Genetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2
Autor(a) principal: | |
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Data de Publicação: | 2003 |
Outros Autores: | , , , , , , |
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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Repositório Institucional da UNIFESP |
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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 |
_version_ |
1814268402235080704 |