Identical sequences found in distant genomes reveal frequent horizontal transfer across the bacterial domain

  1. Michael Sheinman  Is a corresponding author
  2. Ksenia Arkhipova
  3. Peter F Arndt
  4. Bas Dutilh
  5. Rutger Hermsen  Is a corresponding author
  6. Florian Massip  Is a corresponding author
  1. Netherlands Cancer Institute, Netherlands
  2. Utrecht University, Netherlands
  3. Max Planck Institute for Molecular Genetics, Germany
  4. Berlin Institute for Medical Systems Biology, Max Delbrueck Center for Molecular Medicine,, Germany

Abstract

Horizontal Gene Transfer (HGT) is an essential force in microbial evolution. Despite detailed studies on a variety of systems, a global picture of HGT in the microbial world is still missing. Here, we exploit that HGT creates long identical DNA sequences in the genomes of distant species, which can be found efficiently using alignment-free methods. Our pairwise analysis of 93 481 bacterial genomes identified 138 273 HGT events. We developed a model to explain their statistical properties as well as estimate the transfer rate between pairs of taxa. This reveals that long-distance HGT is frequent: our results indicate that HGT between species from different phyla has occurred in at least 8% of the species. Finally, our results confirm that the function of sequences strongly impacts their transfer rate, which varies by more than 3 orders of magnitude between different functional categories. Overall, we provide a comprehensive view of HGT, illuminating a fundamental process driving bacterial evolution.

Data availability

Results of the analysis are provided as supplementary files

The following previously published data sets were used

Article and author information

Author details

  1. Michael Sheinman

    Division of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, Netherlands
    For correspondence
    mishashe@gmail.com
    Competing interests
    The authors declare that no competing interests exist.
  2. Ksenia Arkhipova

    Theoretical Biology and Bioinformatics, Utrecht University, Utrecht, Netherlands
    Competing interests
    The authors declare that no competing interests exist.
  3. Peter F Arndt

    Department of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, Berlin, Germany
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-1762-9836
  4. Bas Dutilh

    Theoretical Biology and Bioinformatics, Utrecht University, Utrecht, Netherlands
    Competing interests
    The authors declare that no competing interests exist.
  5. Rutger Hermsen

    Science faculty, Biology Department, Utrecht University, Utrecht, Netherlands
    For correspondence
    r.hermsen@uu.nl
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-4633-4877
  6. Florian Massip

    Evolutionary and Cancer Genomics, Berlin Institute for Medical Systems Biology, Max Delbrueck Center for Molecular Medicine,, Berlin, Germany
    For correspondence
    florian.massip@mdc-berlin.de
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-5855-0935

Funding

Netherlands Organisation for Scientific Research (Vidi grant 864.14.004)

  • Ksenia Arkhipova
  • Bas Dutilh

H2020 European Research Council (Consolidator Grant 865694: DiversiPHI)

  • Bas Dutilh

Fondation pour la Recherche Médicale (SPE201803005264)

  • Florian Massip

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Reviewing Editor

  1. Richard A Neher, University of Basel, Switzerland

Version history

  1. Received: September 3, 2020
  2. Accepted: June 13, 2021
  3. Accepted Manuscript published: June 14, 2021 (version 1)
  4. Version of Record published: July 9, 2021 (version 2)

Copyright

© 2021, Sheinman et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 3,403
    views
  • 399
    downloads
  • 25
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Michael Sheinman
  2. Ksenia Arkhipova
  3. Peter F Arndt
  4. Bas Dutilh
  5. Rutger Hermsen
  6. Florian Massip
(2021)
Identical sequences found in distant genomes reveal frequent horizontal transfer across the bacterial domain
eLife 10:e62719.
https://doi.org/10.7554/eLife.62719

Share this article

https://doi.org/10.7554/eLife.62719

Further reading

    1. Computational and Systems Biology
    David Geller-McGrath, Kishori M Konwar ... Jason E McDermott
    Tools and Resources

    The reconstruction of complete microbial metabolic pathways using ‘omics data from environmental samples remains challenging. Computational pipelines for pathway reconstruction that utilize machine learning methods to predict the presence or absence of KEGG modules in incomplete genomes are lacking. Here, we present MetaPathPredict, a software tool that incorporates machine learning models to predict the presence of complete KEGG modules within bacterial genomic datasets. Using gene annotation data and information from the KEGG module database, MetaPathPredict employs deep learning models to predict the presence of KEGG modules in a genome. MetaPathPredict can be used as a command line tool or as a Python module, and both options are designed to be run locally or on a compute cluster. Benchmarks show that MetaPathPredict makes robust predictions of KEGG module presence within highly incomplete genomes.

    1. Computational and Systems Biology
    2. Evolutionary Biology
    Kenya Hitomi, Yoichiro Ishii, Bei-Wen Ying
    Research Article

    As the genome encodes the information crucial for cell growth, a sizeable genomic deficiency often causes a significant decrease in growth fitness. Whether and how the decreased growth fitness caused by genome reduction could be compensated by evolution was investigated here. Experimental evolution with an Escherichia coli strain carrying a reduced genome was conducted in multiple lineages for approximately 1000 generations. The growth rate, which largely declined due to genome reduction, was considerably recovered, associated with the improved carrying capacity. Genome mutations accumulated during evolution were significantly varied across the evolutionary lineages and were randomly localized on the reduced genome. Transcriptome reorganization showed a common evolutionary direction and conserved the chromosomal periodicity, regardless of highly diversified gene categories, regulons, and pathways enriched in the differentially expressed genes. Genome mutations and transcriptome reorganization caused by evolution, which were found to be dissimilar to those caused by genome reduction, must have followed divergent mechanisms in individual evolutionary lineages. Gene network reconstruction successfully identified three gene modules functionally differentiated, which were responsible for the evolutionary changes of the reduced genome in growth fitness, genome mutation, and gene expression, respectively. The diversity in evolutionary approaches improved the growth fitness associated with the homeostatic transcriptome architecture as if the evolutionary compensation for genome reduction was like all roads leading to Rome.