Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , , , , , |
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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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 |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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