Feng Kaiyue, Sang He, Jin Han, Song Peng, Xu Wei, Xuan Hongzhuan, Wang Fei
School of Pharmaceutical Sciences and Food Engineering, Liaocheng University, Liaocheng 252059, China.
College of Agriculture and Biology, Liaocheng University, Liaocheng 252059, China.
Microorganisms. 2025 Aug 7;13(8):1844. doi: 10.3390/microorganisms13081844.
Combining antibiotics with propolis is an effective method to combat bacterial drug resistance. Nanoparticles are of interest in the antimicrobial field because of their higher drug stability, solubility, penetration power, and treatment efficacy. In this study, propolis nanoparticles (PNPs) were synthesized, and their antibacterial and anti-biofilm activities against methicillin-resistant (MRSA) in combination with ampicillin sodium (AS) were analyzed. The PNPs had an average particle diameter of 118.0 nm, a polydispersity index of 0.129, and a zeta potential of -28.2 mV. The fractional inhibitory concentration indices of PNPs and AS against tested MRSA strains highlighted this synergy, ranging between 0.375 and 0.5. Crystal violet staining showed that combined PNPs and AS significantly inhibited biofilm formation and reduced existing biofilm biomass. We then discovered that PNPs inhibited bacterial adhesion, extracellular polysaccharide synthesis, and , , and gene expression. These results indicated that PNPs exerted a synergistic antibacterial effect with AS by inhibiting , , and gene expressions to reduce the drug resistance of MRSA. Meanwhile, PNPs weakened bacterial adhesion and aggregation by suppressing gene expression, allowing antibiotics to penetrate the biofilm, and exhibiting significant synergistic anti-biofilm activity. In summary, PNPs are promising candidates for combating MRSA-related diseases.
将抗生素与蜂胶结合是对抗细菌耐药性的有效方法。纳米颗粒因其更高的药物稳定性、溶解性、穿透力和治疗效果而在抗菌领域备受关注。在本研究中,合成了蜂胶纳米颗粒(PNPs),并分析了其与氨苄西林钠(AS)联合对耐甲氧西林金黄色葡萄球菌(MRSA)的抗菌和抗生物膜活性。PNPs的平均粒径为118.0 nm,多分散指数为0.129,zeta电位为-28.2 mV。PNPs和AS对受试MRSA菌株的分数抑菌浓度指数突出了这种协同作用,范围在0.375至0.5之间。结晶紫染色表明,PNPs和AS联合显著抑制生物膜形成并减少现有生物膜生物量。然后我们发现PNPs抑制细菌粘附、胞外多糖合成以及 、 、 和 基因表达。这些结果表明,PNPs通过抑制 、 和 基因表达与AS发挥协同抗菌作用,以降低MRSA的耐药性。同时,PNPs通过抑制 基因表达减弱细菌粘附和聚集,使抗生素能够穿透生物膜,并表现出显著的协同抗生物膜活性。总之,PNPs是对抗MRSA相关疾病的有前景的候选物。