In vitro and in silico studies reveal capsid-mutant Porcine circovirus 2b with novel cytopathogenic and structural characteristics

Detalhes bibliográficos
Autor(a) principal: Cruz, Taís Fukuta [UNESP]
Data de Publicação: 2018
Outros Autores: Magro, Angelo José [UNESP], de Castro, Alessandra M.M.G., Pedraza-Ordoñez, Francisco J., Tsunemi, Miriam Harumi [UNESP], Perahia, David, Araujo, João Pessoa [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.virusres.2018.04.019
http://hdl.handle.net/11449/176303
Resumo: Porcine circovirus 2 (PCV2) is an icosahedral, non-enveloped, and single-stranded circular DNA virus that belongs to the family Circoviridae, genus Circovirus, and is responsible for a complex of different diseases defined as porcine circovirus diseases (PCVDs). These diseases – including postweaning multisystemic wasting syndrome (PMWS), enteric disease, respiratory disease, porcine dermatitis and nephropathy syndrome (PDNS), and reproductive failure – are responsible for large economic losses in the pig industry. After serial passages in swine testicle (ST) cells of a wild-type virus isolated from an animal with PMWS, we identified three PCV2b viruses with capsid protein (known as Cap protein) cumulative mutations, including two novel mutants. The mutant viruses were introduced into new ST cell cultures for reisolation and showed, in comparison to the wild-type PCV2b, remarkable viral replication efficiency (> 1011 DNA copies/ml) and cell death via necrosis, which were clearly related to the accretion of capsid protein mutations. The analysis of a Cap protein/capsid model showed that the mutated residues were located in solvent-accessible positions on the external PCV2b surface. Additionally, the mutated residues were found in linear epitopes and participated in pockets on the capsid surface, indicating that these residues could also be involved in antibody recognition. Taking into account the likely natural emergence of PCV2b variants, it is possible to consider that the results of this work increase knowledge of Circovirus biology and could help to prevent future serious cases of vaccine failure that could lead to heavy losses to the swine industry.
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spelling In vitro and in silico studies reveal capsid-mutant Porcine circovirus 2b with novel cytopathogenic and structural characteristicsAmino acid mutationsCap proteinMolecular modelingPCV2b mutantsPorcine circovirusViral replicationPorcine circovirus 2 (PCV2) is an icosahedral, non-enveloped, and single-stranded circular DNA virus that belongs to the family Circoviridae, genus Circovirus, and is responsible for a complex of different diseases defined as porcine circovirus diseases (PCVDs). These diseases – including postweaning multisystemic wasting syndrome (PMWS), enteric disease, respiratory disease, porcine dermatitis and nephropathy syndrome (PDNS), and reproductive failure – are responsible for large economic losses in the pig industry. After serial passages in swine testicle (ST) cells of a wild-type virus isolated from an animal with PMWS, we identified three PCV2b viruses with capsid protein (known as Cap protein) cumulative mutations, including two novel mutants. The mutant viruses were introduced into new ST cell cultures for reisolation and showed, in comparison to the wild-type PCV2b, remarkable viral replication efficiency (> 1011 DNA copies/ml) and cell death via necrosis, which were clearly related to the accretion of capsid protein mutations. The analysis of a Cap protein/capsid model showed that the mutated residues were located in solvent-accessible positions on the external PCV2b surface. Additionally, the mutated residues were found in linear epitopes and participated in pockets on the capsid surface, indicating that these residues could also be involved in antibody recognition. Taking into account the likely natural emergence of PCV2b variants, it is possible to consider that the results of this work increase knowledge of Circovirus biology and could help to prevent future serious cases of vaccine failure that could lead to heavy losses to the swine industry.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Departamento de Microbiologia e Imunologia Instituto de Biociências (IB) Universidade Estadual Paulista (Unesp)Instituto de Biotecnologia (IBTEC) Universidade Estadual Paulista (Unesp)Departamento de Bioprocessos e Biotecnologia Faculdade de Ciências Agronômicas (FCA) Universidade Estadual Paulista (Unesp)Departamento de Medicina Veterinária Preventiva e Saúde Animal Universidade de São Paulo (USP)Departamento de Salud Animal Universidad de CaldasDepartamento de Bioestatística Instituto de Biociências (IB) Universidade Estadual Paulista (Unesp)Laboratoire de Biologie et de Pharmacologie Appliquée ENS Cachan/Université Paris-SaclayComplexo Educacional Faculdades Metropolitanas Unidas (FMU/HOVET) São Paulo São PauloDepartamento de Microbiologia e Imunologia Instituto de Biociências (IB) Universidade Estadual Paulista (Unesp)Instituto de Biotecnologia (IBTEC) Universidade Estadual Paulista (Unesp)Departamento de Bioprocessos e Biotecnologia Faculdade de Ciências Agronômicas (FCA) Universidade Estadual Paulista (Unesp)Departamento de Bioestatística Instituto de Biociências (IB) Universidade Estadual Paulista (Unesp)FAPESP: 2006/57976-6FAPESP: 2006/59002-9FAPESP: 2013/14530-1Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Universidad de CaldasENS Cachan/Université Paris-SaclaySão PauloCruz, Taís Fukuta [UNESP]Magro, Angelo José [UNESP]de Castro, Alessandra M.M.G.Pedraza-Ordoñez, Francisco J.Tsunemi, Miriam Harumi [UNESP]Perahia, DavidAraujo, João Pessoa [UNESP]2018-12-11T17:20:01Z2018-12-11T17:20:01Z2018-06-02info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article22-33application/pdfhttp://dx.doi.org/10.1016/j.virusres.2018.04.019Virus Research, v. 251, p. 22-33.1872-74920168-1702http://hdl.handle.net/11449/17630310.1016/j.virusres.2018.04.0192-s2.0-850467638482-s2.0-85046763848.pdf0713984768583869Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengVirus Research1,147info:eu-repo/semantics/openAccess2023-11-28T06:15:45Zoai:repositorio.unesp.br:11449/176303Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:57:46.140925Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv In vitro and in silico studies reveal capsid-mutant Porcine circovirus 2b with novel cytopathogenic and structural characteristics
title In vitro and in silico studies reveal capsid-mutant Porcine circovirus 2b with novel cytopathogenic and structural characteristics
spellingShingle In vitro and in silico studies reveal capsid-mutant Porcine circovirus 2b with novel cytopathogenic and structural characteristics
Cruz, Taís Fukuta [UNESP]
Amino acid mutations
Cap protein
Molecular modeling
PCV2b mutants
Porcine circovirus
Viral replication
title_short In vitro and in silico studies reveal capsid-mutant Porcine circovirus 2b with novel cytopathogenic and structural characteristics
title_full In vitro and in silico studies reveal capsid-mutant Porcine circovirus 2b with novel cytopathogenic and structural characteristics
title_fullStr In vitro and in silico studies reveal capsid-mutant Porcine circovirus 2b with novel cytopathogenic and structural characteristics
title_full_unstemmed In vitro and in silico studies reveal capsid-mutant Porcine circovirus 2b with novel cytopathogenic and structural characteristics
title_sort In vitro and in silico studies reveal capsid-mutant Porcine circovirus 2b with novel cytopathogenic and structural characteristics
author Cruz, Taís Fukuta [UNESP]
author_facet Cruz, Taís Fukuta [UNESP]
Magro, Angelo José [UNESP]
de Castro, Alessandra M.M.G.
Pedraza-Ordoñez, Francisco J.
Tsunemi, Miriam Harumi [UNESP]
Perahia, David
Araujo, João Pessoa [UNESP]
author_role author
author2 Magro, Angelo José [UNESP]
de Castro, Alessandra M.M.G.
Pedraza-Ordoñez, Francisco J.
Tsunemi, Miriam Harumi [UNESP]
Perahia, David
Araujo, João Pessoa [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
Universidad de Caldas
ENS Cachan/Université Paris-Saclay
São Paulo
dc.contributor.author.fl_str_mv Cruz, Taís Fukuta [UNESP]
Magro, Angelo José [UNESP]
de Castro, Alessandra M.M.G.
Pedraza-Ordoñez, Francisco J.
Tsunemi, Miriam Harumi [UNESP]
Perahia, David
Araujo, João Pessoa [UNESP]
dc.subject.por.fl_str_mv Amino acid mutations
Cap protein
Molecular modeling
PCV2b mutants
Porcine circovirus
Viral replication
topic Amino acid mutations
Cap protein
Molecular modeling
PCV2b mutants
Porcine circovirus
Viral replication
description Porcine circovirus 2 (PCV2) is an icosahedral, non-enveloped, and single-stranded circular DNA virus that belongs to the family Circoviridae, genus Circovirus, and is responsible for a complex of different diseases defined as porcine circovirus diseases (PCVDs). These diseases – including postweaning multisystemic wasting syndrome (PMWS), enteric disease, respiratory disease, porcine dermatitis and nephropathy syndrome (PDNS), and reproductive failure – are responsible for large economic losses in the pig industry. After serial passages in swine testicle (ST) cells of a wild-type virus isolated from an animal with PMWS, we identified three PCV2b viruses with capsid protein (known as Cap protein) cumulative mutations, including two novel mutants. The mutant viruses were introduced into new ST cell cultures for reisolation and showed, in comparison to the wild-type PCV2b, remarkable viral replication efficiency (> 1011 DNA copies/ml) and cell death via necrosis, which were clearly related to the accretion of capsid protein mutations. The analysis of a Cap protein/capsid model showed that the mutated residues were located in solvent-accessible positions on the external PCV2b surface. Additionally, the mutated residues were found in linear epitopes and participated in pockets on the capsid surface, indicating that these residues could also be involved in antibody recognition. Taking into account the likely natural emergence of PCV2b variants, it is possible to consider that the results of this work increase knowledge of Circovirus biology and could help to prevent future serious cases of vaccine failure that could lead to heavy losses to the swine industry.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:20:01Z
2018-12-11T17:20:01Z
2018-06-02
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://dx.doi.org/10.1016/j.virusres.2018.04.019
Virus Research, v. 251, p. 22-33.
1872-7492
0168-1702
http://hdl.handle.net/11449/176303
10.1016/j.virusres.2018.04.019
2-s2.0-85046763848
2-s2.0-85046763848.pdf
0713984768583869
url http://dx.doi.org/10.1016/j.virusres.2018.04.019
http://hdl.handle.net/11449/176303
identifier_str_mv Virus Research, v. 251, p. 22-33.
1872-7492
0168-1702
10.1016/j.virusres.2018.04.019
2-s2.0-85046763848
2-s2.0-85046763848.pdf
0713984768583869
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Virus Research
1,147
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 22-33
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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