The extradomain a of fibronectin enhances the efficacy of lipopolysaccharide defective Salmonella bacterins as vaccines in mice


Autoria(s): San Román Aberasturi, Beatriz; Lasa Uzcudun, Íñigo; Andrés Cara, Damián de; Amorena Zabalza, Beatriz; Lasarte, Juan José; Grilló Dolset, María Jesús; Garrido, Victoria; Muñoz Álvaro, Pilar María; Arribillaga, Laura; García Martínez, Begoña; Andrés, Ximena de; Zabaleta, Virginia; Mansilla, Cristina; Farrán Blanch, Inmaculada
Contribuinte(s)

IdAB - Instituto de Agrobiotecnología / Agrobioteknologiako Institutua

Gobierno de Navarra / Nafarroako Gobernua: IIM10865.RI1-EP12

Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa

Data(s)

2012

20/06/2014

2012

Resumo

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.

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.

Formato

application/pdf

Identificador

1297-9716 (electronic)

0928-4249 (print)

1277

https://hdl.handle.net/2454/10925

10.1186/1297-9716-43-31

Idioma(s)

eng

Publicador

BioMed Central

Relação

Veterinary Research, 2012, 43:31

https://doi.org/10.1186/1297-9716-43-31

Direitos

© 2012 San Román et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

http://creativecommons.org/licenses/by/2.0

Acceso abierto / Sarbide irekia

info:eu-repo/semantics/openAccess

Palavras-Chave #Biofilm formation #Enteritidis #Veterinary sciences #Mutants #Protein #Infection #Brucella ovis #Extra domain-a #Protective immunity #Enterica serovar typhimurium #Phage-typing scheme
Tipo

Artículo / Artikulua

info:eu-repo/semantics/article

Versión publicada / Argitaratu den bertsioa

info:eu-repo/semantics/publishedVersion