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Detection of Infectious Cryptosporidium Oocysts by Cell Culture Immunofluorescence Assay: Applicability to Environmental Samples

机译:通过细胞培养免疫荧光检测感染性隐孢子虫卵囊:适用于环境样品

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摘要

In the past few years many waterborne outbreaks related to Cryptosporidium have been described. Current methods for detection of Cryptosporidium in water for the most part rely on viability assays which are not informative concerning the infectivity of oocysts. However, for estimation of the risk of infection with Cryptosporidium this information is required. For environmental samples the oocyst counts are often low, and the oocysts have been exposed to unfavorable conditions. Therefore, determination of the infectivity of environmental oocysts requires an assay with a high level of sensitivity. We evaluated the applicability of in vitro cell culture immunofluorescence assays with HCT-8 and Caco-2 cells for determination of oocyst infectivity in naturally contaminated water samples. Cell culture assays were compared with other viability and infectivity assays. Experiments with Cryptosporidium oocysts from different sources revealed that there was considerable variability in infectivity, which was illustrated by variable 50% infective doses, which ranged from 40 to 614 oocysts, and the results indicated that not only relatively large numbers of fresh oocysts but also aged oocysts produced infection in cell cultures. Fifteen Dutch surface water samples were tested, and the cell culture immunofluorescence assays were not capable of determining the infectivity for the low numbers of naturally occurring Cryptosporidium oocysts present in the samples. A comparison with other viability assays, such as the vital dye exclusion assay, demonstrated that surrogate methods overestimate the number of infectious oocysts and therefore the risk of infection with Cryptosporidium. For accurate risk assessment, further improvement of the method for detection of Cryptosporidium in water is needed.
机译:在过去几年中,已经描述了许多与隐孢子虫有关的水源性暴发。当前用于检测水中隐孢子虫的方法大部分依赖于生存力测定,该测定不能提供有关卵囊感染性的信息。但是,为了估计隐孢子虫感染的风险,需要此信息。对于环境样品,卵囊计数通常很低,并且卵囊已经暴露在不利的条件下。因此,确定环境卵囊的感染性需要具有高灵敏度的测定。我们评估了用HCT-8和Caco-2细胞进行的体外细胞培养免疫荧光测定法对确定自然污染水样中卵囊感染性的适用性。将细胞培养测定法与其他存活率和传染性测定法进行了比较。来自不同来源的隐孢子虫卵囊的实验表明,感染性存在相当大的可变性,这可以通过50%的可变感染剂量(范围从40到614个卵囊)来说明,结果表明,不仅相对大量的新鲜卵囊,而且老化卵囊在细胞培养物中产生感染。测试了15个荷兰地表水样品,并且细胞培养免疫荧光测定法无法确定样品中存在的少量天然存在的隐孢子虫卵囊的感染性。与其他活性分析(例如,活性染料排除分析)的比较表明,替代方法高估了感染性卵囊的数量,因此高估了隐孢子虫的感染风险。为了进行准确的风险评估,需要进一步改进水中隐孢子虫的检测方法。

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