Immunogenicity of Proteome-Determined Mycobacterium avium subsp. paratuberculosis-Specific Proteins in Sheep with Paratuberculosis
Mycobacterium avium subsp. paratuberculosis causes paratuberculosis, a chronic granulomatous enteritis. Detecting animals with paratuberculosis infections is difficult because the currently available tools have low sensitivity and lack specificity; these tools are prone to generating spurious positi...
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Veröffentlicht in: | Clinical and Vaccine Immunology 2008-12, Vol.15 (12), p.1824-1833 |
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creator | Hughes, Valerie Bannantine, John P Denham, Susan Smith, Stuart Garcia-Sanchez, Alfredo Sales, Jill Paustian, Michael L Mclean, Kevin Stevenson, Karen |
description | Mycobacterium avium subsp. paratuberculosis causes paratuberculosis, a chronic granulomatous enteritis. Detecting animals with paratuberculosis infections is difficult because the currently available tools have low sensitivity and lack specificity; these tools are prone to generating spurious positive test results caused by exposure to environmental M. avium complex organisms. To generate candidate antigens for incorporation into a specific test for paratuberculosis, subspecies-specific proteins were determined by proteomic comparison of M. avium subsp. paratuberculosis and M. avium subsp. avium. Analysis was aimed at revealing proteins only expressed (or predominant) in the protein profile of M. avium subspecies paratuberculosis. Two-dimensional gel electrophoresis resolved approximately 1,000 protein spots from each subspecies. Proteome analysis identified protein spots whose expression profile appeared markedly increased in M. avium subsp. paratuberculosis, and 32 were identified by analysis of their tryptic peptide profile by matrix-assisted laser desorption ionization-time of flight analysis. Thirty of these proteins were cloned, and their recombinant proteins were expressed. Ovine paratuberculosis sera were used to assess their immunoreactivity by enzyme-linked immunosorbent assay (ELISA), Western blotting, and dot blot analysis. Seventeen proteins were detected in at least one of the immunoassays, and eleven proteins were detected by ELISA with an optical density in excess of the cutoff of 0.1 in four of six sera tested. The immunoreactivity of these proteins indicates their potential as unique diagnostic antigens for the development of a specific serological detection of paratuberculosis. |
doi_str_mv | 10.1128/CVI.00099-08 |
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Detecting animals with paratuberculosis infections is difficult because the currently available tools have low sensitivity and lack specificity; these tools are prone to generating spurious positive test results caused by exposure to environmental M. avium complex organisms. To generate candidate antigens for incorporation into a specific test for paratuberculosis, subspecies-specific proteins were determined by proteomic comparison of M. avium subsp. paratuberculosis and M. avium subsp. avium. Analysis was aimed at revealing proteins only expressed (or predominant) in the protein profile of M. avium subspecies paratuberculosis. Two-dimensional gel electrophoresis resolved approximately 1,000 protein spots from each subspecies. Proteome analysis identified protein spots whose expression profile appeared markedly increased in M. avium subsp. paratuberculosis, and 32 were identified by analysis of their tryptic peptide profile by matrix-assisted laser desorption ionization-time of flight analysis. Thirty of these proteins were cloned, and their recombinant proteins were expressed. Ovine paratuberculosis sera were used to assess their immunoreactivity by enzyme-linked immunosorbent assay (ELISA), Western blotting, and dot blot analysis. Seventeen proteins were detected in at least one of the immunoassays, and eleven proteins were detected by ELISA with an optical density in excess of the cutoff of 0.1 in four of six sera tested. The immunoreactivity of these proteins indicates their potential as unique diagnostic antigens for the development of a specific serological detection of paratuberculosis.</description><identifier>ISSN: 1556-679X</identifier><identifier>ISSN: 1556-6811</identifier><identifier>ISSN: 1098-6588</identifier><identifier>EISSN: 1556-679X</identifier><identifier>DOI: 10.1128/CVI.00099-08</identifier><identifier>PMID: 18845834</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Animals ; Antigens, Bacterial ; Antigens, Bacterial - immunology ; Antigens, Bacterial - isolation & purification ; bacterial antigens ; bacterial enteritis ; bacterial proteins ; Bacterial Proteins - immunology ; Bacterial Proteins - isolation & purification ; diagnosis ; Enzyme-Linked Immunosorbent Assay ; immunology ; isolation & purification ; Microbial Immunology ; microbiology ; Mycobacterium avium subsp. paratuberculosis ; Mycobacterium avium subsp. paratuberculosis - immunology ; paratuberculosis ; Paratuberculosis - diagnosis ; Proteome ; Proteome - immunology ; proteomics ; Recombinant Proteins ; Recombinant Proteins - immunology ; sheep diseases ; Sheep Diseases - diagnosis ; Sheep, Domestic ; Sheep, Domestic - immunology ; Sheep, Domestic - microbiology</subject><ispartof>Clinical and Vaccine Immunology, 2008-12, Vol.15 (12), p.1824-1833</ispartof><rights>Copyright © 2008, American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-31ef4597b49c2f80fe922ebdf895bb5a45a67c07d3e883b226d18940fd3eab913</citedby><cites>FETCH-LOGICAL-c465t-31ef4597b49c2f80fe922ebdf895bb5a45a67c07d3e883b226d18940fd3eab913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2593162/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2593162/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3174,3175,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18845834$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hughes, Valerie</creatorcontrib><creatorcontrib>Bannantine, John P</creatorcontrib><creatorcontrib>Denham, Susan</creatorcontrib><creatorcontrib>Smith, Stuart</creatorcontrib><creatorcontrib>Garcia-Sanchez, Alfredo</creatorcontrib><creatorcontrib>Sales, Jill</creatorcontrib><creatorcontrib>Paustian, Michael L</creatorcontrib><creatorcontrib>Mclean, Kevin</creatorcontrib><creatorcontrib>Stevenson, Karen</creatorcontrib><title>Immunogenicity of Proteome-Determined Mycobacterium avium subsp. paratuberculosis-Specific Proteins in Sheep with Paratuberculosis</title><title>Clinical and Vaccine Immunology</title><addtitle>Clin Vaccine Immunol</addtitle><description>Mycobacterium avium subsp. paratuberculosis causes paratuberculosis, a chronic granulomatous enteritis. Detecting animals with paratuberculosis infections is difficult because the currently available tools have low sensitivity and lack specificity; these tools are prone to generating spurious positive test results caused by exposure to environmental M. avium complex organisms. To generate candidate antigens for incorporation into a specific test for paratuberculosis, subspecies-specific proteins were determined by proteomic comparison of M. avium subsp. paratuberculosis and M. avium subsp. avium. Analysis was aimed at revealing proteins only expressed (or predominant) in the protein profile of M. avium subspecies paratuberculosis. Two-dimensional gel electrophoresis resolved approximately 1,000 protein spots from each subspecies. Proteome analysis identified protein spots whose expression profile appeared markedly increased in M. avium subsp. paratuberculosis, and 32 were identified by analysis of their tryptic peptide profile by matrix-assisted laser desorption ionization-time of flight analysis. Thirty of these proteins were cloned, and their recombinant proteins were expressed. Ovine paratuberculosis sera were used to assess their immunoreactivity by enzyme-linked immunosorbent assay (ELISA), Western blotting, and dot blot analysis. Seventeen proteins were detected in at least one of the immunoassays, and eleven proteins were detected by ELISA with an optical density in excess of the cutoff of 0.1 in four of six sera tested. The immunoreactivity of these proteins indicates their potential as unique diagnostic antigens for the development of a specific serological detection of paratuberculosis.</description><subject>Animals</subject><subject>Antigens, Bacterial</subject><subject>Antigens, Bacterial - immunology</subject><subject>Antigens, Bacterial - isolation & purification</subject><subject>bacterial antigens</subject><subject>bacterial enteritis</subject><subject>bacterial proteins</subject><subject>Bacterial Proteins - immunology</subject><subject>Bacterial Proteins - isolation & purification</subject><subject>diagnosis</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>immunology</subject><subject>isolation & purification</subject><subject>Microbial Immunology</subject><subject>microbiology</subject><subject>Mycobacterium avium subsp. paratuberculosis</subject><subject>Mycobacterium avium subsp. paratuberculosis - immunology</subject><subject>paratuberculosis</subject><subject>Paratuberculosis - diagnosis</subject><subject>Proteome</subject><subject>Proteome - immunology</subject><subject>proteomics</subject><subject>Recombinant Proteins</subject><subject>Recombinant Proteins - immunology</subject><subject>sheep diseases</subject><subject>Sheep Diseases - diagnosis</subject><subject>Sheep, Domestic</subject><subject>Sheep, Domestic - immunology</subject><subject>Sheep, Domestic - microbiology</subject><issn>1556-679X</issn><issn>1556-6811</issn><issn>1098-6588</issn><issn>1556-679X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc-P1CAUxxujcX_ozbM2MfFkR6CUwsXEjKtOssZNxjXeCNDHFNOWCu1u5upfLmMnunrx8t7j8XnfPPhm2ROMVhgT_mr9ZbNCCAlRIH4vO8VVxQpWi6_379Qn2VmM3xCiJeP1w-wEc04rXtLT7Mem7-fB72Bwxk373Nv8KvgJfA_FW5gg9G6AJv-4N14rk85u7nN1c4hx1nFc5aMKapo1BDN3PrpYbEcwzjqzCLkh5m7Ity3AmN-6qc2v_hl4lD2wqovw-JjPs-t3F5_XH4rLT-836zeXhaGsmooSg6WVqDUVhliOLAhCQDeWi0rrStFKsdqguimB81ITwhrMBUU2NZQWuDzPXi-646x7aAwMU1CdHIPrVdhLr5z8-2Zwrdz5G0kqUWJGksCLo0Dw32eIk-xdNNB1agA_R8kEZ2WN8H9ByrAQrKYJfLmAJvgYA9jf22AkD-7K5K785a5EPOFP777gD3y0MwHPF6B1u_bWBZAq9tI0nZO4kpgkkhyoZwtllZdqF1yU11uS9kY4_S-mvPwJlqa59w</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Hughes, Valerie</creator><creator>Bannantine, John P</creator><creator>Denham, Susan</creator><creator>Smith, Stuart</creator><creator>Garcia-Sanchez, Alfredo</creator><creator>Sales, Jill</creator><creator>Paustian, Michael L</creator><creator>Mclean, Kevin</creator><creator>Stevenson, Karen</creator><general>American Society for Microbiology</general><general>American Society for Microbiology (ASM)</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7S9</scope><scope>L.6</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20081201</creationdate><title>Immunogenicity of Proteome-Determined Mycobacterium avium subsp. paratuberculosis-Specific Proteins in Sheep with Paratuberculosis</title><author>Hughes, Valerie ; Bannantine, John P ; Denham, Susan ; Smith, Stuart ; Garcia-Sanchez, Alfredo ; Sales, Jill ; Paustian, Michael L ; Mclean, Kevin ; Stevenson, Karen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-31ef4597b49c2f80fe922ebdf895bb5a45a67c07d3e883b226d18940fd3eab913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Antigens, Bacterial</topic><topic>Antigens, Bacterial - immunology</topic><topic>Antigens, Bacterial - isolation & purification</topic><topic>bacterial antigens</topic><topic>bacterial enteritis</topic><topic>bacterial proteins</topic><topic>Bacterial Proteins - immunology</topic><topic>Bacterial Proteins - isolation & purification</topic><topic>diagnosis</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>immunology</topic><topic>isolation & purification</topic><topic>Microbial Immunology</topic><topic>microbiology</topic><topic>Mycobacterium avium subsp. paratuberculosis</topic><topic>Mycobacterium avium subsp. paratuberculosis - immunology</topic><topic>paratuberculosis</topic><topic>Paratuberculosis - diagnosis</topic><topic>Proteome</topic><topic>Proteome - immunology</topic><topic>proteomics</topic><topic>Recombinant Proteins</topic><topic>Recombinant Proteins - immunology</topic><topic>sheep diseases</topic><topic>Sheep Diseases - diagnosis</topic><topic>Sheep, Domestic</topic><topic>Sheep, Domestic - immunology</topic><topic>Sheep, Domestic - microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hughes, Valerie</creatorcontrib><creatorcontrib>Bannantine, John P</creatorcontrib><creatorcontrib>Denham, Susan</creatorcontrib><creatorcontrib>Smith, Stuart</creatorcontrib><creatorcontrib>Garcia-Sanchez, Alfredo</creatorcontrib><creatorcontrib>Sales, Jill</creatorcontrib><creatorcontrib>Paustian, Michael L</creatorcontrib><creatorcontrib>Mclean, Kevin</creatorcontrib><creatorcontrib>Stevenson, Karen</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical and Vaccine Immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hughes, Valerie</au><au>Bannantine, John P</au><au>Denham, Susan</au><au>Smith, Stuart</au><au>Garcia-Sanchez, Alfredo</au><au>Sales, Jill</au><au>Paustian, Michael L</au><au>Mclean, Kevin</au><au>Stevenson, Karen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunogenicity of Proteome-Determined Mycobacterium avium subsp. paratuberculosis-Specific Proteins in Sheep with Paratuberculosis</atitle><jtitle>Clinical and Vaccine Immunology</jtitle><addtitle>Clin Vaccine Immunol</addtitle><date>2008-12-01</date><risdate>2008</risdate><volume>15</volume><issue>12</issue><spage>1824</spage><epage>1833</epage><pages>1824-1833</pages><issn>1556-679X</issn><issn>1556-6811</issn><issn>1098-6588</issn><eissn>1556-679X</eissn><abstract>Mycobacterium avium subsp. paratuberculosis causes paratuberculosis, a chronic granulomatous enteritis. Detecting animals with paratuberculosis infections is difficult because the currently available tools have low sensitivity and lack specificity; these tools are prone to generating spurious positive test results caused by exposure to environmental M. avium complex organisms. To generate candidate antigens for incorporation into a specific test for paratuberculosis, subspecies-specific proteins were determined by proteomic comparison of M. avium subsp. paratuberculosis and M. avium subsp. avium. Analysis was aimed at revealing proteins only expressed (or predominant) in the protein profile of M. avium subspecies paratuberculosis. Two-dimensional gel electrophoresis resolved approximately 1,000 protein spots from each subspecies. Proteome analysis identified protein spots whose expression profile appeared markedly increased in M. avium subsp. paratuberculosis, and 32 were identified by analysis of their tryptic peptide profile by matrix-assisted laser desorption ionization-time of flight analysis. Thirty of these proteins were cloned, and their recombinant proteins were expressed. Ovine paratuberculosis sera were used to assess their immunoreactivity by enzyme-linked immunosorbent assay (ELISA), Western blotting, and dot blot analysis. Seventeen proteins were detected in at least one of the immunoassays, and eleven proteins were detected by ELISA with an optical density in excess of the cutoff of 0.1 in four of six sera tested. The immunoreactivity of these proteins indicates their potential as unique diagnostic antigens for the development of a specific serological detection of paratuberculosis.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>18845834</pmid><doi>10.1128/CVI.00099-08</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigens, Bacterial Antigens, Bacterial - immunology Antigens, Bacterial - isolation & purification bacterial antigens bacterial enteritis bacterial proteins Bacterial Proteins - immunology Bacterial Proteins - isolation & purification diagnosis Enzyme-Linked Immunosorbent Assay immunology isolation & purification Microbial Immunology microbiology Mycobacterium avium subsp. paratuberculosis Mycobacterium avium subsp. paratuberculosis - immunology paratuberculosis Paratuberculosis - diagnosis Proteome Proteome - immunology proteomics Recombinant Proteins Recombinant Proteins - immunology sheep diseases Sheep Diseases - diagnosis Sheep, Domestic Sheep, Domestic - immunology Sheep, Domestic - microbiology |
title | Immunogenicity of Proteome-Determined Mycobacterium avium subsp. paratuberculosis-Specific Proteins in Sheep with Paratuberculosis |
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