Yang S, Healey M C
Department of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan 84322-5600.
J Parasitol. 1994 Apr;80(2):338-42.
Two experiments were conducted to determine if intraperitoneal (i.p.) and/or subcutaneous (s.c.) injection of Cryptosporidium parvum oocysts could produce patent gut infections in dexamethasone (DEX) or dexamethasone phosphate (DEXp)-immunosuppressed adult female C57BL/6N mice. The results from experiment 1 were suggestive but did not unequivocally demonstrate that i.p. injection of oocysts could produce patent gut infections in these mice. In experiment 2, all mice were individually caged, immunosuppressed with DEXp (groups 1 and 2) or DEX (groups 3 and 4), and administered C. parvum oocysts either by orogastric intubation (groups 1 and 3), i.p. (group 2), or s.c. (group 4). All but 1 mouse in groups 1 and 3 began shedding oocysts in their feces on day 3 post-infection (PI). Mice in these 2 groups continued to shed oocysts until they were killed on day 17 PI. Mice administered oocysts s.c. did not shed oocysts. In group 2, 1 mouse died, 1 failed to shed oocysts, and 1 began shedding oocysts on day 3 PI. The remaining 5 mice started shedding oocysts on either days 8, 10, or 14 PI and continued to shed oocysts until they were killed. We conclude that immunosuppressed adult C57BL/6N mice administered oocysts i.p. can develop patent gut infections with C. parvum.
进行了两项实验,以确定腹腔注射(i.p.)和/或皮下注射(s.c.)微小隐孢子虫卵囊是否能在接受地塞米松(DEX)或磷酸地塞米松(DEXp)免疫抑制的成年雌性C57BL/6N小鼠中引发肠道显性感染。实验1的结果具有一定提示性,但并未明确证明腹腔注射卵囊能在这些小鼠中引发肠道显性感染。在实验2中,所有小鼠单独饲养,用DEXp(第1组和第2组)或DEX(第3组和第4组)进行免疫抑制,并通过灌胃(第1组和第3组)、腹腔注射(第2组)或皮下注射(第4组)给予微小隐孢子虫卵囊。第1组和第3组中除1只小鼠外,所有小鼠在感染后第3天(PI)开始在粪便中排出卵囊。这两组小鼠持续排出卵囊,直到在感染后第17天被处死。皮下注射卵囊的小鼠未排出卵囊。在第2组中,1只小鼠死亡,1只未排出卵囊,1只在感染后第3天开始排出卵囊。其余5只小鼠在感染后第8、10或14天开始排出卵囊,并持续排出卵囊,直到被处死。我们得出结论,腹腔注射卵囊的免疫抑制成年C57BL/6N小鼠可发生微小隐孢子虫肠道显性感染。