Evaluation of the genetic variability found in Brazilian commercial vaccines for infectious bronchitis virus
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | LOCUS Repositório Institucional da UFV |
Texto Completo: | https://doi.org/10.1007/s11262-017-1515-2 http://www.locus.ufv.br/handle/123456789/16514 |
Resumo: | Infectious bronchitis virus (IBV) is currently one of the most important pathogens in the poultry industry. The H120 and Ma5 are the only viral strains approved by the Brazilian government as the constituent of vaccines. Despite the systematic vaccination in Brazil, IBV has not yet been controlled and diseases associated with this virus have been reported in vaccinated chickens. Here, we investigated the genetic variability of H120 and Ma5 strains present in the IBV vaccines from different Brazilian manufacturers. We performed DNA sequencing analyses of the S1 spike glycoprotein gene to investigate its genetic variability and the presence of viral subpopulations among vaccines, between batches, and also in each vaccine after a single passage was performed in chicken embryonated eggs. Our results revealed up to 13 amino acid substitutions among vaccines and some of them were localized in regions of the S1 glycoprotein that play a role in virus–host interaction. Secondary nucleotide peaks identified in the chromatogram for the S1 gene sequence revealed that all original vaccines (H120 and Ma5) were composed by different subpopulations of IBV. Moreover, new viral subpopulations were also found in vaccines after a single passage in chicken embryonated eggs. These findings indicate that H120 and Ma5 viral strains used in vaccines market in Brazil can still mutate very rapidly during replication, leading to amino acid substitutions in proteins involved in the stimulation of the immune response, such as the S1 glycoprotein. Therefore, our data suggest that the genetic variability of these viral strains should be taken into consideration to ensure an effective immune response against IBV. |
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LOCUS Repositório Institucional da UFV |
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Evaluation of the genetic variability found in Brazilian commercial vaccines for infectious bronchitis virusIBVSubpopulationsMa5H120VaccinesControlInfectious bronchitis virus (IBV) is currently one of the most important pathogens in the poultry industry. The H120 and Ma5 are the only viral strains approved by the Brazilian government as the constituent of vaccines. Despite the systematic vaccination in Brazil, IBV has not yet been controlled and diseases associated with this virus have been reported in vaccinated chickens. Here, we investigated the genetic variability of H120 and Ma5 strains present in the IBV vaccines from different Brazilian manufacturers. We performed DNA sequencing analyses of the S1 spike glycoprotein gene to investigate its genetic variability and the presence of viral subpopulations among vaccines, between batches, and also in each vaccine after a single passage was performed in chicken embryonated eggs. Our results revealed up to 13 amino acid substitutions among vaccines and some of them were localized in regions of the S1 glycoprotein that play a role in virus–host interaction. Secondary nucleotide peaks identified in the chromatogram for the S1 gene sequence revealed that all original vaccines (H120 and Ma5) were composed by different subpopulations of IBV. Moreover, new viral subpopulations were also found in vaccines after a single passage in chicken embryonated eggs. These findings indicate that H120 and Ma5 viral strains used in vaccines market in Brazil can still mutate very rapidly during replication, leading to amino acid substitutions in proteins involved in the stimulation of the immune response, such as the S1 glycoprotein. Therefore, our data suggest that the genetic variability of these viral strains should be taken into consideration to ensure an effective immune response against IBV.Virus Genes2018-01-18T17:03:18Z2018-01-18T17:03:18Z2017-11-11info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlepdfapplication/pdf1572-994Xhttps://doi.org/10.1007/s11262-017-1515-2http://www.locus.ufv.br/handle/123456789/16514engNovembro 2017Saraiva, Giuliana LoretoSantos, Marcus RebouçasPereira, Claiton GonçalvesVidigal, Pedro Marcus PereiraFietto, Juliana Lopes RangelMendes, Tiago Antonio de OliveiraBressan, Gustavo CostaSoares-Martins, Jamária A. P.Almeida, Márcia Rogéria deSilva-Júnior, Abelardoinfo:eu-repo/semantics/openAccessreponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFV2024-07-12T07:48:52Zoai:locus.ufv.br:123456789/16514Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452024-07-12T07:48:52LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false |
dc.title.none.fl_str_mv |
Evaluation of the genetic variability found in Brazilian commercial vaccines for infectious bronchitis virus |
title |
Evaluation of the genetic variability found in Brazilian commercial vaccines for infectious bronchitis virus |
spellingShingle |
Evaluation of the genetic variability found in Brazilian commercial vaccines for infectious bronchitis virus Saraiva, Giuliana Loreto IBV Subpopulations Ma5 H120 Vaccines Control |
title_short |
Evaluation of the genetic variability found in Brazilian commercial vaccines for infectious bronchitis virus |
title_full |
Evaluation of the genetic variability found in Brazilian commercial vaccines for infectious bronchitis virus |
title_fullStr |
Evaluation of the genetic variability found in Brazilian commercial vaccines for infectious bronchitis virus |
title_full_unstemmed |
Evaluation of the genetic variability found in Brazilian commercial vaccines for infectious bronchitis virus |
title_sort |
Evaluation of the genetic variability found in Brazilian commercial vaccines for infectious bronchitis virus |
author |
Saraiva, Giuliana Loreto |
author_facet |
Saraiva, Giuliana Loreto Santos, Marcus Rebouças Pereira, Claiton Gonçalves Vidigal, Pedro Marcus Pereira Fietto, Juliana Lopes Rangel Mendes, Tiago Antonio de Oliveira Bressan, Gustavo Costa Soares-Martins, Jamária A. P. Almeida, Márcia Rogéria de Silva-Júnior, Abelardo |
author_role |
author |
author2 |
Santos, Marcus Rebouças Pereira, Claiton Gonçalves Vidigal, Pedro Marcus Pereira Fietto, Juliana Lopes Rangel Mendes, Tiago Antonio de Oliveira Bressan, Gustavo Costa Soares-Martins, Jamária A. P. Almeida, Márcia Rogéria de Silva-Júnior, Abelardo |
author2_role |
author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Saraiva, Giuliana Loreto Santos, Marcus Rebouças Pereira, Claiton Gonçalves Vidigal, Pedro Marcus Pereira Fietto, Juliana Lopes Rangel Mendes, Tiago Antonio de Oliveira Bressan, Gustavo Costa Soares-Martins, Jamária A. P. Almeida, Márcia Rogéria de Silva-Júnior, Abelardo |
dc.subject.por.fl_str_mv |
IBV Subpopulations Ma5 H120 Vaccines Control |
topic |
IBV Subpopulations Ma5 H120 Vaccines Control |
description |
Infectious bronchitis virus (IBV) is currently one of the most important pathogens in the poultry industry. The H120 and Ma5 are the only viral strains approved by the Brazilian government as the constituent of vaccines. Despite the systematic vaccination in Brazil, IBV has not yet been controlled and diseases associated with this virus have been reported in vaccinated chickens. Here, we investigated the genetic variability of H120 and Ma5 strains present in the IBV vaccines from different Brazilian manufacturers. We performed DNA sequencing analyses of the S1 spike glycoprotein gene to investigate its genetic variability and the presence of viral subpopulations among vaccines, between batches, and also in each vaccine after a single passage was performed in chicken embryonated eggs. Our results revealed up to 13 amino acid substitutions among vaccines and some of them were localized in regions of the S1 glycoprotein that play a role in virus–host interaction. Secondary nucleotide peaks identified in the chromatogram for the S1 gene sequence revealed that all original vaccines (H120 and Ma5) were composed by different subpopulations of IBV. Moreover, new viral subpopulations were also found in vaccines after a single passage in chicken embryonated eggs. These findings indicate that H120 and Ma5 viral strains used in vaccines market in Brazil can still mutate very rapidly during replication, leading to amino acid substitutions in proteins involved in the stimulation of the immune response, such as the S1 glycoprotein. Therefore, our data suggest that the genetic variability of these viral strains should be taken into consideration to ensure an effective immune response against IBV. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-11-11 2018-01-18T17:03:18Z 2018-01-18T17:03:18Z |
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 |
1572-994X https://doi.org/10.1007/s11262-017-1515-2 http://www.locus.ufv.br/handle/123456789/16514 |
identifier_str_mv |
1572-994X |
url |
https://doi.org/10.1007/s11262-017-1515-2 http://www.locus.ufv.br/handle/123456789/16514 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Novembro 2017 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
pdf application/pdf |
dc.publisher.none.fl_str_mv |
Virus Genes |
publisher.none.fl_str_mv |
Virus Genes |
dc.source.none.fl_str_mv |
reponame:LOCUS Repositório Institucional da UFV instname:Universidade Federal de Viçosa (UFV) instacron:UFV |
instname_str |
Universidade Federal de Viçosa (UFV) |
instacron_str |
UFV |
institution |
UFV |
reponame_str |
LOCUS Repositório Institucional da UFV |
collection |
LOCUS Repositório Institucional da UFV |
repository.name.fl_str_mv |
LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV) |
repository.mail.fl_str_mv |
fabiojreis@ufv.br |
_version_ |
1822610662877036544 |