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A perspective on the prevalence of DNA enteric virus genomes in anaerobic-digested biological wastes

机译:厌氧消化生物废物中DNA肠道病毒基因组流行的观点

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The major goal of this study is to gain a perspective on the prevalence of DNA enteric virus genomes in mesophilic anaerobic-digested (MAD) sewage sludge and manure by comparing their quantitative PCR (qPCR) concentrations and removals with traditional fecal indicators (Escherichia coli, enterococci, and Bacteroidetes). hi addition, relationships between qPCR and culture, measurements of fecal indicators (FIs) were determined. There was no significant difference between the qPCR concentrations of human adenovirus and E. coli/enterococci in MAD sewage sludge; however, the qPCR concentrations of bovine adenovirus were significantly lower than FIs and bovine polyomavirus (BPyV) in MAD manure. The qPCR concentrations of human polyomavirus were slightly lower than E. coli and enterococci (p<0.05), but no significant difference was observed between the qPCR concentrations of BPyV and FIs. The digestion treatment achieved higher genome removal of bovine DNA enteric viruses than FIs (p<0.05). Significant correlations were observed between qPCR and culture measurements of FIs, but the concentrations and removals of FIs determined by qPCR assays were still significantly different than those determined by culture assays. Overall, we determined that the prevalence of DNA enteric virus genomes in MAD biological wastes was high due to their comparable in qPCR concentrations to FIs, indicating that mesophilic anaerobic digestion treatment alone may not be effective enough to remove DNA viral pathogens in biological wastes.
机译:这项研究的主要目的是通过比较其定量PCR(qPCR)浓度和去除率与传统粪便指标(大肠杆菌,肠球菌和拟杆菌)。另外,确定了qPCR与培养之间的关系,粪便指标(FIs)的测量。 MAD污水污泥中的人腺病毒的qPCR浓度和大肠杆菌/肠球菌的qPCR浓度之间没有显着差异。但是,MAD粪便中牛腺病毒的qPCR浓度明显低于FIs和牛多瘤病毒(BPyV)。人多瘤病毒的qPCR浓度略低于大肠杆菌和肠球菌(p <0.05),但在BPyV和FI的qPCR浓度之间未观察到显着差异。消化处理实现了比FI更高的牛DNA肠病毒基因组去除率(p <0.05)。在qPCR和FI的培养物测量之间观察到显着的相关性,但是通过qPCR测定法确定的FI的浓度和去除与通过培养物测定法确定的FIs的浓度和去除仍然显着不同。总体而言,我们确定MAD生物废物中DNA肠道病毒基因组的流行程度很高,这是由于其qPCR浓度与FI相当,这表明仅中温厌氧消化处理可能不足以有效去除生物废物中的DNA病毒病原体。

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