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Development of an improved competitive ELISA based on a monoclonal antibody against lipopolysaccharide for the detection of bovine brucellosis

BACKGROUND: Brucellosis is the most common bacterial zoonosis, and serological tests are routinely used in brucellosis control and eradication programs. In order to improve the accuracy of serological diagnostic method used in bovine brucellosis detection, this study developed an improved competitiv...

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Autores principales: Wang, Xiaolei, Wang, Yan, Ma, Limei, Zhang, Ran, De, Yanyan, Yang, Xiaowen, Wang, Chuanqing, Wu, Qingmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438517/
https://www.ncbi.nlm.nih.gov/pubmed/25993986
http://dx.doi.org/10.1186/s12917-015-0436-3
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author Wang, Xiaolei
Wang, Yan
Ma, Limei
Zhang, Ran
De, Yanyan
Yang, Xiaowen
Wang, Chuanqing
Wu, Qingmin
author_facet Wang, Xiaolei
Wang, Yan
Ma, Limei
Zhang, Ran
De, Yanyan
Yang, Xiaowen
Wang, Chuanqing
Wu, Qingmin
author_sort Wang, Xiaolei
collection PubMed
description BACKGROUND: Brucellosis is the most common bacterial zoonosis, and serological tests are routinely used in brucellosis control and eradication programs. In order to improve the accuracy of serological diagnostic method used in bovine brucellosis detection, this study developed an improved competitive ELISA with higher specificity and good sensitivity. RESULTS: This study prepared 12 monoclonal antibodies against smooth Brucella lipopolysaccharide. One monoclonal antibody 3 F9, presented C epitope specificity, was used to develop a competitive ELISA for the serological detection of bovine brucellosis. The competitive ELISA, a commercial competitive ELISA kit, the rose-bengal plate agglutination test, and a microplate agglutination test were all used in the detection of 6 hyperimmune antisera against other commonly cross-reacted bacterial pathogens and 110 clinical bovine serum samples. The results of the test comparisons indicated that the competitive ELISA had higher specificity than the commercial competitive ELISA kit and RBT, and comparable sensitivity with the commercial ELISA kit. CONCLUSIONS: This study provided a valuable detection tool with high specificity and good sensitivity, which prevent the wrong-culling of bovines in the eradication campaigns of bovine brucellosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12917-015-0436-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-44385172015-05-21 Development of an improved competitive ELISA based on a monoclonal antibody against lipopolysaccharide for the detection of bovine brucellosis Wang, Xiaolei Wang, Yan Ma, Limei Zhang, Ran De, Yanyan Yang, Xiaowen Wang, Chuanqing Wu, Qingmin BMC Vet Res Methodology Article BACKGROUND: Brucellosis is the most common bacterial zoonosis, and serological tests are routinely used in brucellosis control and eradication programs. In order to improve the accuracy of serological diagnostic method used in bovine brucellosis detection, this study developed an improved competitive ELISA with higher specificity and good sensitivity. RESULTS: This study prepared 12 monoclonal antibodies against smooth Brucella lipopolysaccharide. One monoclonal antibody 3 F9, presented C epitope specificity, was used to develop a competitive ELISA for the serological detection of bovine brucellosis. The competitive ELISA, a commercial competitive ELISA kit, the rose-bengal plate agglutination test, and a microplate agglutination test were all used in the detection of 6 hyperimmune antisera against other commonly cross-reacted bacterial pathogens and 110 clinical bovine serum samples. The results of the test comparisons indicated that the competitive ELISA had higher specificity than the commercial competitive ELISA kit and RBT, and comparable sensitivity with the commercial ELISA kit. CONCLUSIONS: This study provided a valuable detection tool with high specificity and good sensitivity, which prevent the wrong-culling of bovines in the eradication campaigns of bovine brucellosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12917-015-0436-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-05-21 /pmc/articles/PMC4438517/ /pubmed/25993986 http://dx.doi.org/10.1186/s12917-015-0436-3 Text en © Wang et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Wang, Xiaolei
Wang, Yan
Ma, Limei
Zhang, Ran
De, Yanyan
Yang, Xiaowen
Wang, Chuanqing
Wu, Qingmin
Development of an improved competitive ELISA based on a monoclonal antibody against lipopolysaccharide for the detection of bovine brucellosis
title Development of an improved competitive ELISA based on a monoclonal antibody against lipopolysaccharide for the detection of bovine brucellosis
title_full Development of an improved competitive ELISA based on a monoclonal antibody against lipopolysaccharide for the detection of bovine brucellosis
title_fullStr Development of an improved competitive ELISA based on a monoclonal antibody against lipopolysaccharide for the detection of bovine brucellosis
title_full_unstemmed Development of an improved competitive ELISA based on a monoclonal antibody against lipopolysaccharide for the detection of bovine brucellosis
title_short Development of an improved competitive ELISA based on a monoclonal antibody against lipopolysaccharide for the detection of bovine brucellosis
title_sort development of an improved competitive elisa based on a monoclonal antibody against lipopolysaccharide for the detection of bovine brucellosis
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438517/
https://www.ncbi.nlm.nih.gov/pubmed/25993986
http://dx.doi.org/10.1186/s12917-015-0436-3
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