Office of Research and Development, U.S. Environmental Protection Agency, 26 W. Martin Luther King Dr., Cincinnati, OH, 45268, USA.
Office of Research and Development, U.S. Environmental Protection Agency, 26 W. Martin Luther King Dr., Cincinnati, OH, 45268, USA.
Water Res. 2020 Feb 1;169:115213. doi: 10.1016/j.watres.2019.115213. Epub 2019 Oct 19.
Risk-based treatment of onsite wastewaters for decentralized reuse requires information on the occurrence and density of pathogens in source waters, which differ from municipal wastewater due to scaling and dilution effects in addition to variable source contributions. In this first quantitative report of viral enteric pathogens in onsite-collected graywater and wastewater, untreated graywater (n = 50 samples) and combined wastewater (i.e., including blackwater; n = 28) from three decentralized collection systems were analyzed for two norovirus genogroups (GI/GII) and human adenoviruses using droplet digital polymerase chain reaction (ddPCR). Compared to traditional quantitative PCR (qPCR), which had insufficient sensitivity to quantify viruses in graywater, ddPCR allowed quantification of norovirus GII and adenovirus in 4% and 14% of graywater samples, respectively (none quantifiable for norovirus GI). Norovirus GII was routinely quantifiable in combined wastewater by either PCR method (96% of samples), with well-correlated results between the analyses (R = 0.96) indicating a density range of 5.2-7.9 log genome copies/L. These concentrations are greater than typically reported in centralized municipal wastewater, yet agree well with an epidemiology-based model previously used to develop pathogen log-reduction targets (LRTs) for decentralized non-potable water systems. Results emphasize the unique quality of onsite wastewaters, supporting the previous LRTs and further quantitative microbial risk assessment (QMRA) of decentralized water reuse.
基于风险的就地处理废水再利用需要了解水源中病原体的发生和密度信息,由于结垢和稀释效应以及可变的源贡献,这些信息与市政废水不同。在就地收集的灰水和废水的肠道病毒病原体的首次定量报告中,使用液滴数字聚合酶链反应(ddPCR)对三个分散式收集系统中的未经处理的灰水(n=50 个样本)和组合废水(即包括黑水;n=28)分析了两种诺如病毒基因群(GI/GII)和人腺病毒。与传统定量 PCR(qPCR)相比,ddPCR 具有更高的灵敏度,可以定量灰水中的病毒,在 4%的灰水样本中可以定量检测到诺如病毒 GII,在 14%的灰水样本中可以定量检测到腺病毒(诺如病毒 GI 均不可定量)。通过任何一种 PCR 方法均可常规定量检测组合废水中的诺如病毒 GII(96%的样本),两种分析方法的结果相关性很好(R=0.96),表明病毒密度范围为 5.2-7.9 log 基因组拷贝/L。这些浓度高于通常在集中式市政废水中报道的浓度,但与以前用于开发分散式非饮用水系统病原体对数减少目标(LRT)的基于流行病学的模型非常吻合。结果强调了就地废水的独特质量,支持了先前的 LRT 和分散式水再利用的定量微生物风险评估(QMRA)。