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      Distribution of fungi and their toxic metabolites in melon and sesame seeds marketed in two major producing states in Nigeria

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          Abstract

          In this study, melon ( n = 60) and sesame ( n = 60) seeds purchased from markets within Benue and Nasarawa states, respectively, in Nigeria, during two seasons (dry and wet), were analysed for fungal and mycotoxin contamination in order to determine the safety of these foods for human consumption. Molecular analysis revealed the following seven fungal taxonomic groups in the foods: Aspergillus section Candidi, Aspergillus section Flavi, Aspergillus section Nigri, Cladosporium, Fusarium fujikuroi species group, Penicillium, and Pleosporales/Didymellaceae. A total of 78 microbial metabolites, including several mycotoxins, occurred in the foods. The most frequent mycotoxins in melon and sesame were aflatoxin B 1 (occurrence: 76%) and alternariol monomethyl ether (occurrence: 59%), respectively. However, higher mean total aflatoxin levels occurred in sesame (17 μg kg −1) than in melon (11 μg kg −1). About 28 and 5% of melon and sesame, respectively, exceeded the 4 μg kg −1 total aflatoxin limit for oilseeds intended for direct human consumption in the European Union. Additionally, fumonisin B 1 and moniliformin occurred only in sesame, whilst ochratoxins A and B occurred only in melon; ochratoxin B being reported for the first time in this food. Our data indicated seasonal variations in the fungal and mycotoxin contamination levels in both foods.

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          Most cited references64

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          AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS

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            Development of primer sets designed for use with the PCR to amplify conserved genes from filamentous ascomycetes.

            We constructed nine sets of oligonucleotide primers on the basis of the results of DNA hybridization of cloned genes from Neurospora crassa and Aspergillus nidulans to the genomes of select filamentous ascomycetes and deuteromycetes (with filamentous ascomycete affiliations). Nine sets of primers were designed to amplify segments of DNA that span one or more introns in conserved genes. PCR DNA amplification with the nine primer sets with genomic DNA from ascomycetes, deuteromycetes, basidiomycetes, and plants revealed that five of the primer sets amplified a product only from DNA of the filamentous ascomycetes and deuteromycetes. The five primer sets were constructed from the N. crassa genes for histone 3, histone 4, beta-tubulin, and the plasma membrane ATPase. With these five primer sets, polymorphisms were observed in both the size of and restriction enzyme sites in the amplified products from the filamentous ascomycetes. The primer sets described here may provide useful tools for phylogenetic studies and genome analyses in filamentous ascomycetes and deuteromycetes (with ascomycete affiliations), as well as for the rapid differentiation of fungal species by PCR.
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              Impact of food processing and detoxification treatments on mycotoxin contamination

              Mycotoxins are fungal metabolites commonly occurring in food, which pose a health risk to the consumer. Maximum levels for major mycotoxins allowed in food have been established worldwide. Good agricultural practices, plant disease management, and adequate storage conditions limit mycotoxin levels in the food chain yet do not eliminate mycotoxins completely. Food processing can further reduce mycotoxin levels by physical removal and decontamination by chemical or enzymatic transformation of mycotoxins into less toxic products. Physical removal of mycotoxins is very efficient: manual sorting of grains, nuts, and fruits by farmers as well as automatic sorting by the industry significantly lowers the mean mycotoxin content. Further processing such as milling, steeping, and extrusion can also reduce mycotoxin content. Mycotoxins can be detoxified chemically by reacting with food components and technical aids; these reactions are facilitated by high temperature and alkaline or acidic conditions. Detoxification of mycotoxins can also be achieved enzymatically. Some enzymes able to transform mycotoxins naturally occur in food commodities or are produced during fermentation but more efficient detoxification can be achieved by deliberate introduction of purified enzymes. We recommend integrating evaluation of processing technologies for their impact on mycotoxins into risk management. Processing steps proven to mitigate mycotoxin contamination should be used whenever necessary. Development of detoxification technologies for high-risk commodities should be a priority for research. While physical techniques currently offer the most efficient post-harvest reduction of mycotoxin content in food, biotechnology possesses the largest potential for future developments.
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                Author and article information

                Contributors
                chaugez@gmail.com
                Journal
                Mycotoxin Res
                Mycotoxin Res
                Mycotoxin Research
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0178-7888
                1867-1632
                14 July 2020
                14 July 2020
                2020
                : 36
                : 4
                : 361-369
                Affiliations
                [1 ]GRID grid.442581.e, ISNI 0000 0000 9641 9455, Department of Microbiology, , Babcock University, ; Ilishan Remo, Ogun State Nigeria
                [2 ]GRID grid.5173.0, ISNI 0000 0001 2298 5320, Department of Agrobiotechnology (IFA–Tulln), Institute of Bioanalytics and Agro–Metabolomics, , University of Natural Resources and Life Sciences Vienna (BOKU), ; Konrad Lorenzstr. 20, A–3430 Tulln, Austria
                [3 ]GRID grid.4777.3, ISNI 0000 0004 0374 7521, Institute for Global Food Security, School of Biological Sciences, , Queen’s University Belfast, ; University Road, Belfast, Northern Ireland BT7 1NN UK
                Author information
                http://orcid.org/0000-0002-2113-2948
                Article
                400
                10.1007/s12550-020-00400-0
                7536151
                32666399
                89c6e353-6317-47a1-a223-f68ecae2bb90
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 2 August 2019
                : 17 June 2020
                : 7 July 2020
                Funding
                Funded by: University of Natural Resources and Life Sciences Vienna (BOKU)
                Categories
                Original Article
                Custom metadata
                © Society for Mycotoxin (Research Gesellschaft für Mykotoxinforschung e.V.) and Springer-Verlag GmbH Germany, part of Springer Nature 2020

                Toxicology
                food safety,melon,mycology,mycotoxins,sesame
                Toxicology
                food safety, melon, mycology, mycotoxins, sesame

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