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.

  • Review Article
  • Published:

Should we stay or should we go: mechanisms and ecological consequences for biofilm dispersal

Key Points

  • The predominant mode of growth of most bacteria in natural and engineered environments is as a surface-associated community encased in an extracellular matrix, called a biofilm. When conditions within the biofilm become unfavourable, bacteria must be able to disperse to escape and colonize new habitats.

  • The dispersal response of bacterial biofilms is regulated through the production and perception of extracellular and intracellular signalling molecules and in response to environmental cues such as changes in nutrient concentrations. Such signals and cues are translated into changes in gene expression that induce effectors, such as enzymes and surfactants, which break down the biofilm matrix and prepare bacteria for planktonic growth.

  • In addition to releasing bacteria to colonize new sites, dispersal is associated with the formation of genetic variants that may be altered in traits which are important for colonization of and competition in new habitats.

  • The sessile (biofilm) and motile (dispersal) phases of bacterial growth have close analogies to the lifestyles of colonial and holometabolous eukaryotes, including the generation of variants in the dispersal propagules. Biofilms may therefore be useful experimental tools to further explore ecological and evolutionary theories surrounding organisms with sessile and motile life phases.

Abstract

In most environments, bacteria reside primarily in biofilms, which are social consortia of cells that are embedded in an extracellular matrix and undergo developmental programmes resulting in a predictable biofilm 'life cycle'. Recent research on many different bacterial species has now shown that the final stage in this life cycle includes the production and release of differentiated dispersal cells. The formation of these cells and their eventual dispersal is initiated through diverse and remarkably sophisticated mechanisms, suggesting that there are strong evolutionary pressures for dispersal from an otherwise largely sessile biofilm. The evolutionary aspect of biofilm dispersal is now being explored through the integration of molecular microbiology with eukaryotic ecological and evolutionary theory, which provides a broad conceptual framework for the diversity of specific mechanisms underlying biofilm dispersal. Here, we review recent progress in this emerging field and suggest that the merging of detailed molecular mechanisms with ecological theory will significantly advance our understanding of biofilm biology and ecology.

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: The complex structure of bacterial biofilms.
Figure 2: Active biofilm dispersal and variant formation.

Similar content being viewed by others

References

  1. Labbate, M. et al. Quorum sensing-controlled biofilm development in Serratia liquefaciens MG1. J. Bacteriol. 186, 692–698 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Morgan, R., Kohn, S., Hwang, S. H., Hassett, D. J. & Sauer, K. BdlA, a chemotaxis regulator essential for biofilm dispersion in Pseudomonas aeruginosa. J. Bacteriol. 188, 7335–7343 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Southey-Pillig, C. J., Davies, D. G. & Sauer, K. Characterization of temporal protein production in Pseudomonas aeruginosa biofilms. J. Bacteriol. 187, 8114–8126 (2005). This paper shows that differential protein production occurs in specific stages of biofilm development.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Tolker-Nielsen, T. et al. Development and dynamics of Pseudomonas sp. biofilms. J. Bacteriol. 182, 6482–6489 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Kjelleberg, S. & Givskov, M. in The Biofilm Mode of Life: Mechanisms and Adaptations (eds Kjelleberg, S. & Givskov, M.) 5–21 (Horizon Bioscience, 2007).

    Google Scholar 

  6. Flemming, H.-C. & Wingender, J. The biofilm matrix. Nature Rev. Microbiol. 8, 623–633 (2010).

    Article  CAS  Google Scholar 

  7. Monds, R. D. & O'Toole, G. A. The developmental model of microbial biofilms: ten years of a paradigm up for review. Trends Microbiol. 17, 73–87 (2009).

    Article  CAS  PubMed  Google Scholar 

  8. Barken, K. B. et al. Roles of type IV pili, flagellum-mediated motility and extracellular DNA in the formation of mature multicellular structures in Pseudomonas aeruginosa biofilms. Environ. Microbiol. 10, 2331–2343 (2008).

    Article  CAS  PubMed  Google Scholar 

  9. Hall-Stoodley, L., Costerton, J. W. & Stoodley, P. Bacterial biofilms: from the natural environment to infectious diseases. Nature Rev. Microbiol. 2, 95–108 (2004).

    Article  CAS  Google Scholar 

  10. Periasamy, S. & Kolenbrander, P. E. Aggregatibacter actinomycetemcomitans builds mutualistic biofilm communities with Fusobacterium nucleatum and Veillonella Species in saliva. Infect. Immun. 77, 3542–3551 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Kolenbrander, P. E., Palmer, R. J., Periasamy, S. & Jakubovics, N. S. Oral multispecies biofilm development and the key role of cell–cell distance. Nature Rev. Microbiol. 8, 471–480 (2010).

    Article  CAS  Google Scholar 

  12. Ross, P. et al. Regulation of cellulose synthesis in Acetobacter xylinum by cyclic diguanylic acid. Nature 325, 279–281 (1987).

    Article  CAS  PubMed  Google Scholar 

  13. Merighi, M. & Lory, S. in Pseudomonas Vol. 6 (eds Ramos, J. L. & Filloux, A.) 97–138 (Springer, the Netherlands, 2010).

    Book  Google Scholar 

  14. Webb, J. S. et al. Cell death in Pseudomonas aeruginosa biofilm development. J. Bacteriol. 185, 4585–4592 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Mai-Prochnow, A. et al. Biofilm development and cell death in the marine bacterium Pseudoalteromonas tunicata. Appl. Environ. Microbiol. 70, 3232–3238 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Rice, S. A. et al. The biofilm life cycle and virulence of Pseudomonas aeruginosa are dependent on a filamentous prophage. ISME J. 3, 271–282 (2009). This study demonstrates that biofilm development, cell death, stability of the biofilm and the formation of dispersal variants in P. aeruginosa are dependent on the presence of a prophage in the host genome.

    Article  CAS  PubMed  Google Scholar 

  17. Purevdorj-Gage, B., Costerton, W. J. & Stoodley, P. Phenotypic differentiation and seeding dispersal in non-mucoid and mucoid Pseudomonas aeruginosa biofilms. Microbiology 151, 1569–1576 (2005). These authors find that the biofilms of P. aeruginosa undergo active dispersal by means of a motile subpopulation within microcolonies, and that dispersal is dependent on quorum sensing.

    Article  CAS  PubMed  Google Scholar 

  18. Barraud, N. et al. Involvement of nitric oxide in biofilm dispersal of Pseudomonas aeruginosa. J. Bacteriol. 188, 7344–7353 (2006). This article shows that P. areuginosa biofilms produce low levels of NO, which acts as a signal to induce dispersal. This dispersal response is also associated with increased sensitivity to antimicrobials.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Rollet, C., Gal, L. & Guzzo, J. Biofilm-detached cells, a transition from a sessile to a planktonic phenotype: a comparative study of adhesion and physiological characteristics in Pseudomonas aeruginosa. FEMS Microbiol. Lett. 290, 135–142 (2009).

    Article  CAS  PubMed  Google Scholar 

  20. Gjermansen, M., Ragas, P., Sternberg, C., Molin, S. & Tolker-Nielsen, T. Characterization of starvation-induced dispersion in Pseudomonas putida biofilms. Environ. Microbiol. 7, 894–904 (2005). This investigation demonstrates that starvation-induced dispersal of P. putida is mediated via cleavage and release of the adhesin LapA, and that the starvation cue operates via the intracellular second messenger c-di-GMP.

    Article  CAS  PubMed  Google Scholar 

  21. Hunt, S. M., Werner, E. M., Huang, B., Hamilton, M. A. & Stewart, P. S. Hypothesis for the role of nutrient starvation in biofilm detachment. Appl. Environ. Microbiol. 70, 7418–7425 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Sauer, K. et al. Characterization of nutrient-induced dispersion in Pseudomonas aeruginosa PAO1 biofilm. J. Bacteriol. 186, 7312–7326 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Schleheck, D. et al. Pseudomonas aeruginosa PAO1 preferentially grows as aggregates in liquid batch cultures and disperses upon starvation. PLoS Biol. 4, e5513 (2009).

    Google Scholar 

  24. An, S., Wu, J. e. & Zhang, L.-H. Modulation of Pseudomonas aeruginosa biofilm dispersal by a cyclic-di-GMP phosphodiesterase with a putative hypoxia-sensing domain. Appl. Environ. Microbiol. 76, 8160–8173 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Thormann, K. M., Saville, R. M., Shukla, S. & Spormann, A. M. Induction of rapid detachment in Shewanella oneidensis MR-1 biofilms. J. Bacteriol. 187, 1014–1021 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Barraud, N. et al. Nitric oxide-mediated dispersal in single- and multi-species biofilms of clinically and industrially relevant microorganisms. Microb. Biotechnol. 2, 370–378 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Schlag, S., Nerz, C., Birkenstock, T. A., Altenberend, F. & Gotz, F. Inhibition of staphylococcal biofilm formation by nitrite. J. Bacteriol. 189, 7911–7919 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Kaplan, J. B. & Fine, D. H. Biofilm dispersal of Neisseria subflava and other phylogenetically diverse oral bacteria. Appl. Environ. Microbiol. 68, 4943–4950 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Musk, D. J., Banko, D. A. & Hergenrother, P. J. Iron salts perturb biofilm formation and disrupt existing biofilms of Pseudomonas aeruginosa. Chem. Biol. 12, 789–796 (2005).

    Article  CAS  PubMed  Google Scholar 

  30. Glick, R. et al. Increase in rhamnolipid synthesis under iron-limiting conditions influences surface motility and biofilm formation in Pseudomonas aeruginosa. J. Bacteriol. 192, 2973–2980 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Moreau-Marquis, S. et al. The ΔF508-CFTR mutation results in increased biofilm formation by Pseudomonas aeruginosa by increasing iron availability. Am. J. Physiol. Lung Cell. Mol. Physiol. 295, L25–L37 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Kaplan, J. B. Biofilm dispersal: mechanisms, clinical implications, and potential therapeutic uses. Crit. Rev. Oral Biol. Med. 89, 205–218 (2010).

    CAS  Google Scholar 

  33. Lauderdale, K. J., Malone, C. L., Boles, B. R., Morcuende, J. & Horswill, A. R. Biofilm dispersal of community-associated methicillin-resistant Staphylococcus aureus on orthopedic implant material. J. Orthop. Res. 28, 55–61 (2010).

    CAS  PubMed  Google Scholar 

  34. Rice, S. A. et al. Biofilm formation and sloughing in Serratia marcescens are controlled by quorum sensing and nutrient cues. J. Bacteriol. 187, 3477–3485 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Boles, B. R. & Horswill, A. R. agr-mediated dispersal of Staphylococcus aureus biofilms. PLoS Pathog. 4, e1000052 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Crossman, L. & Dow, J. M. Biofilm formation and dispersal in Xanthomonas campestris. Microbes Infect. 6, 623–629 (2004).

    Article  CAS  PubMed  Google Scholar 

  37. Davies, D. G. & Marques, C. N. H. A fatty acid messenger is responsible for inducing dispersion in microbial biofilms. J. Bacteriol. 191, 1393–1403 (2009).

    Article  CAS  PubMed  Google Scholar 

  38. Kolodkin-Gal, I. et al. D-amino acids trigger biofilm disassembly. Science 328, 627–629, (2010). This report describes the role of D -amino acids in triggering biofilm dispersal in B. subtilis and shows that the mode of action is via triggering detachment of amyloid fibres from the membrane. In addition, it shows that D -amino acids inhibit biofilm formation by P. aeruginosa and S. aureus.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Sawyer, L. K. & Hermanowicz, S. W. Detachment of Aeromonas hydrophila and Pseudomonas aeruginosa due to variations in nutrient supply. Water Sci. Technol. 41, 139–145 (2000).

    Article  CAS  Google Scholar 

  40. Delaquis, P. J., Caldwell, D. E., Lawrence, J. R. & Mccurdy, A. R. Detachment of Pseudomonas fluorescens from biofilms on glass surfaces in response to nutrient stress. Microb. Ecol. 18, 199–210 (1989).

    Article  CAS  PubMed  Google Scholar 

  41. Delille, A., Quiles, F. & Humbert, F. In situ monitoring of the nascent Pseudomonas fluorescens biofilm response to variations in the dissolved organic carbon level in low-nutrient water by attenuated total reflectance-fourier transform infrared spectroscopy. Appl. Environ. Microbiol. 73, 5782–5788 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Gjermansen, M., Nilsson, M., Yang, L. & Tolker-Nielsen, T. Characterization of starvation-induced dispersion in Pseudomonas putida biofilms: genetic elements and molecular mechanisms. Mol. Microbiol. 75, 815–826 (2010).

    Article  CAS  PubMed  Google Scholar 

  43. James, G. A., Korber, D. R., Caldwell, D. E. & Costerton, J. W. Digital image-analysis of growth and starvation responses of a surface-colonizing Acinetobacter sp. J. Bacteriol. 177, 907–915 (1995).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Kader, A., Simm, R., Gerstel, U., Morr, M. & Römling, U. Hierarchical involvement of various GGDEF domain proteins in rdar morphotype development of Salmonella enterica serovar Typhimurium. Mol. Microbiol. 60, 602–616 (2006).

    Article  CAS  PubMed  Google Scholar 

  45. Merritt, J. H. et al. Specific control of Pseudomonas aeruginosa surface-associated behaviors by two c-di-GMP diguanylate cyclases. mBio 1, e00183-10 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Paul, R. et al. Cell cycle-dependent dynamic localization of a bacterial response regulator with a novel di-guanylate cyclase output domain. Genes Dev. 18, 715–727 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Barraud, N. et al. Nitric oxide signaling in Pseudomonas aeruginosa biofilms mediates phosphodiesterase activity, decreased cyclic di-GMP levels, and enhanced dispersal. J. Bacteriol. 191, 7333–7342 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Carlson, H. K., Vance, R. E. & Marletta, M. A. H-NOX regulation of c-di-GMP metabolism and biofilm formation in Legionella pneumophila. Mol. Microbiol. 77, 930–942 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  49. Schmidt, I., Steenbakkers, P. J. M., op den Camp, H. J. M., Schmidt, K. & Jetten, M. S. M. Physiologic and proteomic evidence for a role of nitric oxide in biofilm formation by Nitrosomonas europaea and other ammonia oxidizers. J. Bacteriol. 186, 2781–2788 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Potter, A. J. et al. Thioredoxin reductase is essential for protection of Neisseria gonorrhoeae against killing by nitric oxide and for bacterial growth during interaction with cervical epithelial cells. J. Infect. Dis. 199, 227–235 (2009).

    Article  CAS  PubMed  Google Scholar 

  51. Delgado-Nixon, V. M., Gonzalez, G. & Gilles-Gonzalez, M. A. Dos, a heme-binding PAS protein from Escherichia coli, is a direct oxygen sensor. Biochemistry 39, 2685–2691 (2000).

    Article  CAS  PubMed  Google Scholar 

  52. Alexandre, G. Coupling metabolism and chemotaxis-dependent behaviours by energy taxis receptors. Microbiology 156, 2283–2293 (2010).

    Article  CAS  PubMed  Google Scholar 

  53. Giba, Z., Grubišić, D. & Konjević, R. in Nitric Oxide in Plant Growth, Development and Stress Physiology (Plant Cell Monographs) Vol. 5 (eds Lamattina, L. & Polacco, J.) 91–111 (Springer, Berlin, 2007).

    Book  Google Scholar 

  54. Kumar, A., Toledo, J. C., Patel, R. P., Lancaster, J. R. Jr & Steyn, A. J. Mycobacterium tuberculosis DosS is a redox sensor and DosT is a hypoxia sensor. Proc. Natl Acad. Sci. USA 104, 11568–11573 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Bishop, C. D. & Brandhorst, B. P. On nitric oxide signaling, metamorphosis, and the evolution of biphasic life cycles. Evol. Dev. 5, 542–550 (2003).

    Article  CAS  PubMed  Google Scholar 

  56. Davies, D. G. et al. The involvement of cell-to-cell signals in the development of a bacterial biofilm. Science 280, 295–298 (1998). The authors report that quorum sensing signalling is involved in the development of P. aeruginosa biofilms and that biofilms formed by quorum sensing mutants are less stable than those formed by wild-type cells.

    Article  CAS  PubMed  Google Scholar 

  57. Abee, T., Kovasc, A. T., Kuipers, O. P. & van der Veen, S. Biofilm formation and dispersal in Gram-positivie bacteria. Curr. Opin. Biotechnol. 22, 172–179 (2011).

    Article  CAS  PubMed  Google Scholar 

  58. Yarwood, J. M., Bartels, D. J., Volper, E. M. & Greenberg, E. P. Quorum sensing in Staphylococcus aureus biofilms. J. Bacteriol. 186, 1838–1850 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  59. Giacometti, A. et al. RNA III inhibiting peptide inhibits in vivo biofilm formation by drug-resistant Staphylococcus aureus. Antimicrob. Agents Chemother. 47, 1979–1983 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Orent, W. Slime city: where germs talk to each other and execute precise attacks. Discover (17 Jul 2009).

    Google Scholar 

  61. Hammer, B. K. & Bassler, B. L. Quorum sensing controls biofilm formation in Vibrio cholerae. Mol. Microbiol. 50, 101–104 (2003).

    Article  CAS  PubMed  Google Scholar 

  62. Puskas, A., Greenberg, E. P., Kaplan, S. & Schaefer, A. L. A quorum-sensing system in the free-living photosynthetic bacterium Rhodobacter sphaeroides. J. Bacteriol. 179, 7530–7537 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Boles, B. R., Thoendel, M. & Singh, P. K. Rhamnolipids mediate detachment of Pseudomonas aeruginosa from biofilms. Mol. Microbiol. 57, 1210–1223 (2005).

    Article  CAS  PubMed  Google Scholar 

  64. Jobling, M. G. & Holmes, R. K. Characterization of hapR, a positive regulator of the Vibrio cholerae HA/protease gene hap, and its identification as a functional homologue of the Vibrio harveyi luxR gene. Mol. Microbiol. 26, 1023–1034 (1997).

    Article  CAS  PubMed  Google Scholar 

  65. Dow, J. M. et al. Biofilm dispersal in Xanthomonas campestris is controlled by cell–cell signaling and is required for full virulence to plants. Proc. Natl Acad. Sci. USA 100, 10995–11000 (2003). DSF (later chemically determined to be cis -11-methyl-2-dodecenoic acid) is shown to be important for dispersing aggregates of the plant pathogen X. campestris . Additional DSF-like compounds that regulate dispersal in other bacteria have subsequently been identified.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  66. Ryan, R. P. et al. Cell-cell signaling in Xanthomonas campestris involves an HD-GYP domain protein that functions in cyclic di-GMP turnover. Proc. Natl Acad. Sci. USA 103, 6712–6717 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Tao, F., He, Y.-W., Wu, D.-H., Swarup, S. & Zhang, L.-H. The cyclic nucleotide monophosphate domain of Xanthomonas campestris global regulator Clp defines a new class of cyclic di-GMP effectors. J. Bacteriol. 192, 1020–1029 (2010).

    Article  CAS  PubMed  Google Scholar 

  68. Deng, Y., Wu, J. Ä., Tao, F. & Zhang, L.-H. Listening to a new language: DSF-based quorum sensing in Gram-negative bacteria. Chem. Rev. 111, 160–173 (2011).

    Article  CAS  PubMed  Google Scholar 

  69. Huynh, T. T. Carbon starvation induced dispersal of Pseudomonas aeruginosa biofilms. Thesis, Univ. New South Wales (2011).

    Google Scholar 

  70. Lam, H. et al. D-amino acids govern stationary phase cell wall remodeling in bacteria. Science 325, 1552–1555 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  71. Ortzen, D. & Nielsen, P. H. We find them here, we find them there: functional bacterial amyloid. Cell. Mol. Life Sci. 65, 910–927 (2008).

    Article  CAS  Google Scholar 

  72. Karatan, E. & Watnick, P. Signals, regulatory networks, and materials that build and break bacterial biofilms. Microbiol. Mol. Biol. Rev. 73, 310–347 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  73. Allison, D. G., Ruiz, B., SanJose, C., Jaspe, A. & Gilbert, P. Extracellular products as mediators of the formation and detachment of Pseudomonas fluorescens biofilm. FEMS Microbiol. Lett. 167, 179–184 (1998).

    Article  CAS  PubMed  Google Scholar 

  74. Baty, A. M. I., Eastburn, C. C., Techkarnjanaruk, S., Goodman, A. E. & Geesey, G. G. Spatial and temporal variations in chitinolytic gene expression and bacterial biomass production during chitin degradation. Appl. Environ. Microbiol. 66, 3574–3585 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  75. Mann, E. E. et al. Modulation of eDNA release and degradation affects Staphylococcus aureus biofilm maturation. PLoS ONE 4, e5822 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  76. Manuel, S. G. A. Role of active-site residues of dispersin B, a biofilm-releasing β-hexosaminidase from a periodontal pathogen, in substrate hydrolysis. FEBS J. 274, 5987–5999 (2007).

    Article  CAS  PubMed  Google Scholar 

  77. Kaplan, J. B., Meyenhofer, M. F. & Fine, D. H. Biofilm growth and detachment of Actinobacillus actinomycetemcomitans. J. Bacteriol. 185, 1399–1404 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  78. Kaplan, J. B., Ragunath, C., Velliyagounder, K., Fine, D. H. & Ramasubbu, N. Enzymatic detachment of Staphylococcus epidermidis biofilms. Antimicrob. Agents Chemother. 48, 2633–2636 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  79. Chaignon, P. et al. Susceptibility of staphylococcal biofilms to enzymatic treatments depends on their chemical composition. Appl. Microbiol. Biotechnol. 75, 125–132 (2007).

    Article  CAS  PubMed  Google Scholar 

  80. Whitchurch, C. B., Tolker-Nielsen, T., Ragas, P. C. & Mattick, J. S. Extracellular DNA required for bacterial biofilm formation. Science 295, 1487 (2002). This paper describes the role of eDNA as a key component of the extracellular biofilm matrix and shows that enzymatic digestion of eDNA destabilizes P. aeruginosa biofilms.

    Article  CAS  PubMed  Google Scholar 

  81. Boyd, A. & Chakrabarty, A. M. Role of alginate lyase in cell detachment of Pseudomonas aeruginosa. Appl. Environ. Microbiol. 60, 2355–2359 (1994).

    CAS  PubMed  PubMed Central  Google Scholar 

  82. Schooling, S. R., Charaf, U. K., Allison, D. G. & Gilbert, P. A role for rhamnolipid in biofilm dispersion. Biofilms 1, 91–99 (2004).

    Article  Google Scholar 

  83. Kuiper, I. et al. Characterization of two Pseudomonas putida lipopeptide biosurfactants, putisolvin I and II, which inhibit biofilm formation and break down existing biofilms. Mol. Microbiol. 51, 97–113 (2004).

    Article  CAS  PubMed  Google Scholar 

  84. Paul, J. H. Prophages in marine bacteria: dangerous molecular time bombs or the key to survival in the seas? ISME J. 2, 579–589 (2008).

    Article  CAS  PubMed  Google Scholar 

  85. Garcia-Contreras, R., Zhang, X.-S., Kim, Y. & Wood, T. K. Protein translation and cell death: the role of rare tRNAs in biofilm formation and in activating dormant phage killer genes. PLoS ONE 3, e2394 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  86. Sillankorva, S., Neubauer, P. & Azeredo, J. Phage control of dual species biofilms of Pseudomonas fluorescens and Staphylococcus lentus. Biofouling 26, 567–575 (2010).

    Article  PubMed  Google Scholar 

  87. Whiteley, M. et al. Gene expression in Pseudomonas aeruginosa biofilms. Nature 413, 860–864 (2001).

    Article  CAS  PubMed  Google Scholar 

  88. Kirov, S. M. et al. Biofilm differentiation and dispersal in mucoid Pseudomonas aeruginosa isolates from patients with cystic fibrosis. Microbiology 153, 3264–3274 (2007).

    Article  CAS  PubMed  Google Scholar 

  89. Zegans, M. E. et al. Interaction between bacteriophage DMS3 and host CRISPR region inhibits group behaviors of Pseudomonas aeruginosa. J. Bacteriol. 191, 210–219 (2009).

    Article  CAS  PubMed  Google Scholar 

  90. Hughes, K. A., Sutherland, I. W. & Jones, M. V. Biofilm susceptibility to bacteriophage attack: the role of phage-borne polysaccharide depolymerase. Microbiology 144, 3039–3047 (1998).

    Article  CAS  PubMed  Google Scholar 

  91. Hughes, K. A., Sutherland, I. W., Clark, J. & Jones, M. V. Bacteriophage and associated polysaccharide depolymerases: novel tools for study of bacterial biofilms. J. Appl. Microbiol. 85, 583–590 (1998).

    Article  CAS  PubMed  Google Scholar 

  92. Lu, T. K. & Collins, J. J. Dispersing biofilms with engineered enzymatic bacteriophage. Proc. Natl Acad. Sci. USA 104, 11197–11202 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  93. Mitchell, H. L. et al. Treponema denticola biofilm-induced expression of a bacteriophage, toxin–antitoxin systems and transposases. Microbiology 156, 774–788 (2010).

    Article  CAS  PubMed  Google Scholar 

  94. Bowler, D. E. & Benton, T. G. Causes and consequences of animal dispersal strategies: relating individual behaviour to spatial dynamics. Biol. Rev. 80, 205–225 (2005).

    Article  PubMed  Google Scholar 

  95. Ronce, O. How does it feel to be a rolling stone? Ten questions about dispersal evolution. Annu. Rev. Ecol. Evol. Sys. 38, 231–253 (2007). This and reference 94 review some of the key ecological and evolutionary issues in the field of dispersal, with reference 95 in particular being accessible for workers outside the field.

    Article  Google Scholar 

  96. Clobert, J., Le Galliard, J.-F., Cote, J., Meylan, S. & Massot, M. Informed dispersal, heterogeneity in animal dispersal syndromes and the dynamics of spatially structured populations. Ecol. Lett. 12, 197–209 (2009).

    Article  PubMed  Google Scholar 

  97. Rosenberg, E., Kaplan, N., Pines, O., Rosenberg, M. & Gutnick, D. Capsular polysaccharides interfere with adherence of Acinetobacter calcoaceticus to hydrocarbon. FEMS Microbiol. Lett. 17, 157–160 (1983).

    Article  CAS  Google Scholar 

  98. Hentzer, M., Eberl, L. & Givskov, M. Transcriptome analysis of Pseudomonas aeruginosa biofilm development: anaerobic respiration and iron limitation. Biofilms 2, 37–61 (2005).

    Article  Google Scholar 

  99. Ito, A., May, T., Kawata, K. & Okabe, S. Significance of rpoS during maturation of Escherichia coli biofilms. Biotechnol. Bioeng. 99, 1462–1471 (2008).

    Article  CAS  PubMed  Google Scholar 

  100. Banin, E., Brady, K. M. & Greenberg, E. P. Chelator-induced dispersal and killing of Pseudomonas aeruginosa cells in a biofilm. Appl. Environ. Microbiol. 72, 2064–2069 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  101. Rowe, M. C., Withers, H. L. & Swift, S. Uropathogenic Escherichia coli forms biofilm aggregates under iron restriction that disperse upon the supply of iron. FEMS Microbiol. Lett. 307, 102–109 (2010).

    Article  CAS  PubMed  Google Scholar 

  102. Matz, C. & Kjelleberg, S. Off the hook – how bacteria survive protozoan grazing. Trends Microbiol. 13, 302–307 (2005).

    Article  CAS  PubMed  Google Scholar 

  103. Hausner, M. & Wuertz, S. High rates of conjugation in bacterial biofilms as determined by quantitative in situ analysis. Appl. Environ. Microbiol. 65, 3710–3713 (1999).

    CAS  PubMed  PubMed Central  Google Scholar 

  104. Marshall, D. J. & Keough, M. J. The evolutionary ecology of offspring size in marine invertebrates. Adv. Mar. Biol. 53, 1–60 (2007).

    Article  PubMed  Google Scholar 

  105. Strathmann, R. R. Feeding and nonfeeding larval development and life-history evolution in marine invertebrates. Annu. Rev. Ecol. Sys. 16, 339–361 (1985).

    Article  Google Scholar 

  106. Sanchez-Contreras, M. et al. Phenotypic selection and phase variation occur during alfalfa root colonization by Pseudomonas fluorescens F113. J. Bacteriol. 184, 1587–1596 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  107. Webb, J. S., Lau, M. & Kjelleberg, S. Bacteriophage and phenotypic variation in Pseudomonas aeruginosa biofilm development. J. Bacteriol. 186, 8066–8073 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  108. Koh, K. S. et al. Phenotypic diversification and adaptation of Serratia marcescens MG1 biofilm derived morphotypes. J. Bacteriol. 189, 119–130 (2007). This work uncovers the temporally regulated production of morphotypic variants during biofilm development in S. marcescens , and shows that such variants are phentoypically distinct from wild-type cells and also differ in biofilm development.

    Article  CAS  PubMed  Google Scholar 

  109. Koh, K. S. et al. Minimal genetic diversity enhances predation resistance. Mol. Ecol. (in the press).

  110. Benach, J. et al. The structural basis of cyclic diguanylate signal transduction by PilZ domains. EMBO J. 26, 5153–5166 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  111. Christen, M. et al. DgrA is a member of a new family of cyclic diguanosine monophosphate receptors and controls flagellar motor function in Caulobacter crescentus. Proc. Natl Acad. Sci, USA 104, 4112–4117 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  112. Hickman, J. W. & Harwood, C. S. Identification of FleQ from Pseudomonas aeruginosa as a c-di-GMP-responsive transcription factor. Mol. Microbiol. 69, 376–389 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  113. Lee, V. T. et al. A cyclic-di-GMP receptor required for bacterial exopolysaccharide production. Mol. Microbiol. 65, 1474–1484 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  114. Ma, Q., Yang, Z., Pu, M., Peti, W. & Wood, T. K. Engineering a novel c-di-GMP-binding protein for biofilm dispersal. Environ. Microbiol. 13, 631–642 (2011).

    Article  CAS  PubMed  Google Scholar 

  115. Landini, P., Antoniani, D., Burgess, J. & Nijland, R. Molecular mechanisms of compounds affecting bacterial biofilm formation and dispersal. Appl. Microbiol. Biotechnol. 86, 813–823 (2010).

    Article  CAS  PubMed  Google Scholar 

  116. Izano, E. A., Amarante, M. A., Kher, W. B. & Kaplan, J. B. Differential roles of poly-N-acetylglucosamine surface polysaccharide and extracellular DNA in Staphylococcus aureus and Staphylococcus epidermidis biofilms. Appl. Environ. Microbiol. 74, 470–476 (2008).

    Article  CAS  PubMed  Google Scholar 

  117. Elton, C. S. The Ecology of Invasions by Animals and Plants (The University of Chicago Press, Chicago, 1950).

    Google Scholar 

  118. Thorson, G. Reproductive and larval ecology of marine bottom invertebrates. Biol. Rev. 25, 1–45 (1950).

    Article  CAS  PubMed  Google Scholar 

  119. Hughes, R. N. A Functional Biology of Clonal Animals (Chapman and Hall, New York, 1989).

    Google Scholar 

  120. Jackson, J. B. C., Buss, L. W. & Cook, R. E. Population Biology and Evolution of Clonal Organisms (Yale Univ. Press, New Haven, 1985). This and reference 119 provide a comprehensive overview of the biology of modular organisms.

    Google Scholar 

  121. Harrison, P. L. et al. Mass spawning in tropical reef corals. Science 223, 1186–1189 (1984).

    Article  CAS  PubMed  Google Scholar 

  122. Brusca, R. C. & Brusca, G. J. Invertebrates (Sinauer Assoc., Inc., Sunderland, Massachusetts, 2003).

    Google Scholar 

  123. McHugh, D. & Rouse, G. W. Life history evolution of marine invertebrates: new views from phylogenetic systematics. Trends Ecol. Evol., 13, 182–186 (1998).

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The authors acknowledge S. Longford for help with the figures and the Australian Research Council, Environmental Biotechnology Cooperative Research Centre and National Health and Medical Research Council for ongoing and long term support of this research. This is publication number 0058 of the Sydney Institute of Marine Science, Australia.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Staffan Kjelleberg.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Related links

Related links

FURTHER INFORMATION

Centre for Marine bio-innovation, University of New South Wales

Singapore Centre for Environmental Life Sciences Engineering

Glossary

Dispersal

The movement of an individual organism away from the parent organism or population to a new niche.

Cell communication signals

Molecules that are produced and perceived by an organism. Signals are produced at a particular stage of growth under specific conditions or in response to changes in the environment. They accumulate extracellularly and are recognized by a dedicated receptor to induce a concerted response when a critical threshold has been reached. To be classed as cell communication, this response must extend beyond that which is required for metabolism or detoxification of the substance.

Second messenger

An intracellular molecule (usually small and rapidly diffusible) that transmits information from a receptor to a target molecule; for example, cyclic AMP and cyclic di-GMP.

Chemotaxis

The movement of cells or organisms according to chemical concentration gradients in the environment, either towards or away from the stimulus.

Nitric oxide

(NO). A small, reactive gas and a universal signalling molecule in biological systems (as initially discovered in the 1970s, for its role in regulating vasodilation in mammals). In bacteria, NO is generated as a by-product of anaerobic metabolism or by NO synthases (NOSs).

Autoinducing peptides

Extracellular peptides, ranging from 5 to 34 amino acids in length, that are generated by cleavage from precursor peptides and then further post-transcriptionally modified. These peptides are used by Gram-positive bacteria as cell communication signals.

Sensor regulator

A protein that receives and responds to information about changes in the environment, either by binding second messengers or through phosphorylation, to induce transcriptional changes.

Response regulator

The phosphorylation-dependent modulator of a two-component phosphorelay system. The partner sensor protein responds to environmental stimuli to modulate the phosphorylation status of the regulator, and the resultant phosphorylation cascade drives the response through differential expression of target genes.

Lysogenic

Pertaining to a bacteriophage genome: being incorporated into the chromosome of the host bacterium, resulting in transmission to daughter bacterial cells on cell division. Lysogenic phages are referred to as prophages.

Bet hedging

An evolutionary response to variable environments. In the context of dispersal, it is predicted to manifest in a number of ways, including the production of different types of dispersal cells to maximize colonization of different habitats, and spreading dispersal in time to accommodate temporally varying habitats.

Colonial

Of an organism: able to form replicate, more or less identical units ('modules') via asexual means; these units then often connect physically and physiologically to form a colony. Monospecies biofilms are colonial (or modular, or clonal) in this sense.

Holometabolous

Pertaining to an insect: with a life cycle in which there is a larval phase that is morphologically and ecologically distinct from the adult phase and which must undergo 'complete metamorphosis' via a pupal phase before becoming an adult. Examples include butterflies and true flies.

Rights and permissions

Reprints and permissions

About this article

Cite this article

McDougald, D., Rice, S., Barraud, N. et al. Should we stay or should we go: mechanisms and ecological consequences for biofilm dispersal. Nat Rev Microbiol 10, 39–50 (2012). https://doi.org/10.1038/nrmicro2695

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nrmicro2695

This article is cited by

Search

Quick links

Nature Briefing Microbiology

Sign up for the Nature Briefing: Microbiology newsletter — what matters in microbiology research, free to your inbox weekly.

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