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BrSPR20-P1肽与银纳米颗粒对病原菌的协同抗菌活性

Synergistic Antimicrobial Activity of BrSPR20-P1 Peptide and Silver Nanoparticles Against Pathogenic Bacteria.

作者信息

Thongin Thanyamai, Sawatdee Somchai, Songnaka Nuttapon, Uchiyama Jumpei, Wiwasuku Theanchai, Srichana Teerapol, Nakpheng Titpawan, Atipairin Apichart

机构信息

School of Pharmacy, Walailak University, Nakhon Si Thammarat 80161, Thailand.

Drug and Cosmetic Excellence Center, Walailak University, Nakhon Si Thammarat 80161, Thailand.

出版信息

Int J Mol Sci. 2025 Aug 13;26(16):7832. doi: 10.3390/ijms26167832.

Abstract

Bacterial infection is a cause of life-threatening diseases. The emergence of antimicrobial-resistant bacteria exacerbates this situation, highlighting the need for the discovery of new antimicrobial agents. Our previous study identified a novel antimicrobial peptide, BrSPR20-P1 (P1), which showed potential activity against MRSA. Additionally, silver nanoparticles (AgNPs) exhibit broad-spectrum antibacterial activity, capable of killing multidrug-resistant bacteria. The combination of antimicrobial agents presents a novel strategy for combating these pathogens. This study aimed to evaluate the antibacterial activity of the combination of P1 and AgNPs. It revealed that the combinations showed synergy. The P1 and AgNP mixture at a concentration of 1 and 8 µg/mL (1:8) doubled the activity against . and MRSA, while that combination of 64 and 64 µg/mL (64:64) exhibited broad-spectrum activity, expanding to . with a 32-fold increase. These combinations exhibited a bactericidal effect, showing the rapid killing of tested bacteria at 10× MIC, with killing rates during the first 3 h ranging from 4.04 ± 0.01 to 4.31 ± 0.03 h. The P1 and AgNP mixtures caused a low risk of antibacterial resistance up to 30 passages. It was demonstrated that the synergistic activity of P1 and AgNPs occurred through the disruption of cell walls and membranes, leakage of intracellular materials, and cell lysis. Additionally, the mixtures appeared to interact with bacterial genomic DNA, as indicated by a gel retardation assay. These activities of the combinations were concentration-dependent. The 1:8 µg/mL mixture caused low hemolysis and cytotoxicity and did not impede the wound healing process. In contrast, although the 64:64 µg/mL mixture showed excellent antibacterial efficacy, it was toxic to erythrocytes and mammalian cells. It implies that dose optimization is required to balance its efficacy and toxicity. Therefore, the P1 and AgNP combinations exhibit synergistic antimicrobial activity and have the potential to resolve bacterial infections.

摘要

细菌感染是危及生命的疾病的一个病因。抗菌耐药菌的出现加剧了这种情况,凸显了发现新型抗菌剂的必要性。我们之前的研究鉴定出一种新型抗菌肽BrSPR20-P1(P1),其对耐甲氧西林金黄色葡萄球菌(MRSA)显示出潜在活性。此外,银纳米颗粒(AgNPs)表现出广谱抗菌活性,能够杀死多重耐药菌。抗菌剂的联合使用为对抗这些病原体提供了一种新策略。本研究旨在评估P1与AgNPs联合使用的抗菌活性。结果表明联合使用具有协同作用。浓度为1和8 μg/mL(1:8)的P1与AgNP混合物使对……和MRSA的活性提高了一倍,而64和64 μg/mL(64:64)的该组合表现出广谱活性,扩展至……且增加了32倍。这些组合表现出杀菌作用,在10倍最低抑菌浓度(MIC)时能快速杀死受试细菌,在前3小时的杀灭率范围为4.04±0.01至4.31±0.03小时。P1与AgNP混合物在传代30次之前产生抗菌耐药性的风险较低。结果表明P1与AgNPs的协同活性是通过破坏细胞壁和细胞膜、细胞内物质泄漏以及细胞裂解而发生的。此外,凝胶阻滞试验表明混合物似乎与细菌基因组DNA相互作用。这些组合的这些活性具有浓度依赖性。1:8 μg/mL的混合物引起的溶血和细胞毒性较低,并且不妨碍伤口愈合过程。相比之下,尽管64:64 μg/mL的混合物显示出优异的抗菌效果,但它对红细胞和哺乳动物细胞有毒性。这意味着需要进行剂量优化以平衡其疗效和毒性。因此,P1与AgNP组合表现出协同抗菌活性,并且有潜力解决细菌感染问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e276/12386432/de92581ce62c/ijms-26-07832-g001.jpg

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