Furanone at Subinhibitory Concentrations Enhances Staphylococcal Biofilm Formation by luxS Repression

• DOI: 10.1128/aac.01704-08
• Publication Date: 2009-07-21T00:58:33Z
• Authors: Richard Kuehl; Sameer Al-Bataineh; Oliver Gordon; Reto Luginbuehl; Michael Otto; Marcus Textor; Regine Landmann
• Keywords: 0301 basic medicine; Molecular Structure; Staphylococcus; Polysaccharides, Bacterial; biofilm effect; multicellular behaviours; Quorum Sensing; Gene Expression Regulation, Bacterial; Microbial Sensitivity Tests; gram-negative bacteria; Cell Line; Carbon-Sulfur Lyases; Mice; 03 medical and health sciences; Bacterial Proteins; brominated furanones; marine algae; Biofilms; Animals; Furans; staphylococci

ABSTRACT

Brominated furanones from marine algae inhibit multicellular behaviors of gram-negative bacteria such as biofilm formation and quorum sensing (QS) without affecting their growth. The interaction of furanone with QS in gram-positive bacteria is unknown. Staphylococci have two QS systems, agr and luxS , which lower biofilm formation by two different pathways, RNAIII upregulation and bacterial detachment, and polysaccharide intercellular adhesin (PIA) reduction, respectively. We synthesized natural furanone compound 2 [(5 Z )-4-bromo-5-(bromomethylene)-3-butyl-2(5 H )-furanone] from Delisea pulchra and three analogues to investigate their effect on biofilm formation in gram-positive bacteria. Compound 2, but not the analogues, enhanced the biofilms of Staphylococcus epidermidis 1457 and 047 and of S. aureus Newman at concentrations between 1.25 and 20 μM. We show the growth inhibition of S. epidermidis and S. aureus by free furanone and demonstrate bactericidal activity. An induction of biofilm occurred at concentrations of 10 to 20% of the MIC and correlated with an increase in PIA. The biofilm effect was agr independent. It was due to interference with luxS , as shown by reduced luxS expression in the presence of compound 2 and independence of the strong biofilm formation in a luxS mutant upon furanone addition. Poly( l -lysine)-grafted/poly(ethylene glycol)-grafted furanone was ineffective on biofilm and not bactericidal, indicating the necessity for free furanone. Free furanone was similarly toxic for murine fibroblasts as for staphylococci, excluding a therapeutic application of this compound. In summary, we observed a biofilm enhancement by furanone in staphylococci at subinhibitory concentrations, which was manifested by an increase in PIA and dependent on luxS .