School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan 250012, Shandong, China.
School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan 250012, Shandong, China.
Pestic Biochem Physiol. 2023 Sep;195:105556. doi: 10.1016/j.pestbp.2023.105556. Epub 2023 Jul 26.
Azoxystrobin (AZO) is a broad-spectrum strobilurin fungicide widely used in agriculture. However, its use increases the possibility of co-occurrence with mycotoxins such as ochratoxin A (OTA), which poses a significant risk to human health. Therefore, it is imperative to prioritize the evaluation of the combined toxicity of these two compounds. To assess the combined effects of AZO and OTA, the response genes and phenotypes for AZO or OTA exposure were obtained by utilizing Comparative Toxicogenomics Database, and Database for Annotation, Visualization and Integrated Discovery was used for GO and KEGG pathway enrichment analysis. In addition, we provided in-vivo evidence that AZO and OTA, in isolation and combination, could disrupt a variety of biological processes, such as oxidative stress, inflammatory response, apoptosis and thyroid hormone regulation under environmentally relevant concentrations. Notably, our findings suggest that the combined exposure group exhibited greater toxicity, as evidenced by the expression of various markers associated with the aforementioned biological processes, compared to the individual exposure group, which presents potential targets for the underlying mechanisms of induced toxicity. This study provides a novel methodological approach for exploring the mechanism of combined toxicity of a fungicide and a mycotoxin, which can shed light for conducting risk assessment of foodborne toxins.
唑菌胺酯(AZO)是一种广泛应用于农业领域的广谱性 strobilurin 类杀菌剂。然而,其使用增加了与真菌毒素如赭曲霉毒素 A(OTA)共同出现的可能性,这对人类健康构成了重大威胁。因此,优先评估这两种化合物的联合毒性至关重要。为了评估 AZO 和 OTA 的联合效应,我们利用比较毒理学基因组数据库(Comparative Toxicogenomics Database)获得了 AZO 或 OTA 暴露的响应基因和表型,并利用基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路富集分析数据库(Database for Annotation, Visualization and Integrated Discovery)进行了 GO 和 KEGG 通路富集分析。此外,我们提供了体内证据表明,在环境相关浓度下,AZO 和 OTA 无论是单独暴露还是联合暴露,都可能破坏多种生物学过程,如氧化应激、炎症反应、细胞凋亡和甲状腺激素调节。值得注意的是,与单独暴露组相比,联合暴露组的各种与上述生物学过程相关的标志物表达水平更高,表明其毒性更大,这为诱导毒性的潜在机制提供了潜在的靶点。本研究为探索杀菌剂和真菌毒素联合毒性的机制提供了一种新的方法学途径,可为食源毒素的风险评估提供参考。