Studies of Mycobacterium lepraemurium in cell culture. II. Pathogenicity of Mycobacterium lepraemurium maintained in mouse foot pad cell culture and interaction of the bacilli with the infected cells.

Japanese journal of microbiology Pub Date : 1975-08-01
Y Matsuo
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Abstract

A serially diluted bacterial suspension of the Kurume-42 strain of Mycobacterium lepraemurium maintained for 1255 days in a mouse foot pad (MFP) cell culture was inoculated in mice subcutaneously. The ID50 value was estimated at more than 10.7 and less than 85 organisms, indicating that pathogenicity of the organism had been maintained well in a long-term cell culture. The cells infected and maintained for a long period in the cell culture showed all the stages of cell mitosis. This suggests that the bacterial increase in cell cultures of M. lepraemurium is not only due to rephagocytosis of the bacilli released from the infected cells but also to a constant intracellular growth cycle of the bacilli accompanied by mitosis of the infected cells. In acid phosphatase activity, no appreciable differences were noted between the infected and uninfected cells as far as the present cell culture system was concerned. Most of the bacilli within the cells were ultrastructurally normal. Solid bacilli in phagosomes were surrounded by less electron-dense clear zones.

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麻风分枝杆菌细胞培养的研究。2鼠足垫细胞培养中麻风分枝杆菌的致病性及其与感染细胞的相互作用。
将在小鼠足垫(MFP)细胞中培养1255天的连续稀释的麻风分枝杆菌Kurume-42菌株菌悬液接种于小鼠皮下。估计ID50值大于10.7,小于85个生物体,表明该生物体在长期细胞培养中保持了良好的致病性。在细胞培养中感染并维持较长时间的细胞显示出细胞有丝分裂的所有阶段。这表明麻风分枝杆菌细胞培养中细菌数量的增加不仅是由于从感染细胞中释放的杆菌的再吞噬作用,而且还与杆菌的持续细胞内生长周期以及感染细胞的有丝分裂有关。在酸性磷酸酶活性方面,就目前的细胞培养系统而言,感染和未感染的细胞之间没有明显的差异。细胞内大部分杆菌超微结构正常。吞噬体中的固体杆菌被电子密度较小的透明区包围。
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