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首页> 外文期刊>Applied and Environmental Microbiology >Determining UV Inactivation of Toxoplasma gondii Oocysts by Using Cell Culture and a Mouse Bioassay
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Determining UV Inactivation of Toxoplasma gondii Oocysts by Using Cell Culture and a Mouse Bioassay

机译:通过使用细胞培养和小鼠生物测定法确定弓形虫卵囊的紫外线灭活

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The effect of UV exposure on Toxoplasma gondii oocysts has not been completely defined for use in water disinfection. This study evaluated UV-irradiated oocysts by three assays: a SCID mouse bioassay, an in vitro T. gondii oocyst plaque (TOP) assay, and a quantitative reverse transcriptase real-time PCR (RT-qPCR) assay. The results from the animal bioassay show that 1- and 3-log10 inactivation is achieved with 4 mJ/cm2 UV and 10 mJ/cm2 low-pressure UV, respectively. TOP assay results, but not RT-qPCR results, correlate well with bioassay results. In conclusion, a 3-log10 inactivation of T. gondii oocysts is achieved by 10-mJ/cm2 low-pressure UV, and the in vitro TOP assay is a promising alternative to the mouse bioassay.
机译:紫外线对弓形虫卵囊的影响尚未完全确定可用于水消毒。这项研究通过三种检测方法评估了紫外线照射的卵囊:SCID小鼠生物检测,体外弓形虫卵囊菌斑(TOP)检测和定量逆转录酶实时PCR(RT-qPCR)分析。动物生物测定的结果表明,在4 mJ / cm 2 紫外线和10 mJ / cm 2 下实现1-log和3-log 10 灭活。 sup>分别为低压UV。 TOP测定结果(而非RT-qPCR结果)与生物测定结果密切相关。总之, T的3-log 10 失活。弓形虫卵囊是通过10-mJ / cm 2 低压紫外线获得的,而体外 TOP分析是一种有希望的替代小鼠生物分析的方法。

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