Genome sequence of the β-rhizobium Cupriavidus taiwanensis and comparative genomics of rhizobia

  1. Claire Amadou1,6,
  2. Géraldine Pascal1,6,
  3. Sophie Mangenot2,6,
  4. Michelle Glew1,
  5. Cyril Bontemps1,
  6. Delphine Capela1,
  7. Sébastien Carrère1,
  8. Stéphane Cruveiller3,
  9. Carole Dossat2,
  10. Aurélie Lajus3,
  11. Marta Marchetti1,
  12. Véréna Poinsot4,
  13. Zoé Rouy3,
  14. Bertrand Servin5,
  15. Maged Saad1,
  16. Chantal Schenowitz2,
  17. Valérie Barbe2,
  18. Jacques Batut1,
  19. Claudine Médigue3, and
  20. Catherine Masson-Boivin1,7
  1. 1 Laboratoire des Interactions Plantes Micro-organismes (LIPM), UMR CNRS-INRA 2594/441, 31326 Castanet-Tolosan Cedex, France;
  2. 2 C.E.A/IG/Génoscope, 91057 Evry Cedex, France;
  3. 3 CNRS-UMR 8030, 91057 Evry Cedex, France;
  4. 4 Laboratoire des IMRCP, 31062 Toulouse-Cedex, France;
  5. 5 Laboratoire de Génétique Cellulaire, UMR INRA-ENVT, 31326 Castanet-Tolosan Cedex, France

Abstract

We report the first complete genome sequence of a β-proteobacterial nitrogen-fixing symbiont of legumes, Cupriavidus taiwanensis LMG19424. The genome consists of two chromosomes of size 3.42 Mb and 2.50 Mb, and a large symbiotic plasmid of 0.56 Mb. The C. taiwanensis genome displays an unexpected high similarity with the genome of the saprophytic bacterium C. eutrophus H16, despite being 0.94 Mb smaller. Both organisms harbor two chromosomes with large regions of synteny interspersed by specific regions. In contrast, the two species host highly divergent plasmids, with the consequence that C. taiwanensis is symbiotically proficient and less metabolically versatile. Altogether, specific regions in C. taiwanensis compared with C. eutrophus cover 1.02 Mb and are enriched in genes associated with symbiosis or virulence in other bacteria. C. taiwanensis reveals characteristics of a minimal rhizobium, including the most compact (35-kb) symbiotic island (nod and nif) identified so far in any rhizobium. The atypical phylogenetic position of C. taiwanensis allowed insightful comparative genomics of all available rhizobium genomes. We did not find any gene that was both common and specific to all rhizobia, thus suggesting that a unique shared genetic strategy does not support symbiosis of rhizobia with legumes. Instead, phylodistribution analysis of more than 200 Sinorhizobium meliloti known symbiotic genes indicated large and complex variations of their occurrence in rhizobia and non-rhizobia. This led us to devise an in silico method to extract genes preferentially associated with rhizobia. We discuss how the novel genes we have identified may contribute to symbiotic adaptation.

Footnotes

  • 6 These authors equally contributed to this work.

  • 7 Corresponding author.

    7 E-mail catherine.masson{at}toulouse.inra.fr; fax 33-5-61-28-50-61.

  • [Supplemental material is available online at www.genome.org. The sequence data from this study for C. taiwanensis LMG19424 have been submitted to EMBL under accession nos. CU633749 (chromosome 1), CU633750 (chromosome 2), and CU633751 (pRalta).]

  • Article published online before print. Article and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.076448.108.

    • Received January 28, 2008.
    • Accepted May 19, 2008.
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