Malanovic Nermina, Ön Ayse, Pabst Georg, Zellner Alfred, Lohner Karl
Institute of Molecular Biosciences, Biophysics Division, University of Graz, NAWI Graz, Humboldtstrasse 50/III, 8010, Graz, Austria.
Institute of Molecular Biosciences, Biophysics Division, University of Graz, NAWI Graz, Humboldtstrasse 50/III, 8010, Graz, Austria.
Int J Antimicrob Agents. 2020 Nov;56(5):106146. doi: 10.1016/j.ijantimicag.2020.106146. Epub 2020 Aug 25.
Octenidine (OCT) is a widely used antiseptic molecule with an antimicrobial spectrum covering a broad range of bacteria and fungi. However, the detailed molecular mechanism of killing has not yet been elucidated. The objective of our study was to investigate the mode of action of OCT's potent effect on Gram-negative bacteria using Escherichia coli as a model organism as well as corresponding model membranes. The effects of OCT on cellular morphology were observed by electron microscopy, changes affecting membrane integrity (surface charge, fluidity, permeabilisation and depolarisation) by zeta potential, fluorescence microscopy and spectroscopy. Specific interactions of OCT with membrane phospholipids were addressed using differential scanning calorimetry, X-ray scattering and fluorescence techniques. OCT neutralises the surface charge of E. coli leading to disruption of the outer membrane and dramatic loss of the cell wall and further penetrates through the periplasmic space reaching the inner membrane. Model membranes showed that OCT inserts into the hydrophobic fatty acyl chain region of the bilayer, inducing complete lipid disorder. The loss of membrane integrity is also reflected by membrane depolarisation and changes in membrane fluidity as shown by electron microscopy. Insertion of OCT into the outer and inner membrane of E. coli results in a chaotic lipid arrangement that leads to rapid disruption of the cell envelope. We propose that this unspecific mode of action based on purely physical interactions is the basis of the very broad antimicrobial profile and makes it unlikely that resistance to OCT will develop.
奥替尼啶(OCT)是一种广泛使用的抗菌分子,其抗菌谱涵盖多种细菌和真菌。然而,其详细的杀菌分子机制尚未阐明。我们研究的目的是使用大肠杆菌作为模式生物以及相应的模式膜,研究奥替尼啶对革兰氏阴性菌产生强效作用的作用方式。通过电子显微镜观察奥替尼啶对细胞形态的影响,通过zeta电位、荧光显微镜和光谱学观察影响膜完整性(表面电荷、流动性、通透性和去极化)的变化。使用差示扫描量热法、X射线散射和荧光技术研究奥替尼啶与膜磷脂的特异性相互作用。奥替尼啶中和大肠杆菌的表面电荷,导致外膜破坏和细胞壁显著损失,并进一步穿过周质空间到达内膜。模式膜显示,奥替尼啶插入双层膜的疏水脂肪酰链区域,导致脂质完全紊乱。如电子显微镜所示,膜去极化和膜流动性变化也反映了膜完整性的丧失。奥替尼啶插入大肠杆菌的外膜和内膜会导致脂质排列混乱,从而导致细胞壁迅速破坏。我们认为,这种基于纯粹物理相互作用的非特异性作用方式是其广泛抗菌谱的基础,并且不太可能产生对奥替尼啶的耐药性。