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16S rRNA 扩增子测序方案在罗氏/454 高通量钛测序平台上的分析。

Analysis of 16S rRNA amplicon sequencing options on the Roche/454 next-generation titanium sequencing platform.

机构信息

Department of Civil and Environmental Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.

出版信息

PLoS One. 2011;6(9):e25263. doi: 10.1371/journal.pone.0025263. Epub 2011 Sep 23.

Abstract

BACKGROUND

16S rRNA gene pyrosequencing approach has revolutionized studies in microbial ecology. While primer selection and short read length can affect the resulting microbial community profile, little is known about the influence of pyrosequencing methods on the sequencing throughput and the outcome of microbial community analyses. The aim of this study is to compare differences in output, ease, and cost among three different amplicon pyrosequencing methods for the Roche/454 Titanium platform

METHODOLOGY/PRINCIPAL FINDINGS: The following three pyrosequencing methods for 16S rRNA genes were selected in this study: Method-1 (standard method) is the recommended method for bi-directional sequencing using the LIB-A kit; Method-2 is a new option designed in this study for unidirectional sequencing with the LIB-A kit; and Method-3 uses the LIB-L kit for unidirectional sequencing. In our comparison among these three methods using 10 different environmental samples, Method-2 and Method-3 produced 1.5-1.6 times more useable reads than the standard method (Method-1), after quality-based trimming, and did not compromise the outcome of microbial community analyses. Specifically, Method-3 is the most cost-effective unidirectional amplicon sequencing method as it provided the most reads and required the least effort in consumables management.

CONCLUSIONS

Our findings clearly demonstrated that alternative pyrosequencing methods for 16S rRNA genes could drastically affect sequencing output (e.g. number of reads before and after trimming) but have little effect on the outcomes of microbial community analysis. This finding is important for both researchers and sequencing facilities utilizing 16S rRNA gene pyrosequencing for microbial ecological studies.

摘要

背景

16S rRNA 基因焦磷酸测序方法彻底改变了微生物生态学的研究。虽然引物选择和短读长会影响所得微生物群落图谱,但对于焦磷酸测序方法对测序通量和微生物群落分析结果的影响知之甚少。本研究旨在比较罗氏/454 钛平台三种不同扩增子焦磷酸测序方法在输出、易用性和成本方面的差异。

方法/主要发现:本研究选择了以下三种用于 16S rRNA 基因的焦磷酸测序方法:方法 1(标准方法)是使用 LIB-A 试剂盒进行双向测序的推荐方法;方法 2 是本研究设计的新方法,用于使用 LIB-A 试剂盒进行单向测序;方法 3 使用 LIB-L 试剂盒进行单向测序。在使用 10 种不同环境样本对这三种方法进行比较时,经过基于质量的修剪后,方法 2 和方法 3 比标准方法(方法 1)产生了 1.5-1.6 倍的可用读数,并且不会影响微生物群落分析的结果。具体来说,方法 3 是最具成本效益的单向扩增子测序方法,因为它提供了最多的读数,并且在耗材管理方面所需的工作量最少。

结论

我们的研究结果清楚地表明,16S rRNA 基因的替代焦磷酸测序方法可以极大地影响测序输出(例如修剪前后的读数数量),但对微生物群落分析的结果影响很小。这一发现对于利用 16S rRNA 基因焦磷酸测序进行微生物生态学研究的研究人员和测序设施都非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b46a/3179495/0b3ac3e77765/pone.0025263.g001.jpg

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