.en_US.fl_str_mv |
SARS-CoV-2 Epidemic in Brazil Variants displacement Have driven Distinct epidemic waves |
description |
Brazil ranks as third in terms of total number of reported SARS-CoV-2 cases globally. The COVID- 19 epidemic in Brazil was characterised by the co-circulation of multiple variants as a consequence of multiple independent introduction events occurring through time. Here, we describe the SARS-CoV-2 variants that are currently circulating and co-circulating in the country, with the aim to highlight which variants have driven the different epidemic waves. For this purpose, we retrieved metadata information of Coronavirus sequences collected in Brazil and available at the GISAID database. SARS-CoV-2 lineages have been identified along with eleven variants, labelled as VOCs (Alpha, Gamma, Beta, Delta and Omicron) VOIs (Lambda and Mu) VUMs (B.1.1.318) and FMVs (Zeta, Eta and B.1.1.519). Here we show that, in the Brazilian context, after 24 months of sustained transmission and evolution of SARS-CoV-2, local variants (among them the B.1.1.28 and B.1.1.33) were displaced by recently introduced VOCs firstly with the Gamma, followed by Delta and more recently Omicron. The rapid spread of some of those VOCs (such as Gamma and Omicron) was also mirror by a large increase in the number of cases and deaths in the country. This in turn reinforces that, due to the emergence of variants that appear to induce a substantial evasion against neutralizing antibody response, it is important to strengthen genomic effort within the country and how vaccination still remains a critical process to protect the vulnerable population, still at risk of infection and death. |
publishDate |
2022 |
dc.date.issued.fl_str_mv |
2022 |
dc.date.accessioned.fl_str_mv |
2023-01-23T17:34:08Z |
dc.date.available.fl_str_mv |
2023-01-23T17:34:08Z |
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dc.identifier.citation.fl_str_mv |
ALCANTARA, Luiz Carlos Junior et al. SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves. Journal Pre-proof, p. 1 - 11, Apr. 2022. |
dc.identifier.uri.fl_str_mv |
https://www.arca.fiocruz.br/handle/icict/56559 |
identifier_str_mv |
ALCANTARA, Luiz Carlos Junior et al. SARS-CoV-2 epidemic in Brazil: how variants displacement have driven distinct epidemic waves. Journal Pre-proof, p. 1 - 11, Apr. 2022. |
url |
https://www.arca.fiocruz.br/handle/icict/56559 |
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Elsevier B.V. |
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Elsevier B.V. |
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