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Rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food
BACKGROUND: Colistin (polymyxin E) is a kind of peptide antibiotic which has been approved in animal production for the purposes of disease prevention, treatment, and growth promotion. However, the wide use of colistin in animal feed may accelerate the spread of colistin-resistance gene MCR-1 from a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796504/ https://www.ncbi.nlm.nih.gov/pubmed/31636903 http://dx.doi.org/10.1186/s40104-019-0389-7 |
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author | Wang, Jiayi Zhou, Jinyu Chen, Yiqiang Zhang, Xinpei Jin, Yongpeng Cui, Xiaojing He, Dongting Lai, Wenqing He, Lidong |
author_facet | Wang, Jiayi Zhou, Jinyu Chen, Yiqiang Zhang, Xinpei Jin, Yongpeng Cui, Xiaojing He, Dongting Lai, Wenqing He, Lidong |
author_sort | Wang, Jiayi |
collection | PubMed |
description | BACKGROUND: Colistin (polymyxin E) is a kind of peptide antibiotic which has been approved in animal production for the purposes of disease prevention, treatment, and growth promotion. However, the wide use of colistin in animal feed may accelerate the spread of colistin-resistance gene MCR-1 from animal production to human beings, and its residue in animal-origin food may also pose serious health hazards to humans. Thus, it is necessary to develop corresponding analytical methods to monitor the addition of colistin in animal feed and the colistin residue in animal-origin food. RESULTS: A one-step enzyme-linked immunosorbent assay (ELISA) and a lateral flow immunochromatographic assay (LFIA) for colistin were developed based on a newly developed monoclonal antibody. The ELISA showed a 50% inhibition value (IC(50)) of 9.7 ng/mL with assay time less than 60 min, while the LFIA had a strip reader-based detection limit of 0.87 ng/mL in phosphate buffer with assay time less than 15 min. For reducing the non-specific adsorption of colistin onto sample vial, the components of sample extraction solution were optimized and proved to greatly improve the assay accuracy. The spiked recovery experiment showed that the recoveries of colistin from feed, milk and meat samples were in the range of 77.83% to 113.38% with coefficient of variations less than 13% by ELISA analysis and less than 18% by LFIA analysis, respectively. Furthermore, actual sample analysis indicated that the two immunoassays can produce results consistent with instrumental analysis. CONCLUSIONS: The developed assays can be used for rapid qualitative or quantitative detection of colistin in animal feed and food. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-019-0389-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6796504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67965042019-10-21 Rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food Wang, Jiayi Zhou, Jinyu Chen, Yiqiang Zhang, Xinpei Jin, Yongpeng Cui, Xiaojing He, Dongting Lai, Wenqing He, Lidong J Anim Sci Biotechnol Research BACKGROUND: Colistin (polymyxin E) is a kind of peptide antibiotic which has been approved in animal production for the purposes of disease prevention, treatment, and growth promotion. However, the wide use of colistin in animal feed may accelerate the spread of colistin-resistance gene MCR-1 from animal production to human beings, and its residue in animal-origin food may also pose serious health hazards to humans. Thus, it is necessary to develop corresponding analytical methods to monitor the addition of colistin in animal feed and the colistin residue in animal-origin food. RESULTS: A one-step enzyme-linked immunosorbent assay (ELISA) and a lateral flow immunochromatographic assay (LFIA) for colistin were developed based on a newly developed monoclonal antibody. The ELISA showed a 50% inhibition value (IC(50)) of 9.7 ng/mL with assay time less than 60 min, while the LFIA had a strip reader-based detection limit of 0.87 ng/mL in phosphate buffer with assay time less than 15 min. For reducing the non-specific adsorption of colistin onto sample vial, the components of sample extraction solution were optimized and proved to greatly improve the assay accuracy. The spiked recovery experiment showed that the recoveries of colistin from feed, milk and meat samples were in the range of 77.83% to 113.38% with coefficient of variations less than 13% by ELISA analysis and less than 18% by LFIA analysis, respectively. Furthermore, actual sample analysis indicated that the two immunoassays can produce results consistent with instrumental analysis. CONCLUSIONS: The developed assays can be used for rapid qualitative or quantitative detection of colistin in animal feed and food. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-019-0389-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-10-17 /pmc/articles/PMC6796504/ /pubmed/31636903 http://dx.doi.org/10.1186/s40104-019-0389-7 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 | Research Wang, Jiayi Zhou, Jinyu Chen, Yiqiang Zhang, Xinpei Jin, Yongpeng Cui, Xiaojing He, Dongting Lai, Wenqing He, Lidong Rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food |
title | Rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food |
title_full | Rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food |
title_fullStr | Rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food |
title_full_unstemmed | Rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food |
title_short | Rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food |
title_sort | rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796504/ https://www.ncbi.nlm.nih.gov/pubmed/31636903 http://dx.doi.org/10.1186/s40104-019-0389-7 |
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