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通过定量聚合酶链反应测定的原污水和新鲜动物粪便中宿主特异性和通用粪便标志物的浓度。

Concentrations of host-specific and generic fecal markers measured by quantitative PCR in raw sewage and fresh animal feces.

作者信息

Silkie Sarah S, Nelson Kara L

机构信息

Department of Civil and Environmental Engineering, University of California, Berkeley, CA 94720-1710, USA.

出版信息

Water Res. 2009 Nov;43(19):4860-71. doi: 10.1016/j.watres.2009.08.017. Epub 2009 Aug 22.

Abstract

We measured the concentrations of four host-specific (human, dog, cow, and horse Bacteroidales), four generic fecal (16S total Bacteroidales and Escherichia coli, 23S Enterococcus and uidA E. coli,) and two universal bacterial (16S universal and rpoB universal) DNA targets by qPCR in raw sewage and pooled fecal samples from dogs, cows, horses, and Canada Geese. A spiking protocol using the non-fecal bacterium Pseudomonas syringae pph 6 was developed to estimate the recovery of DNA from fecal and environmental samples. The measured fecal marker concentrations were used to calculate baseline ratios and variability of host-specific to generic indicators for each host type. The host-specific markers were found in high concentrations (8-9 log(10)copies/g dry wt.) in their respective hosts' samples, which were equal to or greater than the concentrations of generic E. coli and Enterococcus markers, lending support to the use of host-specific and generic Bacteroidales as sensitive indicators of fecal pollution. The host-specific markers formed a consistent percentage of total Bacteroidales in target host feces and raw sewage, with human-specific comprising 82%, dog-specific 6%, cow-specific 4% and horse-specific 2%. Based on this limited data set, the measurement of host-specific indicators by qPCR has several promising applications. These applications include determining the percentage of total Bacteroidales contributed by a specific host type, using the ratios of host-specific markers to E. coli or Enterococcus to estimate the contribution of each source to these regulated fecal indicator bacteria, and estimating the mass of feces from each host type in environmental samples.

摘要

我们通过定量聚合酶链反应(qPCR)测定了原污水以及来自狗、牛、马和加拿大鹅的混合粪便样本中四种宿主特异性(人类、狗、牛和马拟杆菌目)、四种一般粪便(16S总拟杆菌目和大肠杆菌、23S肠球菌和uidA大肠杆菌)和两种通用细菌(16S通用和rpoB通用)DNA靶标的浓度。开发了一种使用非粪便细菌丁香假单胞菌pph 6的加标方案,以估计粪便和环境样本中DNA的回收率。所测得的粪便标志物浓度用于计算每种宿主类型的宿主特异性指标与一般指标的基线比率和变异性。在各自宿主的样本中发现宿主特异性标志物浓度很高(8 - 9 log(10)拷贝/克干重),这等于或高于一般大肠杆菌和肠球菌标志物的浓度,这支持了将宿主特异性和一般拟杆菌目用作粪便污染敏感指标的做法。宿主特异性标志物在目标宿主粪便和原污水中的总拟杆菌目中所占百分比一致,其中人类特异性占82%、狗特异性占6%、牛特异性占4%、马特异性占2%。基于这个有限的数据集,通过qPCR测量宿主特异性指标有几个有前景的应用。这些应用包括确定特定宿主类型在总拟杆菌目中所占的百分比,利用宿主特异性标志物与大肠杆菌或肠球菌的比率来估计每种来源对这些受监管的粪便指示菌的贡献,以及估计环境样本中每种宿主类型的粪便量。

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