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通过靶向扩增子测序(ITS)方案评估人体肠道中的双歧杆菌群落组成。

Evaluation of bifidobacterial community composition in the human gut by means of a targeted amplicon sequencing (ITS) protocol.

作者信息

Milani Christian, Lugli Gabriele A, Turroni Francesca, Mancabelli Leonardo, Duranti Sabrina, Viappiani Alice, Mangifesta Marta, Segata Nicola, van Sinderen Douwe, Ventura Marco

机构信息

Department of Life Sciences, Laboratory of Probiogenomics, University of Parma, Parma, Italy.

出版信息

FEMS Microbiol Ecol. 2014 Nov;90(2):493-503. doi: 10.1111/1574-6941.12410. Epub 2014 Sep 8.

Abstract

The precise appraisal of the composition of the human gut microbiota still represents a challenging task. The advent of next generation sequencing approaches has opened new ways to dissect the microbial biodiversity of this ecosystem through the use of 16S rRNA gene-based microbiota analysis approaches. However, the detailed representation of specific groups or members of the human gut microbiota, for example Bifidobacteria, may be skewed by the PCR primers employed in the amplification step of the 16S rRNA gene-based microbial profiling pipeline and by the limited resolution of the 16S rRNA gene variable regions. Here, we define the internal transcribed spacer (ITS) sequences of all currently known Bifidobacterium taxa, providing a Bifidobacterium-specific primer pair that targets a hypervariable region within the ITS suitable for precise taxonomic identification of all 48 so far recognized members of the Bifidobacterium genus. In addition, we present an optimized protocol for ITS-based profiling utilizing qiime software, allowing accurate and subspecies-specific compositional reconstruction of the bifidobacterial community in the human gut.

摘要

对人类肠道微生物群组成的精确评估仍然是一项具有挑战性的任务。新一代测序方法的出现为通过使用基于16S rRNA基因的微生物群分析方法来剖析这个生态系统的微生物多样性开辟了新途径。然而,人类肠道微生物群特定群体或成员(例如双歧杆菌)的详细表征可能会因基于16S rRNA基因的微生物谱分析流程扩增步骤中使用的PCR引物以及16S rRNA基因可变区的有限分辨率而产生偏差。在此,我们定义了所有目前已知双歧杆菌类群的内部转录间隔区(ITS)序列,提供了一对双歧杆菌特异性引物,该引物靶向ITS内的一个高变区,适用于对双歧杆菌属目前已识别的所有48个成员进行精确的分类鉴定。此外,我们还展示了一种利用qiime软件进行基于ITS的谱分析的优化方案,可实现对人类肠道中双歧杆菌群落进行准确且亚种特异性的组成重建。

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