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Enterovirus detection from wastewater by RT-PCR and cell culture

机译:通过RT-PCR和细胞培养从废水中检测肠病毒

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This study was carried out first to determine if virus concentration by adsorption to glass wool was suitable for the detection of enterovirus genomes by seminested RT-PCR in treated wastewater and second to compare the presence of infectious enteroviruses and enterovirus genomes. The experiments were performed on 57 treated wastewater samples from two wastewater treatment plants which use different processes. The water samples were analysed directly and after concentration on glass wool. Concerning the effect of a concentration step on glass wool, the results show that after concentration, the number of positive samples increases significantly for both infections enteroviruses (17 vs 0) and enterovirus genomes (37 vs 9). Concerning the comparison of the presence of infectious enteroviruses and enterovirus genomes, it appears for all the samples analysed that the number of positive samples for enterovirus genomes is significantly higher than those for infectious enteroviruses (37 vs 17). Therefore, the presence of enterovirus genomes cannot be considered to be an indicator of the presence of infectious enteroviruses, strictly speaking, but only an indicator of more or less recent viral contamination. However, 3 samples containing infectious enteroviruses are negative by seminested RT-PCR. These false negative results can be explained by the presence of substances that inhibit seminested RT-PCR reactions.
机译:这项研究首先是确定通过吸附在玻璃棉上的病毒浓度是否适合通过半巢式RT-PCR在处理后的废水中检测肠道病毒基因组,其次是比较感染性肠道病毒和肠道病毒基因组的存在。实验是对来自两个使用不同工艺的废水处理厂的57个处理过的废水样品进行的。将水样直接分析,并在玻璃棉上浓缩后进行分析。关于浓缩步骤对玻璃棉的影响,结果表明,浓缩后,感染肠道病毒(17对0)和肠道病毒基因组(37对9)的阳性样品数量均显着增加。关于感染性肠病毒和肠病毒基因组的存在的比较,对于所有分析的样品,似乎肠病毒基因组的阳性样品数量明显高于感染性肠病毒(37 vs 17)。因此,严格地说,肠病毒基因组的存在不能被认为是感染性肠病毒的存在的指示,而仅仅是近期病毒污染的指示。然而,通过半巢式RT-PCR,含有感染性肠病毒的3个样品为阴性。这些假阴性结果可以用抑制半巢式RT-PCR反应的物质来解释。

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