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Detection of enteric viruses in municipal sewage sludge by a combination of the enzymatic virus elution method and RT-PCR

机译:酶病毒洗脱法与RT-PCR相结合检测城市污水污泥中的肠病毒

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摘要

Pathogenic enteric viruses can be retained in municipal sewage sludge as has been reported by many researchers. Although the RT-PCR technique has been extensively employed for the virus detection from various environmental samples, the application of RT-PCR to the detection of viruses in sewage sludge has the difficulty because of inhibitory substances to the gene amplification. However, a combination of the enzymatic virus elution (EVE) method with RT-PCR made it possible to effectively detect viruses in sewage sludge. The enzymatic breakdown of sludge floes in the EVE method enhanced the virus elution from poliovirus 1 (PV1)-inoculated sewage sludge, and the detection of PV1 was performed by RT-PCR without any inhibitions. On the contrary, the application of RT-PCR to the viral assay in the USEPA method using the 10% beef extract solution was not practical because of inhibitions to the viral gene amplification. The combination of the EVE method using lysozyme (polysaccharide-degrading enzyme), papain (protease), and chymotrypsin (protease) with RT-PCR resulted in a virus recovery efficiency of 31%, but a synergistic effect of these enzymes on the virus recovery efficiency was not observed. The EVE method using lysozyme or papain could be a promising procedure for the virus elution from sewage sludge in detecting these viruses with RT-PCR.
机译:如许多研究人员所报道的,致病性肠病毒可以保留在城市污水污泥中。尽管RT-PCR技术已广泛用于从各种环境样品中检测病毒,但是由于RT-PCR技术对基因扩增具有抑制作用,因此难以将其应用于污水污泥中的病毒检测。但是,酶病毒洗脱(EVE)方法与RT-PCR的结合使有效检测污水污泥中的病毒成为可能。 EVE方法中污泥絮凝的酶促分解增强了从脊髓灰质炎病毒1(PV1)接种的污水污泥中的病毒洗脱,并且通过RT-PCR进行了PV1的检测,没有任何抑制作用。相反,由于使用了10%牛肉提取液的USEPA方法,将RT-PCR应用于病毒测定是不切实际的,因为抑制了病毒基因的扩增。使用溶菌酶(多糖降解酶),木瓜蛋白酶(蛋白酶)和胰凝乳蛋白酶(蛋白酶)的EVE方法与RT-PCR结合使用时,病毒的恢复效率为31%,但是这些酶对病毒的恢复具有协同作用没有观察到效率。使用溶菌酶或木瓜蛋白酶的EVE方法可能是一种有前途的方法,可用于通过RT-PCR检测污水中的污泥中的病毒。

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