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Development of a five-plex flow cytometric immunoassay for the simultaneous detection of six coccidiostats in feed and eggs

Coccidiostats are the only veterinary drugs still permitted to be used as feed additives to treat poultry for coccidiosis. To protect consumers, maximum levels for their presence in food and feed have been set by the European Union (EU). To monitor these coccidiostats, a rapid and inexpensive screen...

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Autores principales: Bienenmann-Ploum, Monique E., Huet, Anne-Catherine, Campbell, Katrina, Fodey, Terence L., Vincent, Ursula, Haasnoot, Willem, Delahaut, Philippe, Elliott, Christopher T., Nielen, Michel W. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3426671/
https://www.ncbi.nlm.nih.gov/pubmed/22850895
http://dx.doi.org/10.1007/s00216-012-6214-1
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author Bienenmann-Ploum, Monique E.
Huet, Anne-Catherine
Campbell, Katrina
Fodey, Terence L.
Vincent, Ursula
Haasnoot, Willem
Delahaut, Philippe
Elliott, Christopher T.
Nielen, Michel W. F.
author_facet Bienenmann-Ploum, Monique E.
Huet, Anne-Catherine
Campbell, Katrina
Fodey, Terence L.
Vincent, Ursula
Haasnoot, Willem
Delahaut, Philippe
Elliott, Christopher T.
Nielen, Michel W. F.
author_sort Bienenmann-Ploum, Monique E.
collection PubMed
description Coccidiostats are the only veterinary drugs still permitted to be used as feed additives to treat poultry for coccidiosis. To protect consumers, maximum levels for their presence in food and feed have been set by the European Union (EU). To monitor these coccidiostats, a rapid and inexpensive screening method would be a useful tool. The development of such a screening method, using a flow cytometry-based immunoassay, is described. The assay uses five sets of colour-coded paramagnetic microspheres for the detection of six selected priority coccidiostats. Different coccidiostats, with and without carrier proteins, were covalently coupled onto different bead sets and tested in combination with polyclonal antisera and with a fluorescent-labelled secondary antibody. The five optimal combinations were selected for this multiplex and a simple-to-use sample extraction method was applied for screening blank and spiked eggs and feed samples. A very good correlation (r ranging from 0.995 to 0.999) was obtained with the responses obtained in two different flow cytometers (Luminex 100 and FLEXMAP 3D). The sensitivities obtained were in accordance with the levels set by the EU as the measured limits of detection for narasin/salinomycin, lasalocid, diclazuril, nicarbazin (4,4′-dinitrocarbanilide) and monensin in eggs were 0.01, 0.1, 0.5, 53 and 0.1 μg/kg and in feed 0.1, 0.2, 0.3, 9 and 1.5 μg/kg, respectively. [Figure: see text]
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spelling pubmed-34266712012-08-29 Development of a five-plex flow cytometric immunoassay for the simultaneous detection of six coccidiostats in feed and eggs Bienenmann-Ploum, Monique E. Huet, Anne-Catherine Campbell, Katrina Fodey, Terence L. Vincent, Ursula Haasnoot, Willem Delahaut, Philippe Elliott, Christopher T. Nielen, Michel W. F. Anal Bioanal Chem Original Paper Coccidiostats are the only veterinary drugs still permitted to be used as feed additives to treat poultry for coccidiosis. To protect consumers, maximum levels for their presence in food and feed have been set by the European Union (EU). To monitor these coccidiostats, a rapid and inexpensive screening method would be a useful tool. The development of such a screening method, using a flow cytometry-based immunoassay, is described. The assay uses five sets of colour-coded paramagnetic microspheres for the detection of six selected priority coccidiostats. Different coccidiostats, with and without carrier proteins, were covalently coupled onto different bead sets and tested in combination with polyclonal antisera and with a fluorescent-labelled secondary antibody. The five optimal combinations were selected for this multiplex and a simple-to-use sample extraction method was applied for screening blank and spiked eggs and feed samples. A very good correlation (r ranging from 0.995 to 0.999) was obtained with the responses obtained in two different flow cytometers (Luminex 100 and FLEXMAP 3D). The sensitivities obtained were in accordance with the levels set by the EU as the measured limits of detection for narasin/salinomycin, lasalocid, diclazuril, nicarbazin (4,4′-dinitrocarbanilide) and monensin in eggs were 0.01, 0.1, 0.5, 53 and 0.1 μg/kg and in feed 0.1, 0.2, 0.3, 9 and 1.5 μg/kg, respectively. [Figure: see text] Springer-Verlag 2012-08-01 2012 /pmc/articles/PMC3426671/ /pubmed/22850895 http://dx.doi.org/10.1007/s00216-012-6214-1 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Paper
Bienenmann-Ploum, Monique E.
Huet, Anne-Catherine
Campbell, Katrina
Fodey, Terence L.
Vincent, Ursula
Haasnoot, Willem
Delahaut, Philippe
Elliott, Christopher T.
Nielen, Michel W. F.
Development of a five-plex flow cytometric immunoassay for the simultaneous detection of six coccidiostats in feed and eggs
title Development of a five-plex flow cytometric immunoassay for the simultaneous detection of six coccidiostats in feed and eggs
title_full Development of a five-plex flow cytometric immunoassay for the simultaneous detection of six coccidiostats in feed and eggs
title_fullStr Development of a five-plex flow cytometric immunoassay for the simultaneous detection of six coccidiostats in feed and eggs
title_full_unstemmed Development of a five-plex flow cytometric immunoassay for the simultaneous detection of six coccidiostats in feed and eggs
title_short Development of a five-plex flow cytometric immunoassay for the simultaneous detection of six coccidiostats in feed and eggs
title_sort development of a five-plex flow cytometric immunoassay for the simultaneous detection of six coccidiostats in feed and eggs
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3426671/
https://www.ncbi.nlm.nih.gov/pubmed/22850895
http://dx.doi.org/10.1007/s00216-012-6214-1
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