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Development of Colloidal Gold Immunochromatographic Strips for Detection of Riemerella anatipestifer

Riemerella anatipestifer is one of the most important bacterial pathogen of ducks and causes a contagious septicemia. R. anatipestifer infection causes serositis syndromes similar to other bacterial infections in ducks, including infection by Escherichia coli, Salmonella enterica and Pasteurella mul...

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Autores principales: Hou, Wanwan, Wang, Shaohui, Wang, Xiaolan, Han, Xiangan, Fan, Hongjie, Cao, Shoulin, Yue, Jiaping, Wang, Quan, Jiang, Wei, Ding, Chan, Yu, Shengqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378999/
https://www.ncbi.nlm.nih.gov/pubmed/25822983
http://dx.doi.org/10.1371/journal.pone.0122952
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author Hou, Wanwan
Wang, Shaohui
Wang, Xiaolan
Han, Xiangan
Fan, Hongjie
Cao, Shoulin
Yue, Jiaping
Wang, Quan
Jiang, Wei
Ding, Chan
Yu, Shengqing
author_facet Hou, Wanwan
Wang, Shaohui
Wang, Xiaolan
Han, Xiangan
Fan, Hongjie
Cao, Shoulin
Yue, Jiaping
Wang, Quan
Jiang, Wei
Ding, Chan
Yu, Shengqing
author_sort Hou, Wanwan
collection PubMed
description Riemerella anatipestifer is one of the most important bacterial pathogen of ducks and causes a contagious septicemia. R. anatipestifer infection causes serositis syndromes similar to other bacterial infections in ducks, including infection by Escherichia coli, Salmonella enterica and Pasteurella multocida. Clinically differentiating R. anatipestifer infections from other bacterial pathogen infections is usually difficult. In this study, MAb 1G2F10, a monoclonal antibody against R. anatipestifer GroEL, was used to develop a colloidal gold immunochromatographic strip. Colloidal gold particles were prepared by chemical synthesis to an average diameter of 20±5.26 nm by transmission electron microscope imaging. MAb 1G2F10 was conjugated to colloidal gold particles and the formation of antibody-colloidal gold conjugates was monitored by UV/Vis spectroscopy. Immunochromatographic strips were assembled in regular sequence through different accessories sticked on PVC plate. Strips specifically detected R. anatipestifer within 10 min, but did not detect E. coli, S. enterica and P. multocida. The detection limit for R. anatipestifer was 1×10(6) colony forming units, which was 500 times higher than a conventional agglutination test. Accuracy was 100% match to multiplex PCR. Assay stability and reproducibility were excellent after storage at 4°C for 6 months. The immunochromatographic strips prepared in this study offer a specific, sensitive, and rapid detection method for R. anatipestifer, which is of great importance for the prevention and control of R. anatipestifer infections.
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spelling pubmed-43789992015-04-09 Development of Colloidal Gold Immunochromatographic Strips for Detection of Riemerella anatipestifer Hou, Wanwan Wang, Shaohui Wang, Xiaolan Han, Xiangan Fan, Hongjie Cao, Shoulin Yue, Jiaping Wang, Quan Jiang, Wei Ding, Chan Yu, Shengqing PLoS One Research Article Riemerella anatipestifer is one of the most important bacterial pathogen of ducks and causes a contagious septicemia. R. anatipestifer infection causes serositis syndromes similar to other bacterial infections in ducks, including infection by Escherichia coli, Salmonella enterica and Pasteurella multocida. Clinically differentiating R. anatipestifer infections from other bacterial pathogen infections is usually difficult. In this study, MAb 1G2F10, a monoclonal antibody against R. anatipestifer GroEL, was used to develop a colloidal gold immunochromatographic strip. Colloidal gold particles were prepared by chemical synthesis to an average diameter of 20±5.26 nm by transmission electron microscope imaging. MAb 1G2F10 was conjugated to colloidal gold particles and the formation of antibody-colloidal gold conjugates was monitored by UV/Vis spectroscopy. Immunochromatographic strips were assembled in regular sequence through different accessories sticked on PVC plate. Strips specifically detected R. anatipestifer within 10 min, but did not detect E. coli, S. enterica and P. multocida. The detection limit for R. anatipestifer was 1×10(6) colony forming units, which was 500 times higher than a conventional agglutination test. Accuracy was 100% match to multiplex PCR. Assay stability and reproducibility were excellent after storage at 4°C for 6 months. The immunochromatographic strips prepared in this study offer a specific, sensitive, and rapid detection method for R. anatipestifer, which is of great importance for the prevention and control of R. anatipestifer infections. Public Library of Science 2015-03-30 /pmc/articles/PMC4378999/ /pubmed/25822983 http://dx.doi.org/10.1371/journal.pone.0122952 Text en © 2015 Hou et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hou, Wanwan
Wang, Shaohui
Wang, Xiaolan
Han, Xiangan
Fan, Hongjie
Cao, Shoulin
Yue, Jiaping
Wang, Quan
Jiang, Wei
Ding, Chan
Yu, Shengqing
Development of Colloidal Gold Immunochromatographic Strips for Detection of Riemerella anatipestifer
title Development of Colloidal Gold Immunochromatographic Strips for Detection of Riemerella anatipestifer
title_full Development of Colloidal Gold Immunochromatographic Strips for Detection of Riemerella anatipestifer
title_fullStr Development of Colloidal Gold Immunochromatographic Strips for Detection of Riemerella anatipestifer
title_full_unstemmed Development of Colloidal Gold Immunochromatographic Strips for Detection of Riemerella anatipestifer
title_short Development of Colloidal Gold Immunochromatographic Strips for Detection of Riemerella anatipestifer
title_sort development of colloidal gold immunochromatographic strips for detection of riemerella anatipestifer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378999/
https://www.ncbi.nlm.nih.gov/pubmed/25822983
http://dx.doi.org/10.1371/journal.pone.0122952
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