Temporal expression of agrB, cidA, and alsS in the early development of Staphylococcus aureus UAMS-1 biofilm formation and the structural role of extracellular DNA and carbohydrates

Pathog Dis. 2014 Apr;70(3):414-22. doi: 10.1111/2049-632X.12158. Epub 2014 Mar 11.

Abstract

Extracellular DNA (eDNA) is an important component of the extracellular polymeric substance matrix and is important in the establishment and persistence of Staphylococcus aureus UAMS-1 biofilms. The aim of the study was to determine the temporal expression of genes involved in early biofilm formation and eDNA production. We used qPCR to investigate expression of agrB, which is associated with secreted virulence factors and biofilm dispersal, cidA, which is associated with biofilm adherence and genomic DNA release, and alsS, which is associated with cell lysis, eDNA release and acid tolerance. The contribution of eDNA to the stability of the biofilm matrix was assessed by digesting with DNase I (Pulmozyme) and quantifying structure by confocal microscopy and comstat image analysis. AgrB expression initially increased at 24 h but then dramatically decreased at 72 h in an inverse relationship to biomass, supporting its role in regulating biofilm dispersal. cidA and alsS expression steadily increased over 72 h, suggesting that eDNA was an important component of early biofilm development. DNase I had no effect on biomass, but did cause the biofilms to become more heterogeneous. Carbohydrates in the matrix appeared to play an important role in structural stability.

Keywords: Staphylococcus aureus; agrB; alsS; biofilm; carbohydrate; cidA; eDNA.

MeSH terms

  • Bacterial Proteins / genetics*
  • Biofilms / growth & development*
  • Carbohydrates*
  • DNA, Bacterial*
  • Deoxyribonuclease I / metabolism
  • Extracellular Space / metabolism
  • Gene Expression Regulation, Bacterial*
  • Humans
  • Staphylococcus aureus / isolation & purification
  • Staphylococcus aureus / physiology*

Substances

  • AgrB protein, Staphylococcus aureus
  • Bacterial Proteins
  • Carbohydrates
  • DNA, Bacterial
  • Deoxyribonuclease I