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宏基因组学揭示了基于扩增子的微生物多样性检测中的空白。

Metagenomics uncovers gaps in amplicon-based detection of microbial diversity.

机构信息

Joint Genome Institute, Walnut Creek, California 94598, USA.

出版信息

Nat Microbiol. 2016 Feb 1;1:15032. doi: 10.1038/nmicrobiol.2015.32.

Abstract

Our view of microbial diversity has expanded greatly over the past 40 years, primarily through the wide application of PCR-based surveys of the small-subunit ribosomal RNA (SSU rRNA) gene. Yet significant gaps in knowledge remain due to well-recognized limitations of this method. Here, we systematically survey primer fidelity in SSU rRNA gene sequences recovered from over 6,000 assembled metagenomes sampled globally. Our findings show that approximately 10% of environmental microbial sequences might be missed from classical PCR-based SSU rRNA gene surveys, mostly members of the Candidate Phyla Radiation (CPR) and as yet uncharacterized Archaea. These results underscore the extent of uncharacterized microbial diversity and provide fruitful avenues for describing additional phylogenetic lineages.

摘要

在过去的 40 年中,通过广泛应用基于聚合酶链反应(PCR)的小亚基核糖体 RNA(SSU rRNA)基因调查,我们对微生物多样性的认识有了很大的提高。然而,由于该方法存在明显的局限性,知识仍存在显著的差距。在这里,我们系统地调查了从全球采样的 6000 多个组装宏基因组中回收的 SSU rRNA 基因序列的引物保真度。我们的研究结果表明,大约有 10%的环境微生物序列可能会从基于经典 PCR 的 SSU rRNA 基因调查中丢失,主要是候选门辐射(CPR)和尚未被描述的古菌的成员。这些结果突出了未被描述的微生物多样性的程度,并为描述更多的系统发育谱系提供了有价值的途径。

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