Bacterial morphology: why have different shapes?

Current Opinion in Microbiology

Volumn 10, Issue 6, 2007, Pages 596-600

  Young, Kevin D ^a  

^a UNIVERSITY OF NORTH DAKOTA SCHOOL OF MEDICINE AND HEALTH SCIENCES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL GROWTH; BACTERIAL SURVIVAL; BACTERIUM COMPETENCE; BACTERIUM DETECTION; BACTERIUM IDENTIFICATION; BACTERIVORY; CELL GROWTH; CELL MOTILITY; CELL SHAPE; CELL STRUCTURE; CHEMOTAXIS; ENVIRONMENTAL FACTOR; ESCHERICHIA COLI; EVOLUTIONARY ADAPTATION; MICROBIAL ACTIVITY; MICROMORPHOLOGY; NONHUMAN; NUTRIENT AVAILABILITY; PREDATION; REVIEW; VIBRIO ALGINOLYTICUS;

ADAPTATION, PHYSIOLOGICAL; BACTERIA; BACTERIAL PHYSIOLOGY; MOVEMENT;

BACTERIA (MICROORGANISMS);

EID: 36549043573     PISSN: 13695274     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mib.2007.09.009     Document Type: Review

References (49)

1. Young K.D. The selective value of bacterial shape. Microbiol Mol Biol Rev 70 (2006) 660-703. A comprehensive recent attempt to compile, describe, and classify the ways in which bacteria may utilize morphology to cope with a variety of evolutionary pressures.
2. Beveridge T.J. The bacterial surface: general considerations towards design and function. Can J Microbiol 34 (1988) 363-372
3. Dusenbery D.B. Fitness landscapes for effects of shape on chemotaxis and other behaviors of bacteria. J Bacteriol 180 (1998) 5978-5983. An early review addressing the selective pressures that define bacterial shape, especially with regard to motility.
4. Koch A.L. What size should a bacterium be? A question of scale. Annu Rev Microbiol 50 (1996) 317-348
5. Mitchell J.G. The energetics and scaling of search strategies in bacteria. Am Nat 160 (2002) 727-740. An exquisitely detailed, far-ranging discussion of how the physical requirements imposed by motility influence and constrain bacterial shape.
6. Justice S.S., Hung C., Theriot J.A., Fletcher D.A., Anderson G.G., Footer M.J., and Hultgren S.J. Differentiation and developmental pathways of uropathogenic Escherichia coli in urinary tract pathogenesis. Proc Natl Acad Sci U S A 101 (2004) 1333-1338. The authors observed pathogenesis-associated differentiation, in which E. coli adopts different morphologies during infection of mouse bladder epithelial cells.
7. Stackebrandt E., and Woese C.R. A phylogenetic dissection of the family Micrococcaceae. Curr Microbiol 2 (1979) 317-322
8. Woese C.R., Blanz P., Hespell R.B., and Hahn C.M. Phylogenetic relationships among various helical bacteria. Curr Microbiol 7 (1982) 119-124
9. Siefert J.L., and Fox G.E. Phylogenetic mapping of bacterial morphology. Microbiology 144 (1998) 2803-2808
10. Tamames J., Gonzalez-Moreno M., Mingorance J., Valencia A., and Vicente M. Bringing gene order into bacterial shape. Trends Genet 17 (2001) 124-126
11. Gupta R.S. The phylogeny of proteobacteria: relationships to other eubacterial phyla and eukaryotes. FEMS Microbiol Rev 24 (2000) 367-402
12. Stetter KO: Smallest cell sizes within hyperthermophilic archaea ("Archaebacteria"). In Size Limits of Very Small Microorganisms: Proceedings of a Workshop. Edited by Space 'Studies' Board: National Academic Press; 1999:68-73.
13. Schulz H.N., and Jorgensen B.B. Big bacteria. Annu Rev Microbiol 55 (2001) 105-137
14. Brun Y.V., and Janakiraman R. The dimorphic life cycle of Caulobacter and stalked bacteria. In: Brun Y.V., and Shimkets LJ: (Eds). Prokaryotic Development (2000), American Society for Microbiology 297-317
15. Poindexter J.S. The role of calcium in stalk development and in phosphate acquisition in Caulobacter crescentus. Arch Microbiol 138 (1984) 140-152
16. Poindexter J.S. Role of prostheca development in oligotrophic aquatic bacteria. In: Klug M.J., and Reddy C.A. (Eds). Current Perspectives in Microbial Ecology (1984), ASM Press 33-40
17. Wagner J.K., Setayeshgar S., Sharon L.A., Reilly J.P., and Brun Y.V. A nutrient uptake role for bacterial cell envelope extensions. Proc Natl Acad Sci U S A 103 (2006) 11772-11777. A seminal experimental and mathematical demonstration of how Caulocbacter crescentus responds to nutrient availability by elaborating long, thin prosthecae.
18. Cooper S., and Denny M.W. A conjecture on the relationship of bacterial shape to motility in rod-shaped bacteria. FEMS Microbiol Lett 148 (1997) 227-231
19. Maki N., Gestwicki J.E., Lake E.M., Kiessling L.L., and Adler J. Motility and chemotaxis of filamentous cells of Escherichia coli. J Bacteriol 182 (2000) 4337-4342. A key experiment examining why motile cells have certain lengths by examining motility and chemotaxis in filamentous E. coli.
20. Kearns D.B., and Losick R. Swarming motility in undomesticated Bacillus subtilis. Mol Microbiol 49 (2003) 581-590
21. Julkowska D., Obuchowski M., Holland I.B., and Seror S.J. Branched swarming patterns on a synthetic medium formed by wild-type Bacillus subtilis strain 3610: detection of different cellular morphologies and constellations of cells as the complex architecture develops. Microbiology 150 (2004) 1839-1849. An interesting observation of how one bacterium adopts different morphologies depending on how each cell is positioned within a multi-cell conglomerate.
22. Hay N.A., Tipper D.J., Gygi D., and Hughes C. A novel membrane protein influencing cell shape and multicellular swarming of Proteus mirabilis. J Bacteriol 181 (1999) 2008-2016
23. Kudo S., Imai N., Nishitoba M., Sugiyama S., and Magariyama Y. Asymmetric swimming pattern of Vibrio alginolyticus cells with single polar flagella. FEMS Microbiol Lett 242 (2005) 221-225
24. Magariyama Y., Ichiba M., Nakata K., Baba K., Ohtani T., Kudo S., and Goto T. Difference in bacterial motion between forward and backward swimming caused by the wall effect. Biophys J 88 (2005) 3648-3658. An experimental demonstration of how 'near surface' properties change the pattern of motility in Vibrio alginolyticus, focusing on this organism's peculiar curved motion when swimming backwards.
25. DiLuzio W.R., Turner L., Mayer M., Garstecki P., Weibel D.B., Berg H.C., and Whitesides G.M. Escherichia coli swim on the right-hand side. Nature 435 (2005) 1271-1274. A captivating experimental achievement, showing that non-tumbling E. coli veer rightward when swimming near the planar surface of a thin channel.
26. Lauga E., Diluzio W.R., Whitesides G.M., and Stone H.A. Swimming in circles: motion of bacteria near solid boundaries. Biophys J 90 (2006) 400-412. A computational model describing the effects of bacterial shape on the motility of cells near a planar surface, showing, among other things, that cell length affects the size of the circular path that bacteria traverse in these environments.
27. Robertson B.R., O'Rourke J.L., Neilan B.A., Vandamme P., On S.L., Fox J.G., and Lee A. Mucispirillum schaedleri gen. nov., sp. nov., a spiral-shaped bacterium colonizing the mucus layer of the gastrointestinal tract of laboratory rodents. Int J Syst Evol Microbiol 55 (2005) 1199-1204
28. Atsumi T., Maekawa Y., Yamada T., Kawagishi I., Imae Y., and Homma M. Effect of viscosity on swimming by the lateral and polar flagella of Vibrio alginolyticus. J Bacteriol 178 (1996) 5024-5026
29. Shigematsu M., Umeda A., Fujimoto S., and Amako K. Spirochaete-like swimming mode of Campylobacter jejuni in a viscous environment. J Med Microbiol 47 (1998) 521-526
30. Berg H.C., and Turner L. Movement of microorganisms in viscous environments. Nature 278 (1979) 349-351. Classic treatment of the theoretical reasons that spiral bacteria move efficiently through viscous fluids.
31. Magariyama Y., and Kudo S. A mathematical explanation of an increase in bacterial swimming speed with viscosity in linear-polymer solutions. Biophys J 83 (2002) 733-739
32. Matz C., and Kjelleberg S. Off the hook-how bacteria survive protozoan grazing. Trends Microbiol 13 (2005) 302-307
33. Jürgens K., and Matz C. Predation as a shaping force for the phenotypic and genotypic composition of planktonic bacteria. Antonie Van Leeuwenhoek 81 (2002) 413-434
34. Hahn M.W., and Hofle M.G. Grazing of protozoa and its effect on populations of aquatic bacteria. FEMS Microbiol Ecol 35 (2001) 113-121
35. Sherr E.B., and Sherr B.F. Significance of predation by protists in aquatic microbial food webs. Antonie Van Leeuwenhoek 81 (2002) 293-308
36. Pernthaler J. Predation on prokaryotes in the water column and its ecological implications. Nat Rev Microbiol 3 (2005) 537-546. A particularly accessible review on how protozoan predation fuels bacterial evolution, including the development of several morphological adaptations.
37. Boenigk J., and Arndt H. Bacterivory by heterotrophic flagellates: community structure and feeding strategies. Antonie Van Leeuwenhoek 81 (2002) 465-480
38. Matz C., Bergfeld T., Rice S.A., and Kjelleberg S. Microcolonies, quorum sensing and cytotoxicity determine the survival of Pseudomonas aeruginosa biofilms exposed to protozoan grazing. Environ Microbiol 6 (2004) 218-226
39. Posch T., Simek K., Vrba J., Pernthaler S., Nedoma J., Sattler B., Sonntag B., and Psenner R. Predator-induced changes of bacterial size-structure and productivity studied on an experimental microbial community. Aquat Microb Ecol 18 (1999) 235-246
40. Matz C., and Jurgens K. High motility reduces grazing mortality of planktonic bacteria. Appl Environ Microbiol 71 (2005) 921-929. A well-supported confirmation that efficient and rapid motility helps bacteria evade protozoan predation.
41. Pernthaler J., Posch T., Simek K., Vrba J., Amann R., and Psenner R. Contrasting bacterial strategies to coexist with a flagellate predator in an experimental microbial assemblage. Appl Environ Microbiol 63 (1997) 596-601
42. Simek K., Vrba J., Pernthaler J., Posch T., Hartman P., Nedoma J., and Psenner R. Morphological and compositional shifts in an experimental bacterial community influenced by protists with contrasting feeding modes. Appl Environ Microbiol 63 (1997) 587-595
43. Bianchi M. Unusual bloom of star-like prosthecate bacteria and filaments as a consequence of grazing pressure. Microb Ecol 17 (1989) 137-141
44. DeLeo P.C., and Baveye P. Factors affecting protozoan predation of bacteria clogging laboratory aquifer microcosms. Geomicrobiol J 14 (1997) 127
45. Hahn M.W., and Hofle M.G. Flagellate predation on a bacterial model community: interplay of size-selective grazing, specific bacterial cell size, and bacterial community composition. Appl Environ Microbiol 65 (1999) 4863-4872
46. Jürgens K., Pernthaler J., Schalla S., and Amann R. Morphological and compositional changes in a planktonic bacterial community in response to enhanced protozoan grazing. Appl Environ Microbiol 65 (1999) 1241-1250
47. Posch T., Jezbera J., Vrba J., Simek K., Pernthaler J., Andreatta S., and Sonntag B. Size selective feeding in Cyclidium glaucoma (Ciliophora, Scuticociliatida) and its effects on bacterial community structure: a study from a continuous cultivation system. Microb Ecol 42 (2001) 217-227
48. Mühling M., Harris N., Belay A., and Whitton B.A. Reversal of helix orientation in the cyanobacterium Arthrospira. J Phycol 39 (2003) 360-367
49. Giovannoni S.J., Tripp H.J., Givan S., Podar M., Vergin K.L., Baptista D., Bibbs L., Eads J., Richardson T.H., Noordewier M., et al. Genome streamlining in a cosmopolitan oceanic bacterium. Science 309 (2005) 1242-1245