Epigenetic effects of silver nanoparticles and ionic silver in Tetrahymena thermophila

The widespread use of silver nanoparticles (Ag NPs) has raised substantial health risks, but little is known about the epigenetic toxicity induced by Ag+ and Ag NPs. This study characterized physiological and lncRNA profiles to explore the toxic effects and epigenetic mechanisms in Tetrahymena thermophila on exposure to Ag+ ( in the form of AgNO3) and different Ag NPs for 24 h. The Ag NPs studied varied in size (10 nm and 80 nm) and surface coating (citrate and polyvinylpyrrolidone). We found that both Ag+ and Ag NPs elicited strong growth-inhibiting effects on T. thermophila. The toxicity was mainly caused by high reactive oxygen species (ROS) levels, leading to lipid peroxidation and mitochondrial dysfunction. To combat the oxidative stress, the protist activated an antioxidative response, increasing the activity of glutathione peroxidase and other antioxidants. Notably, 1250 lncRNAs were differentially expressed under Ag+ or Ag NPs exposure relative to the non-exposure control, which were clustered into 15 expression modules in weighted gene co-expression network analysis. These gene modules exhibited toxicant-specific expression patterns, potentially playing regulatory roles, via their co-expressed mRNAs, to inhibit cell growth, activate cell membrane cation channel, and promote oxidoreductase activity. This research illuminates how post-transcriptional mechanisms of a ciliated protozoan regulate responses to Ag+ and Ag NPs toxicities. (C) 2021 Elsevier B.V. All rights reserved.

Automated summary

The study revealed that both Ag+ and Ag NPs exerted growth-inhibiting effects on Tetrahymena thermophila, mainly due to high levels of ROS causing oxidative stress, leading to lipid peroxidation and mitochondrial dysfunction. Additionally, 1250 lncRNAs were differentially expressed under exposure to Ag+ or Ag NPs, potentially regulating cell growth and oxidoreductase activity through co-expressed mRNAs.