Cargando…
Immunochemical detection of mycotoxins in donkey milk
The applicability of enzyme immunoassays (EIA) for aflatoxin M(1) (AFM(1)), ochratoxin A (OTA) and zearalenone (ZEN) to analyse these toxins in donkey milk (Equus asinus) was studied. For AFM(1) and OTA analysis, milk could be analysed by EIA without sample pretreatment. For ZEN, heat treatment at 7...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331496/ https://www.ncbi.nlm.nih.gov/pubmed/30343381 http://dx.doi.org/10.1007/s12550-018-0333-2 |
_version_ | 1783387144218214400 |
---|---|
author | Gross, Madeleine Ploetz, Christian Puck Gottschalk, Christoph |
author_facet | Gross, Madeleine Ploetz, Christian Puck Gottschalk, Christoph |
author_sort | Gross, Madeleine |
collection | PubMed |
description | The applicability of enzyme immunoassays (EIA) for aflatoxin M(1) (AFM(1)), ochratoxin A (OTA) and zearalenone (ZEN) to analyse these toxins in donkey milk (Equus asinus) was studied. For AFM(1) and OTA analysis, milk could be analysed by EIA without sample pretreatment. For ZEN, heat treatment at 78 °C for 30 min prior EIA analysis was required to avoid false positives. To include detection of phase II metabolites of ZEN, samples were additionally treated with glucuronidase/sulfatase for this EIA. Detection limits were 5 ng/kg (AFM(1)), 9 ng/kg (OTA) and 600 ng/kg (ZEN). All donkey milk samples were negative for all three toxins. Satisfactory quantitation was achieved for spiked samples. Analysis of some cereal-containing donkey feed components (pellets, oats) by EIA revealed absence of aflatoxin B(1) (AFB(1), < 3 μg/kg) and OTA (< 4 μg/kg), while ZEN was found in pellets (180 μg/kg) and in oats (7 μg/kg). This is the first one study on multitoxin determination in donkey milk by antibody-based test systems. In general, the results confirm that EIAs are convenient tools for mycotoxin detection in donkey milk. However, false-positive results may occur, possibly due to the high lysozyme content of donkey milk, which may exert inhibitory activity in some competitive EIA systems. Therefore, specific validation of each EIA for this specific matrix is required, and re-analysis after heat treatment of EIA-positive donkey milk is highly recommended. |
format | Online Article Text |
id | pubmed-6331496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-63314962019-01-27 Immunochemical detection of mycotoxins in donkey milk Gross, Madeleine Ploetz, Christian Puck Gottschalk, Christoph Mycotoxin Res Original Article The applicability of enzyme immunoassays (EIA) for aflatoxin M(1) (AFM(1)), ochratoxin A (OTA) and zearalenone (ZEN) to analyse these toxins in donkey milk (Equus asinus) was studied. For AFM(1) and OTA analysis, milk could be analysed by EIA without sample pretreatment. For ZEN, heat treatment at 78 °C for 30 min prior EIA analysis was required to avoid false positives. To include detection of phase II metabolites of ZEN, samples were additionally treated with glucuronidase/sulfatase for this EIA. Detection limits were 5 ng/kg (AFM(1)), 9 ng/kg (OTA) and 600 ng/kg (ZEN). All donkey milk samples were negative for all three toxins. Satisfactory quantitation was achieved for spiked samples. Analysis of some cereal-containing donkey feed components (pellets, oats) by EIA revealed absence of aflatoxin B(1) (AFB(1), < 3 μg/kg) and OTA (< 4 μg/kg), while ZEN was found in pellets (180 μg/kg) and in oats (7 μg/kg). This is the first one study on multitoxin determination in donkey milk by antibody-based test systems. In general, the results confirm that EIAs are convenient tools for mycotoxin detection in donkey milk. However, false-positive results may occur, possibly due to the high lysozyme content of donkey milk, which may exert inhibitory activity in some competitive EIA systems. Therefore, specific validation of each EIA for this specific matrix is required, and re-analysis after heat treatment of EIA-positive donkey milk is highly recommended. Springer Berlin Heidelberg 2018-10-20 2019 /pmc/articles/PMC6331496/ /pubmed/30343381 http://dx.doi.org/10.1007/s12550-018-0333-2 Text en © The Author(s) 2018 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. |
spellingShingle | Original Article Gross, Madeleine Ploetz, Christian Puck Gottschalk, Christoph Immunochemical detection of mycotoxins in donkey milk |
title | Immunochemical detection of mycotoxins in donkey milk |
title_full | Immunochemical detection of mycotoxins in donkey milk |
title_fullStr | Immunochemical detection of mycotoxins in donkey milk |
title_full_unstemmed | Immunochemical detection of mycotoxins in donkey milk |
title_short | Immunochemical detection of mycotoxins in donkey milk |
title_sort | immunochemical detection of mycotoxins in donkey milk |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331496/ https://www.ncbi.nlm.nih.gov/pubmed/30343381 http://dx.doi.org/10.1007/s12550-018-0333-2 |
work_keys_str_mv | AT grossmadeleine immunochemicaldetectionofmycotoxinsindonkeymilk AT ploetzchristianpuck immunochemicaldetectionofmycotoxinsindonkeymilk AT gottschalkchristoph immunochemicaldetectionofmycotoxinsindonkeymilk |