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Zearalenone Biodegradation by the Combination of Probiotics with Cell-Free Extracts of Aspergillus oryzae and its Mycotoxin-Alleviating Effect on Pig Production Performance

In order to remove zearalenone (ZEA) detriment- , and cell-free extracts from were used to degrade ZEA in this study. The orthogonal experiment in vitro showed that the ZEA degradation rate was 92.27% ( < 0.05) under the conditions that , SP1, and SP2 were mixed together at 0.5%, 1.0%, and 1.0%....

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Published in:Toxins 2019-09, Vol.11 (10), p.552
Main Authors: Liu, Chaoqi, Chang, Juan, Wang, Ping, Yin, Qingqiang, Huang, Weiwei, Dang, Xiaowei, Lu, Fushan, Gao, Tianzeng
Format: Article
Language:English
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Summary:In order to remove zearalenone (ZEA) detriment- , and cell-free extracts from were used to degrade ZEA in this study. The orthogonal experiment in vitro showed that the ZEA degradation rate was 92.27% ( < 0.05) under the conditions that , SP1, and SP2 were mixed together at 0.5%, 1.0%, and 1.0%. When cell-free extracts from were combined with the above probiotics at a ratio of 2:1 to make mycotoxin-biodegradation preparation (MBP), the ZEA degradation rate reached 95.15% ( < 0.05). In order to further investigate the MBP effect on relieving the negative impact of ZEA for pig production performance, 120 young pigs were randomly divided into 5 groups, with 3 replicates in each group and 8 pigs for each replicate. Group A was given the basal diet with 86.19 μg/kg ZEA; group B contained 300 μg/kg ZEA without MBP addition; and groups C, D, and E contained 300 μg/kg ZEA added with 0.05%, 0.10%, and 0.15% MBP, respectively. The results showed that MBP addition was able to keep gut microbiota stable. ZEA concentrations in jejunal contents in groups A and D were 89.47% and 80.07% lower than that in group B ( < 0.05), indicating that MBP was effective in ZEA biodegradation. In addition, MBP had no significant effect on pig growth, nutrient digestibility, and the relative mRNA abundance of estrogen receptor alpha ( ) genes in ovaries and the uterus ( > 0.05).
ISSN:2072-6651
2072-6651
DOI:10.3390/toxins11100552