Dunn P L, North R J
Trudeau Institute Inc., Saranac Lake, New York 12983, USA.
Infect Immun. 1995 Sep;63(9):3428-37. doi: 10.1128/iai.63.9.3428-3437.1995.
Three virulent strains of Mycobacterium tuberculosis (H37Rv, Erdman, and NYH-27) and two virulent strains of M. bovis (Ravenel and Branch) were compared in terms of their growth rates in the livers and the lungs of mice, their ability to cause lung pathology, and the time taken for them to cause death. In immunocompetent mice, all strains caused an infection that progressed for 20 days or more and then underwent resolution in the liver but not in the lungs. In the lungs, infection persisted and induced progressive pathology. According to host survival time, Ravenel was the most virulent strain, followed, in decreasing order of virulence, by Branch, H37Rv, Erdman, and NYH-27. The much longer survival times of mice infected with M. tuberculosis strains allowed time for lung histopathology to change from a histiocytic alveolitis to a chronic fibroblastic fibrosis that eventually obliterated most of the lung architecture. By contrast, in mice infected with M. bovis strains, the alveolitis that developed during early infection was rapid and expansive enough to cause death before chronic lung pathology became evident. In mice depleted of CD4+ T cells, increased growth of all virulent strains induced necrotic exudative lung lesions that rapidly filled most of the alveolar sacs with inflammatory cells. These mice died much earlier than infected control mice did. Attenuated strains had longer population doubling times in vivo and failed to cause progressive disease or pathology in the lungs or livers of immunocompetent mice.
对三株结核分枝杆菌强毒株(H37Rv、Erdman和NYH - 27)以及两株牛分枝杆菌强毒株(Ravenel和Branch)在小鼠肝脏和肺脏中的生长速率、引发肺部病变的能力以及导致死亡所需时间方面进行了比较。在免疫功能正常的小鼠中,所有菌株都会引发持续20天或更长时间的感染,之后感染在肝脏中得到缓解,但在肺部却不会。在肺部,感染持续存在并引发进行性病变。根据宿主存活时间,Ravenel是毒性最强的菌株,其次按毒性递减顺序依次为Branch、H37Rv、Erdman和NYH - 27。感染结核分枝杆菌菌株的小鼠存活时间长得多,这使得肺部组织病理学能够从组织细胞性肺泡炎转变为慢性纤维母细胞性纤维化,最终破坏了大部分肺结构。相比之下,在感染牛分枝杆菌菌株的小鼠中,早期感染期间出现的肺泡炎迅速且广泛,足以在慢性肺部病变明显之前导致死亡。在CD4 + T细胞耗竭的小鼠中,所有强毒株的生长增加导致坏死性渗出性肺部病变,炎症细胞迅速充满大部分肺泡囊。这些小鼠比感染的对照小鼠死亡早得多。减毒株在体内的群体倍增时间更长,并且在免疫功能正常的小鼠的肺部或肝脏中不会引发进行性疾病或病变。