| Literature DB >> 32041788 |
Casey M Gries1, Trevor Biddle2, Jeffrey L Bose3, Tammy Kielian4, David D Lo2.
Abstract
Implanted medical device-associated infections pose significant health risks, as they are often the result of bacterial biofilm formation. Staphylococcus aureus is a leading cause of biofilm-associated infections which persist due to mechanisms of device surface adhesion, biofilm accumulation, and reprogramming of host innate immune responses. We found that the S. aureus fibronectin binding protein A (FnBPA) is required for normal biofilm development in mammalian serum and that the SaeRS two-component system is required for functional FnBPA activity in serum. Furthermore, serum-developed biofilms deficient in FnBPA were more susceptible to macrophage invasion, and in a model of biofilm-associated implant infection, we found that FnBPA is crucial for the establishment of infection. Together, these findings show that S. aureus FnBPA plays an important role in physical biofilm development and represents a potential therapeutic target for the prevention and treatment of device-associated infections.Entities:
Keywords: S. aureus; biofilm; fibronectin binding protein; infection
Year: 2020 PMID: 32041788 PMCID: PMC7171244 DOI: 10.1128/IAI.00859-19
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441