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

dc.contributor.authorSoares, R. M.
dc.contributor.authorCortez, A.
dc.contributor.authorHeinemann, M. B.
dc.contributor.authorSakamoto, S. M.
dc.contributor.authorMartins, V. G.
dc.contributor.authorBacci, M.
dc.contributor.authorFernandes, FMD
dc.contributor.authorRichtzenhain, L. J.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade de Brasília (UnB)
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:56:07Z
dc.date.available2014-05-20T13:56:07Z
dc.date.issued2003-06-01
dc.description.abstractThe 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.en
dc.description.affiliationUniv São Paulo, Fac Med Vet & Zootecn, Dept Med Vet Prevent & Saúde Anim, BR-05508900 São Paulo, Brazil
dc.description.affiliationUniv Brasilia, Fac Agron & Med Vet, Brasilia, DF, Brazil
dc.description.affiliationUniv Fed São Paulo, Inst Ciências Biomed, Dept Microbiol Imunol & Parasitol, São Paulo, Brazil
dc.description.affiliationUniv Estadual Paulista, Inst Biociencias, Dept Bioquim, Ctr Estudos Insetos Sociais, Rio Claro, SP, Brazil
dc.description.affiliationUniv São Paulo, Inst Biociencias, Lab Ictiogenet, BR-05508 São Paulo, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Inst Biociencias, Dept Bioquim, Ctr Estudos Insetos Sociais, Rio Claro, SP, Brazil
dc.format.extent1505-1515
dc.identifierhttp://dx.doi.org/10.1099/vir.0.19011-0
dc.identifier.citationJournal of General Virology. Reading: Soc General Microbiology, v. 84, p. 1505-1515, 2003.
dc.identifier.doi10.1099/vir.0.19011-0
dc.identifier.issn0022-1317
dc.identifier.urihttp://hdl.handle.net/11449/20077
dc.identifier.wosWOS:000183372300019
dc.language.isoeng
dc.publisherSoc General Microbiology
dc.relation.ispartofJournal of General Virology
dc.relation.ispartofjcr2.514
dc.relation.ispartofsjr1,325
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.titleGenetic variability of porcine parvovirus isolates revealed by analysis of partial sequences of the structural coding gene VP2en
dc.typeArtigo
dcterms.licensehttp://vir.sgmjournals.org/site/misc/ifora.xhtml#req-copyright
dcterms.rightsHolderSoc General Microbiology
dspace.entity.typePublication
unesp.author.orcid0000-0002-5619-1411[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Rio Claropt
unesp.departmentBioquímica e Microbiologia - IBpt

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