Background: The diagnosis of brucellosis by serological tests is based on antigen suspensions derived from smooth lipopolysaccharide extracts, which can give false-positive results linked to cross-reactivity with other Gram-negative microorganisms, especially Yersinia enterocolitica O:9 and Escherichia coli O157:H7. Objective: The objective of the present study was the characterization by proteomic analysis of specific immunogenic proteins not associated with smooth lipopolysaccharide to improve the diagnostic tests used in the ovine brucellosis eradication programs. Methods: The serum from a sheep positive to Brucella melitensis was treated to eliminate all antibodies against such lipopolysaccharides and highlight the reaction towards the immunoreactive proteins in western blotting. Results: The immunoreactive bands were identified by nLC-MS/MS, and through bioinformatics tools, it was possible to select 12 potential candidates as protein antigens specific for Brucella melitensis. Conclusion: The detection of new antigens not subjected to cross-reactivity with other Gram-negative microorganisms can offer additional tools for the serological diagnosis of such diseases.

Identification of immunogenic candidate for new serological tests for Brucella melitensis by a proteomic approach.

Visciano P.;D'Onofrio F.;Schirone M.
;
Luciani M.
2021-01-01

Abstract

Background: The diagnosis of brucellosis by serological tests is based on antigen suspensions derived from smooth lipopolysaccharide extracts, which can give false-positive results linked to cross-reactivity with other Gram-negative microorganisms, especially Yersinia enterocolitica O:9 and Escherichia coli O157:H7. Objective: The objective of the present study was the characterization by proteomic analysis of specific immunogenic proteins not associated with smooth lipopolysaccharide to improve the diagnostic tests used in the ovine brucellosis eradication programs. Methods: The serum from a sheep positive to Brucella melitensis was treated to eliminate all antibodies against such lipopolysaccharides and highlight the reaction towards the immunoreactive proteins in western blotting. Results: The immunoreactive bands were identified by nLC-MS/MS, and through bioinformatics tools, it was possible to select 12 potential candidates as protein antigens specific for Brucella melitensis. Conclusion: The detection of new antigens not subjected to cross-reactivity with other Gram-negative microorganisms can offer additional tools for the serological diagnosis of such diseases.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11575/115354
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