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Compound mycotoxin detoxifier alleviating aflatoxin B(1) toxic effects on broiler growth performance, organ damage and gut microbiota

The aim of this study was to evaluate the effects of compound mycotoxin detoxifier (CMD) on alleviating the toxic effect of aflatoxin B(1) (AFB(1)) for broiler growth performance. One-kilogram CMD consists of 667 g aflatoxin B(1)-degrading enzyme (ADE, 1,467 U/g), 200 g montmorillonite and 133 g com...

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Detalles Bibliográficos
Autores principales: Guo, Hongwei, Wang, Ping, Liu, Chaoqi, Chang, Juan, Yin, Qingqiang, Wang, Lijun, Jin, Sanjun, Zhu, Qun, Lu, Fushan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811249/
https://www.ncbi.nlm.nih.gov/pubmed/36586389
http://dx.doi.org/10.1016/j.psj.2022.102434
Descripción
Sumario:The aim of this study was to evaluate the effects of compound mycotoxin detoxifier (CMD) on alleviating the toxic effect of aflatoxin B(1) (AFB(1)) for broiler growth performance. One-kilogram CMD consists of 667 g aflatoxin B(1)-degrading enzyme (ADE, 1,467 U/g), 200 g montmorillonite and 133 g compound probiotics (CP). The feeding experiment was divided into 2 stages (1–21 d and 22–42 d). In the early stage, a total of 300 one-day-old Ross broilers were randomly divided into 6 groups, 5 replications for each group, 10 broilers (half male and half female) in each replication. In the later feeding stage, about 240 twenty-two-day-old Ross broilers were randomly divided into 6 groups, 8 replications for each group, 5 broilers in each replication. Group A: basal diet; group B: basal diet with 40 μg/kg AFB(1); group C: basal diet with 1 g/kg CMD; groups D, E, and F: basal diet with 40 μg/kg AFB(1) plus 0.5, 1.0 and 1.5 g/kg CMD, respectively. The results indicated that AFB(1) significantly decreased average daily gain (ADG), protein metabolic rate, organ index of thymus, bursa of Fabricius (BF), superoxide dismutase (SOD), glutathione peroxidase (GSH-PX) and catalase activities in serum, and increased AFB(1) residues in serum and liver (P < 0.05). Hematoxylin-Eosin (HE) staining analysis of jejunum, liver and kidney showed that AFB(1) caused the main pathological changes with different degrees of inflammatory cell infiltration. However, CMD additions could alleviate the negative effects of AFB(1) on the above parameters. The gut microbiota analysis indicated that AFB(1) could significantly increase the abundances of Staphylococcus-xylosu, Esherichia-coli-g-Escherichia-Shigella, and decrease Lactobacillus-aviarius abundance (P < 0.05), but which were adjusted to almost the same levels as the control group by CMD addition. The correlative analysis showed that Lactobacillus-aviarius abundance was positively correlated with ADG, SOD and BF (P < 0.05), whereas Staphylococcus-xylosus abundance was positively correlated with AFB(1) residues in serum and liver (P < 0.05). In conclusion, CMD could keep gut microbiota stable, alleviate histological lesions, increase growth performance, and reduce mycotoxin toxicity. The optimal CMD addition should be 1 g/kg in AFB(1)-contaminated broilers diet.