[溶组织内阿米巴HK 9型多种培养方法的改进]。

Angewandte Parasitologie Pub Date : 1992-08-01
G Luckner, G Ockert
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引用次数: 0

摘要

间接免疫荧光法(IFAT)对肠外溶组织芽胞杆菌感染的血清学诊断需要一种红细胞抗原。这是在我们的实验室通过在含有简单盐混合物(类似林格混合物),小牛血清和大米淀粉的营养培养基中多组分培养溶组织杆菌菌株HK 9生产的。本文中描述的实验目的是寻找一种有用的培养基,在这种培养基中,变形虫可以高密度生长,但不存在干扰抗原产生的物质,如碎片或大米淀粉颗粒。结果表明EAGLE MEM和PARKER的细胞培养基易于操作(与世界上使用的DIAMOND培养基TYI-S-33相反),并取得了良好的效果。经过10次传代培养后,两种培养基都适合于溶组织芽胞杆菌的培养,以制备适合IFAT的抗原。作为一个副作用,我们注意到,当培养基换成另一种完全不同的培养基(从细胞培养基到类似林格溶液)时,变形虫会有一个适应阶段,在此期间变形虫生长缓慢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The improvement of polyxenic cultivation of Entamoeba histolytica type HK 9].

The serological diagnosis of extraintestinal infections with E. histolytica by indirect immunofluorescence (IFAT) requires a corpuscular antigen. This is produced in our laboratory via polyxenic cultivation of E. histolytica strain HK 9 in a nutrient medium containing a simple salt mixture (Resembling the Ringer-mixture), calf serum and rice starch. It was the aim of the experiments described in this paper to search for a useful medium in which the amebae grow in high density but without substances disturbing the antigen production like debris or rice starch granules. It was shown that the cell culture media of EAGLE MEM and PARKER were easy to handle (contrary to the worldwide used DIAMOND medium TYI-S-33) and brought good results. After a period of 10 subcultures both media were suitable for the cultivation of E. histolytica for making an antigen reasonable for IFAT. As a side effect it was noticed that there was an adaptation phase during which the amebae grew slowly when the medium was changed to another which was completely different (from a cell culture medium to a Ringer-like solution).

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