Every four years, the Olympic Games plays host to competitors who have built on their natural talent by training for many years to become the best in their chosen discipline. Similar spirit and endeavour can be found throughout the microbial world, in which every day is a competition to survive and thrive. Microorganisms are trained through evolution to become the fittest and the best adapted to a particular environmental niche or lifestyle, and to innovate when the 'rules of the game' are changed by alterations to their natural habitats. In this Essay, we honour the best competitors in the microbial world by inviting them to take part in the inaugural Microbial Olympics.
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Nyholm, S. V. & McFall-Ngai, M. The winnowing: establishing the squid–vibrio symbiosis. Nature Rev. Microbiol. 2, 632–642 (2004).
Thingstad, T. F. & Lignell, R. Theoretical models for the control of bacterial growth rate, abundance, diversity and carbon demand. Aquat. Microb. Ecol. 13, 19–27 (1997).
Cox, M. M. & Battista, J. R. Deinococcus radiodurans — the consummate survivor. Nature Rev. Microbiol. 3, 882–892 (2005).
Kearns, D. B. A field guide to bacterial swarming motility. Nature Rev. Microbiol. 8, 634–644 (2010).
Russell, A. B. et al. Type VI secretion delivers bacteriolytic effectors to target cells. Nature 475, 343–347 (2011).
Virji, M. Pathogenic neisseriae: surface modulation, pathogenesis and infection control. Nature Rev. Microbiol. 7, 274–286 (2009).
Clauditz, A., Resch, A., Wieland, K. P., Peschel, A. & Gotz, F. Staphyloxanthin plays a role in the fitness of Staphylococcus aureus and its ability to cope with oxidative stress. Infect. Immun. 74, 4950–4953 (2006).
Jarrell, K. F. & McBride, M. J. The surprisingly diverse ways that prokaryotes move. Nature Rev. Microbiol. 6, 466–476 (2008).
Mashburn, L. M., Jett, A. M., Akins, D. R. & Whiteley, M. Staphylococcus aureus serves as an iron source for Pseudomonas aeruginosa during in vivo coculture. J. Bacteriol. 187, 554–566 (2005).
McCormick, J. K., Yarwood, J. M. & Schlievert, P. M. Toxic shock syndrome and bacterial superantigens: an update. Annu. Rev. Microbiol. 55, 77–104 (2001).
Bakaletz, L. O. Developing animal models for polymicrobial diseases. Nature Rev. Microbiol. 2, 552–568 (2004).
Koley, D., Ramsey, M. M., Bard, A. J. & Whiteley, M. Discovery of a biofilm electrocline using real-time 3D metabolite analysis. Proc. Natl Acad. Sci. USA 108, 19996–20001 (2011).
Mashburn, L. M. & Whiteley, M. Membrane vesicles traffic signals and facilitate group activities in a prokaryote. Nature 437, 422–425 (2005).
Chambers, H. F. & Deleo, F. R. Waves of resistance: Staphylococcus aureus in the antibiotic era. Nature Rev. Microbiol. 7, 629–641 (2009).
Sowa, Y. & Berry, R. M. Bacterial flagellar motor. Q. Rev. Biophys. 41, 103–132 (2008).
Porter, S. L. Wadhams, G. H. & Armitage, J. P. Signal processing in complex chemotaxis pathways. Nature Rev. Microbiol. 9, 153–165 (2011).
Valent, B. & Khang, C. H. Recent advances in rice blast effector research. Curr. Opin. Plant Biol. 13, 434–441 (2010).
Robb, E. & Barron, G. Nature's ballistic missile. Science 218, 1221–1222 (1982).
Montal, M. Botulinum neurotoxin: a marvel of protein design. Annu. Rev. Biochem. 79, 591–617 (2010).
Roy, B. A. Floral mimicry by a plant pathogen. Nature 362, 56–58 (1993).
Raguso, R. A. & Roy, B. A. 'Floral' scent production by Puccinia rust fungi that mimic flowers. Mol. Ecol. 7, 1127–1136 (1998).
van Beneden, P. Les Commensaux et les Parasites dans le Regne Animal (G. Ballière, 1875).
Anderson, R. M. & May, R. M. Coevolution of hosts and parasites. Parasitology 85, 411–426 (1982).
Ewald, P. Host-parasite relations, vectors, and the evolution of disease severity. Annu. Rev. Ecol. Syst. 14, 465–485 (1983).
Ewald, P. Evolution of Infectious Disease (Oxford University Press, 1997).
Ruby, E. & Morin, J. G. Specificity of symbiosis between deep-sea fishes and psychrotrophic luminous bacteria. Deep Sea Res. 25, 161–167 (1978).
Villareal, T. A., Woods, S., Moore, J. K. & Culver-Rymsza, K. Vertical migration of Rhizosolenia mats and their significance to NO3− fluxes in the central North Pacific gyre. J. Plankton Res. 18, 1103–1121 (1996).
Than, K. James Cameron completes record-breaking Mariana Trench dive. National Geographic News [online] (2012).
Irgens, R. L., Suzuki, I. & Staley, J. T. Gas vacuolate bacteria obtained from marine waters of Antarctica. Curr. Microbiol. 18, 261–265 (1989).
Bakermans, C. H., et al. Psychrobacter cryohalolentis sp. nov. and Psychrobacter arcticus sp. nov., isolated from Siberian permafrost. Int. J. Syst. Evol. Microbiol. 56, 1285–1291 (2006).
Amato, P., Doyle, S. M., Battista, J. R. & Christner, B. C. Implications of subzero metabolic activity on long-term microbial survival in terrestrial and extraterrestrial permafrost. Astrobiology 10, 789–798 (2010).
Ayala-del-Río, H. L. et al. The genome sequence of Psychrobacter arcticus 273–4, a psychroactive Siberian permafrost bacterium, reveals mechanisms for adaptation to low-temperature growth. Appl. Environ. Microbiol. 76, 2304–2312 (2010).
Wells, L. E. & Deming, J. W. Characterization of a cold-active bacteriophage on two psychrophilic marine hosts. Aquat. Microb. Ecol. 45, 15–29 (2006).
Junge, K., Eicken, H. & Deming, J. W. Motility of Colwellia psychrerythraea strain 34H at subzero temperatures. Appl. Environ. Microbiol. 69, 4282–4284 (2003).
Junge, K., Eicken, Swanson, B. D. & Deming, J. W. Bacterial incorporation of leucine into protein down to −20 °C with evidence for potential activity in subeutectic saline ice formations. Cryobiology 52, 417–429 (2006).
Methe, B. A. et al. The psychrophilic lifestyle as revealed by the genome sequence of Colwellia psychrerythraea 34H through genomic and proteomic analyses. Proc. Natl Acad. Sci. 102, 10913–10918 (2005).
S. Kamoun and S. Hogenhout are supported by The Gatsby Charitable Foundation and the UK Biotechnology and Biological Sciences Research Council.
The authors declare no competing financial interests.
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Youle, M., Rohwer, F., Stacy, A. et al. The Microbial Olympics. Nat Rev Microbiol 10, 583–588 (2012). https://doi.org/10.1038/nrmicro2837
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