Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, United States
Gerard C Krijger
Department of Radiology and Nuclear Medicine, University Medical Centre Utrecht, Utrecht, Netherlands
Ruud M Ramakers
MILabs B.V, Utrecht, Netherlands; Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center, Utrecht, Netherlands; Department of Radiation Science and Technology, Delft University of Technology, Delft, Netherlands
Freek J Beekman
MILabs B.V, Utrecht, Netherlands; Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center, Utrecht, Netherlands; Department of Radiation Science and Technology, Delft University of Technology, Delft, Netherlands
College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, Canada
Marnix GEH Lam
Department of Radiology and Nuclear Medicine, University Medical Centre Utrecht, Utrecht, Netherlands
H Charles Vogely
Department of Orthopedics, University Medical Centre Utrecht, Utrecht, Netherlands
Bart CH van der Wal
Department of Orthopedics, University Medical Centre Utrecht, Utrecht, Netherlands
Jos AG van Strijp
Department of Medical Microbiology, University Medical Centre Utrecht, Utrecht, Netherlands
Alexander R Horswill
Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, United States; Department of Veterans Affairs, Eastern Colorado Health Care System, Denver, United States
Harrie Weinans
Department of Orthopedics, University Medical Centre Utrecht, Utrecht, Netherlands; Department of Biomechanical engineering, TU Delft, Delft, Netherlands
Implant-associated Staphylococcus aureus infections are difficult to treat because of biofilm formation. Bacteria in a biofilm are often insensitive to antibiotics and host immunity. Monoclonal antibodies (mAbs) could provide an alternative approach to improve the diagnosis and potential treatment of biofilm-related infections. Here, we show that mAbs targeting common surface components of S. aureus can recognize clinically relevant biofilm types. The mAbs were also shown to bind a collection of clinical isolates derived from different biofilm-associated infections (endocarditis, prosthetic joint, catheter). We identify two groups of antibodies: one group that uniquely binds S. aureus in biofilm state and one that recognizes S. aureus in both biofilm and planktonic state. Furthermore, we show that a mAb recognizing wall teichoic acid (clone 4497) specifically localizes to a subcutaneously implanted pre-colonized catheter in mice. In conclusion, we demonstrate the capacity of several human mAbs to detect S. aureus biofilms in vitro and in vivo.