Trichothecene Mycotoxins Inhibit Mitochondrial Translation-Implication for the Mechanism of Toxicity

被引:57
作者
Bin-Umer, Mohamed Anwar [1 ]
McLaughlin, John E. [1 ]
Basu, Debaleena [1 ]
McCormick, Susan [2 ]
Tumer, Nilgun E. [1 ]
机构
[1] Rutgers State Univ, Sch Environm & Biol Sci, Dept Plant Biol & Pathol, New Brunswick, NJ 08901 USA
[2] ARS, Bacterial Foodborne Pathogens & Mycol Unit, Natl Ctr Agr Utilizat Res, USDA, Peoria, IL 61604 USA
基金
美国农业部;
关键词
trichothecenes; deoxynivalenol; T-2; toxin; diacetoxyscirpenol; Fusarium; mitochondria; ribosomes; translation; fusion; Fission; ROS; EUKARYOTIC PROTEIN-SYNTHESIS; RIBOTOXIC STRESS-RESPONSE; T-2; TOXIN; CELL-DEATH; PATHWAY; FUSION; DEOXYNIVALENOL; ACTIVATION; INDUCTION; GENE;
D O I
10.3390/toxins3121484
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Fusarium head blight (FHB) reduces crop yield and results in contamination of grains with trichothecene mycotoxins. We previously showed that mitochondria play a critical role in the toxicity of a type B trichothecene. Here, we investigated the direct effects of type A and type B trichothecenes on mitochondrial translation and membrane integrity in Saccharomyces cerevisiae. Sensitivity to trichothecenes increased when functional mitochondria were required for growth, and trichothecenes inhibited mitochondrial translation at concentrations, which did not inhibit total translation. In organello translation in isolated mitochondria was inhibited by type A and B trichothecenes, demonstrating that these toxins have a direct effect on mitochondrial translation. In intact yeast cells trichothecenes showed dose-dependent inhibition of mitochondrial membrane potential and reactive oxygen species, but only at doses higher than those affecting mitochondrial translation. These results demonstrate that inhibition of mitochondrial translation is a primary target of trichothecenes and is not secondary to the disruption of mitochondrial membranes.
引用
收藏
页码:1484 / 1501
页数:18
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