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Development of a colloidal gold immunochromatographic strip for rapid detection of Riemerella anatipestifer in ducks
Riemerella anatipestifer is one of the major bacterial pathogens of ducks and causes significant economic losses in poultry agriculture. Usually, methods for detecting R. anatipestifer infection need specialized equipment and highly skilled personnel. In this study, a novel colloidal gold immunochro...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7598101/ https://www.ncbi.nlm.nih.gov/pubmed/32988508 http://dx.doi.org/10.1016/j.psj.2020.06.035 |
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author | Han, Wenlong Chen, Zongchao Niu, Pengfei Ren, Xiaomei Ding, Chan Yu, Shengqing |
author_facet | Han, Wenlong Chen, Zongchao Niu, Pengfei Ren, Xiaomei Ding, Chan Yu, Shengqing |
author_sort | Han, Wenlong |
collection | PubMed |
description | Riemerella anatipestifer is one of the major bacterial pathogens of ducks and causes significant economic losses in poultry agriculture. Usually, methods for detecting R. anatipestifer infection need specialized equipment and highly skilled personnel. In this study, a novel colloidal gold immunochromatographic strip was developed for rapid detection of R. anatipestifer in ducks. The monoclonal antibodies 2D5 and 2A6 against R. anatipestifer were used as colloidal gold-labeled protein and capture protein, respectively, to recognize the bacteria in tryptic soy broth medium culture and in hearts of infected ducks. The goat anti-mouse IgG antibody was labeled on nitrocellulose membrane as a control for C line. The labeling pH was optimized as 10.0, and the concentration of 2D5 labeled to colloidal gold particles was optimized as 18 μg/mL. The strip specifically detected serotypes 1, 2, and 10 R. anatipestifer strains and showed no cross-reaction with Escherichia coli, Salmonella enterica, and Pasteurella multocida strains. The sensitivity of the strip for detecting R. anatipestifer was 1.0 × 10(6) colony forming unit. The strips remained stable for up to 8 mo at 4°C, and the detection can be completed within 15 min. The strip can detect R. anatipestifer in hearts of the ducks experimentally infected with R. anatipestifer but not infected with E. coli, which were also confirmed with bacterial isolation followed by multiplex polymerase chain reaction. These results suggested that the strips are reliable methods for identification of R. anatipestifer in laboratories and in duck farms. |
format | Online Article Text |
id | pubmed-7598101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75981012020-11-03 Development of a colloidal gold immunochromatographic strip for rapid detection of Riemerella anatipestifer in ducks Han, Wenlong Chen, Zongchao Niu, Pengfei Ren, Xiaomei Ding, Chan Yu, Shengqing Poult Sci Immunology, Health and Disease Riemerella anatipestifer is one of the major bacterial pathogens of ducks and causes significant economic losses in poultry agriculture. Usually, methods for detecting R. anatipestifer infection need specialized equipment and highly skilled personnel. In this study, a novel colloidal gold immunochromatographic strip was developed for rapid detection of R. anatipestifer in ducks. The monoclonal antibodies 2D5 and 2A6 against R. anatipestifer were used as colloidal gold-labeled protein and capture protein, respectively, to recognize the bacteria in tryptic soy broth medium culture and in hearts of infected ducks. The goat anti-mouse IgG antibody was labeled on nitrocellulose membrane as a control for C line. The labeling pH was optimized as 10.0, and the concentration of 2D5 labeled to colloidal gold particles was optimized as 18 μg/mL. The strip specifically detected serotypes 1, 2, and 10 R. anatipestifer strains and showed no cross-reaction with Escherichia coli, Salmonella enterica, and Pasteurella multocida strains. The sensitivity of the strip for detecting R. anatipestifer was 1.0 × 10(6) colony forming unit. The strips remained stable for up to 8 mo at 4°C, and the detection can be completed within 15 min. The strip can detect R. anatipestifer in hearts of the ducks experimentally infected with R. anatipestifer but not infected with E. coli, which were also confirmed with bacterial isolation followed by multiplex polymerase chain reaction. These results suggested that the strips are reliable methods for identification of R. anatipestifer in laboratories and in duck farms. Elsevier 2020-07-03 /pmc/articles/PMC7598101/ /pubmed/32988508 http://dx.doi.org/10.1016/j.psj.2020.06.035 Text en © 2020 Published by Elsevier Inc. on behalf of Poultry Science Association Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Immunology, Health and Disease Han, Wenlong Chen, Zongchao Niu, Pengfei Ren, Xiaomei Ding, Chan Yu, Shengqing Development of a colloidal gold immunochromatographic strip for rapid detection of Riemerella anatipestifer in ducks |
title | Development of a colloidal gold immunochromatographic strip for rapid detection of Riemerella anatipestifer in ducks |
title_full | Development of a colloidal gold immunochromatographic strip for rapid detection of Riemerella anatipestifer in ducks |
title_fullStr | Development of a colloidal gold immunochromatographic strip for rapid detection of Riemerella anatipestifer in ducks |
title_full_unstemmed | Development of a colloidal gold immunochromatographic strip for rapid detection of Riemerella anatipestifer in ducks |
title_short | Development of a colloidal gold immunochromatographic strip for rapid detection of Riemerella anatipestifer in ducks |
title_sort | development of a colloidal gold immunochromatographic strip for rapid detection of riemerella anatipestifer in ducks |
topic | Immunology, Health and Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7598101/ https://www.ncbi.nlm.nih.gov/pubmed/32988508 http://dx.doi.org/10.1016/j.psj.2020.06.035 |
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