Alamiri Feiruz, Riesbeck Kristian, Hakansson Anders P
Division of Experimental Infection Medicine, Department of Translational Medicine, Faculty of Medicine, Lund University, Malmo, Sweden.
Clinical Microbiology, Department of Translational Medicine, Faculty of Medicine, Lund University, Malmo, Sweden.
Antimicrob Agents Chemother. 2019 Sep 9;63(12). doi: 10.1128/AAC.01193-19. Epub 2019 Oct 7.
HAMLET is a protein-lipid complex derived from human milk that was first described for its tumoricidal activity. Later studies showed that HAMLET also has direct bactericidal activity against select species of bacteria, with highest activity against Additionally, HAMLET in combination with various antimicrobial agents can make a broader range of antibiotic-resistant bacterial species sensitive to antibiotics. Here, we show that HAMLET has direct antibacterial activity not only against pneumococci, but also against (GAS) and (GBS). Analogous to pneumococci, HAMLET-treatment of GAS and GBS resulted in depolarization of the bacterial membrane followed by membrane permeabilization and death that could be inhibited by calcium and sodium transport inhibitors. Treatment of clinical antibiotic-resistant isolates of , GAS, and GBS with sublethal concentrations of HAMLET in combination with antibiotics decreased the minimal inhibitory concentrations of the respective antibiotic into the sensitive range. This effect could also be blocked by ion transport inhibitors, suggesting that HAMLET's bactericidal and combination treatment effects used similar mechanisms. Finally, we show that HAMLET potentiated the effects of erythromycin against erythromycin-resistant bacteria more effectively than it potentiated killing by penicillin G of bacteria resistant to penicillin G. These results show for the first time that HAMLET effectively kills three different species of pathogenic using similar mechanisms and also potentiate the activity of macrolides and lincosamides more effectively than combination treatment with beta-lactams. These findings suggest a potential therapeutic role for HAMLET in repurposing antibiotics currently causing treatment failures in patients.
哈姆雷特(HAMLET)是一种源自人乳的蛋白质 - 脂质复合物,最初因其杀肿瘤活性而被描述。后来的研究表明,HAMLET对某些细菌种类也具有直接杀菌活性,对[具体细菌名称未给出]活性最高。此外,HAMLET与各种抗菌剂联合使用可使更广泛的耐抗生素细菌种类对抗生素敏感。在此,我们表明HAMLET不仅对肺炎球菌具有直接抗菌活性,而且对A组链球菌(GAS)和B组链球菌(GBS)也有直接抗菌活性。与肺炎球菌类似,用HAMLET处理GAS和GBS会导致细菌膜去极化,随后膜通透性增加并死亡,而钙和钠转运抑制剂可抑制这种情况。用亚致死浓度的HAMLET与抗生素联合处理临床耐抗生素的[具体细菌名称未给出]、GAS和GBS分离株,可将各自抗生素的最低抑菌浓度降低至敏感范围。这种效应也可被离子转运抑制剂阻断,表明HAMLET的杀菌作用和联合治疗作用使用了相似的机制。最后,我们表明HAMLET增强红霉素对耐红霉素细菌的作用比增强青霉素G对耐青霉素G细菌的杀伤作用更有效。这些结果首次表明,HAMLET使用相似机制有效杀死三种不同种类的致病性[具体细菌名称未给出],并且比与β - 内酰胺类联合治疗更有效地增强大环内酯类和林可酰胺类的活性。这些发现表明HAMLET在重新利用目前导致患者治疗失败的抗生素方面具有潜在的治疗作用。