Abstract:
Biofilm infections can be chronic, life threatening and challenging to eradicate. Understanding <i>in vivo</i> stimuli affecting the biofilm cycle is one step toward targeted prevention strategies. Iron restriction by the host is a stimulus for biofilm formation for some <i>Staphylococcus aureus</i> isolates; however, in some infection scenarios bacteria are exposed to abundant amounts of hemoglobin (Hb), which <i>S. aureus</i> is able to use as iron source. Thus, we hypothesized a role for Hb in the biofilm infection. Microplate "biofilm" assays showed biofilm-matrix production was increased in the presence of hemoglobin when compared to the provision of iron as an inorganic salt. Microscopic analysis of biofilms showed that the provision of iron as hemoglobin consistently caused thicker and more structured biofilms when compared to the effect of the inorganic iron source. Iron responsive biofilm gene expression analysis showed that Agr Quorum Sensing, a known biofilm dispersal marker, was repressed with hemoglobin but induced with an equivalent amount of inorganic iron in the laboratory strain Newman. The gene expression of two biofilm structuring agents, PSMα and PSMβ, differed in the response to the iron source provided and was not correlated to hemoglobin-structured biofilms. A comparison of the model pathogen <i>S. aureus</i> Newman with local clinical isolates demonstrated that while there was a similar phenotypic biofilm response to hemoglobin, there was substantial variation in the expression of key biofilm dispersal markers, suggesting an underappreciated variation in biofilm regulome among <i>S. aureus</i> isolates and that no general inferences can be made by studying the behavior of single strains.
