Protein Purification Laboratory and its Biological Functions; Faculty of Pharmaceutical Sciences, Food and Nutrition; Faculty of Pharmacy, Food and Nutrition; Federal University of Mato Grosso do Sul (UFMS), Campo Grande, Mato Grosso do Sul, Brazil.
Center for Natural and Human Sciences of the Federal University of ABC (UFABC), São Paulo, SP, Brazil.
J Microbiol Biotechnol. 2024 Nov 28;34(11):2231-2244. doi: 10.4014/jmb.2405.05011. Epub 2024 Aug 31.
Recent research has focused on discovering peptides that effectively target multidrug-resistant bacteria while leaving healthy cells unharmed. In this work, we describe the antimicrobial properties of RK8, a peptide composed of eight amino acid residues. Its activity was tested against multidrug-resistant Gram-negative and Gram-positive bacteria. RK8's efficacy in eradicating mature biofilm and increasing membrane permeability was assessed using Sytox Green. Cytotoxicity assays were conducted both in vitro and in vivo models. Circular dichroism analysis revealed that RK8 adopted an extended structure in water and sodium dodecyl sulfate (SDS). RK8 exhibited MICs of 8-64 μM and MBCs of 4-64 μM against various bacteria, with higher effectiveness observed in Methicillin-resistant (MRSA) and KPC+ strains than others. Ciprofloxacin and Vancomycin showed varying MIC and MBC values lower than RK8 for Gram-positive bacteria, but competitive for Gram-negative bacteria. The combination of RK8 and ciprofloxacin showed a synergistic effect. The RK8 peptides could reduce 38% of the mature biofilm. Sytox Green reagent achieved 100% membrane permeation of Gram-positive and Gram-negative bacteria. The RK8 peptide did not show cytotoxic effects against murine macrophages (64 μM), erythrocytes (100 μM) or larvae (960 μM). In the stability test against peptidases, the RK8 peptide was stable, maintaining around 60% of the molecule intact after 120 min of incubation. These results highlight the potential of RK8 to be a promising strategy for developing a new antimicrobial and antibiofilm agent, inspiring and motivating further research in antimicrobial peptides.
最近的研究集中在发现能够有效靶向多药耐药菌而不伤害健康细胞的肽上。在这项工作中,我们描述了由八个氨基酸残基组成的肽 RK8 的抗菌特性。测试了其对多药耐药革兰氏阴性和革兰氏阳性细菌的活性。使用 Sytox Green 评估了 RK8 根除成熟生物膜和增加膜通透性的效果。在体外和体内模型中进行了细胞毒性测定。圆二色性分析表明,RK8 在水中和十二烷基硫酸钠(SDS)中采用扩展结构。RK8 对各种细菌的 MIC 值为 8-64 μM,MBC 值为 4-64 μM,对耐甲氧西林金黄色葡萄球菌(MRSA)和 KPC+菌株的效果更高。环丙沙星和万古霉素对革兰氏阳性菌的 MIC 和 MBC 值低于 RK8,但对革兰氏阴性菌具有竞争性。RK8 和环丙沙星的组合显示出协同作用。RK8 肽可减少 38%的成熟生物膜。Sytox Green 试剂可实现革兰氏阳性和革兰氏阴性细菌 100%的膜通透性。RK8 肽对小鼠巨噬细胞(64 μM)、红细胞(100 μM)或幼虫(960 μM)没有细胞毒性作用。在对抗肽酶的稳定性测试中,RK8 肽是稳定的,孵育 120 分钟后,分子仍保持约 60%的完整性。这些结果突出了 RK8 作为开发新的抗菌和抗生物膜剂的有前途策略的潜力,激励并促进了抗菌肽的进一步研究。