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Published on: December 27, 2016
Evaluation of Antibacterial Effects of Matrix-Induced Silver Ions against Antibiotic-Resistant ESKAPE Pathogens
Ya-Chi Huang1, Tsung-Ying Yang2,3, Bo-Xuan Chen2
1Department of Fragrance and Cosmetic Science, College of Pharmacy, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Abstract:
Recently, drug-resistant bacterial infections, especially ESKAPE pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp.), have become a critical health issue worldwide, highlighting the emerging need for novel antibacterial agents. In this study, silver nanoparticles were extracted from silver-containing mesoporous bioactive glass (MBG-Ag) using four different matrixes, including water, phosphate buffer saline (PBS), tryptic soy broth (TSB), and taurine (Tau). The inductively coupled plasma-mass spectrometer (ICP-MS) results demonstrated that the silver concentration of Tau-Ag was the highest among the four matrixes. The Tau-Ag was also observed to have 87.35% silver ions in its X-ray photoelectron spectrometer (XPS) spectra. The micrograph of transmission electron microscope (TEM) displayed a uniform distribution of silver nanoparticles, which was confined in a smaller size compared to that in TSB-Ag. Moreover, the peak shifts observed in the Fourier-transform infrared spectrometer (FTIR) spectrum implied that the -SO32- and -NH groups in taurine may interact with silver. A low cytotoxicity was noted for Tau-Ag, with approximately 70% of cells surviving at 0.63 mg/mL. Compared to the other three matrix-induced silver agents, Tau-Ag represented a better antibacterial effect against methicillin-resistant Staphylococcus aureus, with a minimum inhibitory concentration (MIC) value of 0.63 mg/mL and a postponed growth of 0.31 mg/mL observed. Further antibacterial examinations illustrated the presence of remarkable antibacterial activities against vancomycin-resistant Enterococcus feacium, carbapenem-resistant Klebsiella pneumoniae, carbapenem-resistant Acinetobacter baumannii, and carbapenem-resistant Pseudomonas aeruginosa. Given our observations and multiple bioactive functions of taurine (prevent patients from inflammation and oxidative-stress injuries), we anticipate that taurine matrix-induced silver ions would be a biomedical material with a high potential for combatting drug-resistant ESKAPE pathogens.
Insights
Taurine-induced silver nanoparticles show potent antibacterial activity against drug-resistant ESKAPE pathogens. This novel material exhibits low cytotoxicity and enhanced efficacy, offering a promising solution for combating critical infections.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Infectious Diseases
Background:
- Rising global threat of drug-resistant bacterial infections, particularly ESKAPE pathogens.
- Urgent need for novel antibacterial agents to address treatment challenges.
Purpose of the Study:
- To extract and characterize silver nanoparticles (AgNPs) from mesoporous bioactive glass using taurine as a matrix.
- To evaluate the antibacterial efficacy and cytotoxicity of taurine-induced AgNPs (Tau-Ag) against multidrug-resistant bacteria.
Main Methods:
- Extraction of AgNPs from mesoporous bioactive glass using water, PBS, TSB, and taurine.
- Characterization using ICP-MS, XPS, TEM, and FTIR.
- Assessment of cytotoxicity and antibacterial activity (MIC, growth inhibition) against ESKAPE pathogens.
Main Results:
- Tau-Ag exhibited the highest silver concentration and a significant presence of silver ions.
- TEM revealed uniform, smaller silver nanoparticles in Tau-Ag compared to TSB-Ag.
- Tau-Ag demonstrated potent antibacterial effects against methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus faecium, and carbapenem-resistant Klebsiella pneumoniae, Acinetobacter baumannii, and Pseudomonas aeruginosa, with low cytotoxicity.
Conclusions:
- Taurine matrix effectively induces silver nanoparticles with enhanced antibacterial properties.
- Tau-Ag presents a promising biomedical material for combating critical drug-resistant ESKAPE pathogens.
- Taurine's inherent bioactive functions may further enhance the therapeutic potential of Tau-Ag.

