Department of Food Chemistry and Toxicology, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Center for Biomedical Research, Medical University of Vienna, Vienna, Austria.
Arch Toxicol. 2024 Oct;98(10):3477-3489. doi: 10.1007/s00204-024-03810-6. Epub 2024 Jun 28.
Natural toxins produced by Alternaria fungi include the mycotoxins alternariol, tenuazonic acid and altertoxins I and II. Several of these toxins have shown high toxicity even at low levels including genotoxic, mutagenic, and estrogenic effects. However, the metabolic effects of toxin exposure from Alternaria are understudied, especially in the liver as a key target. To gain insight into the impact of Alternaria toxin exposure on the liver metabolome, rats (n = 21) were exposed to either (1) a complex culture extract with defined toxin profiles from Alternaria alternata (50 mg/kg body weight), (2) the isolated, highly genotoxic altertoxin-II (ATX-II) (0.7 mg/kg of body weight) or (3) a solvent control. The complex mixture contained a spectrum of Alternaria toxins including a controlled dose of ATX-II, matching the concentration of the isolated ATX-II. Liver samples were collected after 24 h and analyzed via liquid chromatography-high-resolution mass spectrometry (LC-HRMS). Authentic reference standards (> 100) were used to identify endogenous metabolites and exogenous compounds from the administered exposures in tandem with SWATH-acquired MS/MS data which was used for non-targeted analysis/screening. Screening for metabolites produced by Alternaria revealed several compounds solely isolated in the liver of rats exposed to the complex culture, confirming results from a previously performed targeted biomonitoring study. This included the altersetin and altercrasin A that were tentatively identified. An untargeted metabolomics analysis found upregulation of acylcarnitines in rats receiving the complex Alternaria extract as well as downregulation of riboflavin in rats exposed to both ATX-II and the complex mixture. Taken together, this work provides a mechanistic view of Alternari toxin exposure and new suspect screening insights into hardly characterized Alternaria toxins.
由交链孢霉真菌产生的天然毒素包括交链孢酚、 tenuazonic 酸和 alternariol 毒素 I 和 II。这些毒素中的几种即使在低水平下也显示出很高的毒性,包括遗传毒性、致突变性和雌激素效应。然而,交链孢霉毒素暴露的代谢效应研究不足,特别是在肝脏作为关键靶标中。为了深入了解交链孢霉毒素暴露对肝脏代谢组的影响,将大鼠(n=21)暴露于(1)来自Alternaria alternata 的具有定义毒素特征的复杂培养物提取物(50mg/kg 体重),(2)分离的、高度遗传毒性的 alternariol 毒素 II(ATX-II)(0.7mg/kg 体重)或(3)溶剂对照。复杂混合物包含一系列交链孢霉毒素,包括受控剂量的 ATX-II,与分离的 ATX-II 浓度相匹配。暴露 24 小时后收集肝脏样本,并通过液相色谱-高分辨率质谱法(LC-HRMS)进行分析。使用真实的参考标准(>100 种)来鉴定内源性代谢物和外源性化合物,这些化合物来自给予的暴露,并与 SWATH 获得的 MS/MS 数据串联使用,用于非靶向分析/筛选。筛选交链孢霉产生的代谢物发现,几种化合物仅在暴露于复杂培养物的大鼠肝脏中分离出来,这证实了之前进行的靶向生物监测研究的结果。其中包括被暂定为 altersetin 和 altercrasin A 的化合物。非靶向代谢组学分析发现,接受复杂交链孢霉提取物的大鼠的酰基辅酶 A 上调,以及暴露于 ATX-II 和复杂混合物的大鼠的核黄素下调。总之,这项工作提供了交链孢霉毒素暴露的机制观点,并为尚未充分表征的交链孢霉毒素提供了新的可疑筛选见解。