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用于反刍动物无形体体外培养的无血清培养基。

Serum-free media for the in vitro cultivation of Cowdria ruminantium.

作者信息

Zweygarth E, Josemans A I, Horn E

机构信息

Parasitology Division, Onderstepoort Veterinary Institute, South Africa.

出版信息

Ann N Y Acad Sci. 1998 Jun 29;849:307-12. doi: 10.1111/j.1749-6632.1998.tb11063.x.

Abstract

The in vitro culture of Cowdria ruminantium, the causative agent of heartwater in domestic ruminants, was first achieved in 1985; since then, most groups working with this culture system have used media which were supplemented with serum and, in addition, most of them contained tryptose phosphate broth. These undefined products vary from batch to batch and often fail to support the growth of C. ruminantium. We are therefore working towards the development of a completely chemically defined medium for Cowdria culture. We attempted the propagation of the Welgevonden stock of C. ruminantium in bovine endothelial cell cultures in a variety of serum-free culture media. Four synthetic media gave unsatisfactory results, these were: SFRE-199, Iscove's modified Dulbecco's medium, Dulbecco's modified Eagle's medium, and Leibovitz L-15. These media were all supplemented with a proprietary solution A (components solution A of the HL-1 medium kit, containing transferrin, testosterone, sodium selenite, ethanolamine, saturated and unsaturated fatty acids, and stabilizing proteins). Three other serum-free media did support the growth of C. ruminantium: a modified HL-1 medium, Dulbecco's modified Eagle's medium nutrient mixture Ham F-12 (DME/F-12), and RPMI 1640. The chemical composition of DME/F-12 and RPMI 1640 are published, but not that of the HL-1 medium. Each of these media was supplemented with proprietary solution A. Various supplements were investigated as alternative to the incompletely specified solution A; bovine lipoproteins and bovine transferrin were identified as essential supplements which effectively replaced compound solution A. C. ruminantium was propagated in the three growth-supportive media for at least 10 passages.

摘要

反刍动物心水病病原体——反刍兽立克次氏体的体外培养于1985年首次成功;自那时起,大多数使用该培养系统的研究团队都使用了添加血清的培养基,此外,其中大多数还含有胰蛋白胨磷酸盐肉汤。这些成分不明确的产品批次之间存在差异,且常常无法支持反刍兽立克次氏体的生长。因此,我们正在致力于开发一种完全化学成分明确的反刍兽立克次氏体培养基。我们尝试在多种无血清培养基中,在牛内皮细胞培养物中培养反刍兽立克次氏体的韦尔格冯登毒株。四种合成培养基效果不佳,它们分别是:SFRE - 199、伊斯科夫改良的杜尔贝科培养基、杜尔贝科改良的伊格尔培养基和莱博维茨L - 15培养基。这些培养基均添加了一种专利溶液A(HL - 1培养基试剂盒的溶液A成分,含有转铁蛋白、睾酮、亚硒酸钠、乙醇胺、饱和与不饱和脂肪酸以及稳定蛋白)。另外三种无血清培养基确实支持反刍兽立克次氏体的生长:改良的HL - 1培养基、杜尔贝科改良的伊格尔培养基营养混合物哈姆F - 12(DME/F - 12)和RPMI 1640培养基。DME/F - 12和RPMI 1640的化学成分已公布,但HL - 1培养基的化学成分未公布。这些培养基每种都添加了专利溶液A。研究了各种替代成分不明确的溶液A的补充剂;牛脂蛋白和牛转铁蛋白被确定为有效替代复合溶液A的必需补充剂。反刍兽立克次氏体在这三种支持生长的培养基中传代培养了至少10代。

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