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Simvastatin decreases the silver resistance of E. faecalis through compromising the entrapping function of
Jingwen Cui1, Mengting Duan1, Qing Sun1
1The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei‑MOST) and Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan University, 237 Luoyu Road, Wuhan, 430079, People's Republic of China.
Abstract:
Enterococcus faecalis (E. faecalis) is a Gram-positive bacterium closely related to many refractory infections of human and shows the resistant ability against the antibacterial effects of silver. Simvastatin is a semisynthetic compound derived from lovastatin and a hydroxymethyl glutaryl coenzyme A(HMG-COA) reductase inhibitor showing certain inhibitive effects on bacteria. The main purpose of this study was to establish and characterize the Ag+/silver nanoparticles (AgNPs)-resistant E. faecalis, and further evaluate the function of extracellular polymeric substances (EPS) in the silver resistance and the effect of simvastatin on the silver-resistance of E. faecalis. The results showed that the established silver-resistant E. faecalis had strong resistance against both Ag+ and AgNPs and simvastatin could decrease the silver-resistance of both original and Ag+/AgNPs-resistant E. faecalis. The Transmission electron microscopy (TEM), High-angle annular dark-field (HAADF) and mapping images showed that the silver ions or particles aggregated and confined in the EPS on surface areas of the cell membrane when the silver-resistant E. faecalis were incubated with Ag+ or AgNPs. When the simvastatin was added, the silver element was not confined in the EPS and entered the bacteria. These findings may indicate that the silver resistance of E. faecalis was derived from the entrapping function of EPS, but simvastatin could compromise the function of EPS to decrease the silver resistant ability of E. faecalis.
Insights
Simvastatin reduces silver resistance in Enterococcus faecalis by disrupting the extracellular polymeric substances (EPS) that trap silver ions and nanoparticles. This finding offers new insights into combating silver-resistant bacterial infections.
Area of Science:
- Microbiology
- Nanotechnology
- Pharmacology
Background:
- Enterococcus faecalis (E. faecalis) causes refractory infections and exhibits resistance to silver.
- Simvastatin, an HMG-COA reductase inhibitor, shows potential antibacterial properties.
Purpose of the Study:
- Establish and characterize silver-resistant E. faecalis.
- Evaluate the role of extracellular polymeric substances (EPS) in silver resistance.
- Investigate simvastatin's effect on silver resistance in E. faecalis.
Main Methods:
- Development of silver ion (Ag+) and silver nanoparticle (AgNP)-resistant E. faecalis strains.
- Transmission electron microscopy (TEM), High-angle annular dark-field (HAADF), and mapping analyses.
- Incubation of bacteria with silver and simvastatin, followed by elemental analysis.
Main Results:
- Established E. faecalis strains showed high resistance to both Ag+ and AgNPs.
- Simvastatin decreased silver resistance in both original and resistant E. faecalis strains.
- Silver ions/particles were confined within EPS in resistant strains; simvastatin disrupted this, allowing silver entry.
Conclusions:
- Extracellular polymeric substances (EPS) play a crucial role in the silver resistance of E. faecalis.
- Simvastatin compromises EPS function, thereby reducing the bacterium's silver resistance.
- These findings suggest simvastatin as a potential agent to enhance antimicrobial strategies against silver-resistant E. faecalis.
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