首页> 外文期刊>European food research and technology =: Zeitschrift fur Lebensmittel-Untersuchung und -Forschung. A >Detection of GI and GII noroviruses in drinking water and vegetables using filtration and real-time RT-PCR
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Detection of GI and GII noroviruses in drinking water and vegetables using filtration and real-time RT-PCR

机译:使用过滤和实时RT-PCR检测饮用水和蔬菜中的GI和GII诺如病毒

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摘要

The purpose of the study was to provide a rapid and sensitive method for detecting NoV GI and NoV GII in drinking water and vegetables. The method is based on viral concentration by microporous membrane adsorption method before RNA extraction and real-time RT-PCR amplification. Then water and vegetable samples which artificially contaminated with NoV GI and GII stool samples were used to determine the mean virus recoveries and the method sensitivity. The method showed the detection limit of NoV GI was 4.13 x 10(2) copies/500 mL for drinking water and 4.13 x 10(3) copies/15 g for lettuce and coriander. The detection limit of NoV GII was 2.94 x 10(1) copies/500 mL for distilled water, 2.94 x 10(2) copies/500 mL for Mountain spring water and mineral water, and 2.94 x 10(3) copies/15 g for lettuce and coriander. The method described provides a valuable tool for monitoring the potential public health risks associated with noroviruses contamination in drinking water and vegetables.
机译:该研究的目的是提供一种快速灵敏的检测饮用水和蔬菜中NoV GI和NoV GII的方法。该方法基于RNA提取和实时RT-PCR扩增之前通过微孔膜吸附法进行病毒浓缩。然后使用被NoV GI和GII粪便样品人工污染的水和蔬菜样品来确定平均病毒回收率和方法灵敏度。该方法显示,饮用水中NoV GI的检出限为4.13 x 10(2)份/ 500 mL,生菜和香菜的检出限为4.13 x 10(3)份/ 15 g。 NoV GII的检出限为蒸馏水2.94 x 10(1)份/ 500 mL,山泉水和矿泉水为2.94 x 10(2)份/ 500 mL和2.94 x 10(3)份/ 15 g生菜和香菜。所述方法为监测与饮用水和蔬菜中诺如病毒污染相关的潜在公共卫生风险提供了有价值的工具。

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