CoChat
Sign Up
Cited by 477Genomics and Phylogenetic StudiesMicrobial Community Ecology and PhysiologyGut microbiota and health

The DOI matches its Crossref record; 59 of the 59 references it cites were found in a registry or an index.

Microbial abundance, activity and population genomic profiling with mOTUs2

Open access
Milanese, Alessio, Mende, Daniel R, Paoli, Lucas, Salazar, Guillem, Ruscheweyh, Hans-Joachim, Cuenca, Miguelangel, Hingamp, Pascal, Alves, Renato, Costea, Paul I, Coelho, Luis Pedro, Schmidt, Thomas S. B., Almeida, Alexandre, Mitchell, Alex L, Finn, Robert D., Huerta-Cepas, Jaime, Bork, Peer, Zeller, Georg, Sunagawa, Shinichi·2019·Nature Communications
DOI 10.1038/s41467-019-08844-4PMC PMC6399450
Open this paper in CoChat — free accountOpen PDF

Abstract

Metagenomic sequencing has greatly improved our ability to profile the composition of environmental and host-associated microbial communities. However, the dependency of most methods on reference genomes, which are currently unavailable for a substantial fraction of microbial species, introduces estimation biases. We present an updated and functionally extended tool based on universal (i.e., reference-independent), phylogenetic marker gene (MG)-based operational taxonomic units (mOTUs) enabling the profiling of >7700 microbial species. As more than 30% of them could not previously be quantified at this taxonomic resolution, relative abundance estimates based on mOTUs are more accurate compared to other methods. As a new feature, we show that mOTUs, which are based on essential housekeeping genes, are demonstrably well-suited for quantification of basal transcriptional activity of community members. Furthermore, single nucleotide variation profiles estimated using mOTUs reflect those from whole genomes, which allows for comparing microbial strain populations (e.g., across different human body sites).

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1038/s41467-019-08844-4

Cites

59 of 59 references verified0 citation errors · 0 not checkable

Statistics

Figures

Fig. 1 Construction of marker gene-based OTUs (mOTUs) for metagenomic profiling. a Schematic illustration of the mOTUs concept (Methods). b The observed richness of ref-mOTUs (containing exclusively MG sequences from reference genomes; blue) and meta-mOTUs (containing only MG sequences from metagenomes; green) per biome, and c mean cumulative relative abundance of species profiled across 2481 metagenomic samples. d Correspondence between mOTUs and 19,302 metagenome assembled genomes (MAGs) from the human gut. While less than 3% of MAGs are not represented (dark grey bar), mOTUs allow for profiling of 900 species not captured by MAGs. Source data are provided as a Source Data file.
Fig. 1 Construction of marker gene-based OTUs (mOTUs) for metagenomic profiling. a Schematic illustration of the mOTUs concept (Methods). b The observed richness of ref-mOTUs (containing exclusively MG sequences from reference genomes; blue) and meta-mOTUs (containing only MG sequences from metagenomes; green) per biome, and c mean cumulative relative abundance of species profiled across 2481 metagenomic samples. d Correspondence between mOTUs and 19,302 metagenome assembled genomes (MAGs) from the human gut. While less than 3% of MAGs are not represented (dark grey bar), mOTUs allow for profiling of 900 species not captured by MAGs. Source data are provided as a Source Data file.CC BY · PubMed Central
Fig. 2 Evaluation of mOTU profiling on simulated samples. Benchmarks of quantification accuracy (a–g) on ten simulated metagenomic samples (Methods) containing MAGs with (n = 50) and MAGs without (n = 50) a representative reference genome sequence, (h–o) and the CAMI challenge datasets25. a–d A representative simulated metagenome (out of ten; Supplementary Figures 8, 9) analysed with four profilers. e Precision-recall plot, where each data point corresponds to one of the ten simulated samples. Mean absolute error (MAE, also referred to as L1 norm) (f) and differences of the Shannon diversity index (g) from the expected values (error bars in f and g show standard deviation). h–j Average precision-recall values over the two medium complexity samples and (l–n) average precision-recall values over the five high complexity samples of the CAMI dataset (see also Supplementary Figure 10). Each precision-recall plot contains five values for mOTUs2, which correspond to different sets of parameters: high precision (-l 140 -g 6), default (-l 100 -g 3), recall (-l 75 -g 3), high recall (-l 50 -g 2) and maximum recall (-l 30 -g 1), indicating the versatility of mOTUs2 in optimising precision or recall. In (k) and (o), mean absolute errors (MAE; referred to as L1-norm in CAMI) at different taxonomic ranks are shown for several tools. For mOTUs2, results for two options of calculating relative abundances are shown: one with relative abundances re-normalized based on detected taxa, which is enforced in the CAMI evaluation (but artificially deteriorates quantification accuracy), and one without this additional re-normalization (see main text and Supplementary Figure 11 for details). Data are provided in Supplementary Data 3, 4. Other taxonomic profilers (MetaPhyler, TIPP, Taxy-Pro, FOCUS, CLARK, Quickr) evaluated in CAMI25 are denoted by grey dots. Source data are provided as a Source Data file.
Fig. 2 Evaluation of mOTU profiling on simulated samples. Benchmarks of quantification accuracy (a–g) on ten simulated metagenomic samples (Methods) containing MAGs with (n = 50) and MAGs without (n = 50) a representative reference genome sequence, (h–o) and the CAMI challenge datasets25. a–d A representative simulated metagenome (out of ten; Supplementary Figures 8, 9) analysed with four profilers. e Precision-recall plot, where each data point corresponds to one of the ten simulated samples. Mean absolute error (MAE, also referred to as L1 norm) (f) and differences of the Shannon diversity index (g) from the expected values (error bars in f and g show standard deviation). h–j Average precision-recall values over the two medium complexity samples and (l–n) average precision-recall values over the five high complexity samples of the CAMI dataset (see also Supplementary Figure 10). Each precision-recall plot contains five values for mOTUs2, which correspond to different sets of parameters: high precision (-l 140 -g 6), default (-l 100 -g 3), recall (-l 75 -g 3), high recall (-l 50 -g 2) and maximum recall (-l 30 -g 1), indicating the versatility of mOTUs2 in optimising precision or recall. In (k) and (o), mean absolute errors (MAE; referred to as L1-norm in CAMI) at different taxonomic ranks are shown for several tools. For mOTUs2, results for two options of calculating relative abundances are shown: one with relative abundances re-normalized based on detected taxa, which is enforced in the CAMI evaluation (but artificially deteriorates quantification accuracy), and one without this additional re-normalization (see main text and Supplementary Figure 11 for details). Data are provided in Supplementary Data 3, 4. Other taxonomic profilers (MetaPhyler, TIPP, Taxy-Pro, FOCUS, CLARK, Quickr) evaluated in CAMI25 are denoted by grey dots. Source data are provided as a Source Data file.CC BY · PubMed Central
Fig. 3 Reference-extended mOTUs for microbial community diversity profiling. Shannon index was calculated based on 16S rRNA gene (16S) fragments (x-axis) and mOTUs (y-axis), respectively, for 129 human faecal samples (left) and 139 ocean water samples (right). Mean Spearman correlation of diversity estimates based on 16S and three metagenomic profiling tools (Kraken, MetaPhlAn2 and mOTUs2) are shown in the insets. Error bars delineate 95% confidence intervals after bootstrapping. Source data are provided as a Source Data file.
Fig. 3 Reference-extended mOTUs for microbial community diversity profiling. Shannon index was calculated based on 16S rRNA gene (16S) fragments (x-axis) and mOTUs (y-axis), respectively, for 129 human faecal samples (left) and 139 ocean water samples (right). Mean Spearman correlation of diversity estimates based on 16S and three metagenomic profiling tools (Kraken, MetaPhlAn2 and mOTUs2) are shown in the insets. Error bars delineate 95% confidence intervals after bootstrapping. Source data are provided as a Source Data file.CC BY · PubMed Central
Fig. 4 Metatranscriptomic abundance profiling with mOTUs2. a Spearman correlation between matched metagenomic and metatranscriptomic profiles obtained from 36 faecal samples with Kraken, MetaPhlAn2 and mOTUs2. mOTUs2 profiles (red) show significantly higher correlation than the other two methods (paired two-sided Wilcoxon test, boxplots show the median correlation as horizontal lines and interquartile ranges as boxes, whiskers extend at most 1.5 times the interquartile range). b The top-row represents the proportion of cases in which the distance (log-Euclidean) between metagenomic and metatranscriptomic profiles was smallest for the same sample. Below is a taxonomic breakdown (12 most abundant classes) of correlations between metagenomic and metatranscriptomic profiles. For each class, the highest correlation value across the tested methods are shown in bold. Source data are provided as a Source Data file.
Fig. 4 Metatranscriptomic abundance profiling with mOTUs2. a Spearman correlation between matched metagenomic and metatranscriptomic profiles obtained from 36 faecal samples with Kraken, MetaPhlAn2 and mOTUs2. mOTUs2 profiles (red) show significantly higher correlation than the other two methods (paired two-sided Wilcoxon test, boxplots show the median correlation as horizontal lines and interquartile ranges as boxes, whiskers extend at most 1.5 times the interquartile range). b The top-row represents the proportion of cases in which the distance (log-Euclidean) between metagenomic and metatranscriptomic profiles was smallest for the same sample. Below is a taxonomic breakdown (12 most abundant classes) of correlations between metagenomic and metatranscriptomic profiles. For each class, the highest correlation value across the tested methods are shown in bold. Source data are provided as a Source Data file.CC BY · PubMed Central
Fig. 5 Marker gene-based SNV profiles are comparable to those using whole genomes. a Pearson correlation coefficients for MG- and genome-based SNV profiles across species and biomes in the HMP (N = 2807) and ocean dataset (N = 139). Median correlations (Pearson’s r) are shown as horizontal lines and interquartile ranges as boxes. Whiskers extend at most 1.5 times the interquartile range. b Intra- and inter-individual distances of SNV profiles were compared using the area under the receiver operating characteristic curve (AU-ROC) to determine the degree of individuality of microbial strain populations for different human body sites (see also Supplementary Figure 17). Error bars delineate 95% confidence intervals after bootstrapping. Source data are provided as a Source Data file.
Fig. 5 Marker gene-based SNV profiles are comparable to those using whole genomes. a Pearson correlation coefficients for MG- and genome-based SNV profiles across species and biomes in the HMP (N = 2807) and ocean dataset (N = 139). Median correlations (Pearson’s r) are shown as horizontal lines and interquartile ranges as boxes. Whiskers extend at most 1.5 times the interquartile range. b Intra- and inter-individual distances of SNV profiles were compared using the area under the receiver operating characteristic curve (AU-ROC) to determine the degree of individuality of microbial strain populations for different human body sites (see also Supplementary Figure 17). Error bars delineate 95% confidence intervals after bootstrapping. Source data are provided as a Source Data file.CC BY · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 59 references

Cited by

Sorted by citations

Items 201–300 of 477

Related

See all

Metadata

Authors
Milanese, A., Mende, D. R., Paoli, L., Salazar, G., Ruscheweyh, H.-J., Cuenca, M., Hingamp, P., Alves, R., Costea, P. I., Coelho, L. P., Schmidt, T. S. B., Almeida, A., Mitchell, A. L., Finn, R. D., Huerta-Cepas, J., Bork, P., Zeller, G., & Sunagawa, S.
Affiliations
  • European Molecular Biology Laboratory (DE)
  • University of Hawaiʻi at Mānoa (US)
  • SIB Swiss Institute of Bioinformatics (CH)
  • Centre National de la Recherche Scientifique (FR)
  • Heidelberg University (DE)
  • European Bioinformatics Institute (GB)
Corresponding author
  • Zeller, Georg
  • Sunagawa, Shinichi
ORCID
Venue
Nature Communications
Publisher
Springer Science and Business Media LLC
Published
2019-03-04
Volume
10
Issue
1
Pages
1014-1014
ISSN
2041-1723 (ISSN-L)
DOI
10.1038/s41467-019-08844-4
PMC
PMC6399450
OpenAlex
W2920716817
Cited by
446
References
59
Citations by year
2026: 24 · 2025: 43 · 2024: 74 · 2023: 73 · 2022: 89 · 2021: 82 · 2020: 42 · 2019: 17
FWCI
20.03
Type
journal article
Language
en
Open access
Licence
Locations
  • Nature Communications (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • MDC Repository (Max-Delbrueck-Center for Molecular Medicine) (acceptedVersion)
  • HAL (submittedVersion, cc-by)
  • RePEc: Research Papers in Economics (submittedVersion)
  • DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • Online Publication Service of Würzburg University (Würzburg University) (submittedVersion, cc-by)
  • Repository for Publications and Research Data (ETH Zurich) (submittedVersion, cc-by)
  • ETH Zürich Research Collection (cc-by)
Funders
  • European Molecular Biology Organization (GA-2013-609409, ALTF 721-2015, LTFCOFUND2013)
  • Novartis Foundation (LTFCOFUND2013, GA-2013-609409)
  • Bundesministerium für Bildung und Forschung (031A537B)
  • Eidgenössische Technische Hochschule Zürich (PHRT 521)
  • Novartis Stiftung für Medizinisch-Biologische Forschung
  • Helmut Horten Stiftung
  • German Network for Bioinformatics Infrastructure (031 A537B)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
  • Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Keywords
operational taxonomic units, housekeeping genes, microbial community composition, single nucleotide variants, human microbiome, metagenomics
MeSH terms
Host Microbial Interactions, Algorithms, Genetic Markers, Humans, Phylogeny, Cluster Analysis, Sequence Alignment, Genome, Sequence Analysis, DNA, Computational Biology, Genes, Essential, Gene Expression Profiling, Metagenomics, Molecular Sequence Annotation, Microbiota

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review