Different molecular responses of Mytilus mantle to lipopolysaccharide and peptidoglycan challenges

Zilin Yang1, Pingling Cao1, Wenhui Xiao1

  • 1Laboratory of Marine Biology Protein Engineering, Marine Science and Technical College, Zhejiang Ocean University, Zhoushan City, 316022, Zhejiang, China.

PubMed

Insights

Mussel mantle immune responses to peptidoglycan (PGN) and lipopolysaccharide (LPS) differ significantly at the molecular level. Metabolomic analysis reveals distinct impacts on amino acid and lipid metabolism, offering potential biomarkers for immune challenges.

Area of Science:

  • Marine Biology
  • Immunology
  • Metabolomics

Background:

  • Mussels (Mytilus) are sessile filter feeders with mantle tissue crucial for immune defense.
  • Limited understanding of mantle immunity and its molecular responses to microbial stimuli.
  • Peptidoglycan (PGN) and lipopolysaccharide (LPS) are key microbe-associated molecular patterns (MAMPs) triggering immune responses.

Purpose of the Study:

  • To elucidate the molecular regulatory mechanisms in Mytilus mantle under PGN and LPS stress using metabolomics.
  • To evaluate antioxidant capacity, free amino acid profiles, and mucus antimicrobial activity.
  • To identify distinct metabolic signatures and potential biomarkers for PGN and LPS challenges.

Main Methods:

  • Ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS)-based metabolomic profiling of Mytilus mantle.
  • Assessment of antioxidant ability, free amino acid composition, and mantle mucus antimicrobial activity.
  • Comparative analysis of metabolic alterations induced by PGN and LPS.

Main Results:

  • PGN and LPS induced differential changes in mantle free amino acid composition, antioxidant ability, and mucus antimicrobial activity.
  • Both MAMPs altered mantle metabolites including amino acids, phospholipids, and fatty acids.
  • PGN activated amino acid metabolism and inhibited lipid metabolism; LPS activated amino acid metabolism and inhibited arachidonic acid metabolism.
  • PGN vs. LPS showed distinct signaling pathway activation (mTOR, FoxO) and metabolite upregulation (fosfomycin, deoxynojirimycin).

Conclusions:

  • Mussel mantle exhibits distinct metabolomic responses to PGN and LPS, highlighting differential immune regulation.
  • Metabolic profiles provide insights into mussel immune defense mechanisms against specific MAMPs.
  • Identified metabolites responding specifically to PGN and LPS hold potential as biomarkers for immune challenges in mussels.