The multifaceted role of c-di-AMP signaling in the regulation of Porphyromonas gingivalis lipopolysaccharide structure and function

Front Cell Infect Microbiol. 2024 Jun 12:14:1418651. doi: 10.3389/fcimb.2024.1418651. eCollection 2024.

Abstract

Background: This study unveils the intricate functional association between cyclic di-3',5'-adenylic acid (c-di-AMP) signaling, cellular bioenergetics, and the regulation of lipopolysaccharide (LPS) profile in Porphyromonas gingivalis, a Gram-negative obligate anaerobe considered as a keystone pathogen involved in the pathogenesis of chronic periodontitis. Previous research has identified variations in P. gingivalis LPS profile as a major virulence factor, yet the underlying mechanism of its modulation has remained elusive.

Methods: We employed a comprehensive methodological approach, combining two mutants exhibiting varying levels of c-di-AMP compared to the wild type, alongside an optimized analytical methodology that combines conventional mass spectrometry techniques with a novel approach known as FLATn.

Results: We demonstrate that c-di-AMP acts as a metabolic nexus, connecting bioenergetic status to nuanced shifts in fatty acid and glycosyl profiles within P. gingivalis LPS. Notably, the predicted regulator gene cdaR, serving as a potent regulator of c-di-AMP synthesis, was found essential for producing N-acetylgalactosamine and an unidentified glycolipid class associated with the LPS profile.

Conclusion: The multifaceted roles of c-di-AMP in bacterial physiology are underscored, emphasizing its significance in orchestrating adaptive responses to stimuli. Furthermore, our findings illuminate the significance of LPS variations and c-di-AMP signaling in determining the biological activities and immunostimulatory potential of P. gingivalis LPS, promoting a pathoadaptive strategy. The study expands the understanding of c-di-AMP pathways in Gram-negative species, laying a foundation for future investigations into the mechanisms governing variations in LPS structure at the molecular level and their implications for host-pathogen interactions.

Keywords: C-di-AMP signaling; Porphyromonas gingivalis; cellular bioenergetics; lipopolysaccharide; structural variations.

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Dinucleoside Phosphates / metabolism
  • Energy Metabolism
  • Fatty Acids / metabolism
  • Gene Expression Regulation, Bacterial
  • Humans
  • Lipopolysaccharides* / metabolism
  • Porphyromonas gingivalis* / genetics
  • Porphyromonas gingivalis* / metabolism
  • Signal Transduction*
  • Virulence Factors / metabolism

Substances

  • Lipopolysaccharides
  • Virulence Factors
  • Dinucleoside Phosphates
  • Fatty Acids
  • Bacterial Proteins