John P Bannantine, Joseph J Campo, Lingling Li, Arlo Randall, Jozelyn Pablo, Craig A Praul, Juan Antonio Raygoza Garay, Judith R Stabel, Vivek Kapur
{"title":"应用结核分枝杆菌蛋白阵列技术鉴定牛约翰氏病血清反应性抗原。","authors":"John P Bannantine, Joseph J Campo, Lingling Li, Arlo Randall, Jozelyn Pablo, Craig A Praul, Juan Antonio Raygoza Garay, Judith R Stabel, Vivek Kapur","doi":"10.1128/CVI.00081-17","DOIUrl":null,"url":null,"abstract":"<p><p>Johne's disease, a chronic gastrointestinal inflammatory disease caused by <i>Mycobacterium avium</i> subspecies <i>paratuberculosis</i>, 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 <i>M. avium</i> subsp. <i>paratuberculosis</i> and the human pathogen <i>Mycobacterium tuberculosis</i>, here, we applied a whole-proteome <i>M. tuberculosis</i> protein array to identify seroreactive and diagnostic <i>M. avium</i> subsp. <i>paratuberculosis</i> antigens. A genome-scale pairwise analysis of amino acid identity levels between orthologous proteins in <i>M. avium</i> subsp. <i>paratuberculosis</i> and <i>M. tuberculosis</i> showed an average of 62% identity, with more than half the orthologous proteins sharing >75% identity. Analysis of the <i>M. tuberculosis</i> protein array probed with sera from <i>M. avium</i> subsp. <i>paratuberculosis</i>-infected cattle showed antibody binding to 729 <i>M. tuberculosis</i> proteins, with 58% of them having ≥70% identity to <i>M. avium</i> subsp. <i>paratuberculosis</i> orthologs. The results showed that only 4 of the top 40 seroreactive <i>M. tuberculosis</i> antigens were orthologs of previously reported <i>M. avium</i> subsp. <i>paratuberculosis</i> antigens, revealing the existence of a large number of previously unrecognized candidate diagnostic antigens. Enzyme-linked immunosorbent assay (ELISA) testing of 20 <i>M. avium</i> subsp. <i>paratuberculosis</i> recombinant proteins, representing reactive and nonreactive <i>M. tuberculosis</i> orthologs, further confirmed that the <i>M. tuberculosis</i> 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 <i>M. avium</i> subsp. <i>paratuberculosis</i> proteins with potential utility in the next generation of rationally designed Johne's disease diagnostic assays.</p>","PeriodicalId":10271,"journal":{"name":"Clinical and Vaccine Immunology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2017-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1128/CVI.00081-17","citationCount":"9","resultStr":"{\"title\":\"Identification of Novel Seroreactive Antigens in Johne's Disease Cattle by Using the Mycobacterium tuberculosis Protein Array.\",\"authors\":\"John P Bannantine, Joseph J Campo, Lingling Li, Arlo Randall, Jozelyn Pablo, Craig A Praul, Juan Antonio Raygoza Garay, Judith R Stabel, Vivek Kapur\",\"doi\":\"10.1128/CVI.00081-17\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Johne's disease, a chronic gastrointestinal inflammatory disease caused by <i>Mycobacterium avium</i> subspecies <i>paratuberculosis</i>, 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 <i>M. avium</i> subsp. <i>paratuberculosis</i> and the human pathogen <i>Mycobacterium tuberculosis</i>, here, we applied a whole-proteome <i>M. tuberculosis</i> protein array to identify seroreactive and diagnostic <i>M. avium</i> subsp. <i>paratuberculosis</i> antigens. A genome-scale pairwise analysis of amino acid identity levels between orthologous proteins in <i>M. avium</i> subsp. <i>paratuberculosis</i> and <i>M. tuberculosis</i> showed an average of 62% identity, with more than half the orthologous proteins sharing >75% identity. Analysis of the <i>M. tuberculosis</i> protein array probed with sera from <i>M. avium</i> subsp. <i>paratuberculosis</i>-infected cattle showed antibody binding to 729 <i>M. tuberculosis</i> proteins, with 58% of them having ≥70% identity to <i>M. avium</i> subsp. <i>paratuberculosis</i> orthologs. The results showed that only 4 of the top 40 seroreactive <i>M. tuberculosis</i> antigens were orthologs of previously reported <i>M. avium</i> subsp. <i>paratuberculosis</i> antigens, revealing the existence of a large number of previously unrecognized candidate diagnostic antigens. Enzyme-linked immunosorbent assay (ELISA) testing of 20 <i>M. avium</i> subsp. <i>paratuberculosis</i> recombinant proteins, representing reactive and nonreactive <i>M. tuberculosis</i> orthologs, further confirmed that the <i>M. tuberculosis</i> 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. 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Identification of Novel Seroreactive Antigens in Johne's Disease Cattle by Using the Mycobacterium tuberculosis Protein Array.
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.
期刊介绍:
Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.