Vollenbroich D, Pauli G, Ozel M, Vater J
Max-Volmer-Institut für Biophysikalische und Biochemie, Fachgebiet Biochemie und Molekulare Biologie, Technische Universität Berlin, Germany.
Appl Environ Microbiol. 1997 Jan;63(1):44-9. doi: 10.1128/aem.63.1.44-49.1997.
Surfactin, a cyclic lipopeptide antibiotic and biosurfactant produced by Bacillus subtilis, is well-known for its interactions with artificial and biomembrane systems (e.g., bacterial protoplasts or enveloped viruses). To assess the applicability of this antiviral and antibacterial drug, we determined the cytotoxicity of surfactin with a 50% cytotoxic concentration of 30 to 64 microM for a variety of human and animal cell lines in vitro. Concomitantly, we observed an improvement in proliferation rates and changes in the morphology of mycoplasma-contaminated mammalian cells after treatment with this drug. A single treatment over one passage led to complete removal of viable Mycoplasma hyorhinis cells from various adherent cell lines, and Mycoplasma orale was removed from nonadherent human T-lymphoid cell lines by double treatment. This effect was monitored by a DNA fluorescence test, an enzyme-linked immunosorbent assay, and two different PCR methods. Disintegration of the mycoplasma membranes as observed by electron microscopy indicated the mode of action of surfactin. Disintegration is obviously due to a physicochemical interaction of the membrane-active surfactant with the outer part of the lipid membrane bilayer, which causes permeability changes and at higher concentrations leads finally to disintegration of the mycoplasma membrane system by a detergent effect. The low cytotoxicity of surfactin for mammalian cells permits specific inactivation of mycoplasmas without significant deleterious effects on cell metabolism and the proliferation rate in cell culture. These results were used to develop a fast and simple method for complete and permanent inactivation of mycoplasmas in mammalian monolayer and suspension cell cultures.
表面活性素是一种由枯草芽孢杆菌产生的环状脂肽抗生素和生物表面活性剂,因其与人工膜和生物膜系统(如细菌原生质体或包膜病毒)的相互作用而闻名。为了评估这种抗病毒和抗菌药物的适用性,我们测定了表面活性素对多种人和动物细胞系的细胞毒性,其50%细胞毒性浓度在体外为30至64微摩尔。同时,我们观察到用这种药物处理后,支原体污染的哺乳动物细胞的增殖率有所提高,形态也发生了变化。单次传代处理可使各种贴壁细胞系中的猪鼻支原体活细胞完全清除,通过两次处理可从非贴壁人T淋巴细胞系中清除口腔支原体。通过DNA荧光试验、酶联免疫吸附测定和两种不同的PCR方法监测了这种效果。电子显微镜观察到的支原体膜解体表明了表面活性素的作用方式。解体显然是由于膜活性表面活性剂与脂质膜双层外部的物理化学相互作用,这会导致通透性变化,在较高浓度下最终通过去污剂作用导致支原体膜系统解体。表面活性素对哺乳动物细胞的低细胞毒性允许特异性灭活支原体,而对细胞代谢和细胞培养中的增殖率没有明显的有害影响。这些结果被用于开发一种快速简单的方法,用于在哺乳动物单层和悬浮细胞培养中完全和永久地灭活支原体。