Mead J R, Arrowood M J, Sidwell R W, Healey M C
Department of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan 84322-5600.
J Infect Dis. 1991 Jun;163(6):1297-304. doi: 10.1093/infdis/163.6.1297.
Severe combined immune deficient (SCID) and athymic National Institutes of Health (NIH)-III (bg/nu/xid) mice were evaluated for susceptibility to Cryptosporidium parvum infections as neonates and as adults after challenge with inocula of 5 x 10(4) and 1 x 10(6) oocysts/mouse, respectively. SCID and NIH-III nude mice developed chronic infections that persisted over 12 weeks. Cryptosporidial organisms were observed in the small and large intestines of all mice. Colonization of the gallbladder and hepatobiliary duct epithelium occurred in a majority of the NIH-III nude mice and a smaller number of the SCID mice. Severe infections in both mouse strains were associated with clinical deterioration followed by death. Signs in these mice included dehydration, icterus, and emaciation. Deaths apparently resulted from hepatic dysfunction. Control mice experienced transient infections with no clinical signs. Immunodeficient mice should prove useful in studies of disease pathogenesis and in evaluating potential anticryptosporidial agents.
对严重联合免疫缺陷(SCID)小鼠和无胸腺的美国国立卫生研究院(NIH)-III型(bg/nu/xid)小鼠进行评估,观察其作为新生小鼠以及成年小鼠分别接种5×10⁴和1×10⁶个卵囊/小鼠后对微小隐孢子虫感染的易感性。SCID小鼠和NIH-III型裸鼠均发生了持续超过12周的慢性感染。在所有小鼠的小肠和大肠中均观察到隐孢子虫生物体。大多数NIH-III型裸鼠以及较少数量的SCID小鼠出现胆囊和肝胆管上皮定植。两种小鼠品系中的严重感染均与临床状况恶化继而死亡有关。这些小鼠的体征包括脱水、黄疸和消瘦。死亡显然是由肝功能障碍导致的。对照小鼠经历了短暂感染,未出现临床体征。免疫缺陷小鼠在疾病发病机制研究以及评估潜在的抗隐孢子虫药物方面应会被证明是有用的。