Hale T L, Bonventre P F
Infect Immun. 1979 Jun;24(3):879-86. doi: 10.1128/iai.24.3.879-886.1979.
Epithelial cell infection by Shigella flexneri 2a was studied in an in vitro model system. Using the Henle 407 human intestinal epithelial cell line as host cells, a standardized experimental protocol which allowed quantitative measurement of infection was developed. Intravellular residence of infecting organisms was confirmed by indirect fluorescent-antibody staining of unfixed and methanol-fixed (Henle 407) cells and by quantitative bacteriological culture of disrupted host cells after infection. The process of shigella entry into cells was evaluated by chemical or physical modulation of the bacterium under controlled experimental conditions. Shigella were subjected to mild heat, ultraviolet radiation aminoglycoside antibiotics, and immunoglobulins raised against S. flexneri 2a. The data show that heat-stable antigens on the bacterial surface are not solely responsible for infectivity of S. flexneri 2a. Furthermore, it was shown that physiological and synthetic functions of shigellae are required for entry into host cells.
在体外模型系统中研究了福氏志贺菌2a对上皮细胞的感染。以Henle 407人肠道上皮细胞系作为宿主细胞,制定了一种标准化实验方案,可对感染进行定量测量。通过对未固定和甲醇固定的(Henle 407)细胞进行间接荧光抗体染色以及对感染后破碎的宿主细胞进行定量细菌培养,证实了感染性生物体在细胞内的存在。在可控实验条件下,通过对细菌进行化学或物理调节来评估志贺菌进入细胞的过程。对志贺菌进行温和加热、紫外线照射、氨基糖苷类抗生素处理以及用针对福氏志贺菌2a产生的免疫球蛋白处理。数据表明,细菌表面的热稳定抗原并非福氏志贺菌2a感染性的唯一决定因素。此外,研究表明志贺菌进入宿主细胞需要其生理和合成功能。