Niszl I A, Veale R B, Markus M B
Department of Zoology, University of the Witwatersrand, South Africa.
J Parasitol. 1998 Oct;84(5):961-7.
The cytopathic effect (CPE) of southern African, British, and an Asian strain of Acanthamoeba was assessed using a system developed around 2 different mammalian cell (MC) lines. The time taken by the amebae to destroy cell cultures completely was shown to be dependent largely on the size of the amebic inoculum and the cell type. This highlights the need to assess carefully the behavior of cell lines prior to using them for cytopathic testing. Assays performed with conditioned medium collected from both MCs and amebic cells indicated that mechanical destruction may have been primarily responsible for the CPE. Furthermore, not all strains of Acanthamoeba lose cytopathogenicity after being passaged in axenic culture for extended periods. The use of MC cultures was shown to be an accurate, rapid, and repeatable means of assaying the CPE of strains of Acanthamoeba.
使用围绕2种不同哺乳动物细胞(MC)系开发的系统,评估了来自非洲南部、英国和亚洲的棘阿米巴菌株的细胞病变效应(CPE)。结果表明,阿米巴完全破坏细胞培养物所需的时间很大程度上取决于阿米巴接种物的大小和细胞类型。这凸显了在将细胞系用于细胞病变测试之前,仔细评估其行为的必要性。对从MC和阿米巴细胞收集的条件培养基进行的检测表明,机械破坏可能是CPE的主要原因。此外,并非所有棘阿米巴菌株在无共生培养中长期传代后都会丧失细胞致病性。MC培养物被证明是一种准确、快速且可重复的检测棘阿米巴菌株CPE的方法。