The extradomain a of fibronectin enhances the efficacy of lipopolysaccharide defective Salmonella bacterins as vaccines in mice
2012
San Román Aberasturi, Beatriz | Lasa Uzcudun, Íñigo | Andrés Cara, Damián de | Amorena Zabalza, Beatriz | Lasarte, Juan José | Grilló Dolset, María Jesús | Garrido González, Victoria | Muñoz Álvaro, Pilar María | Arribillaga, Laura | García Martínez, Begoña | Andrés, Ximena de | Zabaleta Sanz de Acedo, Virginia | Mansilla, Cristina | Farrán Blanch, Inmaculada | IdAB. Instituto de Agrobiotecnología / Agrobioteknologiako Institutua | Gobierno de Navarra / Nafarroako Gobernua: IIM10865.RI1-EP12 | Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
The Extradomain A from fibronectin (EDA) has an immunomodulatory role as fusion protein with viral and tumor antigens, but its effect when administered with bacteria has not been assessed. Here, we investigated the adjuvant effect of EDA in mice immunizations against Salmonella enterica subspecies enterica serovar Enteritidis (Salmonella Enteritidis). Since lipopolysaccharide (LPS) is a major virulence factor and the LPS O-polysaccharide (O-PS) is the immunodominant antigen in serological diagnostic tests, Salmonella mutants lacking O-PS (rough mutants) represent an interesting approach for developing new vaccines and diagnostic tests to differentiate infected and vaccinated animals (DIVA tests). Here, antigenic preparations (hot-saline extracts and formalin-inactivated bacterins) from two Salmonella Enteritidis rough mutants, carrying either intact (SE Delta waaL) or deep-defective (SE Delta gal) LPS-Core, were used in combination with EDA. Biotinylated bacterins, in particular SE Delta waaL bacterin, decorated with EDAvidin (EDA and streptavidin fusion protein) improved the protection conferred by hot-saline or bacterins alone and prevented significantly the virulent infection at least to the levels of live attenuated rough mutants. These findings demonstrate the adjuvant effect of EDAvidin when administered with biotinylated bacterins from Salmonella Enteritidis lacking O-PS and the usefulness of BEDA-SE Delta waaL as non-live vaccine in the mouse model.
显示更多 [+] 显示较少 [-]This work was funded by Gobierno de Navarra and European Union (project EuroInnova-Navarra reference IIM10865.RI1-EP12). B.S.R., P.M.M. and X.D.A. post-doctoral contracts were granted by Gobierno de Navarra/JAE-doc CSIC, MICINN (Subprograma Juan de la Cierva) and Universidad Pública de Navarra, respectively.
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