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Articles

Survey of mycotoxins in milling oats dedicated for food purposes between 2013 and 2019 by LC–MS/MS

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Pages 1934-1947 | Received 09 May 2021, Accepted 20 Jun 2021, Published online: 30 Jul 2021
 

ABSTRACT

Although the common oat (Avena sativa L.) is well known for its nutritional benefits, it carries the risk of contamination with mycotoxins due to its susceptibility to the growth of various fungi. The procurement of milling oats for food could become more difficult in the coming harvest years due to limited availability, specific quality requirements and the avoidance of mycotoxin contamination. In light of ongoing discussions in the European Commission on regulatory limits for certain mycotoxins including their modified forms, the purpose of this study was to improve the database on their occurrence in milling oats. In particular, we provide data on the predominantly occurring trichothecenes such as deoxynivalenol and its acetylated and modified derivatives (e.g. 3-acetyl-deoxynivalenol, 15-acetyl-deoxynivalenol and deoxynivalenol-3-glucoside) as well as on T-2 and HT-2 toxins. Additionally, the following mycotoxins were analysed: zearalenone, nivalenol, diacetoxyscirpenol, fusarenon-X, ochratoxin A, sterigmatocystin and aflatoxins B1, B2, G1 and G2. Oat samples, (n = 281) pre-selected for their physical properties and DON-content to be less than 1750 µg/kg from 11 European provenances, were analysed for 16 different mycotoxins by LC-MS/MS. Samples were collected from the years of harvest 2013 to 2019. High incidence rates above the limit of quantification of either 5 µg/kg for T-2 and HT-2 toxins or 10 µg/kg for deoxynivalenol were found (98.1, 94.7 and 91.4%, respectively). The mean concentration of the sum of T-2 and HT-2 toxins was 149 µg/kg. The highest level was found in an Irish sample containing 1290 µg/kg for the sum of T-2 and HT-2 toxins. The mean deoxynivalenol concentration was 289 µg/kg, while the highest level was 1414 µg/kg in a Swedish sample. Besides nivalenol other mycotoxins were only present in trace concentrations or not detected.

Acknowledgments

This study was financed by H. & J. Brüggen KG, Lübeck, Germany. We thank Dr. Sari Peltonen (ProAgria), Dr. CG Pettersson (Lantmännen), Dr. Stefan Hoth (Kölln), Dr. Steffen Beuch (Nordsaat) and Dr. Stefanie Boie (University of Lübeck) for their fruitful discussions, information and comments. We thank Norbert Hauf, Axel Rieck, Jutta Koth, Anne Kühne, Sabine Hasse, Ulrike Gerth and Daniel Krause (all H. & J. Brüggen KG) for their technical assistance. Special thanks go to Johannes Meyer and Peter Kowalski for revising the language of this document.

Disclosure statement

The authors do not have any financial interests.

Supplementary material

Supplemental data for this article can be accessed on the publisher’s website.

Additional information

Funding

This work was supported by the H. & J. Brueggen KG [no grant number].

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