Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Evolution of novel cooperative swarming in the bacterium Myxococcus xanthus

Abstract

Cooperation among individuals is necessary for evolutionary transitions to higher levels of biological organization1,2,3. In such transitions, groups of individuals at one level (such as single cells) cooperate to form selective units at a higher level (such as multicellular organisms). Though the evolution of cooperation is difficult to observe directly in higher eukaryotes, microorganisms do offer such an opportunity4. Here we report the evolution of novel cooperative behaviour in experimental lineages of the bacterium Myxococcus xanthus. Wild-type strains of M. xanthus exhibit socially dependent swarming across soft surfaces5 by a mechanism known as ‘S-motility’ that requires the presence of extracellular type IV pili6. In lineages of M. xanthus unable to make pili, a new mechanistic basis for cooperative swarming evolved. Evolved swarming is mediated, at least in part, by enhanced production of an extracellular fibril matrix that binds cells—and their evolutionary interests—together. Though costly to individuals, fibril production greatly enhanced population expansion in groups of interconnected cells. These results show that fundamental transitions to primitive cooperation can readily occur in bacteria.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Swarming rates and phenotypes of ancestral (A1, A2) and evolved (E1–E8) genotypes relative to WT on soft agar.
Figure 2: Swarming rates of WT, A1, A2, E7, E8, cglB and dsp mutants and LS1116 relative to WT on soft agar.
Figure 3
Figure 4: Evolution of fibril production.

Similar content being viewed by others

References

  1. Buss, L. W. The Evolution of Individuality (Princeton Univ. Press, Princeton, NJ, 1987)

    Google Scholar 

  2. Maynard Smith, J. & Szathmáry, E. The Major Transitions in Evolution (W.H. Freeman Spektrum, Oxford/New York, 1995)

    Google Scholar 

  3. Michod, R. E. & Roze, D. Cooperation and conflict in the evolution of multicellularity. Heredity 86, 1–7 (2001)

    Article  CAS  Google Scholar 

  4. Crespi, B. J. The evolution of social behavior in microorganisms. Trends Ecol. Evol. 16, 178–183 (2001)

    Article  Google Scholar 

  5. Shi, W. & Zusman, D. R. The two motility systems of Myxococcus xanthus show different selective advantages on various surfaces. Proc. Natl Acad. Sci. USA 90, 3378–3382 (1993)

    Article  ADS  CAS  Google Scholar 

  6. Wu, S. S. & Kaiser, D. Genetic and functional evidence that Type IV pili are required for social gliding motility in Myxococcus xanthus. Mol. Microbiol. 18, 547–558 (1995)

    Article  CAS  Google Scholar 

  7. Velicer, G. J., Lenski, R. E. & Kroos, L. Rescue of social motility lost during evolution of Myxococcus xanthus in an asocial environment. J. Bacteriol. 184, 2719–2727 (2002)

    Article  CAS  Google Scholar 

  8. Pfeiffer, T. & Bonhoeffer, S. An evolutionary scenario for the transition to undifferentiated multicellularity. Proc. Natl Acad. Sci. USA 100, 1095–1098 (2003)

    Article  ADS  CAS  Google Scholar 

  9. Rainey, P. B. & Rainey, K. Evolution of cooperation and conflict in experimental bacterial populations. Nature 425, 72–74 (2003)

    Article  ADS  CAS  Google Scholar 

  10. Velicer, G. J. Social strife in the microbial world. Trends Microbiol 11, 330–337 (2003)

    Article  CAS  Google Scholar 

  11. Velicer, G. J., Kroos, L. & Lenski, R. E. Loss of social behaviors by Myxococcus xanthus during evolution in an unstructured habitat. Proc. Natl Acad. Sci. USA 95, 12376–12380 (1998)

    Article  ADS  CAS  Google Scholar 

  12. Shimkets, L. J. Intercellular signaling during fruiting-body development of Myxococcus xanthus. Annu. Rev. Microbiol. 53, 525–549 (1999)

    Article  CAS  Google Scholar 

  13. Hodgkin, J. & Kaiser, D. Genetics of gliding motility in Myxococcus xanthus (Myxobacterales): two gene systems control movement. Mol. Gen. Genet. 171, 177–191 (1979)

    Article  Google Scholar 

  14. Behmlander, R. M. & Dworkin, M. Biochemical and structural analyses of the extracellular matrix fibrils of Myxococcus xanthus. J. Bacteriol. 176, 6295–6303 (1994)

    Article  CAS  Google Scholar 

  15. Kearns, D. B., Campbell, B. D. & Shimkets, L. J. Myxococcus xanthus fibril appendages are essential for excitation by a phospholipid attractant. Proc. Natl Acad. Sci. USA 97, 11505–11510 (2000)

    Article  ADS  CAS  Google Scholar 

  16. Li, Y. et al. Extracellular polysaccharides mediate pilus retraction during social motility of Myxococcus xanthus. Proc. Natl Acad. Sci. USA 100, 5443–5448 (2003)

    Article  ADS  CAS  Google Scholar 

  17. Wolgemuth, C., Hoiczyk, E., Kaiser, D. & Oster, G. How myxobacteria glide. Curr. Biol. 12, 369–377 (2002)

    Article  CAS  Google Scholar 

  18. Dana, J. R. & Shimkets, L. J. Regulation of cohesion-dependent cell interactions in Myxococcus xanthus. J. Bacteriol. 175, 3636–3647 (1993)

    Article  CAS  Google Scholar 

  19. Rodriguez, A. M. & Spormann, A. M. Genetic and molecular analysis of cglB, a gene essential for single-cell gliding in Myxococcus xanthus. J. Bacteriol. 181, 4381–4390 (1999)

    CAS  PubMed  PubMed Central  Google Scholar 

  20. Shimkets, L. J. Role of cell cohesion in Myxococcus xanthus fruiting body formation. J. Bacteriol. 166, 842–848 (1986)

    Article  CAS  Google Scholar 

  21. Kearns, D. B. & Shimkets, L. J. Lipid chemotaxis and signal transduction in Myxococcus xanthus. Trends Microbiol. 9, 126–129 (2001)

    Article  CAS  Google Scholar 

  22. Lancero, H. et al. Mapping of Myxococcus xanthus social motility dsp mutations to the dif genes. J. Bacteriol. 184, 1462–1465 (2002)

    Article  CAS  Google Scholar 

  23. Arnold, J. W. & Shimkets, L. J. Inhibition of cell-cell interactions in Myxococcus xanthus by Congo Red. J. Bacteriol. 170, 5765–5770 (1988)

    Article  CAS  Google Scholar 

  24. Kearns, D. B., Bonner, P. J., Smith, D. R. & Shimkets, L. J. An extracellular matrix-associated zinc metalloprotease is required for dilauroyl phosphatidylethanolamine chemotactic excitation in Myxococcus xanthus. J. Bacteriol. 184, 1678–1684 (2002)

    Article  CAS  Google Scholar 

  25. Behmlander, R. M. & Dworkin, M. Extracellular fibrils and contact-mediated cell interactions in Myxococcus xanthus. J. Bacteriol. 173, 7810–7821 (1991)

    Article  CAS  Google Scholar 

  26. Queller, D. C., Ponte, E., Bozzaro, S. & Strassmann, J. E. Single-gene greenbeard effects in the social amoeba Dictyostelium discoideum. Science 299, 105–106 (2003)

    Article  ADS  CAS  Google Scholar 

  27. Cramton, S. E., Ulrich, M., Götz, F. & Doring, G. Anaerobic conditions induce expression of polysaccharide intercellular adhesin in Staphylococcus aureus and Staphylococcus epidermidis. Infect. Immun. 69, 4079–4085 (2001)

    Article  CAS  Google Scholar 

  28. Krause, J. & Ruxton, G. D. Living in Groups (Oxford Univ. Press, Oxford/New York, 2002)

    Google Scholar 

  29. Wu, S. S. & Kaiser, D. Markerless deletions of pil genes in Myxococcus xanthus generated by counterselection with the Bacillus subtilis sacB gene. J. Bacteriol. 178, 5817–5821 (1996)

    Article  CAS  Google Scholar 

  30. Wu, S. S. & Kaiser, D. Regulation of expression of the pilA gene in Myxococcus xanthus. J. Bacteriol. 179, 7748–7758 (1997)

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We are grateful to S. Bonhoeffer, S. Elena, L. Kroos, P. Rainey and W. Shi for discussion or comments, I. Dinkelacker and F. Fiegna for technical assistance, K. Hillesland for construction of strains A1 and A2, D. Kaiser and H. Kaplan for antibodies and plasmids, L. Shimkets for discussion and strains, and J. Berger and H. Schwarz for electron microscopy expertise and assistance.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Gregory J. Velicer.

Ethics declarations

Competing interests

The authors declare that they have no competing financial interests.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Velicer, G., Yu, Yt. Evolution of novel cooperative swarming in the bacterium Myxococcus xanthus. Nature 425, 75–78 (2003). https://doi.org/10.1038/nature01908

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nature01908

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing