Yang Guang, Wang Jingyu, Lu Shengsheng, Chen Zhao, Fan Sheng, Chen Daiwei, Xue Huanxin, Shi Wenyuan, He Jian
Group of Peptides and Natural Products Research, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
The Forsyth Institute, Harvard School of Dental Medicine, Cambridge, Massachusetts, USA.
Br J Pharmacol. 2019 Jun;176(11):1603-1618. doi: 10.1111/bph.14571. Epub 2019 Apr 15.
Propionibacterium acnes (P. acnes) is a Gram-positive bacterium associated with the skin disorder acne. In this study, we determined the importance of fatty acids in the life habitat of P. acnes; we tested our lipopeptide library in an attempt to create potent P. acnes-specific antimicrobial agents.
Antimicrobial activity was determined by the minimal inhibitory concentration (MIC). Lipids from P. acnes were used to explore the mode of action. RAW264.7 cells respectively stimulated with LPS and P. acnes were used to measure the anti-inflammatory activity. Mice ears injected with P. acnes were used to assess the antimicrobial and anti-inflammatory effects of the peptides tested in vivo.
The most potent candidate, C16-KWKW, was observed to be more active against P. acnes, with an MIC of 2 μg·ml , than against other non-targeted bacterial strains, such as Streptococcus mutans, Staphylococcus aureus, and Escherichia coli. The mode of action of C16-KWKW was observed to be through interference with the integrity of bacterial membrane, thereby impairing membrane permeability and causing leakage of the inner contents of bacterial cells. In addition, C16-KWKW inhibited the expression of pro-inflammatory cytokines, such as IL-1β, TNF-α, and inducible NOS, stimulated by both LPS and P. acnes, thus showing potential anti-inflammatory activity, which was further assessed in animal studies in vivo.
C16-KWKW is a lipopeptide displaying both anti-P. acnes and anti-inflammatory effects in vitro and in vivo, and exhibits potential as a treatment for acne vulgaris induced by P. acnes.
痤疮丙酸杆菌是一种与皮肤疾病痤疮相关的革兰氏阳性菌。在本研究中,我们确定了脂肪酸在痤疮丙酸杆菌生存环境中的重要性;我们测试了我们的脂肽文库,试图创制出强效的痤疮丙酸杆菌特异性抗菌剂。
通过最低抑菌浓度(MIC)测定抗菌活性。利用痤疮丙酸杆菌的脂质来探究作用方式。分别用脂多糖(LPS)和痤疮丙酸杆菌刺激的RAW264.7细胞用于测量抗炎活性。给小鼠耳部注射痤疮丙酸杆菌,以评估所测试肽在体内的抗菌和抗炎效果。
观察到最有效的候选物C16-KWKW对痤疮丙酸杆菌的活性更强,其MIC为2μg·ml,而对其他非靶向细菌菌株,如变形链球菌、金黄色葡萄球菌和大肠杆菌的活性较弱。观察到C16-KWKW的作用方式是通过干扰细菌膜的完整性,从而损害膜通透性并导致细菌细胞内内容物泄漏。此外,C16-KWKW抑制了由LPS和痤疮丙酸杆菌刺激产生的促炎细胞因子如IL-1β、TNF-α和诱导型一氧化氮合酶的表达,因此显示出潜在的抗炎活性,这在体内动物研究中得到了进一步评估。
C16-KWKW是一种在体外和体内均表现出抗痤疮丙酸杆菌和抗炎作用的脂肽,具有作为治疗痤疮丙酸杆菌诱导的寻常痤疮的潜力。