D-Galactose as an autoinducer 2 inhibitor to control the biofilm formation of periodontopathogens

J Microbiol. 2016 Sep;54(9):632-637. doi: 10.1007/s12275-016-6345-8. Epub 2016 Aug 31.

Abstract

Autoinducer 2 (AI-2) is a quorum sensing molecule to which bacteria respond to regulate various phenotypes, including virulence and biofilm formation. AI-2 plays an important role in the formation of a subgingival biofilm composed mostly of Gram-negative anaerobes, by which periodontitis is initiated. The aim of this study was to evaluate D-galactose as an inhibitor of AI-2 activity and thus of the biofilm formation of periodontopathogens. In a search for an AI-2 receptor of Fusobacterium nucleatum, D-galactose binding protein (Gbp, Gene ID FN1165) showed high sequence similarity with the ribose binding protein (RbsB), a known AI-2 receptor of Aggregatibacter actinomycetemcomitans. D-Galactose was evaluated for its inhibitory effect on the AI-2 activity of Vibrio harveyi BB152 and F. nucleatum, the major coaggregation bridge organism, which connects early colonizing commensals and late pathogenic colonizers in dental biofilms. The inhibitory effect of D-galactose on the biofilm formation of periodontopathogens was assessed by crystal violet staining and confocal laser scanning microscopy in the absence or presence of AI-2 and secreted molecules of F. nucleatum. D-Galactose significantly inhibited the AI-2 activity of V. harveyi and F. nucleatum. In addition, D-galactose markedly inhibited the biofilm formation of F. nucleatum, Porphyromonas gingivalis, and Tannerella forsythia induced by the AI-2 of F. nucleatum without affecting bacterial growth. Our results demonstrate that the Gbp may function as an AI-2 receptor and that galactose may be used for prevention of the biofilm formation of periodontopathogens by targeting AI-2 activity.

Keywords: AI-2 inhibitor; D-galactose; biofilm; periodontopathogens; quorum sensing.

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Biofilms / drug effects*
  • Calcium-Binding Proteins / genetics
  • Calcium-Binding Proteins / metabolism
  • Fusobacterium nucleatum / drug effects*
  • Fusobacterium nucleatum / genetics
  • Fusobacterium nucleatum / metabolism
  • Galactose / metabolism
  • Galactose / pharmacology*
  • Homoserine / analogs & derivatives*
  • Homoserine / antagonists & inhibitors
  • Homoserine / metabolism
  • Humans
  • Lactones / antagonists & inhibitors*
  • Lactones / metabolism
  • Monosaccharide Transport Proteins / genetics
  • Monosaccharide Transport Proteins / metabolism
  • Periodontitis / microbiology*
  • Periplasmic Binding Proteins / genetics
  • Periplasmic Binding Proteins / metabolism
  • Porphyromonas gingivalis / drug effects*
  • Porphyromonas gingivalis / physiology
  • Vibrio / drug effects
  • Vibrio / physiology

Substances

  • Bacterial Proteins
  • Calcium-Binding Proteins
  • Lactones
  • Monosaccharide Transport Proteins
  • N-octanoylhomoserine lactone
  • Periplasmic Binding Proteins
  • galactose-binding protein
  • Homoserine
  • Galactose