Kumar Manish, Agarwal Mohini, Lakshmi Kavya Anguluri N V, Kaur Amritpal, Mane Pratibha, Sinha O P, Singh Rajni, Bala Kumud
Amity Institute of Biotechnology, Amity University Uttar Pradesh, Noida, India.
Amity Institute of Nanotechnology, Amity University Uttar Pradesh, Noida, India.
Microb Pathog. 2025 Oct;207:107828. doi: 10.1016/j.micpath.2025.107828. Epub 2025 Jun 23.
The escalating global crisis of antimicrobial resistance demands urgent attention. This study, prompted by the World Health Organization's 2020 report foreseeing Acinetobacter baumannii (A. baumannii) as a potential source of future epidemics, explores a sustainable solution. The innovation lies in evaluating Valeriana wallichii's (V. wallichii) methanolic extract nano-conjugate against A. baumannii. High-performance liquid chromatography reveals elevated concentrations of polyphenols- Quercetin, Rutin, and Tannic acid in the extract. Nano-conjugation with silver demonstrates efficacy comparable to tetracycline antibiotic in impeding A. baumannii growth. In-silico studies targeting crucial death receptors of A. baumannii indicate strong binding energies for Tannic acid, Rutin, and Linalool, suggesting their potential as drug candidates. Green-synthesized V. wallichii silver nanoconjugate (Vw-AgNCs), validated by various techniques such as UV-Visible Spectrophotometry, DLS, AFM, SEM, EDX & XRD, significantly enhances A. baumannii restriction compared to the extract alone. Cytotoxicity evaluation on Human Fibroblast cell line (L929) yields an LC50 value of 368 μg/ml, indicating a substantial therapeutic window. Importantly, Vw-AgNCs exhibit superior antimicrobial activity over both the extract and chemically synthesized nanoparticles, positioning them as promising agents against A. baumannii. The antibacterial mechanism of Vw-AgNCs against MDR-A. baumannii was evaluated through multiple parameters, including membrane leakage, DNA fragmentation, Antioxidant enzymatic activities and growth kinetics, all of which demonstrated its potent bactericidal effects. These findings underscore the potential of herbal solutions in addressing the alarming issue of antimicrobial resistance.
全球抗菌药物耐药性危机不断升级,亟需关注。本研究受世界卫生组织2020年报告的启发,该报告预见鲍曼不动杆菌(A. baumannii)可能成为未来疫情的源头,旨在探索一种可持续的解决方案。创新之处在于评估缬草(V. wallichii)甲醇提取物纳米共轭物对鲍曼不动杆菌的作用。高效液相色谱显示提取物中多酚类物质(槲皮素、芦丁和单宁酸)浓度升高。与银的纳米共轭物在抑制鲍曼不动杆菌生长方面显示出与四环素抗生素相当的功效。针对鲍曼不动杆菌关键死亡受体的计算机模拟研究表明,单宁酸、芦丁和芳樟醇具有很强的结合能,表明它们有作为候选药物的潜力。通过紫外可见分光光度法、动态光散射、原子力显微镜、扫描电子显微镜、能谱分析和X射线衍射等多种技术验证的绿色合成缬草银纳米共轭物(Vw-AgNCs),与单独的提取物相比,显著增强了对鲍曼不动杆菌的抑制作用。对人成纤维细胞系(L929)的细胞毒性评估得出LC50值为368μg/ml,表明有较大的治疗窗口。重要的是,Vw-AgNCs在抗菌活性方面优于提取物和化学合成的纳米颗粒,使其成为对抗鲍曼不动杆菌的有前景的药物。通过膜泄漏、DNA片段化、抗氧化酶活性和生长动力学等多个参数评估了Vw-AgNCs对多重耐药鲍曼不动杆菌的抗菌机制,所有这些都证明了其强大的杀菌作用。这些发现强调了草药解决方案在解决令人担忧的抗菌药物耐药性问题方面的潜力。