The Influence of DNA Extraction Procedure and Primer Set on the Bacterial Community Analysis by Pyrosequencing of Barcoded 16S rRNA Gene Amplicons.

Molecular biology international Pub Date : 2014-01-01 Epub Date: 2014-07-10 DOI:10.1155/2014/548683
Ingo C Starke, Wilfried Vahjen, Robert Pieper, Jürgen Zentek
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Abstract

In this study, the effect of different DNA extraction procedures and primer sets on pyrosequencing results regarding the composition of bacterial communities in the ileum of piglets was investigated. Ileal chyme from piglets fed a diet containing different amounts of zinc oxide was used to evaluate a pyrosequencing study with barcoded 16S rRNA PCR products. Two DNA extraction methods (bead beating versus silica gel columns) and two primer sets targeting variable regions of bacterial 16S rRNA genes (8f-534r versus 968f-1401r) were considered. The SEED viewer software of the MG-RAST server was used for automated sequence analysis. A total of 5.2 × 10(5) sequences were used for analysis after processing for read length (150 bp), minimum sequence occurrence (5), and exclusion of eukaryotic and unclassified/uncultured sequences. DNA extraction procedures and primer sets differed significantly in total sequence yield. The distribution of bacterial order and main bacterial genera was influenced significantly by both parameters. However, this study has shown that the results of pyrosequencing studies using barcoded PCR amplicons of bacterial 16S rRNA genes depend on DNA extraction and primer choice, as well as on the manner of downstream sequence analysis.

Abstract Image

Abstract Image

通过对条形码 16S rRNA 基因扩增子进行热测序分析 DNA 提取程序和引物组对细菌群落分析的影响
本研究调查了不同的 DNA 提取程序和引物组对仔猪回肠细菌群落组成的热释光测序结果的影响。使用含有不同量氧化锌的饲料喂养的仔猪的回肠食糜来评估使用条形码 16S rRNA PCR 产物进行的热释光测序研究。研究考虑了两种 DNA 提取方法(打珠法和硅胶柱法)和两套针对细菌 16S rRNA 基因可变区的引物(8f-534r 和 968f-1401r)。MG-RAST 服务器的 SEED 查看器软件用于自动序列分析。在对读取长度(150 bp)、最小序列出现数(5)以及排除真核生物和未分类/未培养序列进行处理后,共有 5.2 × 10(5) 条序列被用于分析。DNA 提取程序和引物组在总序列产量方面存在显著差异。细菌序和主要细菌属的分布受这两个参数的影响很大。不过,本研究表明,使用细菌 16S rRNA 基因条形码 PCR 扩增子进行热测序研究的结果取决于 DNA 提取和引物选择,以及下游序列分析的方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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