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Oral Biofilm Formation on Different Materials for Dental Implants
Published on: June 24, 2018
Methylene Blue Is an Effective Disclosing Agent for Identifying Bacterial Biofilms on Orthopaedic Implants
Jeremy D Shaw1,2, Darrel S Brodke1, Dustin L Williams1,3,4,5
1Department of Orthopaedics, University of Utah School of Medicine, Salt Lake City, Utah.
Background:
Bacterial biofilms pose a challenge in treating implant-associated infections. Biofilms provide bacteria with protection against antimicrobial agents and the immune response and often are invisible to the naked eye. As a biofilm-disclosing agent, methylene blue (MB) has shown promise, but lacks rigorous in vitro evaluation. The purposes of the present study were to assess MB as a biofilm-disclosing agent in vitro for common biofilm-forming organisms and to determine performance characteristics across implant materials and healthy tissue types.
Methods:
Staphylococcus aureus (ATCC 6538) and Pseudomonas aeruginosa (ATCC 27853) biofilms were grown on culture for 2 days in CDC biofilm reactors on titanium, cobalt chromium, polyethylene, and polyether ether ketone (PEEK) coupons. Biofilms were stained with MB solutions of either 0.005% or 0.01% and then were washed with normal saline solution. Digital photographs were obtained to compare the visual sensitivity of the blue dye at these dilutions. Scanning electron microscopy (SEM) was performed to confirm the absence or presence of biofilm on MB-stained areas. Uninoculated controls were also assessed. Healthy adult sheep tissues were also stained to determine the staining characteristics of the host tissue. ImageJ was used to determine the relative blue intensity of stained implants and tissues compared with standard curves.
Results:
S. aureus and P. aeruginosa biofilms stained avidly on titanium, cobalt chromium, polyethylene, and PEEK coupons. There was visible dose-dependent staining based on dye concentration. MB was visible only where biofilms were present as confirmed by SEM. MB did not stain uninoculated controls. Articular cartilage and meniscus demonstrated appreciable staining; bone, tendon, muscle, nerve, and fat did not. Bacterial biofilms demonstrated both dose-dependent and species-specific staining.
Conclusions:
MB is an effective disclosing agent for S. aureus and P. aeruginosa biofilms in vitro. MB did not stain implant materials, nor did it stain most healthy tissues in vitro. MB may allow surgeons to see biofilms and may allow for enhanced debridement once visualized.
Insights
Methylene blue (MB) effectively visualizes bacterial biofilms on implants in vitro. This dye aids in identifying biofilms on common implant materials without staining healthy tissues, potentially improving surgical debridement.
Area of Science:
- Biomaterials science
- Microbiology
- Medical imaging
Background:
- Bacterial biofilms present a significant challenge in treating implant-associated infections due to their resistance to antimicrobials and host defenses.
- Methylene blue (MB) has shown potential as a biofilm-disclosing agent, but requires rigorous in vitro validation.
- Current diagnostic methods often fail to detect biofilms, which are typically invisible to the naked eye.
Purpose of the Study:
- To evaluate methylene blue (MB) as an in vitro biofilm-disclosing agent for common biofilm-forming bacteria.
- To assess the performance characteristics of MB across various implant materials and healthy tissue types.
- To determine the efficacy of MB in visualizing bacterial biofilms in an in vitro setting.
Main Methods:
- Biofilms of Staphylococcus aureus and Pseudomonas aeruginosa were cultivated on titanium, cobalt chromium, polyethylene, and PEEK coupons in CDC biofilm reactors.
- Biofilms were stained with 0.005% or 0.01% methylene blue (MB) solutions, followed by saline washing.
- Digital photography, scanning electron microscopy (SEM), and ImageJ analysis were used to assess biofilm presence, staining intensity, and species-specific staining.
Main Results:
- Staphylococcus aureus and Pseudomonas aeruginosa biofilms stained intensely on all tested implant materials (titanium, cobalt chromium, polyethylene, PEEK).
- Methylene blue (MB) staining was dose-dependent and visible only in the presence of biofilms, confirmed by SEM.
- While MB stained articular cartilage and meniscus, it did not stain bone, tendon, muscle, nerve, or fat, and did not stain uninoculated controls.
Conclusions:
- Methylene blue (MB) is a highly effective in vitro disclosing agent for Staphylococcus aureus and Pseudomonas aeruginosa biofilms.
- MB demonstrated excellent performance on common implant materials, with minimal staining of healthy host tissues.
- The ability of MB to visualize biofilms may enhance surgical debridement by allowing surgeons to identify infected areas.
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