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本文引用的文献

1
Assessment of microbial diversity in human colonic samples by 16S rDNA sequence analysis.16S rDNA 序列分析评估人类结肠样本中的微生物多样性。
FEMS Microbiol Ecol. 2002 Jan 1;39(1):33-9. doi: 10.1111/j.1574-6941.2002.tb00904.x.
2
Host distributions of uncultivated fecal Bacteroidales bacteria reveal genetic markers for fecal source identification.未培养粪便拟杆菌纲细菌的宿主分布揭示了粪便来源鉴定的遗传标记。
Appl Environ Microbiol. 2005 Jun;71(6):3184-91. doi: 10.1128/AEM.71.6.3184-3191.2005.
3
A comparative study of culture-independent, library-independent genotypic methods of fecal source tracking.粪便来源追踪的非培养、非文库依赖型基因分型方法的比较研究
J Water Health. 2003 Dec;1(4):181-94.
4
Evaluation of microbial source tracking methods using mixed fecal sources in aqueous test samples.使用水性测试样品中的混合粪便来源评估微生物源追踪方法。
J Water Health. 2003 Dec;1(4):141-51.
5
ARB: a software environment for sequence data.ARB:一种用于序列数据的软件环境。
Nucleic Acids Res. 2004 Feb 25;32(4):1363-71. doi: 10.1093/nar/gkh293. Print 2004.
6
The use of chemical and molecular microbial indicators for faecal source identification.用于粪便来源鉴定的化学和分子微生物指标
Water Sci Technol. 2003;47(3):39-43.
7
Tiered approach for identification of a human fecal pollution source at a recreational beach: case study at Avalon Bay, Catalina Island, California.在休闲海滩识别人类粪便污染源的分层方法:加利福尼亚州卡特琳娜岛阿瓦隆湾的案例研究
Environ Sci Technol. 2003 Feb 15;37(4):673-80. doi: 10.1021/es025934x.
8
Application of a rapid method for identifying fecal pollution sources in a multi-use estuary.
Water Res. 2003 Feb;37(4):909-13. doi: 10.1016/s0043-1354(02)00384-6.
9
Use of subtractive hybridization for comprehensive surveys of prokaryotic genome differences.利用消减杂交技术对原核生物基因组差异进行全面调查。
FEMS Microbiol Lett. 2002 Jun 4;211(2):175-82. doi: 10.1111/j.1574-6968.2002.tb11221.x.
10
Empirical and theoretical bacterial diversity in four Arizona soils.亚利桑那州四种土壤中的经验性和理论性细菌多样性。
Appl Environ Microbiol. 2002 Jun;68(6):3035-45. doi: 10.1128/AEM.68.6.3035-3045.2002.

用于富集拟杆菌目遗传标记以进行粪便来源鉴定的微孔板消减杂交。

Microplate subtractive hybridization to enrich for bacteroidales genetic markers for fecal source identification.

作者信息

Dick Linda K, Simonich Michael T, Field Katharine G

机构信息

Department of Microbiology, Oregon State University, 220 Nash Hall, Corvallis, Oregon 97331, USA.

出版信息

Appl Environ Microbiol. 2005 Jun;71(6):3179-83. doi: 10.1128/AEM.71.6.3179-3183.2005.

DOI:10.1128/AEM.71.6.3179-3183.2005
PMID:15933019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1151815/
Abstract

The ability to identify sources of fecal pollution plays a key role in the analysis of human health risk and the implementation of water resource management strategies. One approach to this problem involves the identification of bacterial lineages or gene sequences that are found exclusively in a particular host species or group. We used subtractive hybridization to enrich for target host-specific fecal Bacteroidales rRNA gene fragments that were different from those of very closely related reference (subtracter) host sources. Target host rRNA gene fragments were hybridized to subtracter rRNA gene fragments immobilized in a microplate well, and target sequences that did not hybridize were cloned and sequenced for PCR primer design. The use of microplates for DNA immobilization resulted in a one-step subtractive hybridization in which the products could be directly amplified with PCR. The new host-specific primers designed from subtracted target fragments differentiated among very closely related Bacteroidales rRNA gene sequences and distinguished between similar fecal sources, such as elk and cow or human and domestic pet (dog).

摘要

识别粪便污染源的能力在人类健康风险分析和水资源管理策略的实施中起着关键作用。解决这个问题的一种方法是识别仅在特定宿主物种或群体中发现的细菌谱系或基因序列。我们使用消减杂交来富集与密切相关的参考(消减)宿主来源不同的目标宿主特异性粪便拟杆菌属rRNA基因片段。将目标宿主rRNA基因片段与固定在微孔板孔中的消减rRNA基因片段杂交,未杂交的目标序列被克隆并测序以设计PCR引物。使用微孔板固定DNA导致一步消减杂交,其产物可直接用PCR扩增。从消减的目标片段设计的新的宿主特异性引物能够区分密切相关的拟杆菌属rRNA基因序列,并区分相似的粪便来源,如麋鹿和牛或人类和家养宠物(狗)。