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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Susceptibilities of Mycoplasma fermentans and Mycoplasma hyorhinis to membrane-active peptides and enrofloxacin in human tissue cell cultures.
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Susceptibilities of Mycoplasma fermentans and Mycoplasma hyorhinis to membrane-active peptides and enrofloxacin in human tissue cell cultures.

机译:发酵支原体和透明支原体对人组织细胞培养中的膜活性肽和恩诺沙星的敏感性。

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摘要

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.
机译:支原体是无细胞壁的细菌,属于Mollicutes类,对人和动物具有致病性,是组织细胞培养物中的常见污染物。尽管可以使用染色DNA的荧光染料和/或分子探针轻松监测支原体对培养物的污染,但是保护和净化培养物仍然是严峻的挑战。在目前的工作中,我们通过生长抑制和杀伤力测定法研究了发酵支原体和透明支原体对膜活性肽alamethicin,dermaseptin B2,gramicidin S和surfactin的敏感性。在没有血清的情况下,这四种肽以最小的杀菌浓度杀死了支原体,其杀菌浓度为12.5至100 microM,但是在所有情况下,血清的存在都会降低活性。结果,在标准培养条件下(血清浓度为10%),只有alamethicin和gramicidin S能够抑制支原体生长(MIC为50 microM),而septepteptin B2和surfactin无效。此外,用70 microM恩诺沙星对任何一种支原体物种进行实验污染的HeLa细胞培养物的治疗8天可治愈感染的培养物,而单独用alamethicin和gramicidin S的治疗是不可靠的,因为所需的浓度和处理时间对细胞有毒。但是,根据所考虑的支原体和多肽,在治疗30分钟或24小时后,将来美辛或gramicidin S与70 microM恩诺沙星的组合可以根除支原体。实验证明感染了支原体的HeLa细胞培养物应被证明是在接近体内条件下研究抗生素和膜活性肽的抗支原体活性的有用模型。

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