Physiological, cytological and multi-omics analysis revealed the molecular response of Fritillaria cirrhosa to Cd toxicity in Qinghai-Tibet Plateau

J Hazard Mater. 2024 Jul 5:472:134611. doi: 10.1016/j.jhazmat.2024.134611. Epub 2024 May 14.

Abstract

Fritillaria cirrhosa, an endangered plant endemic to plateau regions, faces escalating cadmium (Cd) stress due to pollution in the Qinghai-Tibet Plateau. This study employed physiological, cytological, and multi-omics techniques to investigate the toxic effects of Cd stress and detoxification mechanisms of F. cirrhosa. The results demonstrated that Cd caused severe damage to cell membranes and organelles, leading to significant oxidative damage and reducing photosynthesis, alkaloid and nucleoside contents, and biomass. Cd application increased cell wall thickness by 167.89% in leaves and 445.78% in bulbs, leading to weight percentage of Cd increases of 76.00% and 257.14%, respectively. PER, CESA, PME, and SUS, genes responsible for cell wall thickening, were significantly upregulated. Additionally, the levels of metabolites participating in the scavenging of reactive oxygen species, including oxidized glutathione, D-proline, L-citrulline, and putrescine, were significantly increased under Cd stress. Combined multi-omics analyses revealed that glutathione metabolism and cell wall biosynthesis pathways jointly constituted the detoxification mechanism of F. cirrhosa in response to Cd stress. This study provides a theoretical basis for further screening of new cultivars for Cd tolerance and developing appropriate cultivation strategies to alleviate Cd toxicity.

Keywords: Cadmium; Cell wall; Detoxification mechanisms; Endangered species; Ultrastructure.

MeSH terms

  • Cadmium* / toxicity
  • Cell Wall / drug effects
  • Cell Wall / metabolism
  • Fritillaria* / genetics
  • Fritillaria* / metabolism
  • Glutathione / metabolism
  • Multiomics
  • Oxidative Stress / drug effects
  • Photosynthesis / drug effects
  • Plant Leaves / drug effects
  • Plant Leaves / metabolism
  • Reactive Oxygen Species / metabolism
  • Tibet

Substances

  • Cadmium
  • Glutathione
  • Reactive Oxygen Species