Yamada A, Taguchi F, Fujiwara K
Jpn J Exp Med. 1979 Dec;49(6):413-21.
After intraperitoneal inculation with a virulent mouse hepatitis virus, MHV-3, 50% lethal dose in DDD mice was about 7 log10 higher than that in C3H mice. Histopathologically, splenic lymphocytes especially of the thymus-dependent area were more severely affected in susceptible C3H mice than in DDD mice. In the liver of C3H mice, virus multiplied exponentially after inoculation, attaining 10(6) PFU at moribund stage, while virus multiplication in DDD mice was much less prominent decreasing remarkably at day 5 or later. The virus could multiply in the primary culture of spleen cells from C3H mice but not in those from DDD mice, and cells supporting virus growth seemed to be a theta-positive population of lymphocytes. No difference was observed between the two strains of mice in the ability of peritoneal macrophages to support virus growth in vitro as well as serum interferon levels after infection.
用强毒小鼠肝炎病毒MHV - 3进行腹腔接种后,DDD小鼠的50%致死剂量比C3H小鼠高约7个对数10。组织病理学上,易感的C3H小鼠脾脏淋巴细胞尤其是胸腺依赖区的淋巴细胞比DDD小鼠受到的影响更严重。在C3H小鼠的肝脏中,接种后病毒呈指数增殖,濒死期达到10(6) PFU,而DDD小鼠中的病毒增殖则不那么明显,在第5天或之后显著下降。该病毒能在C3H小鼠脾脏细胞的原代培养物中增殖,但不能在DDD小鼠的脾脏细胞原代培养物中增殖,支持病毒生长的细胞似乎是θ阳性淋巴细胞群体。在腹膜巨噬细胞支持病毒体外生长的能力以及感染后血清干扰素水平方面,两品系小鼠之间未观察到差异。