Immunogenicity and Reactivity of Novel Mycobacterium avium subsp. paratuberculosis PPE MAP1152 and Conserved MAP1156 Proteins with Sera from Experimentally and Naturally Infected Animals

Authors

John Bannantine, USDA-ARSFollow
Avery L. Paulson, University of Nebraska - LincolnFollow
Ofelia Chacon, University of Nebraska - Lincoln
Robert J. Fenton, University of Nebraska - LincolnFollow
Denise Zinniel, University of Nebraska-LincolnFollow
David S. McVey, University of Nebraska - Lincoln
David R. Smith, University of Nebraska at LincolnFollow
Charles J. Czuprynski, University of Wisconsin-Madison
Raúl G. Barletta, University of Nebraska-LincolnFollow

Date of this Version

2010

Citation

CLINICAL AND VACCINE IMMUNOLOGY, Jan. 2011, p. 105–112

doi:10.1128/CVI.00297-10

Comments

2011, American Society for Microbiology.

Abstract

Mycobacterium avium subsp. paratuberculosis causes Johne’s disease (JD) in ruminants. Development of genetic tools and completion of the M. avium subsp. paratuberculosis genome sequencing project have expanded the opportunities for antigen discovery. In this study, we determined the seroreactivities of two proteins encoded at the 5􏰋 and 3􏰋 regions of the MAP1152-MAP1156 gene cluster. MAP1152 encodes a PPE protein, and MAP1156 encodes a diacylglycerol acyltransferase involved in triglyceride metabolism and classified in the uncharacterized protein family UPF0089. Recombinant MAP proteins were overproduced and purified from Escherichia coli as maltose-binding protein (MBP) fusions. Immunoblotting analysis indicated that both MAP1152 and MAP1156 displayed reactivity against sera of mice and rabbits immunized with live M. avium subsp. paratuberculosis cells and against samples from naturally infected cattle. In immunoblot assays, MAP1156 yielded a stronger positive signal than MAP1152 against sera from cattle with JD. An enzyme-linked immunosorbent assay for the recombinant proteins was developed and used to test preclassified positive and negative serum samples from naturally infected and noninfected cattle. Samples, with one exception, displayed no seroreactivity against the MBP-LacZ fusion protein (P > 0.05), the negative-control antigen. MAP1152 displayed seroreactivity against all positive sera but no seroreactivity to the negative sera (P < 0.01). MAP1156 displayed stronger and more variable reactivity than MAP1152, but significant differences were observed between noninfected and infected cattle (P < 0.05). Otherwise, degrees of reactivity followed the same trend as the positive reference antigen. In conclusion, both proteins are immunogenic in mice and rabbits, and M. avium subsp. paratuberculosis-infected cattle mount a humoral response to both MAP1152 and MAP1156 cross- reactive epitopes. These findings have potential applications to diagnostics, vaccine production, and elucida- tion of the immunopathogenesis of JD.