Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Digital do Instituto Evandro Chagas (Patuá) |
Texto Completo: | https://patua.iec.gov.br/handle/iec/4167 |
Resumo: | Noroviruses (NoVs) are enteric viruses that cause acute gastroenteritis, and the pandemic GII.4 genotype is spreading and evolving rapidly. The recombinant GII.P16/GII.4_Sydney strain emerged in 2016, replacing GII.P31/GII.4_Sydney (GII.P31 formerly known as GII.Pe) in some countries. We analyzed the complete genome of 20 NoV strains (17 GII.P31/GII.4_ Sydney and 3 GII.P16/GII.4_Sydney) from Belém and Manaus, Brazil, collected from 2012 to 2016. Phylogenetic trees were constructed by maximum likelihood method from 191 full NoV-VP1 sequences, demonstrated segregation of the Sydney lineage in two larger clades, suggesting that GII.4 strains associated with GII.P16 already have modifications compared with GII.P31/GII.4. Additionally, the Bayesian Markov Chain Monte Carlo method was used to reconstruct a time-scaled phylogenetic tree formed by GII.P16 ORF1 sequences (n = 117) and three complete GII.P16 sequences from Belém. The phylogenetic tree indicated the presence of six clades classified into different capsid genotypes and locations. Evolutionary rates of the ORF1 gene of GII.P16 strains was estimated at 2.01 × 10–3 substitutions/site/year, and the most recent common ancestors were estimated in 2011 (2011–2012, 95% HPD). Comparing the amino acid (AA) sequence coding for ORF1 with the prototype strain GII.P16/GII.4, 36 AA changes were observed, mainly in the non-structural proteins p48, p22, and RdRp. GII.P16/GII.4 strains of this study presented changes in amino acids 310, 333, 373, and 393 of the antigenic sites in the P2 subdomain, and ML tree indicating the division within the Sydney lineage according to the GII.P16 and GII.P31 polymerases. Notably, as noroviruses have high recombination rates and the GII.4 genotype was prevalent for a long time in several locations, additional and continuous evolutionary analyses of this new genotype should be needed in the future. |
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Hernandez, Juliana MercesSilva, Luciana Damascena daSousa Júnior, Edivaldo CostaCardoso, Jedson FerreiraReymão, Tammy Kathlyn AmaralPortela, Ana Caroline RodriguesLima, Clayton Pereira Silva deTeixeira, Dielle MonteiroLucena, Maria Silvia SouzaNunes, Márcio Roberto TeixeiraGabbay, Yvone Benchimol2020-09-01T12:42:11Z2020-09-01T12:42:11Z2020HERNANDEZ, Juliana Merces et al. Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4. Frontiers in Microbiology, v. 11, n. 1870, p. 1-10, Aug. 2020.1664-302Xhttps://patua.iec.gov.br/handle/iec/416710.3389/fmicb.2020.01870Noroviruses (NoVs) are enteric viruses that cause acute gastroenteritis, and the pandemic GII.4 genotype is spreading and evolving rapidly. The recombinant GII.P16/GII.4_Sydney strain emerged in 2016, replacing GII.P31/GII.4_Sydney (GII.P31 formerly known as GII.Pe) in some countries. We analyzed the complete genome of 20 NoV strains (17 GII.P31/GII.4_ Sydney and 3 GII.P16/GII.4_Sydney) from Belém and Manaus, Brazil, collected from 2012 to 2016. Phylogenetic trees were constructed by maximum likelihood method from 191 full NoV-VP1 sequences, demonstrated segregation of the Sydney lineage in two larger clades, suggesting that GII.4 strains associated with GII.P16 already have modifications compared with GII.P31/GII.4. Additionally, the Bayesian Markov Chain Monte Carlo method was used to reconstruct a time-scaled phylogenetic tree formed by GII.P16 ORF1 sequences (n = 117) and three complete GII.P16 sequences from Belém. The phylogenetic tree indicated the presence of six clades classified into different capsid genotypes and locations. Evolutionary rates of the ORF1 gene of GII.P16 strains was estimated at 2.01 × 10–3 substitutions/site/year, and the most recent common ancestors were estimated in 2011 (2011–2012, 95% HPD). Comparing the amino acid (AA) sequence coding for ORF1 with the prototype strain GII.P16/GII.4, 36 AA changes were observed, mainly in the non-structural proteins p48, p22, and RdRp. GII.P16/GII.4 strains of this study presented changes in amino acids 310, 333, 373, and 393 of the antigenic sites in the P2 subdomain, and ML tree indicating the division within the Sydney lineage according to the GII.P16 and GII.P31 polymerases. Notably, as noroviruses have high recombination rates and the GII.4 genotype was prevalent for a long time in several locations, additional and continuous evolutionary analyses of this new genotype should be needed in the future.PAPQ/PROPESP ; PPG-BAIP/UFPA ; Evandro Chagas Institute, Secretary of Health Surveillance, Ministry of Health (IEC/SVS/MS)Federal University of Pará. Institute of Biological Sciences. Program in Biology of Infectious and Parasitic Agents. Belém, PA, Brazil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Federal University of Pará. Institute of Biological Sciences. Program in Biology of Infectious and Parasitic Agents. Belém, PA, Brazil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.engFrontiers MediaEvolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleGastroenterite / virologiaNorovirus / patogenicidadeGenoma / genéticaEvolução MolecularFilogeniainfo:eu-repo/semantics/openAccessreponame:Repositório Digital do Instituto Evandro Chagas (Patuá)instname:Instituto Evandro Chagas (IEC)instacron:IECORIGINALEvolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4.pdfEvolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4.pdfapplication/pdf4486833https://patua.iec.gov.br/bitstreams/dd7db904-6a82-4e51-aca0-77396796c2ad/downloadf634f5bf533e873053d1a2c2a70ad10eMD51LICENSElicense.txtlicense.txttext/plain; charset=utf-82182https://patua.iec.gov.br/bitstreams/687ea01f-2b87-49ba-b563-2a7dc7741236/download11832eea31b16df8613079d742d61793MD52TEXTEvolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4.pdf.txtEvolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4.pdf.txtExtracted texttext/plain51970https://patua.iec.gov.br/bitstreams/1985cdf3-a6c1-4a3a-a56b-91980c6c9a9a/download9aad341a09edf6cc2e51df7b82857401MD55THUMBNAILEvolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4.pdf.jpgEvolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4.pdf.jpgGenerated Thumbnailimage/jpeg5758https://patua.iec.gov.br/bitstreams/cc4dd9a3-44b6-44ce-93ed-61c43085e8b7/download2944cb598a86e57132b338ef31e3e88aMD56iec/41672022-10-20 22:57:37.506oai:patua.iec.gov.br:iec/4167https://patua.iec.gov.brRepositório InstitucionalPUBhttps://patua.iec.gov.br/oai/requestclariceneta@iec.gov.br || Biblioteca@iec.gov.bropendoar:2022-10-20T22:57:37Repositório Digital do Instituto Evandro Chagas (Patuá) - 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dc.title.pt_BR.fl_str_mv |
Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4 |
title |
Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4 |
spellingShingle |
Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4 Hernandez, Juliana Merces Gastroenterite / virologia Norovirus / patogenicidade Genoma / genética Evolução Molecular Filogenia |
title_short |
Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4 |
title_full |
Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4 |
title_fullStr |
Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4 |
title_full_unstemmed |
Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4 |
title_sort |
Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4 |
author |
Hernandez, Juliana Merces |
author_facet |
Hernandez, Juliana Merces Silva, Luciana Damascena da Sousa Júnior, Edivaldo Costa Cardoso, Jedson Ferreira Reymão, Tammy Kathlyn Amaral Portela, Ana Caroline Rodrigues Lima, Clayton Pereira Silva de Teixeira, Dielle Monteiro Lucena, Maria Silvia Souza Nunes, Márcio Roberto Teixeira Gabbay, Yvone Benchimol |
author_role |
author |
author2 |
Silva, Luciana Damascena da Sousa Júnior, Edivaldo Costa Cardoso, Jedson Ferreira Reymão, Tammy Kathlyn Amaral Portela, Ana Caroline Rodrigues Lima, Clayton Pereira Silva de Teixeira, Dielle Monteiro Lucena, Maria Silvia Souza Nunes, Márcio Roberto Teixeira Gabbay, Yvone Benchimol |
author2_role |
author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Hernandez, Juliana Merces Silva, Luciana Damascena da Sousa Júnior, Edivaldo Costa Cardoso, Jedson Ferreira Reymão, Tammy Kathlyn Amaral Portela, Ana Caroline Rodrigues Lima, Clayton Pereira Silva de Teixeira, Dielle Monteiro Lucena, Maria Silvia Souza Nunes, Márcio Roberto Teixeira Gabbay, Yvone Benchimol |
dc.subject.decsPrimary.pt_BR.fl_str_mv |
Gastroenterite / virologia Norovirus / patogenicidade Genoma / genética Evolução Molecular Filogenia |
topic |
Gastroenterite / virologia Norovirus / patogenicidade Genoma / genética Evolução Molecular Filogenia |
description |
Noroviruses (NoVs) are enteric viruses that cause acute gastroenteritis, and the pandemic GII.4 genotype is spreading and evolving rapidly. The recombinant GII.P16/GII.4_Sydney strain emerged in 2016, replacing GII.P31/GII.4_Sydney (GII.P31 formerly known as GII.Pe) in some countries. We analyzed the complete genome of 20 NoV strains (17 GII.P31/GII.4_ Sydney and 3 GII.P16/GII.4_Sydney) from Belém and Manaus, Brazil, collected from 2012 to 2016. Phylogenetic trees were constructed by maximum likelihood method from 191 full NoV-VP1 sequences, demonstrated segregation of the Sydney lineage in two larger clades, suggesting that GII.4 strains associated with GII.P16 already have modifications compared with GII.P31/GII.4. Additionally, the Bayesian Markov Chain Monte Carlo method was used to reconstruct a time-scaled phylogenetic tree formed by GII.P16 ORF1 sequences (n = 117) and three complete GII.P16 sequences from Belém. The phylogenetic tree indicated the presence of six clades classified into different capsid genotypes and locations. Evolutionary rates of the ORF1 gene of GII.P16 strains was estimated at 2.01 × 10–3 substitutions/site/year, and the most recent common ancestors were estimated in 2011 (2011–2012, 95% HPD). Comparing the amino acid (AA) sequence coding for ORF1 with the prototype strain GII.P16/GII.4, 36 AA changes were observed, mainly in the non-structural proteins p48, p22, and RdRp. GII.P16/GII.4 strains of this study presented changes in amino acids 310, 333, 373, and 393 of the antigenic sites in the P2 subdomain, and ML tree indicating the division within the Sydney lineage according to the GII.P16 and GII.P31 polymerases. Notably, as noroviruses have high recombination rates and the GII.4 genotype was prevalent for a long time in several locations, additional and continuous evolutionary analyses of this new genotype should be needed in the future. |
publishDate |
2020 |
dc.date.accessioned.fl_str_mv |
2020-09-01T12:42:11Z |
dc.date.available.fl_str_mv |
2020-09-01T12:42:11Z |
dc.date.issued.fl_str_mv |
2020 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
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article |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
HERNANDEZ, Juliana Merces et al. Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4. Frontiers in Microbiology, v. 11, n. 1870, p. 1-10, Aug. 2020. |
dc.identifier.uri.fl_str_mv |
https://patua.iec.gov.br/handle/iec/4167 |
dc.identifier.issn.-.fl_str_mv |
1664-302X |
dc.identifier.doi.-.fl_str_mv |
10.3389/fmicb.2020.01870 |
identifier_str_mv |
HERNANDEZ, Juliana Merces et al. Evolutionary and molecular analysis of complete genome sequences of norovirus from Brazil: emerging recombinant strain GII.P16/GII.4. Frontiers in Microbiology, v. 11, n. 1870, p. 1-10, Aug. 2020. 1664-302X 10.3389/fmicb.2020.01870 |
url |
https://patua.iec.gov.br/handle/iec/4167 |
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eng |
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eng |
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openAccess |
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Frontiers Media |
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Frontiers Media |
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