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Istituto di scienza dell'alimentazione

Torna all'elenco Contributi in rivista anno 2013

Contributo in rivista

Tipo: Articolo in rivista

Titolo: Non-recombinant display of the B subunit of the heat labile toxin of Escherichia coli on wild type and mutant spores of Bacillus subtilis

Anno di pubblicazione: 2013

Formato: Cartaceo

Autori: Isticato R, Sirec T, Treppiccione L, Maurano F, De Felice M, Rossi M, Ricca E.

Affiliazioni autori: Department of Biology, Federico II University, Naples, Italy Institute of Food Sciences, CNR, Avellino, Italy.

Autori CNR:

  • FRANCESCO MAURANO
  • MAURO ROSSI
  • LUCIA TREPPICCIONE

Lingua: inglese

Abstract: BACKGROUND: Mucosal infections are a major global health problem and it is generally accepted that mucosal vaccination strategies, able to block infection at their entry site, would be preferable with respect to other prevention approaches. However, there are still relatively few mucosal vaccines available, mainly because of the lack of efficient delivery systems and of mucosal adjuvants. Recombinant bacterial spores displaying a heterologous antigen have been shown to induce protective immune responses and, therefore, proposed as a mucosal delivery system. A non-recombinant approach has been recently developed and tested to display antigens and enzymes. RESULTS: We report that the binding subunit of the heat-labile toxin (LTB) of Escherichia coli efficiently adsorbed on the surface of Bacillus subtilis spores. When nasally administered to groups of mice, spore-adsorbed LTB was able to induce a specific immune response with the production of serum IgG, fecal sIgA and of IFN-gamma in spleen and mesenteric lympho nodes (MLN) of the immunized animals. Dot blotting experiments showed that the non-recombinant approach was more efficient than the recombinant system in displaying LTB and that the efficiency of display could be further increased by using mutant spores with an altered surface. In addition, immunofluorescence microscopy experiments showed that only when displayed on the spore surface by the non-recombinant approach LTB was found in its native, pentameric form. CONCLUSION: Our results indicate that non-recombinant spores displaying LTB pentamers can be administered by the nasal route to induce a Th1-biased, specific immune response. Mutant spores with an altered coat are more efficient than wild type spores in adsorbing the antigen, allowing the use of a reduced number of spores in immunization procedures. Efficiency of display, ability to display the native form of the antigen and to induce a specific immune response propose this non-recombinant delivery system as a powerful mucosal vaccine delivery approach.

Lingua abstract: inglese

Pagine da: 98

Rivista:

Microbial cell factories BioMed Central,
Paese di pubblicazione: Regno Unito
Lingua: inglese
ISSN: 1475-2859

Numero volume: 29

Numero fascicolo: 12

Indicizzato da: PubMed [24168229]

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