Development and Evaluation of Epitope-Blocking ELISA for Detection of Antibodies against Contagious Caprine Pleuropneumonia in Goat Sera

Enzyme linked immunosorbent assays (ELISAs) have been developed for the detection of antibodies against contagious caprine pleuropneumonia (CCPP), the causative agent of which is <i>Mycoplasma capricolum</i> subsp. <i>Capripneumoniae</i> (Mccp). The currently available commer...

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Main Authors: Baziki Jean de Dieu, Bodjo S. Charles, Nick Nwankpa, Ethel Chitsungo, Cisse Rahamatou Moustapha Boukary, Naomi Maina, Takele A. Tefera, Rume Veronica Nwankpa, Nduta Mwangi, Yao Mathurin Koffi
Format: Article
Language:English
Published: MDPI AG 2019-10-01
Series:Veterinary Sciences
Subjects:
Online Access:https://www.mdpi.com/2306-7381/6/4/82
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spelling doaj-61c1890db3e54401965b4115d1c607ce2021-04-02T15:06:26ZengMDPI AGVeterinary Sciences2306-73812019-10-01648210.3390/vetsci6040082vetsci6040082Development and Evaluation of Epitope-Blocking ELISA for Detection of Antibodies against Contagious Caprine Pleuropneumonia in Goat SeraBaziki Jean de Dieu0Bodjo S. Charles1Nick Nwankpa2Ethel Chitsungo3Cisse Rahamatou Moustapha Boukary4Naomi Maina5Takele A. Tefera6Rume Veronica Nwankpa7Nduta Mwangi8Yao Mathurin Koffi9African Union-Pan African Veterinary Vaccine Centre (AU-PANVAC), P.O. Box 1746, Debrezeit, EthiopiaAfrican Union-Pan African Veterinary Vaccine Centre (AU-PANVAC), P.O. Box 1746, Debrezeit, EthiopiaAfrican Union-Pan African Veterinary Vaccine Centre (AU-PANVAC), P.O. Box 1746, Debrezeit, EthiopiaAfrican Union-Pan African Veterinary Vaccine Centre (AU-PANVAC), P.O. Box 1746, Debrezeit, EthiopiaAfrican Union-Pan African Veterinary Vaccine Centre (AU-PANVAC), P.O. Box 1746, Debrezeit, EthiopiaMolecular Biology and Biotechnology Department, Pan African University Institute for Basic Sciences, Technology and Innovation (PAUSTI), JKUAT Main Campus, P.O. Box 62000-00200, Nairobi, KenyaResearch and Development Department, National Veterinary Institute, P.O. Box 19, Debrezeit, EthiopiaDepartment of Microbial Cellular and Molecular Biology, Addis Ababa University, P.O. Box 1176, EthiopiaFoot and Mouth Disease Department, Kenya Veterinary Vaccines Production Institute (KEVEVAPI), P.O. Box 53260-00200, Nairobi, KenyaLaboratoire Central Veterinaire, Laboratoire de Virologie, B.P. 206 Bingerville, Côte d’IvoireEnzyme linked immunosorbent assays (ELISAs) have been developed for the detection of antibodies against contagious caprine pleuropneumonia (CCPP), the causative agent of which is <i>Mycoplasma capricolum</i> subsp. <i>Capripneumoniae</i> (Mccp). The currently available commercial CCPP competitive ELISA (CCPP cELISA) kit produced and supplied by IDEXX Company (Westbrook, Maine, United States) is relatively expensive for most African laboratories. To address this issue and provide a variety of choices, a sensitive and specific blocking-ELISA (b-ELISA) test to detect antibodies against CCPP was developed. We describe the newly developed CCPP blocking-ELISA based on the blocking of an epitope of a monoclonal antibody (Mccp-25) by a positive serum sample against the Mccp protein coated on a plate. The Percentage Inhibition (PI) cut-off value for the CCPP b-ELISA was set at 50 using 466 CCPP negative and 84 CCPP positive small ruminant sera. Of the negative sera, 307 were obtained from the Botswana National Veterinary Laboratory (BNVL) and 159 from the Friedrich-Loeffler-Institute (FLI) Germany. The 84 positive sera samples came from experimentally vaccinated goats at the AU-PANVAC facility in Debre-Zeit, Ethiopia. The relative diagnostic sensitivity and specificity of the CCPP b-ELISA was 93% and 88%, respectively. This test result indicated good correlation with that of the commercial CCPP cELISA by IDEXX Company (Westbrook, Maine, United States) with a Cohen&#8217;s &#954; agreement of &#954; agreement of 0.85. The newly developed CCPP b-ELISA will be useful in the detection of antibodies for the diagnosis CCPP and for sero-surveillance during vaccination campaigns.https://www.mdpi.com/2306-7381/6/4/82blocking-elisacut-off valuemonoclonal antibodysensitivity and specificity
collection DOAJ
language English
format Article
sources DOAJ
author Baziki Jean de Dieu
Bodjo S. Charles
Nick Nwankpa
Ethel Chitsungo
Cisse Rahamatou Moustapha Boukary
Naomi Maina
Takele A. Tefera
Rume Veronica Nwankpa
Nduta Mwangi
Yao Mathurin Koffi
spellingShingle Baziki Jean de Dieu
Bodjo S. Charles
Nick Nwankpa
Ethel Chitsungo
Cisse Rahamatou Moustapha Boukary
Naomi Maina
Takele A. Tefera
Rume Veronica Nwankpa
Nduta Mwangi
Yao Mathurin Koffi
Development and Evaluation of Epitope-Blocking ELISA for Detection of Antibodies against Contagious Caprine Pleuropneumonia in Goat Sera
Veterinary Sciences
blocking-elisa
cut-off value
monoclonal antibody
sensitivity and specificity
author_facet Baziki Jean de Dieu
Bodjo S. Charles
Nick Nwankpa
Ethel Chitsungo
Cisse Rahamatou Moustapha Boukary
Naomi Maina
Takele A. Tefera
Rume Veronica Nwankpa
Nduta Mwangi
Yao Mathurin Koffi
author_sort Baziki Jean de Dieu
title Development and Evaluation of Epitope-Blocking ELISA for Detection of Antibodies against Contagious Caprine Pleuropneumonia in Goat Sera
title_short Development and Evaluation of Epitope-Blocking ELISA for Detection of Antibodies against Contagious Caprine Pleuropneumonia in Goat Sera
title_full Development and Evaluation of Epitope-Blocking ELISA for Detection of Antibodies against Contagious Caprine Pleuropneumonia in Goat Sera
title_fullStr Development and Evaluation of Epitope-Blocking ELISA for Detection of Antibodies against Contagious Caprine Pleuropneumonia in Goat Sera
title_full_unstemmed Development and Evaluation of Epitope-Blocking ELISA for Detection of Antibodies against Contagious Caprine Pleuropneumonia in Goat Sera
title_sort development and evaluation of epitope-blocking elisa for detection of antibodies against contagious caprine pleuropneumonia in goat sera
publisher MDPI AG
series Veterinary Sciences
issn 2306-7381
publishDate 2019-10-01
description Enzyme linked immunosorbent assays (ELISAs) have been developed for the detection of antibodies against contagious caprine pleuropneumonia (CCPP), the causative agent of which is <i>Mycoplasma capricolum</i> subsp. <i>Capripneumoniae</i> (Mccp). The currently available commercial CCPP competitive ELISA (CCPP cELISA) kit produced and supplied by IDEXX Company (Westbrook, Maine, United States) is relatively expensive for most African laboratories. To address this issue and provide a variety of choices, a sensitive and specific blocking-ELISA (b-ELISA) test to detect antibodies against CCPP was developed. We describe the newly developed CCPP blocking-ELISA based on the blocking of an epitope of a monoclonal antibody (Mccp-25) by a positive serum sample against the Mccp protein coated on a plate. The Percentage Inhibition (PI) cut-off value for the CCPP b-ELISA was set at 50 using 466 CCPP negative and 84 CCPP positive small ruminant sera. Of the negative sera, 307 were obtained from the Botswana National Veterinary Laboratory (BNVL) and 159 from the Friedrich-Loeffler-Institute (FLI) Germany. The 84 positive sera samples came from experimentally vaccinated goats at the AU-PANVAC facility in Debre-Zeit, Ethiopia. The relative diagnostic sensitivity and specificity of the CCPP b-ELISA was 93% and 88%, respectively. This test result indicated good correlation with that of the commercial CCPP cELISA by IDEXX Company (Westbrook, Maine, United States) with a Cohen&#8217;s &#954; agreement of &#954; agreement of 0.85. The newly developed CCPP b-ELISA will be useful in the detection of antibodies for the diagnosis CCPP and for sero-surveillance during vaccination campaigns.
topic blocking-elisa
cut-off value
monoclonal antibody
sensitivity and specificity
url https://www.mdpi.com/2306-7381/6/4/82
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