Sulfated vizantin causes detachment of biofilms composed mainly of the genus Streptococcus without affecting bacterial growth and viability

BMC Microbiol. 2020 Nov 25;20(1):361. doi: 10.1186/s12866-020-02033-w.

Abstract

Background: Sulfated vizantin, a recently developed immunostimulant, has also been found to exert antibiofilm properties. It acts not as a bactericide, but as a detachment-promoting agent by reducing the biofilm structural stability. This study aimed to investigate the mechanism underlying this activity and its species specificity using two distinct ex vivo oral biofilm models derived from human saliva.

Results: The biofilm, composed mainly of the genus Streptococcus and containing 50 μM of sulfated vizantin, detached significantly from its basal surface with rotation at 500 rpm for only 15 s, even when 0.2% sucrose was supplied. Expression analyses for genes associated with biofilm formation and bacterial adhesion following identification of the Streptococcus species, revealed that a variety of Streptococcus species in a cariogenic biofilm showed downregulation of genes encoding glucosyltransferases involved in the biosynthesis of water-soluble glucan. The expression of some genes encoding surface proteins was also downregulated. Of the two quorum sensing systems involved in the genus Streptococcus, the expression of luxS in three species, Streptococcus oralis, Streptococcus gordonii, and Streptococcus mutans, was significantly downregulated in the presence of 50 μM sulfated vizantin. Biofilm detachment may be facilitated by the reduced structural stability due to these modulations. As a non-specific reaction, 50 μM sulfated vizantin decreased cell surface hydrophobicity by binding to the cell surface, resulting in reduced bacterial adherence.

Conclusion: Sulfated vizantin may be a candidate for a new antibiofilm strategy targeting the biofilm matrix while preserving the resident microflora.

Keywords: Biofilm; Detachment; Functional molecule; Gene expression; Glucosyltransferase; Streptococcus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology*
  • Bacterial Adhesion / drug effects
  • Bacterial Adhesion / genetics
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Biofilms / drug effects*
  • Biofilms / growth & development
  • Dental Caries / microbiology
  • Epithelial Cells / drug effects
  • Gene Expression / drug effects
  • Gingivitis / microbiology
  • Glucosyltransferases / genetics
  • Glucosyltransferases / metabolism
  • Glycolipids / chemistry
  • Glycolipids / pharmacology*
  • Humans
  • Quorum Sensing / drug effects
  • Quorum Sensing / genetics
  • Streptococcus / classification
  • Streptococcus / drug effects
  • Streptococcus / growth & development
  • Streptococcus / physiology*
  • Sulfates / chemistry
  • Trehalose / analogs & derivatives*
  • Trehalose / chemistry
  • Trehalose / pharmacology

Substances

  • 6,6'-bis-O-(3-nonyldodecanoyl)-alpha,alpha'-trehalose
  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Glycolipids
  • Sulfates
  • Trehalose
  • Glucosyltransferases