Comparative transcriptome analysis of the gills of Procambarus clarkii provide novel insights into the response mechanism of ammonia stress tolerance

Mol Biol Rep. 2021 Mar;48(3):2611-2618. doi: 10.1007/s11033-021-06315-y. Epub 2021 Apr 3.

Abstract

Procambarus clarkii is an important model crustacean organism in many researches. Ammonia nitrogen is one of common contaminants in aquatic environment, influencing the health of aquatic organisms. The primary objective of this study was to investigate molecular mechanisms on ammonia stress in gills of P. clarkii to provide new insights into the strategies of aquatic animals in responding to high concentration of ammonia in the environment. Procambarus clarkii were randomly assigned into two groups (ammonia stress group, AG; control group, CG), and gill samples were dependently excised from AG and CG. Then response mechanisms on ammonia stress were investigated based on transcriptome data of P. clarkii. 9237 differentially expressed genes were identified in ammonia stress group. The genes of ion transport enzymes (NKA and SLC6A5S) were significantly up-regulated. Whereas the immune-related genes (e.g. MAP3K7, HSP70, HSP90A, CTSF, CTSL1, CHI and CTL4) and pathways were significantly up-regulated, which played an important role in reacting to ammonia stress. Procambarus clarkii may enhance immune defense to counteract ammonia toxicity by the up-regulation of immune-related genes and signaling pathways. The activities of ion transport enzymes are changed to mobilise signal transduction and ion channel regulation for adapting to ammonia environment. These previous key genes play an important role in resistance to ammonia stress to better prepare for survival in high concentration of ammonia.

Keywords: Ammonia; Environmental toxicology; Gills; Procambarus clarkii; Transcriptomics.

Publication types

  • Comparative Study

MeSH terms

  • Adaptation, Physiological / drug effects
  • Adaptation, Physiological / genetics*
  • Ammonia / toxicity*
  • Animals
  • Antioxidants / metabolism
  • Astacoidea / drug effects
  • Astacoidea / genetics*
  • Astacoidea / immunology
  • Astacoidea / physiology*
  • Energy Metabolism / drug effects
  • Energy Metabolism / genetics
  • Gene Expression Profiling*
  • Gills / metabolism*
  • MAP Kinase Signaling System / genetics
  • Molecular Sequence Annotation
  • Stress, Physiological / drug effects
  • Stress, Physiological / genetics*
  • Transcriptome / drug effects
  • Transcriptome / genetics*

Substances

  • Antioxidants
  • Ammonia