Delphinidin protects colon carcinoma cells against the genotoxic effects of the mycotoxin altertoxin II

• Published in: Toxicology letters 2018-03, Vol.284, p.136-142
• Main Authors: Aichinger, Georg, Puntscher, Hannes, Beisl, Julia, Kütt, Mary-Liis, Warth, Benedikt, Marko, Doris
• Format: Article
• Language: English
• Subjects: Alternaria alternata; Anthocyanin; Combinatory effects; Degradation; Food safety; Mycotoxin
• ISSN: 0378-4274; 1879-3169
• DOI: 10.1016/j.toxlet.2017.12.002

[Display omitted] •The mycotoxin altertoxin II (ATX-II) induces DNA strand breaks in HT-29 cells.•The anthocyanidin delphinidin (DEL) suppresses this genotoxicity of ATX-II.•The presence of DEL diminishes detectable ATX-II levels.•Potential contribution of degradation products of DEL. Alternaria spp. are ubiquitous molds that are able to produce toxic secondary metabolites which may contaminate food globally. One of those is the mycotoxin altertoxin II (ATX-II), a genotoxic and mutagenic compound. In recent years, different flavonoids that may co-occur with mycotoxins in food were demonstrated to temper toxic effects of molds, mostly through their anti-oxidant properties. Thus, in this study, we assessed the influence of the berry anthocyanidin delphinidin on the toxicity of ATX-II in HT-29 colon carcinoma cells. We performed coupled SRB/WST-1 cytotoxicity assays which revealed only weak antagonistic interactions, and single-cell gel electrophoresis (“comet”) assays, where we observed a potent protective effect of delphinidin on the DNA-damaging properties of ATX-II. Furthermore, we investigated the mechanism for this interaction. In the DCF assay delphinidin was found to reduce intracellular oxidative stress levels, which might contribute partly to the latter protection. However, LC-MS experiments showed that co-incubation of the mycotoxin with either delphinidin or its potential degradation product phloroglucinol aldehyde significantly decreased ATX-II concentrations in aqueous solutions, indicating that a direct chemical reaction of ATX-II with these components is likely responsible for the observed loss of toxicity. Our results indicate that delphinidin − and possibly other anthocyanins as well − might play a role in the protection of the gut from Alternaria-induced genotoxicity.