Human monoclonal antibodies against Staphylococcus aureus surface antigens recognize in vitro and in vivo biofilm

Journal Article (2022)
Author(s)

Lisanne de Vor ( University Medical Centre Utrecht)

Bruce van Dijk ( University Medical Centre Utrecht)

Kok van Kessel ( University Medical Centre Utrecht)

Jeffrey S. Kavanaugh (University of Colorado - Anschutz)

Carla de Haas ( University Medical Centre Utrecht)

Piet C. Aerts ( University Medical Centre Utrecht)

Ruud M. Ramakers (TU Delft - RST/Technici Pool, MILabs B.V., University Medical Centre Utrecht)

Freek J. Beekman (TU Delft - RST/Biomedical Imaging, University Medical Centre Utrecht, MILabs B.V.)

Harrie Weinans ( University Medical Centre Utrecht, TU Delft - Biomechanical Engineering, TU Delft - Biomaterials & Tissue Biomechanics)

DOI related publication
https://doi.org/10.7554/eLife.67301 Final published version
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Publication Year
2022
Language
English
Journal title
eLife
Volume number
11
Article number
e67301
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Abstract

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.