新鉴定的Scylla paramamosain抗菌肽Scymicrosin7-26在体外和体内对耐甲氧西林金黄色葡萄球菌具有有效的抗菌活性。

IF 3.8 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2025-05-09 Epub Date: 2025-04-22 DOI:10.1021/acsinfecdis.5c00034
Ying Zhou, Ying Wang, Xiangyu Meng, Ming Xiong, Xianxian Dong, Hui Peng, Fangyi Chen, Ke-Jian Wang
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引用次数: 0

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)是引起皮肤和软组织感染的主要病原体,它严重阻碍伤口愈合过程并导致高死亡率。耐多药细菌的增加,加上新抗生素的供应有限,突出表明迫切需要开发创新的抗微生物物质。抗菌肽(AMPs)具有多靶点和快速抗菌活性,是解决这一危机的有希望的候选人。在这项研究中,我们鉴定了一种新的AMP, Scymicrosin7-26,来源于Scylla paramamosain,它对多种耐多药菌株,特别是MRSA具有有效的抗菌活性。共聚焦显微镜和透射电镜观察表明,Scymicrosin7-26与MRSA结合,并对细胞壁和细胞膜产生破坏作用,迅速穿透并杀死MRSA。值得注意的是,Scymicrosin7-26在各种离子条件、热应力和一定的血清浓度下均表现出良好的稳定性,对HaCaT细胞无明显的毒性作用,其穿透HaCaT细胞的能力表明其具有细胞内靶向治疗的潜力。体外实验中,Scymicrosin7-26显著降低了HaCaT细胞中MRSA的数量,抑制了细胞内MRSA的增殖。在验证了Scymicrosin7-26在海洋模式生物─海洋medaka (Oryzias melastigma)体内的低毒性后,制作了mrsa感染小鼠的伤口模型,并在羟纤维素凝胶中外用Scymicrosin7-26可显著减少细菌负荷,促进伤口愈合。组织学分析证实Scymicrosin7-26减轻了组织损伤,与万古霉素治疗的效果相当。总的来说,Scymicrosin7-26有望治疗MRSA伤口感染,并可能成为对抗抗生素耐药细菌的有价值的补充。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Newly Identified Antimicrobial Peptide Scymicrosin7-26 from Scylla paramamosain Showing Potent Antimicrobial Activity Against Methicillin-Resistant Staphylococcus aureus In Vitro and In Vivo.

Methicillin-resistant Staphylococcus aureus (MRSA) is a predominant pathogen causing skin and soft tissue infections, which significantly hinders the wound healing process and contributes to high mortality rates. The rise of multidrug-resistant bacteria, coupled with the limited availability of new antibiotics, underscores the pressing need for the development of innovative antimicrobial substances. Antimicrobial peptides (AMPs), with their multitargeted and rapid antimicrobial activity, are promising candidates to address this crisis. In this study, we identified a novel AMP, Scymicrosin7-26, derived from Scylla paramamosain, which demonstrated potent antimicrobial activity against a variety of MDR strains, particularly MRSA. Confocal microscopy and transmission electron microscopy observations showed that Scymicrosin7-26 bound to MRSA, and had a disruptive effect on cell walls and cell membranes, rapidly penetrating and killing MRSA. Notably, Scymicrosin7-26 exhibited good stability under various ionic conditions, thermal stresses and certain serum concentration, had no obvious toxic effects on HaCaT cells, and its ability to penetrate HaCaT cells indicated its potential for intracellular targeted therapy. In vitro, Scymicrosin7-26 significantly reduced the number of MRSA in HaCaT cells and inhibited intracellular MRSA proliferation. After verifying the low toxicity of Scymicrosin7-26 in vivo in the Marine model organism─marine medaka (Oryzias melastigma), a wound model of MRSA-infected mice was made, and topical administration of Scymicrosin7-26 in hypromellose gels could significantly reduce bacterial burden and promote wound closure. Histological analysis confirmed that Scymicrosin7-26 alleviated tissue damage and was comparable to the effect of vancomycin treatment. Collectively, Scymicrosin7-26 is promising for the treatment of MRSA wound infections and could be a valuable addition to the arsenal against antibiotic-resistant bacteria.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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