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
Hauptverfasser: Peterson, R.R. (University of Washington, Seattle, WA.), Deeb, B.J, DiGiacomo, R.F
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container_issue 1
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creator Peterson, R.R. (University of Washington, Seattle, WA.)
Deeb, B.J
DiGiacomo, R.F
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
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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. 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source American Society for Microbiology; MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central
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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