4.7 Article

Masked trichothecene and zearalenone mycotoxins withstand digestion and absorption in the upper GI tract but are efficiently hydrolyzed by human gut microbiota in vitro

Journal

MOLECULAR NUTRITION & FOOD RESEARCH
Volume 61, Issue 4, Pages -

Publisher

WILEY
DOI: 10.1002/mnfr.201600680

Keywords

Caco-2; Deoxynivalenol; Glucoside; Hydrolysis; Nivalenol; HT-2 toxin

Funding

  1. Food Standards Agency UK [FS 102101]
  2. Rural and Environment Science and Analytical Services Division (RESAS) of the Scottish Government

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Scope: Cereal grains are commonly contaminated with Fusarium mycotoxins and their plant-derived masked metabolites. The fate of masked mycotoxins in the human gut is poorly understood. Here we assess the metabolism and transport of glucoside metabolites of common trichothecenes (deoxynivalenol, nivalenol, T-2 toxin) and zearalenone compounds (zearalenone, alpha-and beta-zearalenol) in the human gut in vitro. Methods and results: Masked mycotoxins were incubated with artificial digestive juices and absorption was assessed in differentiated Caco-2/TC7 cells. Colonic metabolism was studied using fecal batch cultures from five donors and mycotoxins were detected using LC-MS/MS. All masked mycotoxins were stable under upper GI tract conditions and no absorption was observed. Free trichothecenes were absorbed intact whereas free zearalenone compounds were absorbed and metabolized to undetected compounds by Caco-2/TC7 cells. Human gut microbiota efficiently hydrolyzed all masked mycotoxins. Trichothecenes were fully recovered as parent mycotoxins whereas 40-70% of zearalenone compounds were further metabolized to unknown metabolites. Conclusion: Our results demonstrate that masked trichothecenes will reach the colon intact to be released as parent mycotoxins by gut microbiota, hence contributing to mycotoxin exposure. Masked zearalenone compounds are metabolized by gutmicrobiota and epithelial cells and the identity and toxicity of metabolites remain to be determined.

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