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PhylOTU: A High-Throughput Procedure Quantifies Microbial Community Diversity and Resolves Novel Taxa from Metagenomic Data

机译:PhylOTU:高通量程序量化微生物群落多样性并从元基因组数据中解析出新的分类单元

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摘要

Microbial diversity is typically characterized by clustering ribosomal RNA (SSU-rRNA) sequences into operational taxonomic units (OTUs). Targeted sequencing of environmental SSU-rRNA markers via PCR may fail to detect OTUs due to biases in priming and amplification. Analysis of shotgun sequenced environmental DNA, known as metagenomics, avoids amplification bias but generates fragmentary, non-overlapping sequence reads that cannot be clustered by existing OTU-finding methods. To circumvent these limitations, we developed PhylOTU, a computational workflow that identifies OTUs from metagenomic SSU-rRNA sequence data through the use of phylogenetic principles and probabilistic sequence profiles. Using simulated metagenomic data, we quantified the accuracy with which PhylOTU clusters reads into OTUs. Comparisons of PCR and shotgun sequenced SSU-rRNA markers derived from the global open ocean revealed that while PCR libraries identify more OTUs per sequenced residue, metagenomic libraries recover a greater taxonomic diversity of OTUs. In addition, we discover novel species, genera and families in the metagenomic libraries, including OTUs from phyla missed by analysis of PCR sequences. Taken together, these results suggest that PhylOTU enables characterization of part of the biosphere currently hidden from PCR-based surveys of diversity?
机译:微生物多样性的典型特征是将核糖体RNA(SSU-rRNA)序列聚集成可操作的生物分类单位(OTU)。由于引发和扩增的偏倚,通过PCR进行的环境SSU-rRNA标记的靶向测序可能无法检测到OTU。对散弹枪测序的环境DNA进行的分析(称为宏基因组学)避免了扩增偏差,但会生成片段性的,不重叠的序列读数,而现有的OTU查找方法无法将这些读数进行聚类。为了克服这些限制,我们开发了 PhylOTU ,这是一种计算流程,可通过系统进化原理和概率序列概况从宏基因组SSU-rRNA序列数据中识别OTU。使用模拟宏基因组学数据,我们量化了 PhylOTU 簇读入OTU的准确性。来自全球公海的PCR和shot弹枪测序的SSU-rRNA标记的比较表明,尽管PCR文库每个测序的残基识别出更多的OTU,但是宏基因组文库恢复了更大的OTU分类学多样性。此外,我们在宏基因组库中发现了新物种,属和科,包括通过分析PCR序列而错过的门的OTU。综上所述,这些结果表明 PhylOTU 能够表征当前基于PCR的多样性调查中隐藏的部分生物圈?

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