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Staphylococcus aureus Behavior on Artificial Surfaces Mimicking Bone Environment.
Anaïs Lemaire1, Jennifer Varin-Simon1, Fabien Lamret1
1Biomatériaux et Inflammation en Site Osseux, Université de Reims Champagne-Ardenne, BIOS EA 4691, SFR Cap Santé, 51097 Reims, France.
Pathogens (Basel, Switzerland)
|March 29, 2023
Summary
Biomimetic bone scaffolds made of calcium phosphate (CaP) or collagen can be colonized by Staphylococcus aureus, leading to biofilm formation. Antimicrobial strategies are needed to prevent infections with these bone-regeneration materials.
Area of Science:
- Biomaterials Science
- Infectious Diseases
- Orthopedic Surgery
Background:
- Infections pose a significant challenge to bone regeneration, particularly with biomaterials that may promote bacterial adhesion.
- Calcium phosphate (CaP) and collagen are common substrates for bone regeneration scaffolds but can support Staphylococcus aureus (S. aureus) adhesion.
- S. aureus can form biofilms, which are highly resistant to antibiotics and immune responses, complicating treatment.
Purpose of the Study:
- To compare the adhesion of three S. aureus strains on CaP- and collagen-coated surfaces.
- To evaluate the potential of these bone-mimicking coatings for developing in vitro infection models.
- To assess the risk of bacterial colonization and biofilm development on bone substitute materials.
Main Methods:
- Three S. aureus strains (CIP 53.154, SH1000, USA300) were tested for adhesion on CaP- and collagen-coated surfaces.
- Bacterial adhesion and matrix component formation were quantified.
- Biofilm gene expression was analyzed.
- CaP, collagen, and titanium-mimicking surfaces were simultaneously tested in vitro.
Main Results:
- All three S. aureus strains adhered to both CaP and collagen coatings.
- More visible matrix components were observed on CaP coatings compared to collagen.
- No significant differences in biofilm gene expression were found between CaP and collagen surfaces.
- Simultaneous testing of multiple surfaces did not yield significantly different adhesion results compared to independent testing.
Conclusions:
- CaP and collagen coatings, used as bone substitutes, are susceptible to bacterial colonization, particularly CaP.
- These materials require integration with antimicrobial strategies to prevent biofilm formation.
- The findings highlight the need for careful material selection and infection control in bone regeneration therapies.

