Possemiers Sam, Van Camp John, Bolca Selin, Verstraete Willy
Laboratory of Microbial Ecology and Technology (LabMET), Ghent University, Coupure Links 653, Belgium.
Int J Food Microbiol. 2005 Nov 15;105(1):59-70. doi: 10.1016/j.ijfoodmicro.2005.05.007. Epub 2005 Sep 8.
Sphingosine is known as a natural antimicrobial agent, protecting the human skin from bacterial colonization and possibly affecting the intestinal microbial community after ingestion. In this study we further investigated the antibacterial spectrum of dietary d-eythro-sphingosine in saline towards three intestinal pathogens and to the health promoting lactobacilli and bifidobacteria. The degree of bactericidal effect was studied using plate counts and Live/Dead analysis combined with flow cytometry. To assess activity under complex intestinal conditions, sphingosine was dosed to the Simulator of the Human Intestinal Microbial Ecosystem (SHIME) for a period of 11 days. Finally, we tried to elucidate the factors influencing the activity and the mode of action of sphingosine. In all performed experiments, high correlation occurred between plate counts and Live/Dead analysis. In saline a strong antibacterial effect was seen to all tested species, Gram-negative and Gram-positive, and sphingosine not selectively acted against pathogens, as health promoting bacteria were also affected. Under simulated intestinal conditions however, no shifts in bacterial concentrations were detected. Experiments with individual medium components thought that the effect of sphingosine is very easily neutralized by BSA, stearic acid and surfactants. Based on our results, d-erythro-sphingosine would only be active when protonated and its mode of action would imply electrostatic attraction to the bacteria and disruption of membrane integrity. In conclusion, the application of sphingosine is limited to specific environments, as activity was very sensitive to inhibition. Yet, because of its broad spectrum membrane disrupting activity, it could be very useful under controlled conditions.
鞘氨醇是一种天然抗菌剂,可保护人体皮肤免受细菌定植,并可能在摄入后影响肠道微生物群落。在本研究中,我们进一步研究了膳食d-赤藓型鞘氨醇在生理盐水中对三种肠道病原体以及对促进健康的乳酸菌和双歧杆菌的抗菌谱。使用平板计数法以及结合流式细胞术的死活分析来研究杀菌效果的程度。为了评估在复杂肠道条件下的活性,将鞘氨醇添加到人体肠道微生物生态系统模拟器(SHIME)中11天。最后,我们试图阐明影响鞘氨醇活性和作用方式的因素。在所有进行的实验中,平板计数法与死活分析之间都存在高度相关性。在生理盐水中,对所有测试的革兰氏阴性和革兰氏阳性菌种均观察到强烈的抗菌作用,并且鞘氨醇并非选择性地作用于病原体,因为促进健康的细菌也受到了影响。然而,在模拟肠道条件下,未检测到细菌浓度的变化。对单个培养基成分进行的实验表明,鞘氨醇的作用很容易被牛血清白蛋白、硬脂酸和表面活性剂中和。根据我们的结果,d-赤藓型鞘氨醇仅在质子化时才具有活性,其作用方式意味着对细菌的静电吸引以及膜完整性的破坏。总之,鞘氨醇的应用仅限于特定环境,因为其活性对抑制作用非常敏感。然而,由于其具有广泛的破坏膜活性,在受控条件下可能非常有用。