Isabela Carvalho Brcko, Vinicius Carius de Souza, Gabriela Ribeiro, Alex Ranieri Jeronimo Lima, Antonio Jorge Martins, Claudia Renata Dos Santos Barros, Eneas de Carvalho, James Siqueira Pereira, Loyze Paola Oliveira de Lima, Vincent Louis Viala, Simone Kashima, Debora Glenda Lima de La Roque, Elaine Vieira Santos, Evandra Strazza Rodrigues, Juliana Almeida Nunes, Leandro Spalato Torres, Luiz Artur Vieira Caldeira, Melissa Palmieri, Caio Genovez Medina, Raphael Augusto de Arruda, Renata Beividas Lopes, Geraldo Reple Sobrinho, Daniel Macedo de Melo Jorge, Eurico Arruda, Eladja Christina Bezerra da Silva Mendes, Hazerral de Oliveira Santos, Arabela Leal E Silva de Mello, Felicidade Mota Pereira, Marcela Kelly Astete Gómez, Vanessa Brandão Nardy, Brenno Henrique, Lucas Luiz Vieira, Mariana Matos Roll, Elaine Cristina de Oliveira, Júlia Deffune Profeta Cidin Almeida, Stephanni Figueiredo da Silva, Gleissy Adriane Lima Borges, Katia Cristina de Lima Furtado, Patricia Miriam Sayuri Sato Barros da Costa, Shirley Moreira da Silva Chagas, Esper G Kallás, Daniel Larh, Marta Giovanetti, Svetoslav Nanev Slavov, Sandra Coccuzzo Sampaio, Maria Carolina Elias
{"title":"巴西流感病毒的综合分子流行病学:来自全国分析的见解。","authors":"Isabela Carvalho Brcko, Vinicius Carius de Souza, Gabriela Ribeiro, Alex Ranieri Jeronimo Lima, Antonio Jorge Martins, Claudia Renata Dos Santos Barros, Eneas de Carvalho, James Siqueira Pereira, Loyze Paola Oliveira de Lima, Vincent Louis Viala, Simone Kashima, Debora Glenda Lima de La Roque, Elaine Vieira Santos, Evandra Strazza Rodrigues, Juliana Almeida Nunes, Leandro Spalato Torres, Luiz Artur Vieira Caldeira, Melissa Palmieri, Caio Genovez Medina, Raphael Augusto de Arruda, Renata Beividas Lopes, Geraldo Reple Sobrinho, Daniel Macedo de Melo Jorge, Eurico Arruda, Eladja Christina Bezerra da Silva Mendes, Hazerral de Oliveira Santos, Arabela Leal E Silva de Mello, Felicidade Mota Pereira, Marcela Kelly Astete Gómez, Vanessa Brandão Nardy, Brenno Henrique, Lucas Luiz Vieira, Mariana Matos Roll, Elaine Cristina de Oliveira, Júlia Deffune Profeta Cidin Almeida, Stephanni Figueiredo da Silva, Gleissy Adriane Lima Borges, Katia Cristina de Lima Furtado, Patricia Miriam Sayuri Sato Barros da Costa, Shirley Moreira da Silva Chagas, Esper G Kallás, Daniel Larh, Marta Giovanetti, Svetoslav Nanev Slavov, Sandra Coccuzzo Sampaio, Maria Carolina Elias","doi":"10.1093/ve/veae102","DOIUrl":null,"url":null,"abstract":"<p><p>Influenza A and B viruses represent significant global health threats, contributing substantially to morbidity and mortality rates. However, a comprehensive understanding of the molecular epidemiology of these viruses in Brazil, a continental-size country and a crucial hub for the entry, circulation, and dissemination of influenza viruses within South America, still needs to be improved. This study addresses this gap by consolidating data and samples across all Brazilian macroregions, as part of the Center for Viral Surveillance and Serological Assessment project, together with an extensive number of other Brazilian sequences provided by a public database during the epidemic seasons spanning 2021-23. Phylogenetic analysis of the hemagglutinin segment of influenza A/H1N1pdm09, A/H3N2, and influenza B/Victoria-lineage viruses revealed that in 2021 and in the first semester of 2022, the A/H3N2 2a.3 strain was the predominant circulating strain. Subsequently, the A/H3N2 2b became the prevalent strain until October, when it was substituted by A/H1N1pdm09 5a.2a and 5a.2a.1 lineages. This scenario was maintained during the year of 2023. B/Victoria emerged and circulated at low levels between December 2021 and September 2022 and then became coprevalent with A/H1N1pdm09 5a.2a and 5a.2a.1 lineages. The comparison between the vaccine strain A/Darwin/9/2021 and circulating viruses revealed shared mutations to aspartic acid at residues 186 and 225 across all A/H3N2 lineages from 2021 to 2023, altering the charge in the receptor-binding domain. For A/H1N1pdm09, the 2022 consensus of 5a.2a.1 and the vaccine strain A/Victoria/2570/2019 showed 14 amino acid substitutions. Key residues H180, D187, K219, R223, E224, and T133 are involved in hydrogen interactions with sialic acids, while N130, K142, and D222 may contribute to distance interactions based on docking analyses. Importantly, distinct influenza A lineage frequency patterns were observed across Brazil's macroregions, underscoring the regional variations in virus circulation. This study characterizes influenza A and B viruses circulating in Brazil, providing insights into their circulation patterns and dynamics across Brazilian macroregions. These findings hold significant implications for public health interventions, informing strategies to mitigate transmission risks, optimize vaccination efforts, and enhance outbreak control measures.</p>","PeriodicalId":56026,"journal":{"name":"Virus Evolution","volume":"11 1","pages":"veae102"},"PeriodicalIF":5.5000,"publicationDate":"2024-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11711486/pdf/","citationCount":"0","resultStr":"{\"title\":\"Comprehensive molecular epidemiology of influenza viruses in Brazil: insights from a nationwide analysis.\",\"authors\":\"Isabela Carvalho Brcko, Vinicius Carius de Souza, Gabriela Ribeiro, Alex Ranieri Jeronimo Lima, Antonio Jorge Martins, Claudia Renata Dos Santos Barros, Eneas de Carvalho, James Siqueira Pereira, Loyze Paola Oliveira de Lima, Vincent Louis Viala, Simone Kashima, Debora Glenda Lima de La Roque, Elaine Vieira Santos, Evandra Strazza Rodrigues, Juliana Almeida Nunes, Leandro Spalato Torres, Luiz Artur Vieira Caldeira, Melissa Palmieri, Caio Genovez Medina, Raphael Augusto de Arruda, Renata Beividas Lopes, Geraldo Reple Sobrinho, Daniel Macedo de Melo Jorge, Eurico Arruda, Eladja Christina Bezerra da Silva Mendes, Hazerral de Oliveira Santos, Arabela Leal E Silva de Mello, Felicidade Mota Pereira, Marcela Kelly Astete Gómez, Vanessa Brandão Nardy, Brenno Henrique, Lucas Luiz Vieira, Mariana Matos Roll, Elaine Cristina de Oliveira, Júlia Deffune Profeta Cidin Almeida, Stephanni Figueiredo da Silva, Gleissy Adriane Lima Borges, Katia Cristina de Lima Furtado, Patricia Miriam Sayuri Sato Barros da Costa, Shirley Moreira da Silva Chagas, Esper G Kallás, Daniel Larh, Marta Giovanetti, Svetoslav Nanev Slavov, Sandra Coccuzzo Sampaio, Maria Carolina Elias\",\"doi\":\"10.1093/ve/veae102\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Influenza A and B viruses represent significant global health threats, contributing substantially to morbidity and mortality rates. However, a comprehensive understanding of the molecular epidemiology of these viruses in Brazil, a continental-size country and a crucial hub for the entry, circulation, and dissemination of influenza viruses within South America, still needs to be improved. This study addresses this gap by consolidating data and samples across all Brazilian macroregions, as part of the Center for Viral Surveillance and Serological Assessment project, together with an extensive number of other Brazilian sequences provided by a public database during the epidemic seasons spanning 2021-23. Phylogenetic analysis of the hemagglutinin segment of influenza A/H1N1pdm09, A/H3N2, and influenza B/Victoria-lineage viruses revealed that in 2021 and in the first semester of 2022, the A/H3N2 2a.3 strain was the predominant circulating strain. Subsequently, the A/H3N2 2b became the prevalent strain until October, when it was substituted by A/H1N1pdm09 5a.2a and 5a.2a.1 lineages. This scenario was maintained during the year of 2023. B/Victoria emerged and circulated at low levels between December 2021 and September 2022 and then became coprevalent with A/H1N1pdm09 5a.2a and 5a.2a.1 lineages. The comparison between the vaccine strain A/Darwin/9/2021 and circulating viruses revealed shared mutations to aspartic acid at residues 186 and 225 across all A/H3N2 lineages from 2021 to 2023, altering the charge in the receptor-binding domain. For A/H1N1pdm09, the 2022 consensus of 5a.2a.1 and the vaccine strain A/Victoria/2570/2019 showed 14 amino acid substitutions. Key residues H180, D187, K219, R223, E224, and T133 are involved in hydrogen interactions with sialic acids, while N130, K142, and D222 may contribute to distance interactions based on docking analyses. Importantly, distinct influenza A lineage frequency patterns were observed across Brazil's macroregions, underscoring the regional variations in virus circulation. 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Comprehensive molecular epidemiology of influenza viruses in Brazil: insights from a nationwide analysis.
Influenza A and B viruses represent significant global health threats, contributing substantially to morbidity and mortality rates. However, a comprehensive understanding of the molecular epidemiology of these viruses in Brazil, a continental-size country and a crucial hub for the entry, circulation, and dissemination of influenza viruses within South America, still needs to be improved. This study addresses this gap by consolidating data and samples across all Brazilian macroregions, as part of the Center for Viral Surveillance and Serological Assessment project, together with an extensive number of other Brazilian sequences provided by a public database during the epidemic seasons spanning 2021-23. Phylogenetic analysis of the hemagglutinin segment of influenza A/H1N1pdm09, A/H3N2, and influenza B/Victoria-lineage viruses revealed that in 2021 and in the first semester of 2022, the A/H3N2 2a.3 strain was the predominant circulating strain. Subsequently, the A/H3N2 2b became the prevalent strain until October, when it was substituted by A/H1N1pdm09 5a.2a and 5a.2a.1 lineages. This scenario was maintained during the year of 2023. B/Victoria emerged and circulated at low levels between December 2021 and September 2022 and then became coprevalent with A/H1N1pdm09 5a.2a and 5a.2a.1 lineages. The comparison between the vaccine strain A/Darwin/9/2021 and circulating viruses revealed shared mutations to aspartic acid at residues 186 and 225 across all A/H3N2 lineages from 2021 to 2023, altering the charge in the receptor-binding domain. For A/H1N1pdm09, the 2022 consensus of 5a.2a.1 and the vaccine strain A/Victoria/2570/2019 showed 14 amino acid substitutions. Key residues H180, D187, K219, R223, E224, and T133 are involved in hydrogen interactions with sialic acids, while N130, K142, and D222 may contribute to distance interactions based on docking analyses. Importantly, distinct influenza A lineage frequency patterns were observed across Brazil's macroregions, underscoring the regional variations in virus circulation. This study characterizes influenza A and B viruses circulating in Brazil, providing insights into their circulation patterns and dynamics across Brazilian macroregions. These findings hold significant implications for public health interventions, informing strategies to mitigate transmission risks, optimize vaccination efforts, and enhance outbreak control measures.
期刊介绍:
Virus Evolution is a new Open Access journal focusing on the long-term evolution of viruses, viruses as a model system for studying evolutionary processes, viral molecular epidemiology and environmental virology.
The aim of the journal is to provide a forum for original research papers, reviews, commentaries and a venue for in-depth discussion on the topics relevant to virus evolution.