Detection of antibodies to Pasteurella multocida by capture enzyme immunoassay using a monoclonal antibody against P37 antigen
As infection with Pasteurella multocida is common in rabbits, an enzyme immunoassay (EIA) was developed for its detection. A murine immunoglobulin G monoclonal antibody was used to capture a 37-kDa polypeptide of P. multocida serotype A:12 in an EIA to detect antibodies to P. multocida. The 37-kDa a...
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Veröffentlicht in: | Journal of Clinical Microbiology 1997-01, Vol.35 (1), p.208-212 |
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description | As infection with Pasteurella multocida is common in rabbits, an enzyme immunoassay (EIA) was developed for its detection. A murine immunoglobulin G monoclonal antibody was used to capture a 37-kDa polypeptide of P. multocida serotype A:12 in an EIA to detect antibodies to P. multocida. The 37-kDa antigen was selected since it was previously shown to be a major immunogen during P. multocida infection in rabbits. The sensitivity of the P37 EIA, determined with sera from 56 rabbits infected with P. multocida, was 98%. Specificity, evaluated with sera from 62 rabbits from colonies free of P. multocida,was 92%. Titration curves of sera from rabbits immunized with P. multocida serotype A:3 or A:12 coincided, indicating that the P37 EIA was equally efficient in detecting antibodies to the two major serotypes of the organism. Comparison of the P37 EIA with the current serodiagnostic test, a bacterial lysate EIA, revealed relatively good correlation (r = 0.68). However, specificity was greatly improved, as 34% of uninfected rabbits were falsely positive by the lysate EIA whereas only 3% of uninfected rabbits were falsely positive by the P37 EIA. The coefficient of variation for same-day tests was 10%, and that for interday tests was 15%, indicating good reproducibility. The greater sensitivity and specificity of the P37 EIA should significantly enhance diagnostic capability to identify rabbits infected with P. multocida |
doi_str_mv | 10.1128/jcm.35.1.208-212.1997 |
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(University of Washington, Seattle, WA.) ; Deeb, B.J ; DiGiacomo, R.F</creator><creatorcontrib>Peterson, R.R. (University of Washington, Seattle, WA.) ; Deeb, B.J ; DiGiacomo, R.F</creatorcontrib><description>As infection with Pasteurella multocida is common in rabbits, an enzyme immunoassay (EIA) was developed for its detection. A murine immunoglobulin G monoclonal antibody was used to capture a 37-kDa polypeptide of P. multocida serotype A:12 in an EIA to detect antibodies to P. multocida. The 37-kDa antigen was selected since it was previously shown to be a major immunogen during P. multocida infection in rabbits. The sensitivity of the P37 EIA, determined with sera from 56 rabbits infected with P. multocida, was 98%. Specificity, evaluated with sera from 62 rabbits from colonies free of P. multocida,was 92%. Titration curves of sera from rabbits immunized with P. multocida serotype A:3 or A:12 coincided, indicating that the P37 EIA was equally efficient in detecting antibodies to the two major serotypes of the organism. Comparison of the P37 EIA with the current serodiagnostic test, a bacterial lysate EIA, revealed relatively good correlation (r = 0.68). However, specificity was greatly improved, as 34% of uninfected rabbits were falsely positive by the lysate EIA whereas only 3% of uninfected rabbits were falsely positive by the P37 EIA. The coefficient of variation for same-day tests was 10%, and that for interday tests was 15%, indicating good reproducibility. The greater sensitivity and specificity of the P37 EIA should significantly enhance diagnostic capability to identify rabbits infected with P. multocida</description><identifier>ISSN: 0095-1137</identifier><identifier>EISSN: 1098-660X</identifier><identifier>DOI: 10.1128/jcm.35.1.208-212.1997</identifier><identifier>PMID: 8968909</identifier><identifier>CODEN: JCMIDW</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Animal bacterial diseases ; Animals ; Antibodies, Bacterial - immunology ; Antibodies, Monoclonal - immunology ; Antigens, Bacterial - immunology ; Bacterial diseases ; Biological and medical sciences ; Immunoenzyme Techniques ; Infectious diseases ; Medical sciences ; Mice ; Pasteurella Infections - diagnosis ; Pasteurella Infections - immunology ; Pasteurella Infections - microbiology ; PASTEURELLA MULTOCIDA ; Pasteurella multocida - immunology ; Pasteurella multocida - isolation & purification ; Rabbits</subject><ispartof>Journal of Clinical Microbiology, 1997-01, Vol.35 (1), p.208-212</ispartof><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c509t-6a4e91373f5c88991212225747b6e6037c4553489e1cf45a21bd8a3ba0257ae03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC229540/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC229540/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,3176,4010,27900,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2511143$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8968909$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peterson, R.R. (University of Washington, Seattle, WA.)</creatorcontrib><creatorcontrib>Deeb, B.J</creatorcontrib><creatorcontrib>DiGiacomo, R.F</creatorcontrib><title>Detection of antibodies to Pasteurella multocida by capture enzyme immunoassay using a monoclonal antibody against P37 antigen</title><title>Journal of Clinical Microbiology</title><addtitle>J Clin Microbiol</addtitle><description>As infection with Pasteurella multocida is common in rabbits, an enzyme immunoassay (EIA) was developed for its detection. A murine immunoglobulin G monoclonal antibody was used to capture a 37-kDa polypeptide of P. multocida serotype A:12 in an EIA to detect antibodies to P. multocida. The 37-kDa antigen was selected since it was previously shown to be a major immunogen during P. multocida infection in rabbits. The sensitivity of the P37 EIA, determined with sera from 56 rabbits infected with P. multocida, was 98%. Specificity, evaluated with sera from 62 rabbits from colonies free of P. multocida,was 92%. Titration curves of sera from rabbits immunized with P. multocida serotype A:3 or A:12 coincided, indicating that the P37 EIA was equally efficient in detecting antibodies to the two major serotypes of the organism. Comparison of the P37 EIA with the current serodiagnostic test, a bacterial lysate EIA, revealed relatively good correlation (r = 0.68). However, specificity was greatly improved, as 34% of uninfected rabbits were falsely positive by the lysate EIA whereas only 3% of uninfected rabbits were falsely positive by the P37 EIA. The coefficient of variation for same-day tests was 10%, and that for interday tests was 15%, indicating good reproducibility. The greater sensitivity and specificity of the P37 EIA should significantly enhance diagnostic capability to identify rabbits infected with P. multocida</description><subject>Animal bacterial diseases</subject><subject>Animals</subject><subject>Antibodies, Bacterial - immunology</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Antigens, Bacterial - immunology</subject><subject>Bacterial diseases</subject><subject>Biological and medical sciences</subject><subject>Immunoenzyme Techniques</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Pasteurella Infections - diagnosis</subject><subject>Pasteurella Infections - immunology</subject><subject>Pasteurella Infections - microbiology</subject><subject>PASTEURELLA MULTOCIDA</subject><subject>Pasteurella multocida - immunology</subject><subject>Pasteurella multocida - isolation & purification</subject><subject>Rabbits</subject><issn>0095-1137</issn><issn>1098-660X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUuLFDEUhQtRxnb0DwgDWYi7KvOoVJKFCxmfMOCADrgLt9Kp6gxVSZukRtqFv9203TbOylXg3u-c5ORU1QXBDSFUvro1c8N4QxqKZU0JbYhS4kG1IljJuuvwt4fVCmPFa0KYeFw9SekWY9K2nJ9VZ1J1UmG1qn69tdma7IJHYUDgs-vD2tmEckDXkLJdop0mQPMy5WDcGlC_Qwa2ucyR9T93s0VunhcfICXYoSU5P6LCBx_MFDxMf013CEZwPmV0zcSf4Wj90-rRAFOyz47neXXz_t3Xy4_11ecPny7fXNWGY5XrDlqrSgw2cCOlUqTkpZSLVvSd7TATpsRirVSWmKHlQEm_lsB6wAUCi9l59frgu1362a6N9TnCpLfRzRB3OoDT9zfebfQY7jSlird7_cujPobvi01Zzy6Z_c94G5akhRSdoEL-FyRcdoKLroD8AJoYUop2OD2GYL0vWJeCNeOa6FKwLoH1vuCiu_g3yUl1bLTsXxz3kAxMQwRvXDphlBNCWlYwdMA2btz8cNFqSPO9Kwvy_IAMEDSMsbjcfFGCSk4o-w17McTW</recordid><startdate>199701</startdate><enddate>199701</enddate><creator>Peterson, R.R. (University of Washington, Seattle, WA.)</creator><creator>Deeb, B.J</creator><creator>DiGiacomo, R.F</creator><general>American Society for Microbiology</general><scope>FBQ</scope><scope>IQODW</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>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>199701</creationdate><title>Detection of antibodies to Pasteurella multocida by capture enzyme immunoassay using a monoclonal antibody against P37 antigen</title><author>Peterson, R.R. (University of Washington, Seattle, WA.) ; Deeb, B.J ; DiGiacomo, R.F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-6a4e91373f5c88991212225747b6e6037c4553489e1cf45a21bd8a3ba0257ae03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animal bacterial diseases</topic><topic>Animals</topic><topic>Antibodies, Bacterial - immunology</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Antigens, Bacterial - immunology</topic><topic>Bacterial diseases</topic><topic>Biological and medical sciences</topic><topic>Immunoenzyme Techniques</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Pasteurella Infections - diagnosis</topic><topic>Pasteurella Infections - immunology</topic><topic>Pasteurella Infections - microbiology</topic><topic>PASTEURELLA MULTOCIDA</topic><topic>Pasteurella multocida - immunology</topic><topic>Pasteurella multocida - isolation & purification</topic><topic>Rabbits</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peterson, R.R. 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(University of Washington, Seattle, WA.)</au><au>Deeb, B.J</au><au>DiGiacomo, R.F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of antibodies to Pasteurella multocida by capture enzyme immunoassay using a monoclonal antibody against P37 antigen</atitle><jtitle>Journal of Clinical Microbiology</jtitle><addtitle>J Clin Microbiol</addtitle><date>1997-01</date><risdate>1997</risdate><volume>35</volume><issue>1</issue><spage>208</spage><epage>212</epage><pages>208-212</pages><issn>0095-1137</issn><eissn>1098-660X</eissn><coden>JCMIDW</coden><abstract>As infection with Pasteurella multocida is common in rabbits, an enzyme immunoassay (EIA) was developed for its detection. A murine immunoglobulin G monoclonal antibody was used to capture a 37-kDa polypeptide of P. multocida serotype A:12 in an EIA to detect antibodies to P. multocida. The 37-kDa antigen was selected since it was previously shown to be a major immunogen during P. multocida infection in rabbits. The sensitivity of the P37 EIA, determined with sera from 56 rabbits infected with P. multocida, was 98%. Specificity, evaluated with sera from 62 rabbits from colonies free of P. multocida,was 92%. Titration curves of sera from rabbits immunized with P. multocida serotype A:3 or A:12 coincided, indicating that the P37 EIA was equally efficient in detecting antibodies to the two major serotypes of the organism. Comparison of the P37 EIA with the current serodiagnostic test, a bacterial lysate EIA, revealed relatively good correlation (r = 0.68). However, specificity was greatly improved, as 34% of uninfected rabbits were falsely positive by the lysate EIA whereas only 3% of uninfected rabbits were falsely positive by the P37 EIA. The coefficient of variation for same-day tests was 10%, and that for interday tests was 15%, indicating good reproducibility. The greater sensitivity and specificity of the P37 EIA should significantly enhance diagnostic capability to identify rabbits infected with P. multocida</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>8968909</pmid><doi>10.1128/jcm.35.1.208-212.1997</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal bacterial diseases Animals Antibodies, Bacterial - immunology Antibodies, Monoclonal - immunology Antigens, Bacterial - immunology Bacterial diseases Biological and medical sciences Immunoenzyme Techniques Infectious diseases Medical sciences Mice Pasteurella Infections - diagnosis Pasteurella Infections - immunology Pasteurella Infections - microbiology PASTEURELLA MULTOCIDA Pasteurella multocida - immunology Pasteurella multocida - isolation & purification Rabbits |
title | Detection of antibodies to Pasteurella multocida by capture enzyme immunoassay using a monoclonal antibody against P37 antigen |
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