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Identification of Novel Seroreactive Antigens in Johne's Disease Cattle by Using the Mycobacterium tuberculosis Protein Array.
Bannantine, John P; Campo, Joseph J; Li, Lingling; Randall, Arlo; Pablo, Jozelyn; Praul, Craig A; Raygoza Garay, Juan Antonio; Stabel, Judith R; Kapur, Vivek.
Afiliación
  • Bannantine JP; U.S. Department of Agriculture, Agricultural Research Service, National Animal Disease Center, Ames, Iowa, USA john.bannantine@ars.usda.gov vkapur@psu.edu.
  • Campo JJ; Antigen Discovery, Inc., Irvine, California, USA.
  • Li L; Pennsylvania State University, University Park, Pennsylvania, USA.
  • Randall A; Antigen Discovery, Inc., Irvine, California, USA.
  • Pablo J; Antigen Discovery, Inc., Irvine, California, USA.
  • Praul CA; Pennsylvania State University, University Park, Pennsylvania, USA.
  • Raygoza Garay JA; Pennsylvania State University, University Park, Pennsylvania, USA.
  • Stabel JR; U.S. Department of Agriculture, Agricultural Research Service, National Animal Disease Center, Ames, Iowa, USA.
  • Kapur V; Pennsylvania State University, University Park, Pennsylvania, USA john.bannantine@ars.usda.gov vkapur@psu.edu.
Clin Vaccine Immunol ; 24(7)2017 Jul.
Article en En | MEDLINE | ID: mdl-28515134
ABSTRACT
Johne's disease, a chronic gastrointestinal inflammatory disease caused by Mycobacterium avium subspecies paratuberculosis, is endemic in dairy cattle and other ruminants worldwide and remains a challenge to diagnose using traditional serological methods. Given the close phylogenetic relationship between M. avium subsp. paratuberculosis and the human pathogen Mycobacterium tuberculosis, here, we applied a whole-proteome M. tuberculosis protein array to identify seroreactive and diagnostic M. avium subsp. paratuberculosis antigens. A genome-scale pairwise analysis of amino acid identity levels between orthologous proteins in M. avium subsp. paratuberculosis and M. tuberculosis showed an average of 62% identity, with more than half the orthologous proteins sharing >75% identity. Analysis of the M. tuberculosis protein array probed with sera from M. avium subsp. paratuberculosis-infected cattle showed antibody binding to 729 M. tuberculosis proteins, with 58% of them having ≥70% identity to M. avium subsp. paratuberculosis orthologs. The results showed that only 4 of the top 40 seroreactive M. tuberculosis antigens were orthologs of previously reported M. avium subsp. paratuberculosis antigens, revealing the existence of a large number of previously unrecognized candidate diagnostic antigens. Enzyme-linked immunosorbent assay (ELISA) testing of 20 M. avium subsp. paratuberculosis recombinant proteins, representing reactive and nonreactive M. tuberculosis orthologs, further confirmed that the M. tuberculosis array has utility as a screening tool for identifying candidate antigens for Johne's disease diagnostics. Additional ELISA testing of field serum samples collected from dairy herds around the United States revealed that MAP2942c had the strongest seroreactivity with Johne's disease-positive samples. Collectively, our studies have considerably expanded the number of candidate M. avium subsp. paratuberculosis proteins with potential utility in the next generation of rationally designed Johne's disease diagnostic assays.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Paratuberculosis / Mycobacterium avium subsp. paratuberculosis / Anticuerpos Antibacterianos / Antígenos Bacterianos Tipo de estudio: Diagnostic_studies País/Región como asunto: America do norte Idioma: En Revista: Clin Vaccine Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2017 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Paratuberculosis / Mycobacterium avium subsp. paratuberculosis / Anticuerpos Antibacterianos / Antígenos Bacterianos Tipo de estudio: Diagnostic_studies País/Región como asunto: America do norte Idioma: En Revista: Clin Vaccine Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2017 Tipo del documento: Article