• Pestka, J. Toxicological mechanisms and potential health effects of deoxynivalenol and nivalenol. World Mycotoxin J. 3, 323–347 (2010).


    Google Scholar
     

  • Ndiaye, S. et al. Current review of mycotoxin biodegradation and bioadsorption: microorganisms, mechanisms, and main important applications. Toxins 14, 729 (2022).


    Google Scholar
     

  • Alassane-Kpembi, I. et al. Co-exposure to low doses of the food contaminants deoxynivalenol and nivalenol has a synergistic inflammatory effect on intestinal explants. Arch. Toxicol. 91, 2677–2687 (2017).


    Google Scholar
     

  • Hasuda, A. L. et al. Deoxynivalenol induces apoptosis and inflammation in the liver: analysis using precision-cut liver slices. Food Chem. Toxicol. 163, 112930 (2022).


    Google Scholar
     

  • Wang, P. et al. Effective protective agents against organ toxicity of deoxynivalenol and their detoxification mechanisms: a review. Food Chem. Toxicol. 182, 114121 (2023).


    Google Scholar
     

  • Zhang, Y. et al. Deoxynivalenol: occurrence, toxicity, and degradation. Food Control 155, 110027 (2024).


    Google Scholar
     

  • Murtaza, B. et al. Recalling the reported toxicity assessment of deoxynivalenol, mitigating strategies and its toxicity mechanisms: comprehensive review. Chem.-Biol. Interact. 387, 110799 (2024).


    Google Scholar
     

  • Tu, Y., Liu, S., Cai, P. & Shan, T. Global distribution, toxicity to humans and animals, biodegradation, and nutritional mitigation of deoxynivalenol: a review. Compr. Rev. Food Sci. Food Saf. 22, 3951–3983 (2023).


    Google Scholar
     

  • Oguz, H. et al. In vitro mycotoxin binding capacities of clays, glucomannan and their combinations. Toxicon 214, 93–103 (2022).


    Google Scholar
     

  • Tapingkae, W. et al. IndustriaL-scale production of mycotoxin binder from the red yeast Sporidiobolus pararoseus KM281507. J. Fungi 8, 353 (2022).


    Google Scholar
     

  • Tian, Y. et al. Elimination of Fusarium mycotoxin deoxynivalenol (DON) via microbial and enzymatic strategies: Current status and future perspectives. Trends Food Sci. Technol. 124, 96–107 (2022).


    Google Scholar
     

  • Ben Taheur, F., Kouidhi, B., Al Qurashi, Y. M. A., Ben Salah-Abbès, J. & Chaieb, K. Review: Biotechnology of mycotoxins detoxification using microorganisms and enzymes. Toxicon 160, 12–22 (2019).


    Google Scholar
     

  • Recharla, N., Park, S., Kim, M., Kim, B. & Jeong, J. Y. Protective effects of biological feed additives on gut microbiota and the health of pigs exposed to deoxynivalenol: a review. J. Anim. Sci. Technol. 64, 640–653 (2022).


    Google Scholar
     

  • Jeong, J. Y., Kim, J., Kim, M. & Park, S. Efficacy of high-dose synbiotic additives for deoxynivalenol detoxification: effects on blood biochemistry, histology, and intestinal microbiome in weaned piglets. Biology 13, 889 (2024).


    Google Scholar
     

  • Wang, X., Yong, C. C. & Oh, S. Metabolites of Latilactobacillus curvatus BYB3 and indole activate aryl hydrocarbon receptor to attenuate lipopolysaccharide-induced intestinal barrier dysfunction. Food Sci. Anim. Resour. 42, 1046–1060 (2022).


    Google Scholar
     

  • Khalid, F. et al. Potential of Bacillus velezensis as a probiotic in animal feed: a review. J. Microbiol. 59, 627–633 (2021).


    Google Scholar
     

  • Li, C. et al. Screening and characterization of Bacillus velezensis LB-Y-1 toward selection as a potential probiotic for poultry with multi-enzyme production property. Front. Microbiol. 14, https://doi.org/10.3389/fmicb.2023.1143265 (2023).

  • Dhouib, H. et al. Potential of a novel endophytic Bacillus velezensis in tomato growth promotion and protection against Verticillium wilt disease. Biol. Control 139, 104092 (2019).


    Google Scholar
     

  • Zeng, J., Huang, W., Tian, X., Hu, X. & Wu, Z. Brewer’s spent grain fermentation improves its soluble sugar and protein as well as enzymatic activities using Bacillus velezensis. Process Biochem. 111, 12–20 (2021).


    Google Scholar
     

  • Liu, Y. et al. Dietary Bacillus velezensis KNF-209 supplementation improves growth performance, enhances immunity, and promotes gut health in broilers. Poultry Sci. 103, 103946 (2024).


    Google Scholar
     

  • Chen, J., Zhang, X., He, Z., Xiong, D. & Long, M. Damage on intestinal barrier function and microbial detoxification of deoxynivalenol: a review. J. Integr. Agric. 23, 2507–2524 (2024).


    Google Scholar
     

  • Liu, M. et al. Chitosan oligosaccharide alleviates DON-induced liver injury via suppressing ferroptosis in mice. Ecotoxicol. Environ. Saf. 290, 117530 (2025).


    Google Scholar
     

  • Bai, Y. et al. Lactobacillus rhamnosus GG ameliorates DON-induced intestinal damage depending on the enrichment of beneficial bacteria in weaned piglets. J. Anim. Sci. Biotechnol. 13, 90 (2022).


    Google Scholar
     

  • Pabst, O. et al. Gut-liver axis: barriers and functional circuits. Nat. Rev. Gastroenterol. Hepatol. 20, 447–461 (2023).


    Google Scholar
     

  • Zheng, Z. & Wang, B. The gut-liver axis in health and disease: the role of gut microbiota-derived signals in liver injury and regeneration. Front. Immunol. 12, https://doi.org/10.3389/fimmu.2021.775526 (2021).

  • Farid, W. et al. Gastrointestinal transit tolerance, cell surface hydrophobicity, and functional attributes of Lactobacillus Acidophilus strains isolated from Indigenous Dahi. Food Sci. Nutr. 9, 5092–5102 (2021).


    Google Scholar
     

  • Li, S. et al. Oral delivery of bacteria: Basic principles and biomedical applications. J. Control. Release 327, 801–833 (2020).


    Google Scholar
     

  • Tsang, R. S. W. et al. Culture-Confirmed Invasive meningococcal disease in Canada, 2010 to 2014: characterization of Serogroup B Neisseria meningitidis strains and their predicted coverage by the 4CMenB vaccine. mSphere 5, https://doi.org/10.1128/mSphere.00883-19 (2020).

  • Deng, Y. et al. Deoxynivalenol: emerging toxic mechanisms and control strategies, current and future perspectives. J. Agricult. Food Chem. 71, 10901–10915 (2023).


    Google Scholar
     

  • Liu, D., Wang, Q., He, W., Ge, L. & Huang, K. Deoxynivalenol aggravates the immunosuppression in piglets and PAMs under the condition of PEDV infection through inhibiting TLR4/NLRP3 signaling pathway. Ecotoxicol. Environ. Saf. 231, 113209 (2022).


    Google Scholar
     

  • Zhao, W. et al. Modulating effects of Astragalus polysaccharide on immune disorders via gut microbiota and the TLR4/NF-κB pathway in rats with syndrome of dampness stagnancy due to spleen deficiency. J. Zhejiang Univ. Sci. B 24, 650–662 (2023).


    Google Scholar
     

  • Kamle, M. et al. Deoxynivalenol: an overview on occurrence, chemistry, biosynthesis, health effects and its detection, management, and control strategies in food and feed. Microbiol. Res. 13, 292–314 (2022).


    Google Scholar
     

  • Zhao, X. et al. Contamination and biotransformation of deoxynivalenol (DON) in common commercial foods: current status, challenges and future perspectives. Green Synth. Catal. https://doi.org/10.1016/j.gresc.2025.04.008 (2025).

  • Wang, L. L. et al. Food raw materials and food production occurrences of deoxynivalenol in different regions. Trends Food Sci. Technol. 83, 41–52 (2019).


    Google Scholar
     

  • Zhu La, A. T. et al. A New Bacillus velezensis strain CML532 improves chicken growth performance and reduces intestinal clostridium perfringens colonization. Microorganisms 12, https://doi.org/10.3390/microorganisms12040771 (2024).

  • Dong, W. et al. Isolation of Bacillus licheniformis and its protective effect on liver oxidative stress and apoptosis induced by aflatoxin B1. Poultry Sci. 103, 104079 (2024).


    Google Scholar
     

  • Zhang, Q. et al. Characterization and antioxidant activity of released exopolysaccharide from potential probiotic Leuconostoc mesenteroides LM187. J. Microbiol. Biotechnol. 31, 1144–1153 (2021).


    Google Scholar
     

  • Bai, Y. et al. Gut microbiota mediates Lactobacillus rhamnosus GG alleviation of deoxynivalenol-induced anorexia. J. Agricult. Food Chem. 71, 8164–8181 (2023).


    Google Scholar
     

  • Broekaert, N., Devreese, M., De Baere, S., De Backer, P. & Croubels, S. Modified Fusarium mycotoxins unmasked: From occurrence in cereals to animal and human excretion. Food Chem. Toxicol. 80, 17–31 (2015).


    Google Scholar
     

  • Zhang, Y. et al. Deoxynivalenol: occurrence, toxicity, and degradation. Food Control 155,110027 (2024).

  • Monastero, R. N. & Pentyala, S. Cytokines as biomarkers and their respective clinical cutoff levels. Int. J. Inflamm. 2017, 4309485 (2017).


    Google Scholar
     

  • Ma, R. et al. Detoxification of DON-induced hepatotoxicity in mice by cold atmospheric plasma. Ecotoxicol. Environ. Saf. 280, 116547 (2024).


    Google Scholar
     

  • Kiela, P. R. & Ghishan, F. K. Physiology of intestinal absorption and secretion. Best Pract. Res. Clin. Gastroenterol. 30, 145–159 (2016).


    Google Scholar
     

  • Hanyu, H. et al. Mycotoxin deoxynivalenol has different impacts on intestinal barrier and stem cells by its route of exposure. Toxins 12, 610 (2020).


    Google Scholar
     

  • Zeisel, M. B., Dhawan, P. & Baumert, T. F. Tight junction proteins in gastrointestinal and liver disease. Gut 68, 547–561 (2019).


    Google Scholar
     

  • Liao, S. et al. Chloroquine improves deoxynivalenol-induced inflammatory response and intestinal mucosal damage in piglets. Oxid. Med. Cel. Longev. 2020, 1–13 (2020).


    Google Scholar
     

  • Ge, L. et al. Nontoxic-dose deoxynivalenol aggravates lipopolysaccharides-induced inflammation and tight junction disorder in IPEC-J2 cells through activation of NF-κB and LC3B. Food Chem. Toxicol. 145, 111712 (2020).


    Google Scholar
     

  • Selwyn, F. P., Cheng, S. L., Klaassen, C. D. & Cui, J. Y. Regulation of hepatic drug-metabolizing enzymes in germ-free mice by conventionalization and probiotics. Drug Metabol. Dispos. 44, 262–274 (2016).


    Google Scholar
     

  • Chen, B. et al. Complete genome analysis of Bacillus velezensis TS5 and its potential as a probiotic strain in mice. Front. Microbiol. 14, https://doi.org/10.3389/fmicb.2023.1322910 (2023).

  • Chelakkot, C., Ghim, J. & Ryu, S. H. Mechanisms regulating intestinal barrier integrity and its pathological implications. Exp. Mol. Med. 50, 1–9 (2018).


    Google Scholar
     

  • Wan, S. et al. Baicalin ameliorates the gut barrier function and intestinal microbiota of broiler chickens. Acta Biochim. Biophys. Sin. 56, 634–644 (2024).


    Google Scholar
     

  • Lin, R. et al. Lactobacillus rhamnosus GG supplementation modulates the gut microbiota to promote butyrate production, protecting against deoxynivalenol exposure in nude mice. Biochem. Pharmacol. 175, 113868 (2020).


    Google Scholar
     

  • Ma, K. et al. Lactobacillus rhamnosus GG ameliorates deoxynivalenol-induced kidney oxidative damage and mitochondrial injury in weaned piglets. Food Funct. 13, 3905–3916 (2022).


    Google Scholar
     

  • Hays, K. E., Pfaffinger, J. M. & Ryznar, R. The interplay between gut microbiota, short-chain fatty acids, and implications for host health and disease. Gut Microbes 16, 2393270 (2024).


    Google Scholar
     

  • Yao, Y. et al. The role of short-chain fatty acids in immunity, inflammation and metabolism. Crit. Rev. Food Sci. Nutr. 62, 1–12 (2022).


    Google Scholar
     

  • Bruneau, A., Hundertmark, J., Guillot, A. & Tacke, F. Molecular and cellular mediators of the gut-liver axis in the progression of liver diseases. Front. Med. 8, https://doi.org/10.3389/fmed.2021.725390 (2021).

  • Pestka, J. & Zhou, H.-R. Toll-like receptor priming sensitizes macrophages to proinflammatory cytokine gene induction by deoxynivalenol and other toxicants. Toxicol. Sci. 92, 445–455 (2006).


    Google Scholar
     

  • Fang, J., Yang, Y. & Xie, W. Chinese expert consensus on the application of live combined Bifidobacterium, Lactobacillus, and Enterococcus powder/capsule in digestive system diseases (2021). J. Gastroenterol. Hepatol. 38, 1089–1098 (2023).


    Google Scholar
     

  • Yi, R., Zhou, X., Liu, T., Xue, R. & Yang, Z. Amelioration effect of Lactobacillus plantarum KFY02 on low-fiber diet-induced constipation in mice by regulating gut microbiota. Front. Nutr. 9, https://doi.org/10.3389/fnut.2022.938869 (2022).

  • Al-Sadi, R. et al. Lactobacillus acidophilus induces a strain- specific and toll-like receptor 2-dependent enhancement of intestinal epithelial tight junction barrier and protection against intestinal inflammation. Am. J. Pathol. 191, 872–884 (2021).


    Google Scholar
     

  • Niu, H. et al. Effect of Lactobacillus rhamnosus MN-431 producing indole derivatives on complementary feeding-induced diarrhea rat pups through the enhancement of the intestinal barrier function. Mol. Nutr. Food Res. 66, 2100619 (2022).


    Google Scholar
     

  • Lai, H. C. et al. Gut microbiota modulates COPD pathogenesis: role of anti-inflammatory Parabacteroides goldsteinii lipopolysaccharide. Gut 71, 309–321 (2022).


    Google Scholar
     

  • Tan, H., Zhao, J., Zhang, H., Zhai, Q. & Chen, W. Novel strains of Bacteroides fragilis and Bacteroides ovatus alleviate the LPS-induced inflammation in mice. Appl. Microbiol. Biotechnol. 103, 2353–2365 (2019).


    Google Scholar
     

  • Liu, C. et al. Epigallocatechin gallate alleviates Staphylococcal Enterotoxin A-induced intestinal barrier damage by regulating gut microbiota and inhibiting the TLR4-NF-κB/MAPKs-NLRP3 inflammatory cascade. J. Agricult. Food Chem. 71, 16286–16302 (2023).


    Google Scholar
     

  • Mao, X. et al. Deoxynivalenol induces caspase-3/GSDME-dependent pyroptosis and inflammation in mouse liver and HepaRG cells. Arch. Toxicol. 96, 3091–3112 (2022).


    Google Scholar
     

  • Mennah-Govela, Y. A., Swackhamer, C. & Bornhorst, G. M. Gastric secretion rate and protein concentration impact intragastric pH and protein hydrolysis during dynamic in vitro gastric digestion. Food Hydrocoll. Health 1, 100027 (2021).


    Google Scholar
     

  • Jiang, Y. et al. Oral administration of Bacillus cereus GW-01 alleviates the accumulation and detrimental effects of ?-cypermethrin in mice. Chemosphere 312, 137333 (2023).


    Google Scholar
     

  • Qi, N. et al. Isolation and characterization of a novel hydrolase-producing probiotic Bacillus licheniformis and its application in the fermentation of soybean meal. Front. Nutr. 10, https://doi.org/10.3389/fnut.2023.1123422 (2023).

  • Zhao, J. et al. Mechanism of β-cypermethrin metabolism by Bacillus cereus GW-01. Chem. Eng. J. 430, 132961 (2022).


    Google Scholar
     

  • Kuebutornye, F. K. A. et al. In vitro assessment of the probiotic characteristics of three Bacillus species from the gut of Nile Tilapia, Oreochromis niloticus. Probiot. Antimicrob. Proteins 12, 412–424 (2020).


    Google Scholar
     

  • Fernández, M. F., Boris, S. & Barbés, C. Probiotic properties of human lactobacilli strains to be used in the gastrointestinal tract. J. Appl. Microbiol. 94, 449–455 (2003).


    Google Scholar
     

  • Kang, R. et al. Toxicokinetics of deoxynivalenol in Dezhou male donkeys after oral administration. Toxins 15, https://doi.org/10.3390/toxins15070426 (2023).

  • Luo, J., Xiao, S., Wang, B., Cai, Y. & Wang, J. In vitro fermentation of pineapple-whey protein fermentation product on human intestinal microbiota derived from fecal microbiota transplant donors. LWT-Food Sci. Technol. 191, 115637 (2024).


    Google Scholar