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从人类粪便样本中恢复宏基因组信息受测序深度和分析方法的影响。

Metagenomic Information Recovery from Human Stool Samples Is Influenced by Sequencing Depth and Profiling Method.

机构信息

Diversigen Inc., Houston, TX 77021, USA.

Alkek Center for Metagenomics and Microbiome Research, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Genes (Basel). 2020 Nov 21;11(11):1380. doi: 10.3390/genes11111380.

Abstract

Sequencing of the 16S rRNA gene (16S) has long been a go-to method for microbiome characterization due to its accessibility and lower cost compared to shotgun metagenomic sequencing (SMS). However, 16S sequencing rarely provides species-level resolution and cannot provide direct assessment of other taxa (e.g., viruses and fungi) or functional gene content. Shallow shotgun metagenomic sequencing (SSMS) has emerged as an approach to bridge the gap between 16S sequencing and deep metagenomic sequencing. SSMS is cost-competitive with 16S sequencing, while also providing species-level resolution and functional gene content insights. In the present study, we evaluated the effects of sequencing depth on marker gene-mapping- and alignment-based annotation of bacteria in healthy human stool samples. The number of identified taxa decreased with lower sequencing depths, particularly with the marker gene-mapping-based approach. Other annotations, including viruses and pathways, also showed a depth-dependent effect on feature recovery. These results refine the understanding of the suitability and shortcomings of SSMS, as well as annotation tools for metagenomic analyses in human stool samples. Results may also translate to other sample types and may open the opportunity to explore the effect of sequencing depth and annotation method.

摘要

16S rRNA 基因测序(16S)长期以来一直是微生物组特征描述的首选方法,因为与 shotgun 宏基因组测序(SMS)相比,它具有可及性和更低的成本。然而,16S 测序很少提供物种水平的分辨率,并且不能直接评估其他分类群(例如病毒和真菌)或功能基因含量。浅层 shotgun 宏基因组测序(SSMS)已成为一种在 16S 测序和深度宏基因组测序之间架起桥梁的方法。SSMS 与 16S 测序具有成本竞争力,同时还提供了物种水平的分辨率和功能基因含量的见解。在本研究中,我们评估了测序深度对健康人粪便样本中基于标记基因映射和比对的细菌标记基因映射和比对注释的影响。随着测序深度的降低,鉴定的分类群数量减少,特别是基于标记基因映射的方法。其他注释,包括病毒和途径,也显示出对特征恢复的深度依赖性。这些结果细化了对 SSMS 以及用于人类粪便样本宏基因组分析的注释工具的适用性和缺点的理解。结果也可能转化为其他样本类型,并可能为探索测序深度和注释方法的影响提供机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4354/7700633/83bff6915051/genes-11-01380-g001.jpg

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