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聚合酶链式反应(PCR)扩增子大小对克隆文库微生物多样性和群落结构评估的影响。

Effect of PCR amplicon size on assessments of clone library microbial diversity and community structure.

作者信息

Huber Julie A, Morrison Hilary G, Huse Susan M, Neal Phillip R, Sogin Mitchell L, Mark Welch David B

机构信息

Josephine Bay Paul Center, Marine Biological Laboratory, Woods Hole, MA 02543, USA.

出版信息

Environ Microbiol. 2009 May;11(5):1292-302. doi: 10.1111/j.1462-2920.2008.01857.x. Epub 2009 Feb 9.

DOI:10.1111/j.1462-2920.2008.01857.x
PMID:19220394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2716130/
Abstract

PCR-based surveys of microbial communities commonly use regions of the small-subunit ribosomal RNA (SSU rRNA) gene to determine taxonomic membership and estimate total diversity. Here we show that the length of the target amplicon has a significant effect on assessments of microbial richness and community membership. Using operational taxonomic unit (OTU)- and taxonomy-based tools, we compared the V6 hypervariable region of the bacterial SSU rRNA gene of three amplicon libraries of c. 100, 400 and 1000 base pairs (bp) from each of two hydrothermal vent fluid samples. We found that the smallest amplicon libraries contained more unique sequences, higher diversity estimates and a different community structure than the other two libraries from each sample. We hypothesize that a combination of polymerase dissociation, cloning bias and mispriming due to secondary structure accounts for the differences. While this relationship is not linear, it is clear that the smallest amplicon libraries contained more different types of sequences, and accordingly, more diverse members of the community. Because divergent and lower abundant taxa can be more readily detected with smaller amplicons, they may provide better assessments of total community diversity and taxonomic membership than longer amplicons in molecular studies of microbial communities.

摘要

基于聚合酶链式反应(PCR)的微生物群落调查通常使用小亚基核糖体RNA(SSU rRNA)基因区域来确定分类归属并估计总多样性。在此我们表明,目标扩增子的长度对微生物丰富度和群落组成的评估有显著影响。使用基于操作分类单元(OTU)和分类学的工具,我们比较了来自两个热液喷口流体样本的三个扩增子文库的细菌SSU rRNA基因V6高变区,每个文库的长度约为100、400和1000个碱基对(bp)。我们发现,与每个样本的其他两个文库相比,最小的扩增子文库包含更多独特序列、更高的多样性估计值以及不同的群落结构。我们推测,聚合酶解离、克隆偏差以及二级结构导致的错配引发共同造成了这些差异。虽然这种关系不是线性的,但很明显,最小的扩增子文库包含更多不同类型的序列,因此也包含群落中更多样化的成员。由于较小的扩增子能够更轻易地检测到分化程度高且丰度较低的分类群,在微生物群落的分子研究中,与较长的扩增子相比,它们可能能更好地评估群落总多样性和分类归属。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64ca/2716130/6fa31d7ad915/nihms108948f6.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64ca/2716130/6fa31d7ad915/nihms108948f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64ca/2716130/4ac1f6723cb3/nihms108948f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64ca/2716130/80301e96b5e9/nihms108948f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64ca/2716130/a9b153801c5d/nihms108948f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64ca/2716130/b6e7332903b7/nihms108948f4.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64ca/2716130/6fa31d7ad915/nihms108948f6.jpg

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2
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3
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4
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