Yan-Qi Ning , Zhe Peng , Yu Zhang , Alainaa Refaie , Jing-Hui Ge , Li-Jia Guo , Wen-Jie Yang , Lv-Hui Sun
{"title":"A novel mycotoxin-degrading enzyme complex can biodegrade AFB1, DON, and ZEN co-contamination in both in vitro and in vivo experiments","authors":"Yan-Qi Ning , Zhe Peng , Yu Zhang , Alainaa Refaie , Jing-Hui Ge , Li-Jia Guo , Wen-Jie Yang , Lv-Hui Sun","doi":"10.1016/j.toxicon.2025.108539","DOIUrl":null,"url":null,"abstract":"<div><div>A novel mycotoxin-degrading enzyme complex (MDE), developed via a microcapsule coating process and containing three degrading enzymes, exhibits the ability to biodegrade aflatoxin B<sub>1</sub> (AFB<sub>1</sub>), deoxynivalenol (DON) and zearalenone (ZEN). This study aims to evaluate the efficacy of MDE against AFB<sub>1</sub>, DON, and ZEN through <em>in vitro</em> and <em>in vivo</em> experiments. <strong><em>In vitro</em> simulated digestion</strong> experiments revealed that <strong>the</strong> MDE degraded the concentrations of AFB<sub>1</sub>, DON, and ZEN by 76.27 %, 74.04 %, and 60.77 %, respectively. <em>In vivo</em> experiments were conducted using 39 one-day-old male Cobb broilers allocated into three groups: a basal diet group (BD; CON), a BD group supplemented with 50 μg/kg AFB<sub>1</sub>, 3.0 mg/kg DON, and 1.5 mg/kg ZEN (Toxins), and a BD plus Toxins diet with 0.02 % MDE (Toxins + MDE), with the experiment lasting for 14 days. Compared to the Toxins group, the Toxins + MDE group showed a tendency to increase (<em>P</em> = 0.09) the body weight on day 7. Moreover, the Toxins treatment increased the serum alanine aminotransferase (ALT) activities, aspartate aminotransferase (AST) activities, and blood urea nitrogen (BUN) concentrations, and decreased creatinine (CREA) concentrations. Interestingly, dietary supplementation with 0.02 % MDE alleviated these adverse effects. Additionally, the Toxins and Toxins + MDE groups exhibited slight lymphocytic infiltration and mucosal epithelial detachment in the glandular stomach and the villi layer. Notably, dietary supplementation with 0.02 % MDE decreased gastric AFB<sub>1</sub>, DON, and ZEN concentrations by 40.1 %, 37.7 %, and 29.1 %, respectively. In conclusion, MDE effectively degrades the concentrations of AFB<sub>1</sub>, DON, and ZEN through <em>in vitro</em> simulated pig digestion and <em>in vivo</em> chick experiments.</div></div>","PeriodicalId":23289,"journal":{"name":"Toxicon","volume":"266 ","pages":"Article 108539"},"PeriodicalIF":2.4000,"publicationDate":"2025-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Toxicon","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0041010125003149","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
A novel mycotoxin-degrading enzyme complex (MDE), developed via a microcapsule coating process and containing three degrading enzymes, exhibits the ability to biodegrade aflatoxin B1 (AFB1), deoxynivalenol (DON) and zearalenone (ZEN). This study aims to evaluate the efficacy of MDE against AFB1, DON, and ZEN through in vitro and in vivo experiments. In vitro simulated digestion experiments revealed that the MDE degraded the concentrations of AFB1, DON, and ZEN by 76.27 %, 74.04 %, and 60.77 %, respectively. In vivo experiments were conducted using 39 one-day-old male Cobb broilers allocated into three groups: a basal diet group (BD; CON), a BD group supplemented with 50 μg/kg AFB1, 3.0 mg/kg DON, and 1.5 mg/kg ZEN (Toxins), and a BD plus Toxins diet with 0.02 % MDE (Toxins + MDE), with the experiment lasting for 14 days. Compared to the Toxins group, the Toxins + MDE group showed a tendency to increase (P = 0.09) the body weight on day 7. Moreover, the Toxins treatment increased the serum alanine aminotransferase (ALT) activities, aspartate aminotransferase (AST) activities, and blood urea nitrogen (BUN) concentrations, and decreased creatinine (CREA) concentrations. Interestingly, dietary supplementation with 0.02 % MDE alleviated these adverse effects. Additionally, the Toxins and Toxins + MDE groups exhibited slight lymphocytic infiltration and mucosal epithelial detachment in the glandular stomach and the villi layer. Notably, dietary supplementation with 0.02 % MDE decreased gastric AFB1, DON, and ZEN concentrations by 40.1 %, 37.7 %, and 29.1 %, respectively. In conclusion, MDE effectively degrades the concentrations of AFB1, DON, and ZEN through in vitro simulated pig digestion and in vivo chick experiments.
期刊介绍:
Toxicon has an open access mirror Toxicon: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. An introductory offer Toxicon: X - full waiver of the Open Access fee.
Toxicon''s "aims and scope" are to publish:
-articles containing the results of original research on problems related to toxins derived from animals, plants and microorganisms
-papers on novel findings related to the chemical, pharmacological, toxicological, and immunological properties of natural toxins
-molecular biological studies of toxins and other genes from poisonous and venomous organisms that advance understanding of the role or function of toxins
-clinical observations on poisoning and envenoming where a new therapeutic principle has been proposed or a decidedly superior clinical result has been obtained.
-material on the use of toxins as tools in studying biological processes and material on subjects related to venom and antivenom problems.
-articles on the translational application of toxins, for example as drugs and insecticides
-epidemiological studies on envenoming or poisoning, so long as they highlight a previously unrecognised medical problem or provide insight into the prevention or medical treatment of envenoming or poisoning. Retrospective surveys of hospital records, especially those lacking species identification, will not be considered for publication. Properly designed prospective community-based surveys are strongly encouraged.
-articles describing well-known activities of venoms, such as antibacterial, anticancer, and analgesic activities of arachnid venoms, without any attempt to define the mechanism of action or purify the active component, will not be considered for publication in Toxicon.
-review articles on problems related to toxinology.
To encourage the exchange of ideas, sections of the journal may be devoted to Short Communications, Letters to the Editor and activities of the affiliated societies.