Luraschi Roberto, Muñoz-Villagrán Claudia, Cornejo Fabián A, Pugin Benoit, Tobar Fernanda Contreras, Sandoval Juan Marcelo, Rivas-Pardo Jaime Andrés, Vera Carlos, Arenas Felipe
Laboratorio de Microbiología Molecular, Facultad de Química y Biología, Universidad de Santiago de Chile, Santiago 9170022, Chile.
Laboratory of Food Biotechnology, Department of Health Sciences and Technology, ETH Zürich, 8092 Zürich, Switzerland.
Int J Mol Sci. 2025 Jul 28;26(15):7287. doi: 10.3390/ijms26157287.
Tellurite (TeO) is a highly soluble and toxic oxyanion that inhibits the growth of at concentrations as low as ~1 µg/mL. This toxicity has been primarily attributed to the generation of reactive oxygen species (ROS) during its intracellular reduction by thiol-containing molecules and NAD(P)H-dependent enzymes. However, under anaerobic conditions, exhibits significantly increased tellurite tolerance-up to 100-fold in minimal media-suggesting the involvement of additional, ROS-independent mechanisms. In this study, we combined chemical-genomic screening, untargeted metabolomics, and targeted biochemical assays to investigate the effects of tellurite under both aerobic and anaerobic conditions. Our findings reveal that tellurite perturbs amino acid and nucleotide metabolism, leading to intracellular imbalances that impair protein synthesis. Additionally, tellurite induces notable changes in membrane lipid composition, particularly in phosphatidylethanolamine derivatives, which may influence biophysical properties of the membrane, such as fluidity or curvature. This membrane remodeling could contribute to the increased resistance observed under anaerobic conditions, although direct evidence of altered membrane fluidity remains to be established. Overall, these results demonstrate that tellurite toxicity extends beyond oxidative stress, impacting central metabolic pathways and membrane-associated functions regardless of oxygen availability.
亚碲酸盐(TeO)是一种高度可溶且有毒的含氧阴离子,在低至约1 µg/mL的浓度下就能抑制其生长。这种毒性主要归因于含硫醇分子和NAD(P)H依赖性酶在细胞内将其还原过程中产生的活性氧(ROS)。然而,在厌氧条件下,其对亚碲酸盐的耐受性显著提高——在基本培养基中高达100倍——这表明存在其他不依赖ROS的机制。在本研究中,我们结合化学基因组筛选、非靶向代谢组学和靶向生化分析,来研究有氧和厌氧条件下亚碲酸盐的影响。我们的研究结果表明,亚碲酸盐扰乱氨基酸和核苷酸代谢,导致细胞内失衡,进而损害蛋白质合成。此外,亚碲酸盐会引起膜脂组成的显著变化,尤其是磷脂酰乙醇胺衍生物,这可能会影响膜的生物物理性质,如流动性或曲率。这种膜重塑可能有助于在厌氧条件下观察到的抗性增加,尽管膜流动性改变的直接证据仍有待确定。总体而言,这些结果表明,亚碲酸盐的毒性不仅限于氧化应激,无论氧气是否存在,都会影响中心代谢途径和与膜相关的功能。