Genetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2

Detalhes bibliográficos
Autor(a) principal: Soares, Rodrigo M.
Data de Publicação: 2003
Outros Autores: Cortez, Adriana, Heinemann, Marcos B., Sakamoto, Sidnei Myioshi [UNIFESP], Martins, Vanderlei G., Bacci, Mauricio, Fernandes, Flora Maria de Campos, Richtzenhain, Leonardo J.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1099/vir.0.19011-0
http://repositorio.unifesp.br/handle/11600/27261
Resumo: The 3'-terminal 853 nt (and the putative 283 aa) sequence of the VP2-encoding gene from 29 field strains of porcine parvovirus (PPV) were determined and compared both to each other and with other published sequences. Sequences were examined using maximum-parsimony and statistical analyses for nucleotide diversity and sequence variability. Among the nucleotide sequences of the PPV field strains, 26 polymorphic sites were encountered; 22 polymorphic sites were detected in the putative amino acid sequence. Mapping polymorphic sites of protein data onto the three-dimensional (3D) structure of PPV VP2 revealed that almost all substitutions were located on the external surface of the viral capsid. Mapping amino acid substitutions to the alignment between PPV VP2 sequences and the 3D structure of canine parvovirus (CPV) capsid, many PPV substitutions were observed to map to regions of recognized antigenicity and/or to contain phenotypically important residues for CPV and other parvoviruses. in spite of the high sequence similarity, genetic analysis has shown the existence of at least two virus lineages among the samples. in conclusion, these results highlight the need for close surveillance on PPV genetic drift, with an assessment of its potential ability to modify the antigenic make-up of the virus.
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spelling Genetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2The 3'-terminal 853 nt (and the putative 283 aa) sequence of the VP2-encoding gene from 29 field strains of porcine parvovirus (PPV) were determined and compared both to each other and with other published sequences. Sequences were examined using maximum-parsimony and statistical analyses for nucleotide diversity and sequence variability. Among the nucleotide sequences of the PPV field strains, 26 polymorphic sites were encountered; 22 polymorphic sites were detected in the putative amino acid sequence. Mapping polymorphic sites of protein data onto the three-dimensional (3D) structure of PPV VP2 revealed that almost all substitutions were located on the external surface of the viral capsid. Mapping amino acid substitutions to the alignment between PPV VP2 sequences and the 3D structure of canine parvovirus (CPV) capsid, many PPV substitutions were observed to map to regions of recognized antigenicity and/or to contain phenotypically important residues for CPV and other parvoviruses. in spite of the high sequence similarity, genetic analysis has shown the existence of at least two virus lineages among the samples. in conclusion, these results highlight the need for close surveillance on PPV genetic drift, with an assessment of its potential ability to modify the antigenic make-up of the virus.Univ São Paulo, Fac Med Vet & Zootecn, Dept Med Vet Prevent & Saude Anim, BR-05508900 São Paulo, BrazilUniv Brasilia, Fac Agron & Med Vet, Brasilia, DF, BrazilUniversidade Federal de São Paulo, Inst Ciencias Biomed, Dept Microbiol Imunol & Parasitol, São Paulo, BrazilUniv Estadual Paulista, Inst Biociencias, Dept Bioquim, Ctr Estudos Insetos Sociais, Rio Claro, SP, BrazilUniv São Paulo, Inst Biociencias, Lab Ictiogenet, BR-05508 São Paulo, BrazilUniversidade Federal de São Paulo, Inst Ciencias Biomed, Dept Microbiol Imunol & Parasitol, São Paulo, BrazilWeb of ScienceSoc General MicrobiologyUniversidade de São Paulo (USP)Universidade de Brasília (UnB)Universidade Federal de São Paulo (UNIFESP)Univ Estadual PaulistaSoares, Rodrigo M.Cortez, AdrianaHeinemann, Marcos B.Sakamoto, Sidnei Myioshi [UNIFESP]Martins, Vanderlei G.Bacci, MauricioFernandes, Flora Maria de CamposRichtzenhain, Leonardo J.2016-01-24T12:33:51Z2016-01-24T12:33:51Z2003-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1505-1515http://dx.doi.org/10.1099/vir.0.19011-0Journal of General Virology. Reading: Soc General Microbiology, v. 84, p. 1505-1515, 2003.10.1099/vir.0.19011-00022-1317http://repositorio.unifesp.br/handle/11600/27261WOS:000183372300019engJournal of General Virologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T10:33:51Zoai:repositorio.unifesp.br/:11600/27261Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652016-01-24T10:33:51Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Genetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2
title Genetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2
spellingShingle Genetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2
Soares, Rodrigo M.
title_short Genetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2
title_full Genetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2
title_fullStr Genetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2
title_full_unstemmed Genetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2
title_sort Genetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2
author Soares, Rodrigo M.
author_facet Soares, Rodrigo M.
Cortez, Adriana
Heinemann, Marcos B.
Sakamoto, Sidnei Myioshi [UNIFESP]
Martins, Vanderlei G.
Bacci, Mauricio
Fernandes, Flora Maria de Campos
Richtzenhain, Leonardo J.
author_role author
author2 Cortez, Adriana
Heinemann, Marcos B.
Sakamoto, Sidnei Myioshi [UNIFESP]
Martins, Vanderlei G.
Bacci, Mauricio
Fernandes, Flora Maria de Campos
Richtzenhain, Leonardo J.
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade de Brasília (UnB)
Universidade Federal de São Paulo (UNIFESP)
Univ Estadual Paulista
dc.contributor.author.fl_str_mv Soares, Rodrigo M.
Cortez, Adriana
Heinemann, Marcos B.
Sakamoto, Sidnei Myioshi [UNIFESP]
Martins, Vanderlei G.
Bacci, Mauricio
Fernandes, Flora Maria de Campos
Richtzenhain, Leonardo J.
description The 3'-terminal 853 nt (and the putative 283 aa) sequence of the VP2-encoding gene from 29 field strains of porcine parvovirus (PPV) were determined and compared both to each other and with other published sequences. Sequences were examined using maximum-parsimony and statistical analyses for nucleotide diversity and sequence variability. Among the nucleotide sequences of the PPV field strains, 26 polymorphic sites were encountered; 22 polymorphic sites were detected in the putative amino acid sequence. Mapping polymorphic sites of protein data onto the three-dimensional (3D) structure of PPV VP2 revealed that almost all substitutions were located on the external surface of the viral capsid. Mapping amino acid substitutions to the alignment between PPV VP2 sequences and the 3D structure of canine parvovirus (CPV) capsid, many PPV substitutions were observed to map to regions of recognized antigenicity and/or to contain phenotypically important residues for CPV and other parvoviruses. in spite of the high sequence similarity, genetic analysis has shown the existence of at least two virus lineages among the samples. in conclusion, these results highlight the need for close surveillance on PPV genetic drift, with an assessment of its potential ability to modify the antigenic make-up of the virus.
publishDate 2003
dc.date.none.fl_str_mv 2003-06-01
2016-01-24T12:33:51Z
2016-01-24T12:33:51Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1099/vir.0.19011-0
Journal of General Virology. Reading: Soc General Microbiology, v. 84, p. 1505-1515, 2003.
10.1099/vir.0.19011-0
0022-1317
http://repositorio.unifesp.br/handle/11600/27261
WOS:000183372300019
url http://dx.doi.org/10.1099/vir.0.19011-0
http://repositorio.unifesp.br/handle/11600/27261
identifier_str_mv Journal of General Virology. Reading: Soc General Microbiology, v. 84, p. 1505-1515, 2003.
10.1099/vir.0.19011-0
0022-1317
WOS:000183372300019
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of General Virology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1505-1515
dc.publisher.none.fl_str_mv Soc General Microbiology
publisher.none.fl_str_mv Soc General Microbiology
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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