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      Deciphering the Anti-Aflatoxinogenic Properties of Eugenol Using a Large-Scale q-PCR Approach

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          Abstract

          Produced by several species of Aspergillus, Aflatoxin B 1 (AFB 1) is a carcinogenic mycotoxin contaminating many crops worldwide. The utilization of fungicides is currently one of the most common methods; nevertheless, their use is not environmentally or economically sound. Thus, the use of natural compounds able to block aflatoxinogenesis could represent an alternative strategy to limit food and feed contamination. For instance, eugenol, a 4-allyl-2-methoxyphenol present in many essential oils, has been identified as an anti-aflatoxin molecule. However, its precise mechanism of action has yet to be clarified. The production of AFB 1 is associated with the expression of a 70 kB cluster, and not less than 21 enzymatic reactions are necessary for its production. Based on former empirical data, a molecular tool composed of 60 genes targeting 27 genes of aflatoxin B 1 cluster and 33 genes encoding the main regulatory factors potentially involved in its production, was developed. We showed that AFB 1 inhibition in Aspergillus flavus following eugenol addition at 0.5 mM in a Malt Extract Agar (MEA) medium resulted in a complete inhibition of the expression of all but one gene of the AFB 1 biosynthesis cluster. This transcriptomic effect followed a down-regulation of the complex composed by the two internal regulatory factors, AflR and AflS. This phenomenon was also influenced by an over-expression of veA and mtfA, two genes that are directly linked to AFB 1 cluster regulation.

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          Coordination of secondary metabolism and development in fungi: the velvet family of regulatory proteins.

          Filamentous fungi produce a number of small bioactive molecules as part of their secondary metabolism ranging from benign antibiotics such as penicillin to threatening mycotoxins such as aflatoxin. Secondary metabolism can be linked to fungal developmental programs in response to various abiotic or biotic external triggers. The velvet family of regulatory proteins plays a key role in coordinating secondary metabolism and differentiation processes such as asexual or sexual sporulation and sclerotia or fruiting body formation. The velvet family shares a protein domain that is present in most parts of the fungal kingdom from chytrids to basidiomycetes. Most of the current knowledge derives from the model Aspergillus nidulans where VeA, the founding member of the protein family, was discovered almost half a century ago. Different members of the velvet protein family interact with each other and the nonvelvet protein LaeA, primarily in the nucleus. LaeA is a methyltransferase-domain protein that functions as a regulator of secondary metabolism and development. A comprehensive picture of the molecular interplay between the velvet domain protein family, LaeA and other nuclear regulatory proteins in response to various signal transduction pathway starts to emerge from a jigsaw puzzle of several recent studies. © 2011 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved.
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            Current Situation of Mycotoxin Contamination and Co-occurrence in Animal Feed—Focus on Europe

            Mycotoxins are secondary metabolites produced by fungi especially those belonging to the genus Aspergillus, Penicillum and Fusarium. Mycotoxin contamination can occur in all agricultural commodities in the field and/or during storage, if conditions are favourable to fungal growth. Regarding animal feed, five mycotoxins (aflatoxins, deoxynivalenol, zearalenone, fumonisins and ochratoxin A) are covered by EU legislation (regulation or recommendation). Transgressions of these limits are rarely observed in official monitoring programs. However, low level contamination by Fusarium toxins is very common (e.g., deoxynivalenol (DON) is typically found in more than 50% of the samples) and co-contamination is frequently observed. Multi-mycotoxin studies reported 75%–100% of the samples to contain more than one mycotoxin which could impact animal health at already low doses. Co-occurrence of mycotoxins is likely to arise for at least three different reasons (i) most fungi are able to simultaneously produce a number of mycotoxins, (ii) commodities can be contaminated by several fungi, and (iii) completed feed is made from various commodities. In the present paper, we reviewed the data published since 2004 concerning the contamination of animal feed with single or combinations of mycotoxins and highlighted the occurrence of these co-contaminations.
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              Regulation of secondary metabolism in filamentous fungi.

              Fungal secondary metabolites are of intense interest to humankind due to their pharmaceutical (antibiotics) and/or toxic (mycotoxins) properties. In the past decade, tremendous progress has been made in understanding the genes that are associated with production of various fungal secondary metabolites. Moreover, the regulatory mechanisms controlling biosynthesis of diverse groups of secondary metabolites have been unveiled. In this review, we present the current understanding of the genetic regulation of secondary metabolism from clustering of biosynthetic genes to global regulators balancing growth, sporulation, and secondary metabolite production in selected fungi with emphasis on regulation of metabolites of agricultural concern. Particularly, the roles of G protein signaling components and developmental regulators in the mycotoxin sterigmatocystin biosynthesis in the model fungus Aspergillus nidulans are discussed in depth.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Toxins (Basel)
                Toxins (Basel)
                toxins
                Toxins
                MDPI
                2072-6651
                26 April 2016
                May 2016
                : 8
                : 5
                : 123
                Affiliations
                [1 ]Toxalim, Université de Toulouse, INRA, ENVT, INP Purpan, UPS, Toulouse, France; isauracaceres@ 123456hotmail.com (I.C.); rhodakhoury@ 123456gmail.com (R.E.K.); yannick.lippi@ 123456toulouse.inra.fr (Y.L.); claire.naylies@ 123456toulouse.inra.fr (C.N.); ioswald@ 123456toulouse.inra.fr (I.P.O.); olivier.puel@ 123456toulouse.inra.fr (O.P.)
                [2 ]Laboratoire de Mycologie et Sécurité des Aliments (LMSA), Département de Biochimie, Faculté des Sciences, Université Saint-Joseph, P.O. Box 11-514, Beirut 1107 2050, Lebanon; andre.khoury@ 123456usj.edu.lb
                [3 ]Applied Mycology Group, School of Energy, Environment and AgriFood, Cranfield University, Cranfield MK43 0AL, Bedfordshire, UK; a.medinavaya@ 123456cranfield.ac.uk
                [4 ]Laboratory of Microbiology, Department of Natural Sciences and Earth, Faculty of Sciences I, Lebanese University, Hadath Campus, P.O. Box 11-8281, Beirut, Lebanon; a.atoui@ 123456cnrs.edu.lb
                Author notes
                [* ]Correspondence: jd.bailly@ 123456envt.fr ; Tel.: +33-56-1193-229
                [†]

                These authors contributed equally to this work.

                Article
                toxins-08-00123
                10.3390/toxins8050123
                4885038
                27128940
                8e25043d-dad1-470c-bcf4-67dfe25ee4da
                © 2016 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 31 March 2016
                : 18 April 2016
                Categories
                Article

                Molecular medicine
                aflatoxin b1,aspergillus flavus,aflatoxinogenesis,molecular tool,gene regulation,eugenol

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