School of Life Sciences, B.S. Abdur Rahman Crescent Institute of Science and Technology, GST Road, Vandalur, Chennai, Tamil Nadu, 600 048, India.
Appl Biochem Biotechnol. 2024 Apr;196(4):2031-2052. doi: 10.1007/s12010-023-04630-7. Epub 2023 Jul 18.
The silver nanoparticles (AgNPs) were produced by employing a biogenic loom and tested for antipathogenic assets against multi-drug-resistant (MDR) ESKAPE bacteria. Biogenically synthesized AgNPs were characterized adopting various high-throughput techniques such as UHRTEM, SEM with EDX, DLS, TGA-DTA, and XRD and spectroscopic analysis showed polydispersion of nanoparticles. In this context, AgNPs with the attribute of spherical-shaped nanoparticles with an average size of 26 nm were successfully synthesized utilizing bacterial supernatant. The antipathogenic activities of AgNPs were assessed against 11 strains of MDR ESKAPE bacteria including Enterococcus faecium; methicillin-resistant Staphylococcus aureus; Klebsiella pneumonia; Acinetobacter baumannii; Pseudomonas aeruginosa; Enterobacter aerogenes; and Enterobacter species. The exposure of biogenic AgNPs in a well diffusion assay showed all the growth inhibitions of ESKAPE bacteria at 200 μg/ml after 18 h of incubation. Growth kinetics demonstrated maximum killing at 60 μg/ml after 4 h of completion. The highest biofilm depletions were found at 100 μg/ml in adhesion assay. Live/dead assays showed effective killing of the ESKAPE bacteria at 10 μg/ml in pre-existing biofilms. The effective inhibitory concentrations of AgNPs were investigated ranging from 10 to 200 μg/ml. The selected pathogens found sensitive to AgNPs are statistically significant (P < 0.05) than that of cefotaxime/AgNO. Consequently, a broad spectrum of antimicrobial potentials of AgNPs can be alternative to conventional antimicrobial agents for future medicine.
采用生物纺丝法制备了银纳米粒子(AgNPs),并测试了其对多药耐药(MDR)ESKAPE 细菌的抗病原生物特性。采用超高速透射电子显微镜(UHRTEM)、SEM-EDX、DLS、TGA-DTA 和 XRD 等多种高通量技术对生物合成的 AgNPs 进行了表征,光谱分析显示纳米粒子具有多分散性。在这种情况下,利用细菌上清液成功合成了具有球形纳米粒子特性的 AgNPs,平均粒径为 26nm。采用琼脂扩散法评估了 AgNPs 对 11 株 MDR ESKAPE 细菌(包括屎肠球菌;耐甲氧西林金黄色葡萄球菌;肺炎克雷伯菌;鲍曼不动杆菌;铜绿假单胞菌;产气肠杆菌;和肠杆菌属)的抗病原生物活性。在 18 小时孵育后,生物合成 AgNPs 在 200μg/ml 时对所有 ESKAPE 细菌的生长均表现出抑制作用。动力学研究表明,在 4 小时完成时,最大杀菌浓度为 60μg/ml。在黏附试验中,发现生物膜减少量最高为 100μg/ml。活/死检测显示,在预先存在的生物膜中,AgNPs 在 10μg/ml 时可有效杀死 ESKAPE 细菌。AgNPs 的有效抑制浓度范围为 10 至 200μg/ml。发现对 AgNPs 敏感的选定病原体在统计学上(P<0.05)比头孢噻肟/AgNO 更显著。因此,AgNPs 的广谱抗菌潜力可以替代传统的抗菌药物,用于未来的医学。