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Accurate and universal delineation of prokaryotic species

Nature Methods volume 10, pages 881–884 (2013)Cite this article

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Abstract

The exponentially increasing number of sequenced genomes necessitates fast, accurate, universally applicable and automated approaches for the delineation of prokaryotic species. We developed specI (species identification tool; http://www.bork.embl.de/software/specI/), a method to group organisms into species clusters based on 40 universal, single-copy phylogenetic marker genes. Applied to 3,496 prokaryotic genomes, specI identified 1,753 species clusters. Of 314 discrepancies with a widely used taxonomic classification, >62% were resolved by literature support.

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Figure 1: Comparative performance assessment of specI.
Figure 2: Phylogenetic trees and species-level clustering of Prochlorococcus displaying discrepancies with the NCBI Taxonomy data.

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Acknowledgements

We thank the members of the Bork group for helpful discussions and Y. Yuan and members of the European Molecular Biology Laboratory information technology core facility for managing the high-performance computing resources. We acknowledge funding provided by the CancerBiome project (European Research Council project reference 268985), the 'METACARDIS' project (FP7-HEALTH-2012-INNOVATION-I-305312) and the International Human Microbiome Standards project (HEALTH-F4-2010-261376).

Author information

Authors and Affiliations

  1. European Molecular Biology Laboratory, Heidelberg, Germany

    Daniel R Mende, Shinichi Sunagawa, Georg Zeller & Peer Bork

  2. Max Delbrück Centre for Molecular Medicine, Berlin, Germany

    Peer Bork

Authors
  1. Daniel R Mende
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  2. Shinichi Sunagawa
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  3. Georg Zeller
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  4. Peer Bork
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Contributions

P.B., D.R.M., S.S. and G.Z. designed the study. D.R.M. developed and implemented the program, D.R.M. and G.Z. performed the experiments, D.R.M., S.S. and G.Z. analyzed the data, and D.R.M., S.S., G.Z. and P.B. wrote the manuscript.

Corresponding author

Correspondence to Peer Bork.

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Competing interests

The authors declare no competing financial interests.

Supplementary information

Supplementary Text and Figures

Supplementary Figures 1–8, Supplementary Tables 1–3, 5–7, 15, 17, 19 and 20, and Supplementary Note (PDF 1573 kb)

Supplementary Table 4

NCBI Taxonomy information of type strains listed on the list of prokaryotic names with standing in nomenclature (LPSN;http://www.bacterio.net/) that could be linked to NCBI, including their sequencing status (XLS 365 kb)

Supplementary Table 8

ANIb values of Prochlorococcusmarinus (XLS 19 kb)

Supplementary Table 9

ANIm values of Prochlorococcusmarinus (XLS 14 kb)

Supplementary Table 10

ANIb values of the Serratia and Rahnella clades (XLS 14 kb)

Supplementary Table 11

ANIm values of the Serratia and Rahnella clades (XLS 14 kb)

Supplementary Table 12

ANIb values of the Buchnera clade (XLS 15 kb)

Supplementary Table 13

ANIm values of the Buchnera clade (XLS 15 kb)

Supplementary Table 14

Cluster assignments for the 3,496 genomes used in this study (XLS 496 kb)

Supplementary Table 16

Literature-based reclassifications of species assignments of NCBI Taxonomy database (XLS 94 kb)

Supplementary Table 18

Assignments of genomes were previously not assigned to a named species to known species using the species clustering strategy presented in this publication (XLS 28 kb)

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Mende, D., Sunagawa, S., Zeller, G. et al. Accurate and universal delineation of prokaryotic species. Nat Methods 10, 881–884 (2013). https://doi.org/10.1038/nmeth.2575

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