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用于土壤法医鉴别分析的随机全宏基因组测序

Random whole metagenomic sequencing for forensic discrimination of soils.

作者信息

Khodakova Anastasia S, Smith Renee J, Burgoyne Leigh, Abarno Damien, Linacre Adrian

机构信息

School of Biological Sciences, Flinders University, Adelaide, Australia.

School of Biological Sciences, Flinders University, Adelaide, Australia; Forensic Science South Australia, Adelaide, Australia.

出版信息

PLoS One. 2014 Aug 11;9(8):e104996. doi: 10.1371/journal.pone.0104996. eCollection 2014.

Abstract

Here we assess the ability of random whole metagenomic sequencing approaches to discriminate between similar soils from two geographically distinct urban sites for application in forensic science. Repeat samples from two parklands in residential areas separated by approximately 3 km were collected and the DNA was extracted. Shotgun, whole genome amplification (WGA) and single arbitrarily primed DNA amplification (AP-PCR) based sequencing techniques were then used to generate soil metagenomic profiles. Full and subsampled metagenomic datasets were then annotated against M5NR/M5RNA (taxonomic classification) and SEED Subsystems (metabolic classification) databases. Further comparative analyses were performed using a number of statistical tools including: hierarchical agglomerative clustering (CLUSTER); similarity profile analysis (SIMPROF); non-metric multidimensional scaling (NMDS); and canonical analysis of principal coordinates (CAP) at all major levels of taxonomic and metabolic classification. Our data showed that shotgun and WGA-based approaches generated highly similar metagenomic profiles for the soil samples such that the soil samples could not be distinguished accurately. An AP-PCR based approach was shown to be successful at obtaining reproducible site-specific metagenomic DNA profiles, which in turn were employed for successful discrimination of visually similar soil samples collected from two different locations.

摘要

在此,我们评估随机全宏基因组测序方法区分来自两个地理上不同城市地点的相似土壤的能力,以用于法医学。采集了来自两个位于居民区、相距约3公里的公园绿地的重复样本,并提取了DNA。然后使用鸟枪法、全基因组扩增(WGA)和基于单引物DNA扩增(AP-PCR)的测序技术来生成土壤宏基因组图谱。接着将完整和抽样的宏基因组数据集与M5NR/M5RNA(分类学分类)和SEED子系统(代谢分类)数据库进行比对注释。使用多种统计工具进行了进一步的比较分析,包括:层次凝聚聚类(CLUSTER);相似性剖面分析(SIMPROF);非度量多维尺度分析(NMDS);以及在分类学和代谢分类的所有主要层面上的主坐标典型分析(CAP)。我们的数据表明,基于鸟枪法和WGA的方法为土壤样本生成了高度相似的宏基因组图谱,以至于无法准确区分土壤样本。结果显示,基于AP-PCR的方法成功获得了可重复的特定地点宏基因组DNA图谱,进而成功区分了从两个不同地点采集的外观相似的土壤样本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1160/4128759/ba94158a75ba/pone.0104996.g001.jpg

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