The removal of mycotoxins from contaminated feed using lactic acid bacteria (LAB) has been proposed as an inexpensive, safe, and promising mycotoxin decontamination strategy. In this study, viable and heat-inactivated L. acidophilus CIP 76.13T and L. delbrueckii subsp. bulgaricus CIP 101027T cells were investigated for their ability to remove aflatoxin B1 (AFB1), ochratoxin A (OTA), zearalenone (ZEA), and deoxynivalenol (DON) from MRS medium and PBS buffer over a 24 h period at 37 °C. LAB decontamination activity was also assessed in a ZEA-contaminated liquid feed (LF). Residual mycotoxin concentrations were determined by UHPLC-FLD/DAD analysis. In PBS, viable L. acidophilus CIP 76.13T and L. delbrueckii subsp. bulgaricus CIP 101027T cells removed up to 57% and 30% of ZEA and DON, respectively, while AFB1 and OTA reductions were lower than 15%. In MRS, 28% and 33% of ZEA and AFB1 were removed, respectively; OTA and DON reductions were small (≤15%). Regardless of the medium, heat-inactivated cells produced significantly lower mycotoxin reductions than those obtained with viable cells. An adsorption mechanism was suggested to explain the reductions in AFB1 and OTA, while biodegradation could be responsible for the removal of ZEA and DON. Both viable LAB strains reduced ZEA by 23% in contaminated LF after 48 h of incubation. These findings suggest that LAB strains of L. acidophilus CIP 76.13T and L. delbrueckii subsp. bulgaricus CIP 101027T may be applied in the feed industry to reduce mycotoxin contamination.

The present study evaluated the effect of gamma irradiation on the stability of ochratoxin A (OTA) under various conditions. The effects of the physical state of OTA (solid vs aqueous), initial OTA concentration, irradiation dose and dose rate as well as the presence of model substances simulating food matrix compounds on OTA radiostability were investigated. First, pure OTA with and without food model compounds including α-D-glucose (monosaccharide), Methyl α-D-glucopyranoside (starch) and the amino acid derivatives N-α-acetyl-L-lysine methyl ester and N-α-acetyl-L-cysteine methyl ester (protein models) were irradiated with doses of 2, 4 and 8 kGy applied at 15.117 and 108.24 Gy/min. Secondly, artificially OTA-contaminated wheat with different moisture content (11, 14 and 16%) was irradiated with doses of 2, 4 and 8 kGy applied at 63.39 Gy/min. Residual OTA levels were analysed using ultra-high performance liquid chromatography coupled with tandem mass spectrometry. Solid OTA (50 and 3,200 ng/ml)showed great irradiation stability, even with irradiation doses up to 8 kGy. Under dry conditions, the presence of food model components did not affect OTA radiostability. However, in an aqueous solution, complete reduction was achieved at the initial OTA concentration of 50 ng/ml and irradiation dose of 2 kGy. Applying gamma irradiation to cereal-based food model systems produced a significant OTA reduction (5,000 µg/kg) of 47.2% in moistened wheat kernels (16%) with an absorbed dose of 8 kGy but failed to reduce the OTA content of low moisture content wheat (11%). These model experiments offered a useful tool to assess the main key factors affecting gamma irradiation-induced OTA reduction. Gamma irradiation is promising since the irradiation doses applied could partially reduce OTA contamination. Nevertheless, its efficacy was largely affected by initial moisture content and could be dangerous if toxic by-products are produced or nutritive quality is lost and needs further study.

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The objective of this study was the evaluation of the effects of different gamma irradiation doses on the survival of natural mycoflora as well as on the reduction of mycotoxin contamination (ochratoxin A [OTA] and aflatoxin B1 [AFB1]) in naturally contaminated sorghum samples. Mycotoxin levels were determined by ultra-highperformance liquid chromatography coupled to triple quadrupole tandem mass spectrometry (UHPLC-QqQ-MS/MS). The results have demonstrated that the dose of 3 kGy was sufficient to eliminate 90% of the natural fungal load of sorghum. Increasing gamma irradiation dose showed significant effects (p < .05) on initial mycotoxin content. At radiation dose of 10 kGy, maximum reduction of 59% and 32% were achieved in naturally contaminated sorghum for AFB1 and OTA, respectively. The obtained results clearly showed that gamma irradiation can be a promising method to control fungal and mycotoxin contamination in sorghum.

Gamma irradiation is a useful technology for degrading mycotoxins. The purpose of this study was to investigate the effect of irradiation on ochratoxin A (OTA) stability under different conditions. OTA was irradiated in methanolic solution and on millet flour at doses of 2 and 4 kGy. Residual OTA concentrations and possible degradation products in irradiated samples were analyzed by high-performance liquid chromatography with fluorescence detection and liquid chromatography coupled to mass spectrometry. The extent of in vitro cytotoxicity of OTA to HepG2 cells, with and without irradiation treatment, was assessed with an MTT assay. OTA was more sensitive to gamma radiation on Tunisian millet flour than in methanolic solutions. After irradiation of naturally contaminated millet flour, the OTA concentration was significantly reduced by 48 and 62% at a dose of 2 and 4 kGy, respectively. However, in the methanolic solution, OTA at concentrations of 1 and 5 μg mL−1 was relatively stable even at a dose of 4 kGy, with no degradation products detected in the chemical analysis. Analytical results were confirmed by cell culture assays. The remaining cytotoxicity (MTT assay) of OTA following irradiation was not significantly affected compared with the controls. These findings indicate that gamma irradiation could offer a solution for OTA decontamination in the postharvest processing chain of millet flour. However, the associated toxicological hazard of decontaminated food matrices needs more investigation.