Matsuo Y
Jpn J Microbiol. 1975 Aug;19(4):319-25.
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.
将在小鼠足垫(MFP)细胞培养物中连续传代培养1255天的鼠麻风杆菌久留米-42株的系列稀释细菌悬液皮下接种到小鼠体内。估计半数感染剂量(ID50)值大于10.7且小于85个菌,这表明该菌在长期细胞培养中仍保持良好的致病性。在细胞培养物中长时间感染并维持的细胞呈现出细胞有丝分裂的各个阶段。这表明鼠麻风杆菌细胞培养物中细菌数量的增加不仅是由于被感染细胞释放的杆菌的再吞噬,还归因于杆菌持续的细胞内生长周期以及被感染细胞的有丝分裂。就目前的细胞培养系统而言,在酸性磷酸酶活性方面,未观察到感染细胞与未感染细胞之间有明显差异。细胞内的大多数杆菌在超微结构上是正常的。吞噬小体中的固态杆菌被电子密度较低的透明区域包围。