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Validation of host-specific Bacteroidales quantitative PCR assays and their application to microbial source tracking of drinking water sources in the Kathmandu Valley, Nepal.验证针对特定宿主的拟杆菌定量 PCR 检测方法及其在尼泊尔加德满都谷地饮用水源微生物溯源中的应用。
J Appl Microbiol. 2018 Aug;125(2):609-619. doi: 10.1111/jam.13884. Epub 2018 May 23.
2
Global Distribution of Human-Associated Fecal Genetic Markers in Reference Samples from Six Continents.全球六大陆参考样本中人源粪便遗传标记的分布。
Environ Sci Technol. 2018 May 1;52(9):5076-5084. doi: 10.1021/acs.est.7b04438. Epub 2018 Apr 16.
3
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J Environ Qual. 2017 Jul;46(4):760-766. doi: 10.2134/jeq2016.11.0432.
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Human fecal and pathogen exposure pathways in rural Indian villages and the effect of increased latrine coverage.印度农村村庄的人类粪便与病原体暴露途径以及增加厕所覆盖率的影响
Water Res. 2016 Sep 1;100:232-244. doi: 10.1016/j.watres.2016.05.015. Epub 2016 May 4.
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rrnDB: improved tools for interpreting rRNA gene abundance in bacteria and archaea and a new foundation for future development.rrnDB:用于解释细菌和古细菌中rRNA基因丰度的改进工具以及未来发展的新基础。
Nucleic Acids Res. 2015 Jan;43(Database issue):D593-8. doi: 10.1093/nar/gku1201. Epub 2014 Nov 20.
6
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Performance characteristics of qPCR assays targeting human- and ruminant-associated bacteroidetes for microbial source tracking across sixteen countries on six continents.针对来自六大洲十六个国家的微生物源追踪,qPCR 检测方法在靶向人类和反刍动物相关拟杆菌方面的性能特征。
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Evaluation of genetic markers from the 16S rRNA gene V2 region for use in quantitative detection of selected Bacteroidales species and human fecal waste by qPCR.评估 16S rRNA 基因 V2 区的遗传标记,用于通过 qPCR 定量检测选定的拟杆菌目物种和人粪便废物。
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Evaluation of new gyrB-based real-time PCR system for the detection of B. fragilis as an indicator of human-specific fecal contamination.评价基于新 gyrB 的实时 PCR 系统检测脆弱拟杆菌作为人源粪便污染指示菌的效果。
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日本河水中微生物溯源的宿主特异性拟杆菌门遗传标记的评估和应用。

Assessment and application of host-specific Bacteroidales genetic markers for microbial source tracking of river water in Japan.

机构信息

Interdisciplinary Center for River Basin Environment, Graduate Faculty of Interdisciplinary Research, University of Yamanashi, Kofu, Yamanashi, Japan.

Department of Civil and Environmental Engineering, Faculty of Engineering, University of Yamanashi, Kofu, Yamanashi, Japan.

出版信息

PLoS One. 2018 Nov 16;13(11):e0207727. doi: 10.1371/journal.pone.0207727. eCollection 2018.

DOI:10.1371/journal.pone.0207727
PMID:30444920
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6239337/
Abstract

Microbial source tracking using host-specific microbial genetic markers is considered a promising approach to determine fecal contamination sources of aquatic environments. This study aimed to assess the application of previously developed host-specific Bacteroidales quantitative PCR assays to microbial source tracking of river water samples in Yamanashi Prefecture, Japan. Various types of fecal-source samples, such as raw sewage, secondary-treated sewage of a wastewater treatment plant, and cattle feces, were used for three human-, two ruminant- and two pig-specific Bacteroidales quantitative PCR assays. Our results demonstrated that BacHum, BacR and Pig2Bac assays as suitable human-, ruminant- and pig-specific assays, with an accuracy of 86%, 94% and 77%, respectively. These selected assays were used for microbial source tracking of 63 river water samples collected at nine sites in two river basins. From these sites, there were 48 (76%), 34 (54%) and 9 (14%) positive samples using the BacHum, BacR and Pig2Bac assays, respectively. These assays revealed the effects of humans and animals on fecal contamination of river water.

摘要

利用宿主特异性微生物遗传标记进行微生物溯源被认为是确定水生环境粪便污染来源的一种很有前途的方法。本研究旨在评估先前开发的宿主特异性 Bacteroidales 定量 PCR 检测方法在日本山梨县河水样本微生物溯源中的应用。本研究使用了各种粪便源样本,如未经处理的污水、污水处理厂的二级处理污水和牛粪便,用于三种人源、两种反刍动物源和两种猪源 Bacteroidales 定量 PCR 检测。我们的结果表明,BacHum、BacR 和 Pig2Bac 检测方法分别作为合适的人源、反刍动物源和猪源特异性检测方法,其准确性分别为 86%、94%和 77%。这些选定的检测方法用于对从两个流域的九个地点采集的 63 个河水样本进行微生物溯源。从这些地点中,BacHum、BacR 和 Pig2Bac 检测方法的阳性样本分别为 48(76%)、34(54%)和 9(14%)。这些检测方法揭示了人类和动物对河水粪便污染的影响。