<i>Staphylococcus aureus</i> Adhesion on Hydrophobin Coatings: Adhesion Forces and the Influence of Surface Charge

<i>Staphylococcus aureus</i> (<i>S. aureus</i>) is one of the bacterial species capable of forming multilayered biofilms on implants. Such biofilms formed on implanted medical devices often require the removal of the implant in order to avoid sepsis or, in the worst case, even the death of the patient. To address the problem of unwanted <i>S. aureus</i> biofilm formation, its first step, i.e., adhesion, must be understood and prevented. Thus, the development of adhesion-reducing surface coatings for implant materials is of utmost importance. In this work, we used single-cell force spectroscopy to analyze the adhesion of the biofilm-forming <i>S. aureus</i> strain SA113 on naive and protein-coated silicon surfaces (SiO<sub>2</sub>). In addition to the wild type, we used the SA113 Δ<i>dltA</i> knockout mutant to further investigate the effect of d-alanylation of lipoteichoic acids of the cell wall. In order to examine how the surface charge affects adhesion, we coated silanized SiO<sub>2</sub> surfaces with amphiphilic class II hydrophobins. The naturally occurring hydrophobin HFBI was used as well as the HFBI variant D40Q/D43N, which is less negatively charged at physiological pH due to the exchange of two acidic aspartate residues. These two types of hydrophobin-coated surfaces resemble each other in roughness and wettability but differ only in charge. By measurement of the forces with which each <i>S. aureus</i> strain binds to hydrophobin-coated surfaces, we show that the adhesion of <i>S. aureus</i> at surfaces can be influenced by the charges exposed by the target surfaces. Therefore, in addition to hydrogen bonding, electrostatic interactions between the cell and the hydrophilic surface govern adhesion on these surfaces. Moreover, we found that for both HFBI coatings, the adhesion strength of <i>S. aureus</i> is reduced by nearly a factor of 30 compared to silanized SiO<sub>2</sub> surfaces. Therefore, hydrophobin coatings are of great interest for further use in the field of biomedical surface coating.

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Journal
ACS Omega
Published
2025-08-20
DOI
https://doi.org/10.1021/acsomega.4c11010
Primary Topic
Bacterial biofilms and quorum sensing
Type
article
Field-Weighted Citation Impact
0.00

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article

Staphylococcus aureus Adhesion on Hydrophobin Coatings: Adhesion Forces and the Influence of Surface Charge

Kirstin Kochems, Karin Jacobs, Philipp Jung, Markus Bischoff et al.
ACS Omega
Bacterial biofilms and quorum sensing
article

Staphylococcus aureus Adhesion on Hydrophobin Coatings: Adhesion Forces and the Influence of Surface Charge

Kirstin Kochems, Karin Jacobs, Philipp Jung, Markus Bischoff, Ben Wieland, Michael Lienemann, Hendrik Hähl, Friederike Nolle, Hannah Heintz
article en

Abstract

<i>Staphylococcus aureus</i> (<i>S. aureus</i>) is one of the bacterial species capable of forming multilayered biofilms on implants. Such biofilms formed on implanted medical devices often require the removal of the implant in order to avoid sepsis or, in the worst case, even the death of the patient. To address the problem of unwanted <i>S. aureus</i> biofilm formation, its first step, i.e., adhesion, must be understood and prevented. Thus, the development of adhesion-reducing surface coatings for implant materials is of utmost importance. In this work, we used single-cell force spectroscopy to analyze the adhesion of the biofilm-forming <i>S. aureus</i> strain SA113 on naive and protein-coated silicon surfaces (SiO<sub>2</sub>). In addition to the wild type, we used the SA113 Δ<i>dltA</i> knockout mutant to further investigate the effect of d-alanylation of lipoteichoic acids of the cell wall. In order to examine how the surface charge affects adhesion, we coated silanized SiO<sub>2</sub> surfaces with amphiphilic class II hydrophobins. The naturally occurring hydrophobin HFBI was used as well as the HFBI variant D40Q/D43N, which is less negatively charged at physiological pH due to the exchange of two acidic aspartate residues. These two types of hydrophobin-coated surfaces resemble each other in roughness and wettability but differ only in charge. By measurement of the forces with which each <i>S. aureus</i> strain binds to hydrophobin-coated surfaces, we show that the adhesion of <i>S. aureus</i> at surfaces can be influenced by the charges exposed by the target surfaces. Therefore, in addition to hydrogen bonding, electrostatic interactions between the cell and the hydrophilic surface govern adhesion on these surfaces. Moreover, we found that for both HFBI coatings, the adhesion strength of <i>S. aureus</i> is reduced by nearly a factor of 30 compared to silanized SiO<sub>2</sub> surfaces. Therefore, hydrophobin coatings are of great interest for further use in the field of biomedical surface coating.

ACS OmegaVol. 10(34)
Trier University of Applied Sciences (DE), Max Planck Institute for Medical Research (DE), BioChem Technology (United States) (US), Institute of Medical Microbiology and Hygiene (DE), Applied BioPhysics (United States) (US), Max Planck Institute for the Structure and Dynamics of Matter (DE), United Medix Laboratories (Finland) (FI), VTT Technical Research Centre of Finland (FI), Universität Trier (DE), Saarland University (DE)
Deutsche Forschungsgemeinschaft, Academy of Finland, Bundesministerium für Bildung und Forschung
Openalex Percentile: Top 81%
Bacterial biofilms and quorum sensing
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