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SARS-CoV-2 epidemic in Brazil: how the displacement of variants has driven distinct epidemic waves.
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.
  • Alcantara LCJ; Laboratório de Flavivírus, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil; Laboratório de Genética Celular e Molecular, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil. Electronic address: luiz.alcantara@ioc.fiocruz.
  • Nogueira E; Laboratório de Genética Celular e Molecular, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Shuab G; Laboratório de Flavivírus, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
  • Tosta S; Laboratório de Genética Celular e Molecular, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Fristch H; Laboratório de Genética Celular e Molecular, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Pimentel V; Global Health and Tropical Medicine (GHTM), Instituto de Higiene e Medicina Tropical/Universidade Nova de Lisboa (IHMT/UNL), Portugal.
  • Souza-Neto JA; São Paulo State University (UNESP), School of Agricultural Sciences, Botucatu, Brazil.
  • Coutinho LL; University of São Paulo, Centro de Genômica Funcional da ESALQ, Piracicaba, SP, Brazil.
  • Fukumasu H; Department of Veterinary Medicine, School of Animal Science and Food Engineering, University of Sao Paulo, Pirassununga, Sao Paulo, Brazil.
  • Sampaio SC; Butantan Institute, São Paulo, Brazil.
  • Elias MC; Butantan Institute, São Paulo, Brazil.
  • Kashima S; University of São Paulo, Ribeirão Preto Medical School, Blood Center of Ribeirão Preto, Ribeirão Preto, SP, Brazil.
  • Slavov SN; University of São Paulo, Ribeirão Preto Medical School, Blood Center of Ribeirão Preto, Ribeirão Preto, SP, Brazil.
  • Ciccozzi M; Medical Statistic and Molecular Epidemiology Unit, University of Biomedical Campus, Rome, Italy.
  • Cella E; Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL, USA.
  • Lourenco J; Department of Zoology, Peter Medawar Building, University of Oxford, Oxford, UK; Biosystems and Integrative Sciences Institute (BioISI), Universidade de Lisboa, Portugal.
  • Fonseca V; Organização Pan-Americana da Saúde/Organização Mundial da Saúde, Brasília, Distrito Federal, Brazil; 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. E
  • Giovanetti M; Laboratório de Flavivírus, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil; Laboratório de Genética Celular e Molecular, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil; Department of Science and Technology for Humans
Virus Res ; 315: 198785, 2022 07 02.
Article in English | MEDLINE | ID: covidwho-1860141
ABSTRACT
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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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Country/Region as subject: South America / Brazil Language: English Journal: Virus Res Journal subject: Virology Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Country/Region as subject: South America / Brazil Language: English Journal: Virus Res Journal subject: Virology Year: 2022 Document Type: Article