Nir-Paz Ran, Prévost Marie-Christine, Nicolas Pierre, Blanchard Alain, Wróblewski Henri
Unité d'Oncologie Virale, Institut Pasteur, Paris, France.
Antimicrob Agents Chemother. 2002 May;46(5):1218-25. doi: 10.1128/AAC.46.5.1218-1225.2002.
Mycoplasmas, which are bacteria that are devoid of a cell wall and which belong to the class Mollicutes, are pathogenic for humans and animals and are frequent contaminants of tissue cell cultures. Although contamination of cultures with mycoplasma can easily be monitored with fluorescent dyes that stain DNA and/or with molecular probes, protection and decontamination of cultures remain serious challenges. In the present work, we investigated the susceptibilities of Mycoplasma fermentans and Mycoplasma hyorhinis to the membrane-active peptides alamethicin, dermaseptin B2, gramicidin S, and surfactin by growth inhibition and lethality assays. In the absence of serum, the four peptides killed mycoplasmas at minimal bactericidal concentrations that ranged from 12.5 to 100 microM, but in all cases the activities were decreased by the presence of serum. As a result, under standard culture conditions (10% serum) only alamethicin and gramicidin S were able to inhibit mycoplasma growth (MICs, 50 microM), while dermaseptin B2 and surfactin were ineffective. Furthermore, 8 days of treatment of HeLa cell cultures experimentally contaminated with either mycoplasma species with 70 microM enrofloxacin cured the cultures of infection, whereas treatment with alamethicin and gramicidin S alone was not reliable because the concentrations and treatment times required were toxic to the cells. However, combination of alamethicin or gramicidin S with 70 microM enrofloxacin allowed mycoplasma eradication after 30 min or 24 h of treatment, depending on the mycoplasma and peptide considered. HeLa cell cultures experimentally infected with mycoplasmas should prove to be a useful model for study of the antimycoplasma activities of antibiotics and membrane-active peptides under conditions close to those found in vivo.
支原体是一类没有细胞壁的细菌,属于柔膜菌纲,可导致人类和动物致病,并且是组织细胞培养中常见的污染物。尽管用能对DNA进行染色的荧光染料和/或分子探针能够很容易地监测支原体对培养物的污染情况,但是对培养物的保护和净化仍然是严峻的挑战。在本研究中,我们通过生长抑制和致死率试验,研究了发酵支原体和猪鼻支原体对膜活性肽短杆菌肽A、皮肤抗菌肽B2、短杆菌肽S和表面活性素的敏感性。在无血清的情况下,这四种肽在最低杀菌浓度为12.5至100微摩尔时可杀死支原体,但在所有情况下,血清的存在都会降低其活性。因此,在标准培养条件(10%血清)下,只有短杆菌肽A和短杆菌肽S能够抑制支原体生长(最小抑菌浓度为50微摩尔),而皮肤抗菌肽B2和表面活性素则无效。此外,用70微摩尔恩诺沙星对被任一支原体物种实验性污染的HeLa细胞培养物进行8天的处理可治愈感染,而单独使用短杆菌肽A和短杆菌肽S进行处理并不可靠,因为所需的浓度和处理时间对细胞有毒性。然而,将短杆菌肽A或短杆菌肽S与70微摩尔恩诺沙星联合使用时,根据所考虑的支原体和肽的不同,在处理30分钟或24小时后可根除支原体。在接近体内实际情况的条件下,实验性感染支原体的HeLa细胞培养物应可成为研究抗生素和膜活性肽抗支原体活性的有用模型。