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基于16S rRNA扩增子测序的粪便微生物特征分析指导方案

Guided Protocol for Fecal Microbial Characterization by 16S rRNA-Amplicon Sequencing.

作者信息

Di Segni Ayelet, Braun Tzipi, BenShoshan Marina, Farage Barhom Sarit, Glick Saar Efrat, Cesarkas Karen, Squires James E, Keller Nathan, Haberman Yael

机构信息

Sheba Medical Center.

Children's Hospital of Pittsburgh of UPMC.

出版信息

J Vis Exp. 2018 Mar 19(133):56845. doi: 10.3791/56845.

Abstract

The human intestinal microbiome plays a central role in protecting cells from injury, in processing energy and nutrients, and in promoting immunity. Deviations from what is considered a healthy microbiota composition (dysbiosis) may impair vital functions leading to pathologic conditions. Recent and ongoing research efforts have been directed toward the characterization of associations between microbial composition and human health and disease. Advances in high-throughput sequencing technologies enable characterization of the gut microbial composition. These methods include 16S rRNA-amplicon sequencing and shotgun sequencing. 16S rRNA-amplicon sequencing is used to profile taxonomical composition, while shotgun sequencing provides additional information about gene predictions and functional annotation. An advantage in using a targeted sequencing method of the 16S rRNA gene variable region is its substantially lower cost compared to shotgun sequencing. Sequence differences in the 16S rRNA gene are used as a microbial fingerprint to identify and quantify different taxa within an individual sample. Major international efforts have enlisted standards for 16S rRNA-amplicon sequencing. However, several studies report a common source of variation caused by batch effect. To minimize this effect, uniformed protocols for sample collection, processing, and sequencing must be implemented. This protocol proposes the integration of broadly used protocols starting from fecal sample collection to data analyses. This protocol includes a column-free, direct-PCR approach that enables simultaneous handling and DNA extraction of large numbers of fecal samples, along with PCR amplification of the V4 region. In addition, the protocol describes the analysis pipeline and provides a script using the latest version of QIIME (QIIME 2 version 2017.7.0 and DADA2). This step-by-step protocol is aimed to guide those interested in initiating the use of 16S rRNA-amplicon sequencing in a robust, reproductive, easy to use, detailed way.

摘要

人类肠道微生物群在保护细胞免受损伤、处理能量和营养以及促进免疫方面发挥着核心作用。与被认为是健康微生物群组成(生态失调)的情况出现偏差可能会损害重要功能,导致病理状况。最近和正在进行的研究工作一直致力于表征微生物组成与人类健康和疾病之间的关联。高通量测序技术的进步使得能够对肠道微生物组成进行表征。这些方法包括16S rRNA扩增子测序和鸟枪法测序。16S rRNA扩增子测序用于分析分类组成,而鸟枪法测序提供有关基因预测和功能注释的额外信息。使用16S rRNA基因可变区靶向测序方法的一个优点是与鸟枪法测序相比成本大幅降低。16S rRNA基因中的序列差异被用作微生物指纹,以识别和量化单个样本中的不同分类群。主要的国际努力已经制定了16S rRNA扩增子测序的标准。然而,几项研究报告了由批次效应引起的常见变异来源。为了尽量减少这种效应,必须实施统一的样本采集、处理和测序方案。本方案建议整合从粪便样本采集到数据分析的广泛使用的方案。本方案包括一种无柱直接PCR方法,该方法能够同时处理和提取大量粪便样本的DNA,并对V4区域进行PCR扩增。此外,该方案描述了分析流程,并提供了一个使用最新版本QIIME(QIIME 2版本2017.7.0和DADA2)的脚本。这个逐步的方案旨在以一种稳健、可重复、易于使用且详细的方式指导那些有兴趣开始使用16S rRNA扩增子测序的人。

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