Machine learning prioritization of antibiotic residues in aquatic foods reveals exposure-driven genotoxic risk mediated by BCL2
- Food Chem X. 2026 Feb 8:34:103646. doi: 10.1016/j.fochx.2026.103646.
- 1. Department of Preventive Medicine, School of Public Health, Guangzhou Medical University, Xinzao, Panyu District, Guangzhou, China.
- 2. Guangzhou Institute for Food Inspection, 53 Jiejin 2nd Road, Panyu District, Guangzhou, China.
- 3. Guangdong Provincial Key Laboratory of Major Obstetric Diseases, Guangdong Provincial Clinical Research Center for Obstetrics and Gynecology, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Antibiotic residues in aquatic foods pose genotoxic risks. Traditional monitoring focuses on individual Maximum Residue Limit (MRL) compliance, often overlooking cumulative multi-residue risks. We developed an interpretable machine learning (ML) framework integrating surveillance data (3719 samples, 17 Antibiotics) with mechanistic validation to prioritize risks in Guangzhou (2021-2023). Exposure metrics and in silico hazard predictions were analyzed via clustering and ranking. Enrofloxacin, sulfamethoxazole, and 3-amino-2-oxazolidinone were prioritized, with risk drivers deconstructed via Explainable AI (SHAP). In L-02 hepatocytes, prioritized mixtures reduced viability (70.21 ± 7.49%), increased Apoptosis (7.12 ± 2.75%), and induced DNA damage (tail DNA% 5.25 ± 1.03%) (all p < 0.05). BCL2 overexpression significantly attenuated this damage (tail DNA% 2.90 ± 2.65%, p < 0.05), confirming its role as a key functional mediator. This surveillance-to-mechanism workflow provides a data-driven paradigm for identifying mechanistic biomarkers and prioritizing food safety interventions, surpassing traditional compliance-based monitoring.
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Cat. No.Product NameDescriptionTargetResearch Area
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Research Areas: Infection
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Calcium Ionophore Antibiotic, Methanogenic Bacteria Inhibitor
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Research Areas: Infection
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Research Areas: Infection
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target: Monoamine Oxidase
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target: Drug MetaboliteResearch Areas: Infection
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target: Drug MetaboliteResearch Areas: Others