Yeast fractions can mitigate the risk of zearalenone
Yeast fractions have shown to be an effective solution to minimise the negative effects of certain mycotoxins. What makes YCW’s effective as mycotoxin adsorbents?
BY VIRGINIE MARQUIS, PHD, TOXICOLOGY AND PATHOGENS R&D MANAGER, PHILEO BY LESAFFRE
T In vitro single
concentration study In vitro isotherm study
he global impact of mycotoxins is a constant food and feed safety issue, creating hazards which result in economic losses in farm animal production. Effective decontamination strategies have been
developed to counter this problem, with the most used methods involving the addition of mycotoxin detoxifiers to
Table 1 – Efficacy of Safwall in adsorbing ZEA. Conditions
Incubation at 37°C, pH3 and pH7, 1ppm ZEA
Incubation at 37°C, pH 3 or 7, ZEA concentrations ranging from 100ppb to 20ppm.
feed. As part of this process, mycotoxins are physically bound by binding agent which decreases the gastrointestinal absorption of toxins. In addition to their efficiency as postbiotics, delivering probiotic effects on microbiota and immunity, yeast cell walls (YCW’s) are widely used by the animal feed industry as mycotoxin adsorbents. Several studies have shown that most YCW’s, when tested in vitro, display evident mycotoxin reducing effects, but with differing levels of consistency. Our focus, therefore, is directed towards the mechanism of mycotoxin adsorption and what makes YCW’s an efficient mycotoxin adsorbent.
Mechanism of mycotoxin adsorption The interactive mechanism between yeasts and mycotoxins is complex, being determined by the structure and composition
Results 76% adsorption at pH3 80% adsorption at pH7.
2,5 3
1,5 2
0,5 1
0 0 1 2 3 Ceq (mg/L)
In vitro conditions simulating GIT
Incubation at 39°C, one step mimicking the stomach at pH 2.5 followed by intestine at pH 6.5, 1ppm ZEA.
In vivo toxicokinetic study Cross-over design, ZEA (5mg/kg BW) administered orally with or in broiler chickens
In vivo trial in gilts
without the YCW (0.2 or 0.5g/kg BW). Plasma concentrations of ZEA and metabolites quantified by LC-MS.
Trial period of 28 days. 600µg ZEA/kg feed. Parameters measured: vulva size, organs weight, ZEA and metabolites content in liver.
Isotherm of ZEA adsorption on different YCW’s (different composition, strain, origin, and structure). 78% adsorption.
Bioavailability reduced by more than 90% for 0.5g/kg BW Safwall dosage and by 60% for the dose 0.2g/kg BW.
Vulva size and relative weight of reproductive organs increased due to ZEA but
decreased to control value with Safwall addition. ZEA, α-ZEL and β-ZEL content decreased in liver in presence of Safwall compared to ZEA treatment alone.
40 ▶ MYCOTOXINS | NOVEMBER 2021 4 5 6 Safwall
Qeq(mg/g)
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