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首页> 外文期刊>BMC Microbiology >Design of targeted primers based on 16S rRNA sequences in meta-transcriptomic datasets and identification of a novel taxonomic group in the Asgard archaea
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Design of targeted primers based on 16S rRNA sequences in meta-transcriptomic datasets and identification of a novel taxonomic group in the Asgard archaea

机译:基于16S rRNA序列在荟萃转录组数据集中的靶向引物的设计及Asgard Archaea中新型分类组的鉴定

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摘要

Amplification of small subunit (SSU) rRNA genes with universal primers is a common method used to assess microbial populations in various environmental samples. However, owing to limitations in coverage of these universal primers, some microorganisms remain unidentified. The present study aimed to establish a method for amplifying nearly full-length SSU rRNA gene sequences of previously unidentified prokaryotes, using newly designed targeted primers via primer evaluation in meta-transcriptomic datasets. Primer binding regions of universal primer 8F/Arch21F for bacteria or archaea were used for primer evaluation of SSU rRNA sequences in meta-transcriptomic datasets. Furthermore, targeted forward primers were designed based on SSU rRNA reads from unclassified groups unmatched with the universal primer 8F/Arch21F, and these primers were used to amplify nearly full-length special SSU rRNA gene sequences along with universal reverse primer 1492R. Similarity and phylogenetic analysis were used to confirm their novel status. Using this method, we identified unclassified SSU rRNA sequences that were not matched with universal primer 8F and Arch21F. A new group within the Asgard superphylum was amplified by the newly designed specific primer based on these unclassified SSU rRNA sequences by using mudflat samples. We showed that using specific primers designed based on universal primer evaluation from meta-transcriptomic datasets, identification of novel taxonomic groups from a specific environment is possible.
机译:具有通用引物的小亚基(SSU)RRNA基因的扩增是用于评估各种环境样品中的微生物群的常用方法。然而,由于这些通用引物的覆盖范围的局限性,一些微生物仍未认定。本研究旨在建立一种用于扩增先前未识别的原核生物的几乎全长SSU rRNA基因序列的方法,通过在Meta-Transcrapmic数据集中的引物评价中使用新设计的靶向引物。用于细菌或古痤疮的通用引物8F / Arch21f的引物结合区域用于Meta-Transcraphy Datasets中SSU RRNA序列的引物评价。此外,基于由通用引物8F / ARC21F离立的未分类基团的SSU RRNA读取的靶向前引物,并且这些引物用于扩增几乎全长特殊的SSU rRNA基因序列以及通用反向引物1492R。相似性和系统发育分析用于确认它们的新颖状态。使用该方法,我们鉴定了与通用底漆8F和Arch21f不匹配的未分类的SSU rRNA序列。通过使用Mudflat样品,通过基于这些未分类的SSU rRNA序列的新设计的特异性引物进行ASGARD超星系中的新组。我们表明,使用基于荟萃转录组数据集的通用引物评估设计的特定引物,可以从特定环境中识别新的分类分类群。

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