Li Zhongjie, Wang Huayi, Li Shasha, Deng Bo, Zhang Wenlu, Wu Pengfei, Li Wanwu, Xin Pengyang, Zhao Lingyu, Gao Shegan
Henan Provincial Key Laboratory of Microbiota and Esophageal Cancer Prevention and Control, Henan University of Science and Technology, Luoyang, 471000, China.
The First Affiliated Hospital of Henan University of Science and Technology, Luoyang, 471000, Henan, China.
Probiotics Antimicrob Proteins. 2025 Jul 3. doi: 10.1007/s12602-025-10590-7.
The increasing infection and antibiotic resistance of Pseudomonas aeruginosa has become a major threat to public health, making exploring new and effective antimicrobial agents particularly important. In this study, the scorpion-derived cationic peptide GK8 was designed, which showed effectiveness against P. aeruginosa including clinical resistance strains with low hemolytic activity. In the mouse skin subcutaneous infection model, GK8 significantly decreased the number of P. aeruginosa cells and inflammatory infiltration in the infected area. Mechanism research showed that GK8 killed P. aeruginosa in a concentration- and time-dependent manner, damaging the membrane integrity and membrane potential, inducing ROS accumulation, and interacting with nucleic acids. Moreover, GK8 could inhibit the pathogenic factors of P. aeruginosa, including inhibiting adhesion, motility, pyocyanin production, protease and elastase activities, and biofilm formation. Taken together, GK8 could be a potential alternative anti-infective agent against skin infection caused by P. aeruginosa.
铜绿假单胞菌感染的不断增加及其对抗生素的耐药性已成为对公众健康的重大威胁,这使得探索新型有效的抗菌剂尤为重要。在本研究中,设计了一种源自蝎子的阳离子肽GK8,它对铜绿假单胞菌包括临床耐药菌株有效,且溶血活性较低。在小鼠皮肤皮下感染模型中,GK8显著减少了感染区域的铜绿假单胞菌细胞数量和炎性浸润。机制研究表明,GK8以浓度和时间依赖性方式杀死铜绿假单胞菌,破坏膜完整性和膜电位,诱导活性氧积累,并与核酸相互作用。此外,GK8可抑制铜绿假单胞菌的致病因素,包括抑制黏附、运动性、绿脓菌素产生、蛋白酶和弹性蛋白酶活性以及生物膜形成。综上所述,GK8可能是一种针对铜绿假单胞菌引起的皮肤感染的潜在替代抗感染剂。