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Ducks as a potential reservoir for Pasteurella multocida infection detected using a new rOmpH-based ELISA
Pasteurella multocida is an important pathogen of numerous domestic poultry and wild animals and is associated with a variety of diseases including fowl cholera. The aim of this study was to develop an indirect enzyme-linked immunosorbent assay (ELISA) based on recombinant outer-membrane protein H (...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559375/ https://www.ncbi.nlm.nih.gov/pubmed/28626158 http://dx.doi.org/10.1292/jvms.17-0124 |
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author | LIU, Rongchang CHEN, Cuiteng CHENG, Longfei LU, Ronghui FU, Guanghua SHI, Shaohua CHEN, Hongmei WAN, Chunhe LIN, Jiansheng FU, Qiuling HUANG, Yu |
author_facet | LIU, Rongchang CHEN, Cuiteng CHENG, Longfei LU, Ronghui FU, Guanghua SHI, Shaohua CHEN, Hongmei WAN, Chunhe LIN, Jiansheng FU, Qiuling HUANG, Yu |
author_sort | LIU, Rongchang |
collection | PubMed |
description | Pasteurella multocida is an important pathogen of numerous domestic poultry and wild animals and is associated with a variety of diseases including fowl cholera. The aim of this study was to develop an indirect enzyme-linked immunosorbent assay (ELISA) based on recombinant outer-membrane protein H (rOmpH) for detection of anti-P. multocida antibodies in serum to determine their prevalence in Chinese ducks. The P. multocida ompH gene was cloned into pET32a, and rOmpH was expressed in Escherichia coli BL21 (DE3). Western blotting revealed that purified rOmpH was recognized by duck antisera against P. multocida, and an indirect ELISA was established. During analysis of serum samples (n=115) from ducks, the rOmpH ELISA showed 95.0% specificity, 100% sensitivity and a 92.0% κ coefficient (95% confidence interval 0.844–0.997) as compared with a microtiter agglutination test. Among 165 randomly selected serum samples, which were collected in 2015 and originated from six duck farms across Fujian Province, China, anti-P. multocida antibodies were detected in 22.42% of apparently healthy ducks, including 25 of 90 sheldrakes (27.8%), eight of 50 Peking ducks (16.0%) and four of 25 Muscovy ducks (16%). Overall, the data suggest that rOmpH is a suitable candidate antigen for the development of an indirect ELISA for detection of P. multocida in ducks; moreover, our results showed that ducks could serve as a potential reservoir for P. multocida infection. |
format | Online Article Text |
id | pubmed-5559375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55593752017-08-25 Ducks as a potential reservoir for Pasteurella multocida infection detected using a new rOmpH-based ELISA LIU, Rongchang CHEN, Cuiteng CHENG, Longfei LU, Ronghui FU, Guanghua SHI, Shaohua CHEN, Hongmei WAN, Chunhe LIN, Jiansheng FU, Qiuling HUANG, Yu J Vet Med Sci Bacteriology Pasteurella multocida is an important pathogen of numerous domestic poultry and wild animals and is associated with a variety of diseases including fowl cholera. The aim of this study was to develop an indirect enzyme-linked immunosorbent assay (ELISA) based on recombinant outer-membrane protein H (rOmpH) for detection of anti-P. multocida antibodies in serum to determine their prevalence in Chinese ducks. The P. multocida ompH gene was cloned into pET32a, and rOmpH was expressed in Escherichia coli BL21 (DE3). Western blotting revealed that purified rOmpH was recognized by duck antisera against P. multocida, and an indirect ELISA was established. During analysis of serum samples (n=115) from ducks, the rOmpH ELISA showed 95.0% specificity, 100% sensitivity and a 92.0% κ coefficient (95% confidence interval 0.844–0.997) as compared with a microtiter agglutination test. Among 165 randomly selected serum samples, which were collected in 2015 and originated from six duck farms across Fujian Province, China, anti-P. multocida antibodies were detected in 22.42% of apparently healthy ducks, including 25 of 90 sheldrakes (27.8%), eight of 50 Peking ducks (16.0%) and four of 25 Muscovy ducks (16%). Overall, the data suggest that rOmpH is a suitable candidate antigen for the development of an indirect ELISA for detection of P. multocida in ducks; moreover, our results showed that ducks could serve as a potential reservoir for P. multocida infection. The Japanese Society of Veterinary Science 2017-06-15 2017-07 /pmc/articles/PMC5559375/ /pubmed/28626158 http://dx.doi.org/10.1292/jvms.17-0124 Text en ©2017 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Bacteriology LIU, Rongchang CHEN, Cuiteng CHENG, Longfei LU, Ronghui FU, Guanghua SHI, Shaohua CHEN, Hongmei WAN, Chunhe LIN, Jiansheng FU, Qiuling HUANG, Yu Ducks as a potential reservoir for Pasteurella multocida infection detected using a new rOmpH-based ELISA |
title | Ducks as a potential reservoir for Pasteurella multocida infection detected using a new rOmpH-based ELISA |
title_full | Ducks as a potential reservoir for Pasteurella multocida infection detected using a new rOmpH-based ELISA |
title_fullStr | Ducks as a potential reservoir for Pasteurella multocida infection detected using a new rOmpH-based ELISA |
title_full_unstemmed | Ducks as a potential reservoir for Pasteurella multocida infection detected using a new rOmpH-based ELISA |
title_short | Ducks as a potential reservoir for Pasteurella multocida infection detected using a new rOmpH-based ELISA |
title_sort | ducks as a potential reservoir for pasteurella multocida infection detected using a new romph-based elisa |
topic | Bacteriology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559375/ https://www.ncbi.nlm.nih.gov/pubmed/28626158 http://dx.doi.org/10.1292/jvms.17-0124 |
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