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dc.contributor.authorDe Medeiros, Beatriz Maria Machado-
dc.contributor.authorCangiani, E. E.-
dc.contributor.authorHiguti, L.-
dc.contributor.authorSatomi, L. C.-
dc.contributor.authorSouza, C. D.-
dc.contributor.authorSilva, A. R C-
dc.contributor.authorMaia, J. M L-
dc.contributor.authorFalcão, D. P.-
dc.date.accessioned2014-05-27T11:22:05Z-
dc.date.accessioned2016-10-25T18:23:12Z-
dc.date.available2014-05-27T11:22:05Z-
dc.date.available2016-10-25T18:23:12Z-
dc.date.issued2006-12-01-
dc.identifierhttp://serv-bib.fcfar.unesp.br/seer/index.php/Cien_Farm/article/view/385-
dc.identifier.citationRevista de Ciencias Farmaceuticas Basica e Aplicada, v. 27, n. 3, p. 221-227, 2006.-
dc.identifier.issn1808-4532-
dc.identifier.urihttp://hdl.handle.net/11449/69342-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/69342-
dc.description.abstractIt is known that the invasin molecule of Yersinia pseudotuberculosis stimulates human peripheral B cells in vitro. In this work we evaluated the in vivo role of invasin as polyclonal activator of B lymphocytes in the mouse experimental model, by comparing strains of Y. pseudotuberculosis expressing invasin and isogenic inv mutants. Swiss mice were infected intravenously with two strains expressing invasin (YpIII pIB1 and an isogenic virulence plasmid-cured strain, YpIII) and with two invasin mutant strains (Yp100 pIB1 and Yp100, plasmid-cured). Spleen cells were sampled on days 7, 14, 21 and 28 after infection. Immunoglobulin (Ig)-secreting spleen cells were detected by protein A plaque assay and specific antibodies were detected in sera by ELISA. The virulent strain YPIII pIB1 (wild type) did not provoke polyclonal activation of B lymphocytes in vivo. In general, fewer Ig-secreting spleen cells of all isotypes were found in the infected animals than in the control animals. Specific IgG antibodies were detected in the sera of animals infected with all strains. The peak response occurred on the 21 st day post-infection, and the Yp100 strain provoked the highest level of these antibodies. We concluded that invasin is not a polyclonal activator of murine B cells.en
dc.format.extent221-227-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectB lymphocytes-
dc.subjectInvasin-
dc.subjectPolyclonal activation-
dc.subjectSpecific antibodies-
dc.subjectYersinia pseudotuberculosis-
dc.subjectimmunoglobulin-
dc.subjectinvasin-
dc.subjectprotein A-
dc.subjectanalytic method-
dc.subjectanimal experiment-
dc.subjectB lymphocyte activation-
dc.subjectbacterial strain-
dc.subjectcomparative study-
dc.subjectcontrolled study-
dc.subjectenzyme linked immunosorbent assay-
dc.subjectfemale-
dc.subjectmouse-
dc.subjectnonhuman-
dc.subjectspleen cell-
dc.titleInvasin of Yersinia pseudotuberculosis is not a polyclonal activator of mouse B lymphocytesen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Biological Sciences School of Pharmaceutical Sciences São Paulo State University, UNESP, Araraquara, SP-
dc.description.affiliationDepartamento de Ciências Biológicas Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista, UNESP, Rodovia Araraquara-Jaú, km 1, CEP: 14801-902 - Araraquara - SP-
dc.description.affiliationUnespDepartment of Biological Sciences School of Pharmaceutical Sciences São Paulo State University, UNESP, Araraquara, SP-
dc.description.affiliationUnespDepartamento de Ciências Biológicas Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista, UNESP, Rodovia Araraquara-Jaú, km 1, CEP: 14801-902 - Araraquara - SP-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-34948873791.pdf-
dc.relation.ispartofRevista de Ciências Farmacêuticas Básica e Aplicada-
dc.identifier.scopus2-s2.0-34948873791-
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