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Intact Cryptosporidium parvum oocysts isolated after in vitro excystation are infectious to neonatal mice.
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Detection of infectious Cryptosporidium parvum oocysts in surface and filter backwash water samples by immunomagnetic separation and integrated cell culture-PCR.通过免疫磁珠分离和细胞培养-聚合酶链反应联用技术检测地表水和滤池反冲洗水样本中感染性微小隐孢子虫卵囊
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Enzyme immunoassay detection of Cryptosporidium parvum inhibition by sinefungin in sporozoite infected HCT-8 enterocytic cells.
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Infectivity of Cryptosporidium parvum oocysts stored in water at environmental temperatures.微小隐孢子虫卵囊在环境温度下于水中储存后的感染性。
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Viable Cryptosporidium parvum oocysts exposed to chlorine or other oxidising conditions may lack identifying epitopes.暴露于氯或其他氧化条件下的活微小隐孢子虫卵囊可能缺乏识别表位。
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新生小鼠模型中微小隐孢子虫卵囊最大感染性的定量流式细胞术评估

Quantitative flow cytometric evaluation of maximal Cryptosporidium parvum oocyst infectivity in a neonate mouse model.

作者信息

Delaunay A, Gargala G, Li X, Favennec L, Ballet J J

机构信息

Laboratoire d'Immunologie et Immunopathologie, UPRES-EA 2128, CHU, 14033 Caen, France.

出版信息

Appl Environ Microbiol. 2000 Oct;66(10):4315-7. doi: 10.1128/AEM.66.10.4315-4317.2000.

DOI:10.1128/AEM.66.10.4315-4317.2000
PMID:11010875
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC92301/
Abstract

The importance of waterborne transmission of Cryptosporidium parvum to humans has been highlighted by recent outbreaks of cryptosporidiosis. The first step in a survey of contaminated water currently consists of counting C. parvum oocysts. Data suggest that an accurate risk evaluation should include a determination of viability and infectivity of counted oocysts in water. In this study, oocyst infectivity was addressed by using a suckling mouse model. Four-day-old NMRI (Naval Medical Research Institute) mice were inoculated per os with 1 to 1,000 oocysts in saline. Seven days later, the number of oocysts present in the entire small intestine was counted by flow cytometry using a fluorescent, oocyst-specific monoclonal antibody. The number of intestinal oocysts was directly related to the number of inoculated oocysts. For each dose group, infectivity of oocysts, expressed as the percentage of infected animals, was 100% for challenge doses between 25 and 1,000 oocysts and about 70% for doses ranging from 1 to 10 oocysts/animal. Immunofluorescent flow cytometry was useful in enhancing the detection sensitivity in the highly susceptible NMRI suckling mouse model and so was determined to be suitable for the evaluation of maximal infectivity risk.

摘要

近期隐孢子虫病的爆发凸显了微小隐孢子虫经水传播给人类的重要性。目前对受污染水进行调查的第一步是对微小隐孢子虫卵囊进行计数。数据表明,准确的风险评估应包括对水中所计数卵囊的活力和感染性的测定。在本研究中,通过使用乳鼠模型来研究卵囊的感染性。将4日龄的NMRI(海军医学研究所)小鼠经口接种1至1000个用生理盐水稀释的卵囊。7天后,使用荧光、卵囊特异性单克隆抗体通过流式细胞术对整个小肠中的卵囊数量进行计数。肠道卵囊的数量与接种卵囊的数量直接相关。对于每个剂量组,以感染动物的百分比表示的卵囊感染性,在25至1000个卵囊的攻击剂量下为100%,在1至10个卵囊/动物的剂量下约为70%。免疫荧光流式细胞术有助于提高在高度易感的NMRI乳鼠模型中的检测灵敏度,因此被确定适用于评估最大感染风险。