Abstract

Mycotoxins are toxic substances naturally produced by various fungi, and these compounds not only inflict economic damage, but also pose risks to human and animal health. The goal of the present study was to optimize the QuEChERS-based extraction and liquid chromatography–tandem mass spectrometry (LC–MS/MS) method for the analysis of 11 mycotoxins, such as aflatoxins (AFs), ochratoxin A (OTA), fumonisins (FBs), T-2 toxin, HT-2 toxin, zearalenone (ZEN), and deoxynivalenol (DON), commonly found in feed. The QuEChERS method, characterized by being “quick, easy, cheap, effective, rugged, and safe”, has become one of the most common extractions and clean-up procedures for mycotoxin analyses in food. Therefore, in this experiment, an optimal method for the analysis of 11 mycotoxins in feed was established by modifying the general QuEChERS method. In this process, it was confirmed that even if feed samples of different weights were extracted, the quantitative value of mycotoxins in the feed was not affected. To reduce matrix effects, 13C-labeled compounds and deuterium were used as internal standards. This optimized method was then applied in the determination of 11 mycotoxins in 736 feed ingredients and compound feeds obtained from South Korea. The results showed that the occurrence rates of FBs, ZEN, and DON were 59.4%, 38.0%, and 32.1%, respectively, and OTA, AFs, and T-2 toxin and HT-2 toxin were found in fewer than 1% of the 736 feeds. The mean concentration ranges of FBs, ZEN, and DON were 757–2387, 44–4552, and 248–9680 μg/kg, respectively. Among the samples in which DON and ZEN were detected, 10 and 12 samples exceeded the management recommendation standards presented by the Ministry of Agriculture, Food and Rural Affairs (MAFRA). However, when the detected concentrations of DON and ZEN were compared with guideline levels in foreign countries, such as the US, Japan, China, and the EU, the number of positive samples changed. In addition, the co-occurrence of mycotoxins in the feed was analyzed, and the results showed that 43.8% of the samples were contaminated with two or three mycotoxins, among which the co-occurrence rate of FBs, ZEN, and DON was the highest. In conclusion, these results suggest the need for stricter management standards for FBs, DON, and ZEN in South Korea, and emphasize the importance of the continuous monitoring of feeds.

Highlights

  • Mycotoxins are toxic secondary metabolites formed by fungi in genera such as Alternaria, Aspergillus, Fusarium, and Penicillium [1]

  • MAFRA specifies that samples that have passed through a 20-mesh (850 μm) sieve should be used for the analysis of mycotoxins present in feeds [24]

  • In order to establish the optimal homogeneity of the feed sample, we used 1 kg samples containing aflatoxins B1 and B2 and ochratoxin A to perform a homogeneity test after they were ground to a level of 30 mesh (600 μm)

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Summary

Introduction

Mycotoxins are toxic secondary metabolites formed by fungi in genera such as Alternaria, Aspergillus, Fusarium, and Penicillium [1]. The International Agency for Research on Cancer (IARC) has classified DON, T-2 toxin, HT-2 toxin, and ZEN as possible human carcinogens (Group 3); FBs and ochratoxin A (OTA) as human carcinogens (Group 2B); and AF as a human carcinogen (Group 1) [17] These toxic substances are chemically stable and do not degrade at high temperatures, and a single fungal species can produce various types of mycotoxins [18,19]. The sampling procedure and the homogenization process in the preparation stage before sample extraction can significantly affect the measurement of mycotoxins [23] For this reason, the Ministry of Agriculture, Food and Rural Affairs (MAFRA) recommends passing the pulverized feed through a sieve of 20 mesh (850 μm), and the weight of the feed used for pretreatment should be set to 25 g [24]. The third factor is that feed is a complex matrix because various materials are included, and any interfering substances that remain after extraction can affect instrument analysis; matrix effects must be reduced through a clean-up process [18,22,25]

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