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Influence of DNA Extraction Method 16S rRNA Targeted Hypervariable Regions and Sample Origin on Microbial Diversity Detected by 454 Pyrosequencing in Marine Chemosynthetic Ecosystems

机译:DNA提取方法靶向16S rRNA的高变区和样品来源对454化学测序法检测海洋化学合成生态系统中微生物多样性的影响

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摘要

Next-generation sequencing (NGS) opens up exciting possibilities for improving our knowledge of environmental microbial diversity, allowing rapid and cost-effective identification of both cultivated and uncultivated microorganisms. However, library preparation, sequencing, and analysis of the results can provide inaccurate representations of the studied community compositions. Therefore, all these steps need to be taken into account carefully. Here we evaluated the effects of DNA extraction methods, targeted 16S rRNA hypervariable regions, and sample origins on the diverse microbes detected by 454 pyrosequencing in marine cold seep and hydrothermal vent sediments. To assign the reads with enough taxonomic precision, we built a database with about 2,500 sequences from Archaea and Bacteria from deep-sea marine sediments, affiliated according to reference publications in the field. Thanks to statistical and diversity analyses as well as inference of operational taxonomic unit (OTU) networks, we show that (i) while DNA extraction methods do not seem to affect the results for some samples, they can lead to dramatic changes for others; and (ii) the choice of amplification and sequencing primers also considerably affects the microbial community detected in the samples. Thereby, very different proportions of pyrosequencing reads were obtained for some microbial lineages, such as the archaeal ANME-1, ANME-2c, and MBG-D and deltaproteobacterial subgroups. This work clearly indicates that the results from sequencing-based analyses, such as pyrosequencing, should be interpreted very carefully. Therefore, the combination of NGS with complementary approaches, such as fluorescence in situ hybridization (FISH)/catalyzed reporter deposition (CARD)-FISH or quantitative PCR (Q-PCR), would be desirable to gain a more comprehensive picture of environmental microbial communities.
机译:下一代测序(NGS)为改善我们对环境微生物多样性的了解开辟了令人兴奋的可能性,从而可以快速,经济高效地鉴定培养的微生物和未培养的微生物。但是,文库的制备,测序和结果分析可能无法提供所研究社区组成的准确表示。因此,所有这些步骤都需要仔细考虑。在这里,我们评估了DNA提取方法,靶向16S rRNA高变区以及样品来源对通过454焦磷酸测序在海洋冷渗流和热液喷口沉积物中检测到的多种微生物的影响。为了以足够的分类学精度分配读物,我们建立了一个数据库,该数据库包含来自深海海洋沉积物的古细菌和细菌的约2500个序列,并根据该领域的参考出版物提供了相关信息。通过统计和多样性分析以及可操作分类单元(OTU)网络的推断,我们表明:(i)尽管DNA提取方法似乎对某些样品的结果没有影响,但它们可能导致其他样品的巨大变化; (ii)扩增引物和测序引物的选择也极大地影响了样品中检测到的微生物群落。因此,对于某些微生物谱系,例如古细菌ANME-1,ANME-2c,MBG-D和德尔塔蛋白菌亚组,焦磷酸测序读数的比例非常不同。这项工作清楚地表明,基于测序的分析(例如焦磷酸测序)的结果应非常仔细地解释。因此,将NGS与互补方法(例如荧光原位杂交(FISH)/催化的报道分子沉积(CARD)-FISH或定量PCR(Q-PCR))相结合,对于获得更全面的环境微生物群落图景将是理想的。

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