Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal

Detalhes bibliográficos
Autor(a) principal: Borges, Vítor
Data de Publicação: 2020
Outros Autores: Isidro, Joana, Cortes-Martins, Helena, Duarte, Sílvia, Vieira, Luís, Leite, Ricardo, Gordo, Isabel, Caetano, Constantino P., Nunes, Baltazar, Sá, Regina, Oliveira, Ana, Guiomar, Raquel, Portuguese network for SARS-CoV-2 genomics, Gomes, João Paulo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.18/7607
Resumo: Genomic surveillance of SARS-CoV-2 was rapidly implemented in Portugal by the National Institute of Health in collaboration with a nationwide consortium of >50 hospitals/laboratories. Here, we track the geotemporal spread of a SARS-CoV-2 variant with a mutation (D839Y) in a potential host-interacting region involving the Spike fusion peptide, which is a target motif of anti-viral drugs that plays a key role in SARS-CoV-2 infectivity. The Spike Y839 variant was most likely imported from Italy in mid-late February and massively disseminated in Portugal during the early epidemic, becoming prevalent in the Northern and Central regions of Portugal where it represented 22% and 59% of the sampled genomes, respectively, by 30 April. Based on our high sequencing sampling during the early epidemics [15.5% (1275/8251) and 6.0% (1500/24987) of all confirmed cases until the end of March and April, respectively], we estimate that, between 14 March and 9 April (covering the epidemic exponential phase) the relative frequency of the Spike Y839 variant increased at a rate of 12.1% (6.1%-18.2%, CI 95%) every three days, being potentially associated with 24.8% (20.8-29.7%, CI 95%; 3177-4542 cases, CI 95%) of all COVID-19 cases in Portugal during this period. Our data supports population/epidemiological (founder) effects contributing to the Y839 variant superspread. The potential existence of selective advantage is also discussed, although experimental validation is required. Despite huge differences in genome sampling worldwide, SARS-CoV-2 Spike D839Y has been detected in 13 countries in four continents, supporting the need for close surveillance and functional assays of Spike variants.
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spelling Massive dissemination of a SARS-CoV-2 Spike Y839 variant in PortugalCOVID-19Epidemiological MonitoringGenomicsHigh-Throughput Nucleotide SequencingHumansPhylogenyPortugalSARS-CoV-2Severity of Illness IndexSpike Glycoprotein, CoronavirusGenome, ViralMutationPandemicsInfecções RespiratóriasEstados de Saúde e de DoençaGenomic surveillance of SARS-CoV-2 was rapidly implemented in Portugal by the National Institute of Health in collaboration with a nationwide consortium of >50 hospitals/laboratories. Here, we track the geotemporal spread of a SARS-CoV-2 variant with a mutation (D839Y) in a potential host-interacting region involving the Spike fusion peptide, which is a target motif of anti-viral drugs that plays a key role in SARS-CoV-2 infectivity. The Spike Y839 variant was most likely imported from Italy in mid-late February and massively disseminated in Portugal during the early epidemic, becoming prevalent in the Northern and Central regions of Portugal where it represented 22% and 59% of the sampled genomes, respectively, by 30 April. Based on our high sequencing sampling during the early epidemics [15.5% (1275/8251) and 6.0% (1500/24987) of all confirmed cases until the end of March and April, respectively], we estimate that, between 14 March and 9 April (covering the epidemic exponential phase) the relative frequency of the Spike Y839 variant increased at a rate of 12.1% (6.1%-18.2%, CI 95%) every three days, being potentially associated with 24.8% (20.8-29.7%, CI 95%; 3177-4542 cases, CI 95%) of all COVID-19 cases in Portugal during this period. Our data supports population/epidemiological (founder) effects contributing to the Y839 variant superspread. The potential existence of selective advantage is also discussed, although experimental validation is required. Despite huge differences in genome sampling worldwide, SARS-CoV-2 Spike D839Y has been detected in 13 countries in four continents, supporting the need for close surveillance and functional assays of Spike variants.This study is co-funded by Fundação para a Ciência e a Tecnologia and Agência de Investigação Clínica e Inovação Biomédica [grant number 234_596874175] on behalf of the Research 4 COVID-19 call. This work is also a result of the GenomePT project [grant number POCI-01-0145- FEDER-022184], supported by COMPETE 2020 –Operational Programme for Competitiveness and Internationalisation (POCI), Lisboa Portugal Regional Operational Programme (Lisboa2020), Algarve Portugal Regional Operational Programme (CRESC Algarve2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF), and by Fundação para a Ciência e a Tecnologia (FCT).Taylor & Francis/ Shanghai Shangyixun Cultural CommunicationRepositório Científico do Instituto Nacional de SaúdeBorges, VítorIsidro, JoanaCortes-Martins, HelenaDuarte, SílviaVieira, LuísLeite, RicardoGordo, IsabelCaetano, Constantino P.Nunes, BaltazarSá, ReginaOliveira, AnaGuiomar, RaquelPortuguese network for SARS-CoV-2 genomicsGomes, João Paulo2021-03-31T14:52:22Z2020-122020-12-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.18/7607engEmerg Microbes Infect. 2020 Dec;9(1):2488-2496. doi: 10.1080/22221751.2020.18445522222-175110.1080/22221751.2020.1844552info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-20T15:42:06Zoai:repositorio.insa.pt:10400.18/7607Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:42:14.066315Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal
title Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal
spellingShingle Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal
Borges, Vítor
COVID-19
Epidemiological Monitoring
Genomics
High-Throughput Nucleotide Sequencing
Humans
Phylogeny
Portugal
SARS-CoV-2
Severity of Illness Index
Spike Glycoprotein, Coronavirus
Genome, Viral
Mutation
Pandemics
Infecções Respiratórias
Estados de Saúde e de Doença
title_short Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal
title_full Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal
title_fullStr Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal
title_full_unstemmed Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal
title_sort Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal
author Borges, Vítor
author_facet Borges, Vítor
Isidro, Joana
Cortes-Martins, Helena
Duarte, Sílvia
Vieira, Luís
Leite, Ricardo
Gordo, Isabel
Caetano, Constantino P.
Nunes, Baltazar
Sá, Regina
Oliveira, Ana
Guiomar, Raquel
Portuguese network for SARS-CoV-2 genomics
Gomes, João Paulo
author_role author
author2 Isidro, Joana
Cortes-Martins, Helena
Duarte, Sílvia
Vieira, Luís
Leite, Ricardo
Gordo, Isabel
Caetano, Constantino P.
Nunes, Baltazar
Sá, Regina
Oliveira, Ana
Guiomar, Raquel
Portuguese network for SARS-CoV-2 genomics
Gomes, João Paulo
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Nacional de Saúde
dc.contributor.author.fl_str_mv Borges, Vítor
Isidro, Joana
Cortes-Martins, Helena
Duarte, Sílvia
Vieira, Luís
Leite, Ricardo
Gordo, Isabel
Caetano, Constantino P.
Nunes, Baltazar
Sá, Regina
Oliveira, Ana
Guiomar, Raquel
Portuguese network for SARS-CoV-2 genomics
Gomes, João Paulo
dc.subject.por.fl_str_mv COVID-19
Epidemiological Monitoring
Genomics
High-Throughput Nucleotide Sequencing
Humans
Phylogeny
Portugal
SARS-CoV-2
Severity of Illness Index
Spike Glycoprotein, Coronavirus
Genome, Viral
Mutation
Pandemics
Infecções Respiratórias
Estados de Saúde e de Doença
topic COVID-19
Epidemiological Monitoring
Genomics
High-Throughput Nucleotide Sequencing
Humans
Phylogeny
Portugal
SARS-CoV-2
Severity of Illness Index
Spike Glycoprotein, Coronavirus
Genome, Viral
Mutation
Pandemics
Infecções Respiratórias
Estados de Saúde e de Doença
description Genomic surveillance of SARS-CoV-2 was rapidly implemented in Portugal by the National Institute of Health in collaboration with a nationwide consortium of >50 hospitals/laboratories. Here, we track the geotemporal spread of a SARS-CoV-2 variant with a mutation (D839Y) in a potential host-interacting region involving the Spike fusion peptide, which is a target motif of anti-viral drugs that plays a key role in SARS-CoV-2 infectivity. The Spike Y839 variant was most likely imported from Italy in mid-late February and massively disseminated in Portugal during the early epidemic, becoming prevalent in the Northern and Central regions of Portugal where it represented 22% and 59% of the sampled genomes, respectively, by 30 April. Based on our high sequencing sampling during the early epidemics [15.5% (1275/8251) and 6.0% (1500/24987) of all confirmed cases until the end of March and April, respectively], we estimate that, between 14 March and 9 April (covering the epidemic exponential phase) the relative frequency of the Spike Y839 variant increased at a rate of 12.1% (6.1%-18.2%, CI 95%) every three days, being potentially associated with 24.8% (20.8-29.7%, CI 95%; 3177-4542 cases, CI 95%) of all COVID-19 cases in Portugal during this period. Our data supports population/epidemiological (founder) effects contributing to the Y839 variant superspread. The potential existence of selective advantage is also discussed, although experimental validation is required. Despite huge differences in genome sampling worldwide, SARS-CoV-2 Spike D839Y has been detected in 13 countries in four continents, supporting the need for close surveillance and functional assays of Spike variants.
publishDate 2020
dc.date.none.fl_str_mv 2020-12
2020-12-01T00:00:00Z
2021-03-31T14:52:22Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.18/7607
url http://hdl.handle.net/10400.18/7607
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Emerg Microbes Infect. 2020 Dec;9(1):2488-2496. doi: 10.1080/22221751.2020.1844552
2222-1751
10.1080/22221751.2020.1844552
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Taylor & Francis/ Shanghai Shangyixun Cultural Communication
publisher.none.fl_str_mv Taylor & Francis/ Shanghai Shangyixun Cultural Communication
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
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