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利用生物合成的银纳米颗粒-抗生素组合抑制生物膜形成介导的耐甲氧西林和毒力基因

Impeding Biofilm-Forming Mediated Methicillin-Resistant and Virulence Genes Using a Biosynthesized Silver Nanoparticles-Antibiotic Combination.

作者信息

Fareid Mohamed A, El-Sherbiny Gamal M, Askar Ahmed A, Abdelaziz Amer M, Hegazy Asmaa M, Ab Aziz Rosilah, Hamada Fatma A

机构信息

Clinical Laboratory Science Department, Applied Medical Science College, University of Ha'il, Hail 2440, Saudi Arabia.

Botany and Microbiology Department, Faculty of Science, Al-Azhar University, Cairo 11884, Egypt.

出版信息

Biomolecules. 2025 Feb 11;15(2):266. doi: 10.3390/biom15020266.

Abstract

Methicillin-resistant (MRSA) continues to represent a significant clinical challenge, characterized by consistently elevated rates of morbidity and mortality. Care regimen success is still difficult and necessitates assessing new antibiotics as well as supplemental services, including source control and searching for alternative approaches to combating it. Hence, we propose to synthesize silver nanoparticles (Ag-NPs) by employing a cell-free filter (CFF) of sp. to augment antibiotic activity and combat biofilm-forming MRSA. Seven bacterial isolates from clinical samples were identified, antibiotics were profiled with Vitek-2, and the phenotypic detecting of biofilm with Congo red medium and microplate assay was carried out. The PCR technique was used for detecting genes ( and ) coded in biofilm forming. The characterization of Ag-NPs was performed using several analytical methods, such as UV spectroscopy, dynamic light scattering (DLS), zeta potential measurement, transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). The antibacterial properties of Ag-NPs and oxacillin-Ag-NPs were assessed against standard strains and clinical isolates by employing the agar well diffusion technique and the microdilution assay. The biogenic synthesis Ag-NPs resulted in uniformly spherical particles, with an average size of 20 nm. These Ag-NPs demonstrated significant activity against biofilm-forming MRSA, with minimum inhibitory concentrations (MICs) ranging from 12 to 15 μg/mL. Additionally, Ag-NPs completely impede biofilm formation by MRSA at sublethal doses of 0.75 MICs. The expression levels of the and genes were reduced by 1.9- to 2.2- and 2.4- to 2.8-fold, respectively. A significant synergistic effect was noted when Ag-NPs were used in combination with oxacillin, leading to reduced MICs of 1.87 μg/mL for oxacillin and 4.0 μg/mL for Ag-NPs against MRSA. The FICi of 0.375 further validated the synergistic relationship between oxacillin and Ag-NPs at the concentrations of 1.87 and 4 μg/mL. Findings from the time-kill test demonstrated the highest reduction in log (CFU)/mL of the initial MRSA inoculum after 12-hour exposure. The cytotoxicity analysis of Ag-NPs revealed no significant cytotoxic effects on the human skin cell line HFB-4 at low concentrations, with IC values of 61.40 µg/mL for HFB-4 and 34.2 µg/mL for HepG-2. Comparable with oxacillin-Ag-NPs, Ag-NPs showed no cytotoxic effects on HFB-4 at different concentrations and exhibited an IC value of 31.2 against HepG-2-cells. In conclusion, the biosynthesis of Ag-NPs has demonstrated effective antibacterial activity against MRSA and has completely hindered biofilm formation, suggesting a valuable alternative for clinical applications.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)仍然是一个重大的临床挑战,其特征是发病率和死亡率持续居高不下。护理方案的成功仍然困难,需要评估新的抗生素以及补充服务,包括源头控制和寻找对抗它的替代方法。因此,我们建议通过使用sp.的无细胞滤器(CFF)合成银纳米颗粒(Ag-NPs),以增强抗生素活性并对抗形成生物膜的MRSA。从临床样本中鉴定出7株细菌分离株,用Vitek-2对其进行抗生素谱分析,并采用刚果红培养基和微孔板法对生物膜进行表型检测。PCR技术用于检测生物膜形成中编码的基因(和)。使用多种分析方法对Ag-NPs进行表征,如紫外光谱、动态光散射(DLS)、zeta电位测量、透射电子显微镜(TEM)、X射线衍射(XRD)和傅里叶变换红外光谱(FTIR)。通过琼脂孔扩散技术和微量稀释法评估Ag-NPs和奥沙西林-Ag-NPs对标准菌株和临床分离株的抗菌性能。生物合成的Ag-NPs产生均匀的球形颗粒,平均尺寸为20nm。这些Ag-NPs对形成生物膜的MRSA表现出显著活性,最低抑菌浓度(MICs)范围为12至15μg/mL。此外,Ag-NPs在亚致死剂量0.75 MICs时完全阻止MRSA形成生物膜。和基因的表达水平分别降低了1.9至2.2倍和2.4至2.8倍。当Ag-NPs与奥沙西林联合使用时,观察到显著的协同作用,导致奥沙西林对MRSA的MICs降低至1.87μg/mL,Ag-NPs降低至4.0μg/mL。0.375的FICi进一步验证了奥沙西林和Ag-NPs在1.87和4μg/mL浓度下的协同关系。时间杀菌试验的结果表明,在暴露于初始MRSA接种物12小时后,log(CFU)/mL的降低最为显著。Ag-NPs的细胞毒性分析表明,在低浓度下对人皮肤细胞系HFB-4没有显著的细胞毒性作用,HFB-4的IC值为61.40μg/mL,HepG-2的IC值为34.2μg/mL。与奥沙西林-Ag-NPs相比,Ag-NPs在不同浓度下对HFB-4没有细胞毒性作用,对HepG-2细胞的IC值为31.2。总之,Ag-NPs的生物合成已证明对MRSA具有有效的抗菌活性,并完全阻碍了生物膜的形成,为临床应用提供了一种有价值的替代方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e45/11852608/cde5a3b5bf6d/biomolecules-15-00266-g001.jpg

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