首页> 外文期刊>The American Journal of Tropical Medicine and Hygiene >Leishmania spp: completely defined medium without serum and macromolecules (CDM/LP) for the continuous in vitro cultivation of infective promastigote forms.
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Leishmania spp: completely defined medium without serum and macromolecules (CDM/LP) for the continuous in vitro cultivation of infective promastigote forms.

机译:利什曼原虫(Leishmania spp):完全定义的不含血清和大分子(CDM / LP)的培养基,用于连续体外培养感染性前鞭毛体形式。

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The elimination of serum or of serum-derived macromolecules that supplant the fetal calf serum requirement from Leishmania culture media could decrease costs and improve the feasibility of large-scale production of well-defined parasite material. We report a completely defined medium, without serum-derived protein and/or macromolecules as a serum substitute, of common, available, and inexpensive constituents that can be used in place of serum-supplemented media for the continuous in vitro cultivation of promastigote forms of various Leishmania species. Typical promastigote morphology was observed in Giemsa-stained smears, regardless of the strain analyzed. Electrophoretic analysis showed that the proteinase patterns of aserically grown promastigote forms were similar to those obtained in serum-supplemented RPMI 1640 medium for all Leishmania studied. Similar antigenic profiles were recognized in immunoblots by sera from hosts with visceral or cutaneous leishmaniasis after growing promastigotes in the two different culture media. For parasites causing both cutaneous and visceral leishmaniasis, the absence of serum and macromolecules in the culture medium did not markedly change their in vitro infectivity for resident mouse macrophages and their virulence in animals compared with parasites cultivated in nondefined medium. Serum-free technology will be increasingly important in providing stability and reproducibility as research using promastigote moves closer to therapeutic applications.
机译:从利什曼原虫培养基中消除血清或代替胎牛血清需求的血清衍生大分子可以降低成本,并提高大规模生产明确的寄生虫材料的可行性。我们报告了一种完全定义的培养基,其中没有血清来源的蛋白质和/或大分子作为血清替代品,具有常见,可用和廉价的成分,可以代替补充血清的培养基用于连续体外培养的前鞭毛体形式的各种利什曼原虫。在吉姆萨染色涂片中观察到典型的前鞭毛体形态,与所分析的菌株无关。电泳分析表明,对于所有研究的利什曼原虫,非肠道生长的前鞭毛体形式的蛋白酶模式与在补充血清的RPMI 1640培养基中获得的模式相似。在两种不同培养基中生长前鞭毛体后,内脏或皮肤利什曼病的宿主血清中的免疫印迹可识别相似的抗原谱。对于同时引起皮肤利什曼病和内脏利什曼病的寄生虫,与在非确定性培养基中培养的寄生虫相比,培养基中血清和大分子的缺失不会显着改变其对常驻小鼠巨噬细胞的体外感染性及其在动物体内的毒力。随着使用前鞭毛体的研究越来越接近于治疗应用,无血清技术在提供稳定性和可重复性方面将变得越来越重要。

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