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Papel das proteínas Yops de Yersinia pseudotuberculosis na ativação dos linfócitos B

dc.contributor.authorMedeiros, Beatriz Maria Machado [UNESP]
dc.contributor.authorSouza, Cleide Dos Santos
dc.contributor.authorHiguti, L. [UNESP]
dc.contributor.authorMaia, Jose Mario Lourenco [UNESP]
dc.contributor.authorSilva, Eloisa Elena Cangiani [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal da Bahia (UFBA)
dc.date.accessioned2014-05-27T11:21:00Z
dc.date.available2014-05-27T11:21:00Z
dc.date.issued2003-12-01
dc.description.abstractThe virulence plasmid common to pathogenic Yersinia species encodes a number of secreted proteins denoted Yops (Yersinia outer proteins). The Yops effectors have been related to a set of biological properties, including resistance to phagocytosis, cytotoxicity and dephosphorilation of host proteins. However, the interaction of Yops with the adaptive immune response is not clear. Yops secreted by Yersinia enterocolitica O:3 provoke policlonal activation of B lymphocyte, when inoculated in mice. In this work, Yops secreted by K pseudotuberculosis were inoculated by intravenous route in SPF Swiss mice, with the purpose of verify the in vivo role of these proteins in the splenic B lymphocyte activation. The kinetics of production of specific and nonspecific immunoglobulins of the different isotypes (IgG, IgA and IgM), was investigated by the technique of ELISPOT The presence of specific anu-Yersinia antibodies in the serum of the inoculated animals was also investigated by ELISA. It was observed a significant increase only in the number of nonspecific IgG-secreting lymphocytes, on the 21 st day after inoculation (a 2.5-fold increase compared to control). The number of lymphocytes secreting other isotypes of Ig was similar to the controls, with exception of IgA, which was 3.1-fold impaired on the 7th day after inoculation. Turning to specific Ig-secreting cells, the response of the animal was very individual. In some inoculated mice, it was detected anu-Yersinia IgG-secreting cells on the 7 th and 14 th days after inoculation and IgM-secreting cells on the 7 th and 28 th days after inoculation. On the other hand, IgG anù-Yersinia antibodies were detected in the sera of all inoculated mice on all days after inoculation, with a peak on the 28 th day; IgM anti- Yersinia were detected only on the 7th day after inoculation. These results demonstrate that it exist a difference in the immunomodulatory capability of Yops secreted by Y. pseudotuberculosis and Y. enterocolitica.en
dc.description.affiliationDepartamento de Ciencias Biologicas Faculdade de Ciencias Farmaceuticas UNESP, 14801-902 - Araraquara - SP
dc.description.affiliationPIBIC/CNPq
dc.description.affiliationFAPESP
dc.description.affiliationUnespDepartamento de Ciencias Biologicas Faculdade de Ciencias Farmaceuticas UNESP, 14801-902 - Araraquara - SP
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.format.extent53-60
dc.identifier.citationRevista de Ciencias Farmaceuticas, v. 24, n. 1, p. 53-60, 2003.
dc.identifier.issn0101-3793
dc.identifier.scopus2-s2.0-4644230891
dc.identifier.urihttp://hdl.handle.net/11449/67571
dc.language.isopor
dc.relation.ispartofRevista de Ciencias Farmaceuticas
dc.rights.accessRightsAcesso restritopt
dc.sourceScopus
dc.subjectExperimental infection
dc.subjectPoliclonal activation
dc.subjectSpecific antibodies
dc.subjectYersinia pseudotuberculosis
dc.subjectYops
dc.subjectantibody
dc.subjectbacterial protein
dc.subjectimmunoglobulin A
dc.subjectimmunoglobulin G
dc.subjectimmunoglobulin M
dc.subjectunclassified drug
dc.subjectyops protein
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectantibody production
dc.subjectantibody specificity
dc.subjectB lymphocyte
dc.subjectB lymphocyte activation
dc.subjectbacterial virulence
dc.subjectcontrolled study
dc.subjectcytotoxicity
dc.subjectdephosphorylation
dc.subjectenzyme linked immunosorbent assay
dc.subjectenzyme linked immunospot assay
dc.subjectimmune response
dc.subjectimmunoglobulin producing cell
dc.subjectimmunoglobulin production
dc.subjectimmunomodulation
dc.subjectin vivo study
dc.subjectmouse
dc.subjectmouse strain
dc.subjectnonhuman
dc.subjectphagocytosis
dc.subjectplasmid
dc.subjectpolyclonal activation
dc.subjectprotein interaction
dc.subjectprotein secretion
dc.subjectspleen cell
dc.subjectYersinia
dc.subjectYersinia enterocolitica
dc.titlePapel das proteínas Yops de Yersinia pseudotuberculosis na ativação dos linfócitos Bpt
dc.title.alternativeRole of Yops of Yersinia pseudotuberculosis in B lymphocyte activationen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublication5004bcab-94af-4939-b980-091ae9d0a19e
relation.isDepartmentOfPublication.latestForDiscovery5004bcab-94af-4939-b980-091ae9d0a19e
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentCiências Biológicas - FCFpt

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