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Fecal source tracking in water using a mitochondrial DNA microarray

机译:使用线粒体DNA微阵列追踪水中的粪便来源

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摘要

A mitochondrial-based microarray (mitoArray) was developed for rapid identification of the presence of 28 animals and one family (cervidae) potentially implicated in fecal pollution in mixed activity watersheds. Oligonucleotide probes for genus or subfamily-level identification were targeted within the 12S rRNA - Val tRNA - 16S rRNA region in the mitochondrial genome. This region, called MI-50, was selected based on three criteria: 1) the ability to be amplified by universal primers 2) these universal primer sequences are present in most commercial and domestic animals of interest in source tracking, and 3) that sufficient sequence variation exists within this region to meet the minimal requirements for microarray probe discrimination. To quantify the overall level of mitochondrial DNA (mtDNA) in samples, a quantitative-PCR (Q-PCR) universal primer pair was also developed. Probe validation was performed using DNA extracted from animal tissues and, for many cases, animal-specific fecal samples. To reduce the amplification of potentially interfering fish mtDNA sequences during the MI-50 enrichment step, a clamping PCR method was designed using a fish-specific peptide nucleic acid. DNA extracted from 19 water samples were subjected to both array and independent PCR analyses. Our results confirm that the mitochondrial microarray approach method could accurately detect the dominant animals present in water samples emphasizing the potential for this methodology in the parallel scanning of a large variety of animals normally monitored in fecal source tracking.
机译:基于线粒体的微阵列(mitoArray)被开发用于快速识别28种动物和一个家族(鹿科)的存在,这些家族可能与混合活动分水岭的粪便污染有关。用于属或亚家族水平鉴定的寡核苷酸探针靶向线粒体基因组中的12S rRNA-Val tRNA-16S rRNA区域。根据三个条件选择此区域,称为MI-50:1)通用引物扩增的能力2)这些通用引物序列在源追踪中存在于大多数目标商业动物中,并且3)足够该区域内存在序列变异,以满足微阵列探针识别的最低要求。为了量化样品中线粒体DNA(mtDNA)的总体水平,还开发了定量PCR(Q-PCR)通用引物对。使用从动物组织中提取的DNA进行探针验证,在许多情况下,还使用动物特异性粪便样品。为了减少在MI-50富集步骤​​中可能干扰鱼类mtDNA序列的扩增,设计了使用鱼类特异性肽核酸的钳制PCR方法。从19个水样中提取的DNA进行了阵列和独立PCR分析。我们的结果证实,线粒体微阵列方法可以准确检测水样中存在的优势动物,从而强调了这种方法在并行扫描通常在粪便来源跟踪中监测的多种动物中的潜力。

著录项

  • 来源
    《Water Research》 |2013年第1期|16-30|共15页
  • 作者单位

    Biotechnology Research Institute, National Research Council of Canada, Montreal, QC H4P 2R2, Canada,Departement of Microbiology and Immunology, University of Montreal, Montreal, QC H3T 1/4, Canada;

    INRS-Institut Armand-Frappier, 531 Boulevard des Prairies, Laval, QC H7V 1B7, Canada;

    INRS-Institut Armand-Frappier, 531 Boulevard des Prairies, Laval, QC H7V 1B7, Canada;

    Biotechnology Research Institute, National Research Council of Canada, Montreal, QC H4P 2R2, Canada,Departement of Microbiology and Immunology, University of Montreal, Montreal, QC H3T 1/4, Canada;

    Agriculture and Agri-Food Canada, 1391 Sandford Street, London, ON N5V 4T3, Canada;

    Biotechnology Research Institute, National Research Council of Canada, Montreal, QC H4P 2R2, Canada,Departement of Microbiology and Immunology, University of Montreal, Montreal, QC H3T 1/4, Canada;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    mitochondria; DNA microarray; source tracking; fecal; peptide nucleic acid; PCR clamping; quantitative PCR;

    机译:线粒体DNA芯片源跟踪;粪便肽核酸PCR钳位;定量PCR;
  • 入库时间 2022-08-17 13:45:34

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