4.8 Article

Cultivation-independent genomes greatly expand taxonomic-profiling capabilities of mOTUs across various environments

期刊

MICROBIOME
卷 10, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s40168-022-01410-z

关键词

Metagenomics; Microbial community; Benchmarking; Taxonomic profiling; Marker gene; Metagenome-assembled genome; Single-cell genome; Reference genome

资金

  1. Swiss Federal Institute of Technology Zurich
  2. Swiss National Foundation
  3. NCCR Microbiomes [205321_184955]
  4. Strategic Focal Area Personalized Health and Related Technologies (PHRT ) of the ETH Domain [51NF40_180575]
  5. European Molecular Biology Laboratory [2018-521]
  6. German Federal Ministry of Education and Research (BMBF, the de.NBI network)
  7. [031A537B]
  8. [031L0181A]
  9. Swiss National Science Foundation (SNF) [205321_184955] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

We developed mOTUs3, a command line tool that enables accurate species-level profiling of metagenomes. It provides a more comprehensive view of prokaryotic community diversity, especially for underexplored microbiomes. The tool leverages the reconstruction of over 600,000 draft genomes, including metagenome-assembled genomes (MAGs), to address the lack of reference genomes for many microbial species. mOTUs3 is found to be more accurate and congruent with 16S rRNA gene-based methods, and it increases the resolution of microbial groups and identifies differentially abundant taxa in comparative metagenomic studies.
BackgroundTaxonomic profiling is a fundamental task in microbiome research that aims to detect and quantify the relative abundance of microorganisms in biological samples. Available methods using shotgun metagenomic data generally depend on the deposition of sequenced and taxonomically annotated genomes, usually from cultures of isolated strains, in reference databases (reference genomes). However, the majority of microorganisms have not been cultured yet. Thus, a substantial fraction of microbial community members remains unaccounted for during taxonomic profiling, particularly in samples from underexplored environments. To address this issue, we developed the mOTU profiler, a tool that enables reference genome-independent species-level profiling of metagenomes. As such, it supports the identification and quantification of both known and unknown species based on a set of select marker genes. ResultsWe present mOTUs3, a command line tool that enables the profiling of metagenomes for > 33,000 species-level operational taxonomic units. To achieve this, we leveraged the reconstruction of > 600,000 draft genomes, most of which are metagenome-assembled genomes (MAGs), from diverse microbiomes, including soil, freshwater systems, and the gastrointestinal tract of ruminants and other animals, which we found to be underrepresented by reference genomes. Overall, two thirds of all species-level taxa lacked a reference genome. The cumulative relative abundance of these newly included taxa was low in well-studied microbiomes, such as the human body sites (6-11%). By contrast, they accounted for substantial proportions (ocean, freshwater, soil: 43-63%) or even the majority (pig, fish, cattle: 60-80%) of the relative abundance across diverse non-human-associated microbiomes. Using community-developed benchmarks and datasets, we found mOTUs3 to be more accurate than other methods and to be more congruent with 16S rRNA gene-based methods for taxonomic profiling. Furthermore, we demonstrate that mOTUs3 increases the resolution of well-known microbial groups into species-level taxa and helps identify new differentially abundant taxa in comparative metagenomic studies. ConclusionsWe developed mOTUs3 to enable accurate species-level profiling of metagenomes. Compared to other methods, it provides a more comprehensive view of prokaryotic community diversity, in particular for currently underexplored microbiomes. To facilitate comparative analyses by the research community, it is released with > 11,000 precomputed profiles for publicly available metagenomes and is freely available at: .

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据