4.7 Article

Integration of transcriptomics and metabolomics reveals damage and recovery mechanisms of fish gills in response to nanosilver exposure

Journal

AQUATIC TOXICOLOGY
Volume 237, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.aquatox.2021.105895

Keywords

Silver nanoparticles; Common carp; Ecotoxicology; Transcriptome; Metabolome

Funding

  1. National Natural Science Foundation of China [22066026, 21567029]

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The study found that the toxicity of silver nanoparticles on fish gills showed potential recoverability at molecular and phenotype levels, as indicated by changes in gene and metabolite expression and the recovery of TCA cycle activity in common carp gills after exposure to AgNPs.
Toxic effects of silver nanoparticles (AgNPs) on fish gills have been widely reported but the recoverability of AgNPs-induced fish gill injuries is still unknown. In this study, combined multiomics and conventional toxicological analytical methods were used to investigate the changes in the gills of common carp responses to AgNPs (0.1 mg/L) toxicity after 24 h exposure and 7-day recovery. Conventional toxicological results showed that AgNPs exposure significantly increased silver content in gills and caused epithelial hyperplasia and lamellar fusion. After the recovery period, the silver content in fish gills significantly decreased; accompanied by the disappearance of histopathological characteristics in fish gills. Multiomics results revealed that AgNPs exposure resulted in the differential expression of 687 genes and 96 metabolites in fish gills. These differentially expressed genes (DEGs) and metabolites mainly participate in amino acid, carbohydrate, and lipid metabolisms, and are significantly enriched in the tricarboxylic acid (TCA) cycle. After the recovery period, the number of DEGs and metabolites in gills decreased to 33 and 90, respectively. Moreover, DEGs and metabolites in the TCA cycle recovered to control levels. In summary, the present study found that AgNPs-induced fish gill toxicity showed potential recoverability at molecular and phenotype levels.

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