Association of proteases of Porphyromonas (Bacteroides) gingivalis with its adhesion to Actinomyces viscosus

J Dent Res. 1991 Feb;70(2):82-6. doi: 10.1177/00220345910700021501.


P. gingivalis adheres to A. viscosus on mineral surfaces mimicking teeth. To study whether P. gingivalis proteases contribute to its binding, mutants of P. gingivalis deficient in proteases were compared with their parent strain and a P. gingivalis-type strain for their adherence to A. viscosus on saliva-coated hydroxyapatite by manipulating a radio-isotope binding assay. Adherence of P. gingivalis 2561 to A. viscosus was studied by tests of the effects of incubation temperature and known inhibitors or promoters of proteases. Controls were handled by the assay run in PBS buffer at 22 degrees C. Two mutants deficient in trypsin-like protease were found to be deficient in adherence (% attachment relative to control: 3.2 +/- 0.1% and 11.2 +/- 0.4%), while a collagenase-deficient mutant had an adherence score (51.6 +/- 8.4) closer to that of the parent strain (75.6 +/- 7.2%). Heating P. gingivalis at 70 degrees C decreased its subsequent adherence at 22 degrees C by 80%. Adherence decreased by 60% when the assay was run at 4 degrees C, but increased by 70% at 37 degrees C. Reducing agents (dithiothreitol, cysteine, and mercaptoethanol) enhanced P. gingivalis adherence by 50 to 60%. Protease inhibitors (BZMD, SBTI, TPCK, TLCK, CMPS, PMSF) decreased adherence by 10 to 50%. Also, Hg2+ and Zn2+ decreased adherence by 30 to 50%, and arginine decreased it by 50%. Most of these effects on P. gingivalis adherence were statistically significant (p less than 0.05). Analysis of these data suggests that P. gingivalis proteases may contribute to the cohesion of P. gingivalis and A. viscosus.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actinomyces / metabolism*
  • Analysis of Variance
  • Arginine / pharmacology
  • Bacterial Adhesion / drug effects
  • Bacterial Adhesion / physiology*
  • Bacterial Proteins / metabolism
  • Bacteroides / enzymology*
  • Endopeptidases / metabolism*
  • Metals / pharmacology
  • Microbial Collagenase / metabolism
  • Protease Inhibitors / pharmacology
  • Protein Binding
  • Stimulation, Chemical


  • Bacterial Proteins
  • Metals
  • Protease Inhibitors
  • Arginine
  • Endopeptidases
  • Microbial Collagenase