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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/5291
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dc.contributor.authorCandresse, Thierry-
dc.contributor.authorLot, Herve-
dc.contributor.authorGerman-Retana, Sylvie-
dc.contributor.authorKrause-Sakate, Renate-
dc.contributor.authorThomas, John-
dc.contributor.authorSouche, Sylvie-
dc.contributor.authorDelaunay, Thierry-
dc.contributor.authorLanneau, Maryvonne-
dc.contributor.authorLe Gall, Olivier-
dc.date.accessioned2014-05-20T13:19:46Z-
dc.date.accessioned2016-10-25T16:41:19Z-
dc.date.available2014-05-20T13:19:46Z-
dc.date.available2016-10-25T16:41:19Z-
dc.date.issued2007-09-01-
dc.identifierhttp://dx.doi.org/10.1099/vir.0.82980-0-
dc.identifier.citationJournal of General Virology. Reading: Soc General Microbiology, v. 88, p. 2605-2610, 2007.-
dc.identifier.issn0022-1317-
dc.identifier.urihttp://hdl.handle.net/11449/5291-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/5291-
dc.description.abstractA panel of 19 monoclonal antibodies (mAbs) was used to study the immunological variability of Lettuce mosaic virus (LMV), a member of the genus Potyvirus, and to perform a first epitope characterization of this virus. Based on their specificity of recognition against a panel of 15 LMV isolates, the mAbs could be clustered in seven reactivity groups. Surface plasmon resonance analysis indicated the presence, on the LMV particles, of at least five independent recognition/ binding regions, correlating with the seven mAbs reactivity groups. The results demonstrate that LMV shows significant serological variability and shed light on the LMV epitope structure. The various mAbs should prove a new and efficient tool for LIVIV diagnostic and field epidemiology studies.en
dc.format.extent2605-2610-
dc.language.isoeng-
dc.publisherSoc General Microbiology-
dc.sourceWeb of Science-
dc.titleAnalysis of the serological variability of Lettuce mosaic virus using monoclonal antibodies and surface plasmon resonance technologyen
dc.typeoutro-
dc.contributor.institutionINRA-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionDept Primary Ind & Fisheries-
dc.description.affiliationINRA, IBVM, UMR GDPP INRA Bordeaux 2, F-33883 Villenave Dornon, France-
dc.description.affiliationINRA, F-84143 Montfavet, France-
dc.description.affiliationUNESP FCA, Dept Producao Vegetal, BR-18603970 Botucatu, SP, Brazil-
dc.description.affiliationDept Primary Ind & Fisheries, Indooroopilly, Qld 4068, Australia-
dc.description.affiliationUnespUNESP FCA, Dept Producao Vegetal, BR-18603970 Botucatu, SP, Brazil-
dc.identifier.doi10.1099/vir.0.82980-0-
dc.identifier.wosWOS:000249226400029-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of General Virology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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