Williams A, McBride B W, Hall G, Fitzgeorge R B, Farrar G H
Centre for Applied Microbiology and Research (CAMR), Porton Down, Salisbury, Wiltshire.
J Med Microbiol. 1995 Jun;42(6):433-41. doi: 10.1099/00222615-42-6-433.
A new small animal model of experimental Legionnaires' disease is described in which the reconstitution of SCID-Beige mice with human peripheral blood leucocytes permits the in-vivo growth of Legionella pneumophila in the lungs of aerosol-challenged mice. Following infection, viable bacterial counts within the lungs of mice increased from 10(5) cfu/lung at the time of inoculation to a maximum of 10(10) cfu/lung by 48 h post-inoculation. Two types of disease were detected in the lungs of infected SCID-Beige mice. An acute exudative bronchiolitis and bronchopneumonia were seen in the most severely affected mice and, in the less severely affected mice, lesions of subacute or chronic disease were seen with thickening of alveolar walls and consolidation of lung tissue. Human cells did not appear to be involved directly in the pathology but were required for the establishment of infection. Immunohistological staining of lung tissue revealed substantial amounts of bacterial antigen distributed in a pattern similar to that seen in human Legionnaires' disease.
本文描述了一种新的实验性军团病小动物模型,其中用人外周血白细胞重建SCID-米色小鼠,可使嗜肺军团菌在经气溶胶攻击的小鼠肺部进行体内生长。感染后,小鼠肺部的活菌计数从接种时的每肺10(5) cfu增加到接种后48小时的每肺最高10(10) cfu。在感染的SCID-米色小鼠肺部检测到两种类型的疾病。在受影响最严重的小鼠中可见急性渗出性细支气管炎和支气管肺炎,在受影响较轻的小鼠中可见亚急性或慢性疾病病变,伴有肺泡壁增厚和肺组织实变。人类细胞似乎未直接参与病理过程,但却是感染建立所必需的。肺组织的免疫组织化学染色显示大量细菌抗原以与人类军团病相似的模式分布。