
ABSTRACT Due to their abilities to form strong biofilms, Staphylococcus aureus and Staphylococcus epidermidis are the most frequently isolated pathogens in persistent and chronic implant-associated infections. As biofilm-embedded bacteria are more resistant to antibiotics and the immune system, they are extremely difficult to treat. Therefore, biofilm-active antibiotics are a major challenge. Here we investigated the effect of the lantibiotic gallidermin on two representative biofilm-forming staphylococcal species. Gallidermin inhibits not only the growth of staphylococci in a dose-dependent manner but also efficiently prevents biofilm formation by both species. The effect on biofilm might be due to repression of biofilm-related targets, such as ica (intercellular adhesin) and atl (major autolysin). However, gallidermin's killing activity on 24-h and 5-day-old biofilms was significantly decreased. A subpopulation of 0.1 to 1.0% of cells survived, comprising “persister” cells of an unknown genetic and physiological state. Like many other antibiotics, gallidermin showed only limited activity on cells within mature biofilms.
570, Staphylococcus aureus, Microbial Viability, 610, Microbial Sensitivity Tests, N-Acetylmuramoyl-L-alanine Amidase, Bacteriocins, Biofilms, Staphylococcus epidermidis, Adhesins, Bacterial, Peptides
570, Staphylococcus aureus, Microbial Viability, 610, Microbial Sensitivity Tests, N-Acetylmuramoyl-L-alanine Amidase, Bacteriocins, Biofilms, Staphylococcus epidermidis, Adhesins, Bacterial, Peptides
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