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Natural antibacterial agent-based nanoparticles for effective treatment of intracellular MRSA infection
Xinshu Zou1, Shuang Cai1, Tingting Wang1
1College of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, PR China; Heilongjiang Key Laboratory for Animal Disease Control and Pharmaceutical Development, Harbin 150030, PR China.
Abstract:
Intracellular MRSA is extremely difficult to eradicate by traditional antibiotics, leading to infection dissemination and drug resistance. A general lack of facile and long-term strategies to effectively eliminate intracellular MRSA. In this study, glabridin (GLA)-loaded pH-responsive nanoparticles (NPs) were constructed using cinnamaldehyde (CA)-dextran conjugates as carriers. These NPs targeted infected macrophages/MRSA via dextran mediation and effectively accumulated at the MRSA infection site. The NPs were then destabilized in response to the low pH of the lysosomes, which triggered the release of CA and GLA. The released CA downregulated the expression of cytotoxic pore-forming toxins, thereby decreasing the damage of macrophage and risk of the intracellular bacterial dissemination. Meanwhile, GLA could rapidly kill intracellularly entrapped MRSA with a low possibility of developing resistance. Using a specific combination of the natural antibacterial agents CA and GLA, NPs effectively eradicated intracellular MRSA with low toxicity to normal tissues in a MRSA-induced peritonitis model. This strategy presents a potential alternative for enhancing intracellular MRSA therapy, particularly for repeated and long-term clinical applications. STATEMENT OF SIGNIFICANCE: Intracellular MRSA infections are a growing threat to public health, and there is a general lack of a facile strategy for efficiently eliminating intracellular MRSA while reducing the ever-increasing drug resistance. In this study, pH-responsive and macrophage/MRSA-targeting nanoparticles were prepared by conjugating the phytochemical cinnamaldehyde to dextran to encapsulate the natural antibacterial agent glabridin. Using a combination of traditional Chinese medicine, the NPs significantly increased drug accumulation in MRSA and showed superior intracellular and extracellular bactericidal activity. Importantly, the NPs can inhibit potential intracellular bacteria dissemination and reduce the development of drug resistance, thus allowing for repeated treatment. Natural antibacterial agent-based drug delivery systems are an attractive alternative for facilitating the clinical treatment of intracellular MRSA infections.
Insights
New nanoparticles effectively target and eliminate intracellular MRSA (methicillin-resistant Staphylococcus aureus) infections. This approach uses natural compounds to kill bacteria, reduce toxin damage, and prevent drug resistance, offering a promising therapy for difficult-to-treat infections.
Area of Science:
- Nanomedicine
- Antimicrobial Therapy
- Drug Delivery Systems
Background:
- Intracellular MRSA (methicillin-resistant Staphylococcus aureus) poses a significant challenge due to its resistance to conventional antibiotics, leading to infection spread and treatment failure.
- Existing strategies for eradicating intracellular MRSA are limited, lacking facile and long-term solutions.
- A critical need exists for novel therapeutic approaches to combat intracellular MRSA infections effectively and mitigate the development of antibiotic resistance.
Purpose of the Study:
- To develop pH-responsive nanoparticles (NPs) loaded with glabridin (GLA) and cinnamaldehyde (CA) for targeted intracellular MRSA eradication.
- To investigate the efficacy of these NPs in delivering therapeutic agents to infected macrophages and reducing MRSA burden.
- To evaluate the potential of this strategy as an alternative for enhancing intracellular MRSA therapy, particularly for chronic or recurrent infections.
Main Methods:
- Construction of pH-responsive nanoparticles using cinnamaldehyde (CA)-dextran conjugates as carriers for glabridin (GLA).
- Dextran-mediated targeting of NPs to infected macrophages and MRSA accumulation at infection sites.
- pH-triggered destabilization of NPs in lysosomes, releasing CA and GLA to exert antibacterial effects and reduce host cell damage.
Main Results:
- The developed NPs effectively targeted infected macrophages and accumulated at MRSA infection sites.
- Released CA downregulated cytotoxic pore-forming toxins, reducing macrophage damage and bacterial dissemination.
- GLA demonstrated rapid killing of intracellular MRSA with a low potential for resistance development, leading to effective eradication in a peritonitis model with low host toxicity.
Conclusions:
- The combination of natural antibacterial agents GLA and CA within pH-responsive NPs offers a potent strategy for eradicating intracellular MRSA.
- This nanoparticle-based approach demonstrates low toxicity to normal tissues and holds promise for repeated and long-term clinical applications.
- The developed drug delivery system represents an attractive alternative for facilitating the clinical treatment of challenging intracellular MRSA infections.
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