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The Metabolic Fate of Deoxynivalenol and Its Acetylated Derivatives in a Wheat Suspension Culture: Identification and Detection of DON-15-O-Glucoside, 15-Acetyl-DON-3-O-Glucoside and 15-Acetyl-DON-3-Sulfate

Overview
Journal Toxins (Basel)
Publisher MDPI
Specialty Toxicology
Date 2015 Aug 15
PMID 26274975
Citations 11
Authors
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Abstract

Deoxynivalenol (DON) is a protein synthesis inhibitor produced by the Fusarium species, which frequently contaminates grains used for human or animal consumption. We treated a wheat suspension culture with DON or one of its acetylated derivatives, 3-acetyl-DON (3-ADON), 15-acetyl-DON (15-ADON) and 3,15-diacetyl-DON (3,15-diADON), and monitored the metabolization over a course of 96 h. Supernatant and cell extract samples were analyzed using a tailored LC-MS/MS method for the quantification of DON metabolites. We report the formation of tentatively identified DON-15-O-β-D-glucoside (D15G) and of 15-acetyl-DON-3-sulfate (15-ADON3S) as novel deoxynivalenol metabolites in wheat. Furthermore, we found that the recently identified 15-acetyl-DON-3-O-β-D-glucoside (15-ADON3G) is the major metabolite produced after 15-ADON challenge. 3-ADON treatment led to a higher intracellular content of toxic metabolites after six hours compared to all other treatments. 3-ADON was exclusively metabolized into DON before phase II reactions occurred. In contrast, we found that 15-ADON was directly converted into 15-ADON3G and 15-ADON3S in addition to metabolization into deoxynivalenol-3-O-β-D-glucoside (D3G). This study highlights significant differences in the metabolization of DON and its acetylated derivatives.

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References
1.
Warth B, Fruhmann P, Wiesenberger G, Kluger B, Sarkanj B, Lemmens M . Deoxynivalenol-sulfates: identification and quantification of novel conjugated (masked) mycotoxins in wheat. Anal Bioanal Chem. 2014; 407(4):1033-9. PMC: 4305104. DOI: 10.1007/s00216-014-8340-4. View

2.
Fruhmann P, Skrinjar P, Weber J, Mikula H, Warth B, Sulyok M . Sulfation of deoxynivalenol, its acetylated derivatives, and T2-toxin. Tetrahedron. 2014; 70(34):5260-5266. PMC: 4082130. DOI: 10.1016/j.tet.2014.05.064. View

3.
Alexander N, McCormick S, Waalwijk C, van der Lee T, Proctor R . The genetic basis for 3-ADON and 15-ADON trichothecene chemotypes in Fusarium. Fungal Genet Biol. 2011; 48(5):485-95. DOI: 10.1016/j.fgb.2011.01.003. View

4.
Varga E, Wiesenberger G, Hametner C, Ward T, Dong Y, Schofbeck D . New tricks of an old enemy: isolates of Fusarium graminearum produce a type A trichothecene mycotoxin. Environ Microbiol. 2014; 17(8):2588-600. PMC: 4950012. DOI: 10.1111/1462-2920.12718. View

5.
Kluger B, Bueschl C, Lemmens M, Michlmayr H, Malachova A, Koutnik A . Biotransformation of the mycotoxin deoxynivalenol in fusarium resistant and susceptible near isogenic wheat lines. PLoS One. 2015; 10(3):e0119656. PMC: 4361057. DOI: 10.1371/journal.pone.0119656. View