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用单个微小隐孢子虫卵囊感染免疫抑制的C57BL/6N成年小鼠。

Infection of immunosuppressed C57BL/6N adult mice with a single oocyst of Cryptosporidium parvum.

作者信息

Yang S, Benson S K, Du C, Healey M C

机构信息

Department of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan 84322-5600, USA.

出版信息

J Parasitol. 2000 Aug;86(4):884-7. doi: 10.1645/0022-3395(2000)086[0884:IOICAM]2.0.CO;2.

DOI:10.1645/0022-3395(2000)086[0884:IOICAM]2.0.CO;2
PMID:10958482
Abstract

The present study was designed to determine the minimum number of Cryptosporidium parvum oocysts capable of producing patent infections in immunosuppressed C57BL/6N adult mice. Sixty-four female mice were divided into 6 groups of 8 mice each, except group 1 that contained 24 mice. Mice in groups 1-3 were immunosuppressed with dexamethasone and inoculated with 1, 5, and 10 oocysts per mouse, respectively. The accuracy of the inoculum size was microscopically confirmed. Mice in groups 4-6 served as controls: they received either only oocyst inoculation (group 4), or immunosuppression (group 5), or no treatments (group 6). Fecal oocyst shedding was monitored daily for each mouse using an indirect immunofluorescent assay. Parasite colonization in the terminal ileum of each mouse was evaluated histologically. Four of 24 mice in group 1 developed patent infections, with a prepatent period of approximately 6 days. All mice in groups 2 and 3 developed patent infections, with prepatent periods ranging from 4 to 7 days. Mice in groups 4-6 remained uninfected. Parasite colonization was observed in the terminal ilea of all mice in groups 1-3 that shed fecal oocysts. The present study experimentally demonstrates that a single viable oocyst can induce patent C. parvum infections in immunosuppressed C57BL/6N adult mice and indicates that this mouse model could be used for the parasite genotype or isolate cloning.

摘要

本研究旨在确定能够在免疫抑制的C57BL/6N成年小鼠中产生显性感染的最小微小隐孢子虫卵囊数量。64只雌性小鼠被分为6组,每组8只,但第1组包含24只小鼠。第1 - 3组的小鼠用 dexamethasone进行免疫抑制,分别每只小鼠接种1、5和10个卵囊。接种量的准确性通过显微镜确认。第4 - 6组的小鼠作为对照:它们要么仅接受卵囊接种(第4组),要么接受免疫抑制(第5组),要么不接受任何处理(第6组)。每天使用间接免疫荧光测定法监测每只小鼠的粪便卵囊排出情况。对每只小鼠回肠末端的寄生虫定植情况进行组织学评估。第1组的24只小鼠中有4只出现显性感染,潜伏期约为6天。第2组和第3组的所有小鼠均出现显性感染,潜伏期为4至7天。第4 - 6组的小鼠未被感染。在第1 - 3组所有排出粪便卵囊的小鼠的回肠末端观察到寄生虫定植。本研究通过实验证明,单个活卵囊可在免疫抑制的C57BL/6N成年小鼠中诱导微小隐孢子虫显性感染,并表明该小鼠模型可用于寄生虫基因型或分离株的克隆。

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