Cartron Michaël L, England Simon R, Chiriac Alina Iulia, Josten Michaele, Turner Robert, Rauter Yvonne, Hurd Alexander, Sahl Hans-Georg, Jones Simon, Foster Simon J
The Krebs Institute, Department of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield, United Kingdom.
Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, United Kingdom.
Antimicrob Agents Chemother. 2014 Jul;58(7):3599-609. doi: 10.1128/AAC.01043-13. Epub 2014 Apr 7.
Human skin fatty acids are a potent aspect of our innate defenses, giving surface protection against potentially invasive organisms. They provide an important parameter in determining the ecology of the skin microflora, and alterations can lead to increased colonization by pathogens such as Staphylococcus aureus. Harnessing skin fatty acids may also give a new avenue of exploration in the generation of control measures against drug-resistant organisms. Despite their importance, the mechanism(s) whereby skin fatty acids kill bacteria has remained largely elusive. Here, we describe an analysis of the bactericidal effects of the major human skin fatty acid cis-6-hexadecenoic acid (C6H) on the human commensal and pathogen S. aureus. Several C6H concentration-dependent mechanisms were found. At high concentrations, C6H swiftly kills cells associated with a general loss of membrane integrity. However, C6H still kills at lower concentrations, acting through disruption of the proton motive force, an increase in membrane fluidity, and its effects on electron transfer. The design of analogues with altered bactericidal effects has begun to determine the structural constraints on activity and paves the way for the rational design of new antistaphylococcal agents.
人体皮肤脂肪酸是我们先天防御的一个重要方面,为抵御潜在的入侵微生物提供表面保护。它们是确定皮肤微生物群落生态的一个重要参数,其改变可能导致金黄色葡萄球菌等病原体的定植增加。利用皮肤脂肪酸也可能为开发针对耐药生物的控制措施提供一条新的探索途径。尽管它们很重要,但皮肤脂肪酸杀死细菌的机制在很大程度上仍然不清楚。在这里,我们描述了对主要人体皮肤脂肪酸顺式-6-十六碳烯酸(C6H)对人体共生菌和病原体金黄色葡萄球菌的杀菌作用的分析。发现了几种C6H浓度依赖性机制。在高浓度下,C6H迅速杀死细胞,伴随着膜完整性的普遍丧失。然而,C6H在较低浓度下仍能杀死细菌,其作用方式是破坏质子动力、增加膜流动性以及对电子传递的影响。具有改变杀菌效果的类似物的设计已开始确定活性的结构限制,并为合理设计新的抗葡萄球菌药物铺平了道路。