The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Microanatomy at Cellular Resolution and Spatial Order of Physiological Differentiation in a Bacterial Biofilm
Open accessAbstract
Bacterial biofilms are highly structured multicellular communities whose formation involves flagella and an extracellular matrix of adhesins, amyloid fibers, and exopolysaccharides. Flagella are produced by still-dividing rod-shaped Escherichia coli cells during postexponential growth when nutrients become suboptimal. Upon entry into stationary phase, however, cells stop producing flagella, become ovoid, and generate amyloid curli fibers. These morphological changes, as well as accompanying global changes in gene expression and cellular physiology, depend on the induction of the stationary-phase sigma subunit of RNA polymerase, σ S (RpoS), the nucleotide second messengers cyclic AMP (cAMP), ppGpp, and cyclic-di-GMP, and a biofilm-controlling transcription factor, CsgD. Using flagella, curli fibers, a CsgD::GFP reporter, and cell morphology as “anatomical” hallmarks in fluorescence and scanning electron microscopy, different physiological zones in macrocolony biofilms of E. coli K-12 can be distinguished at cellular resolution. Small ovoid cells encased in a network of curli fibers form the outer biofilm layer. Inner regions are characterized by heterogeneous CsgD::GFP and curli expression. The bottom zone of the macrocolonies features elongated dividing cells and a tight mesh of entangled flagella, the formation of which requires flagellar motor function. Also, the cells in the outer-rim growth zone produce flagella, which wrap around and tether cells together. Adjacent to this growth zone, small chains and patches of shorter curli-surrounded cells appear side by side with flagellated curli-free cells before curli coverage finally becomes confluent, with essentially all cells in the surface layer being encased in “curli baskets.” IMPORTANCE Heterogeneity or cellular differentiation in biofilms is a commonly accepted concept, but direct evidence at the microscale has been difficult to obtain. Our study reveals the microanatomy and microphysiology of an Escherichia coli macrocolony biofilm at an unprecedented cellular resolution, with physiologically different zones and strata forming as a function of known global regulatory networks that respond to biofilm-intrinsic gradients of nutrient supply. In addition, this study identifies zones of heterogeneous and potentially bistable CsgD and curli expression, shows bacterial curli networks to strikingly resemble Alzheimer plaques, and suggests a new role of flagella as an architectural element in biofilms.
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Cites
Fruiting body formation by Bacillus subtilis
Branda, S. S., González-Pastor, J. E., Ben-Yehuda, S., Losick, R., & Kolter, R. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191384198 · Cited by 1,129
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Innate and Induced Resistance Mechanisms of Bacterial Biofilms
Anderson, G. G., & O'Toole, G. A. (2008) · Current Topics in Microbiology and Immunology · doi:10.1007/978-3-540-75418-3_5 · Cited by 438
Diversity, biogenesis and function of microbial amyloids
Blanco, L. P., Evans, M. L., Smith, D. R., Badtke, M. P., & Chapman, M. R. (2012) · Trends in Microbiology · doi:10.1016/j.tim.2011.11.005 · Cited by 320
Mechanism of amyloid plaque formation suggests an intracellular basis of Aβ pathogenicity
Friedrich, R. P., Tepper, K., Rönicke, R., Soom, M., Westermann, M., Reymann, K., Kaether, C., & Fändrich, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904532106 · Cited by 303
Global Transcriptional Programs Reveal a Carbon Source Foraging Strategy by Escherichia coli
Liu, M., Durfee, T., Cabrera, J. E., Zhao, K., Jin, D. J., & Blattner, F. R. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m414050200 · Cited by 209
A short-time scale colloidal system reveals early bacterial adhesion dynamics
Beloin, C., Houry, A., Froment, M., Ghigo, J.-M., & Henry, N. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060167 · Cited by 58
Cited by
Cyclic di-GMP: second messenger extraordinaire
Jenal, U., Reinders, A., & Lori, C. (2017) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.190 · Cited by 1,039
Hobley, L., Harkins, C., MacPhee, C. E., & Stanley-Wall, N. R. (2015) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuv015 · Cited by 581
“Mutation of either fliC or motA (the flagellar filament protein and one of the motor proteins) rendered E. coli unable to make a fully ringed patterned colony (Serra et al. 2013b).”
BackgroundMethodResultInfluentialBiofilm-associated persistence of food-borne pathogens
Bridier, A., Sanchez-Vizuete, P., Guilbaud, M., Piard, J.-C., Naïtali, M., & Briandet, R. (2015) · Food Microbiology · doi:10.1016/j.fm.2014.04.015 · Cited by 507
The dental plaque biofilm matrix
Jakubovics, N. S., Goodman, S. D., Mashburn‐Warren, L., Stafford, G. P., & Cieplik, F. (2021) · Periodontology 2000 · doi:10.1111/prd.12361 · Cited by 488
Cellulose as an Architectural Element in Spatially Structured Escherichia coli Biofilms
Serra, D. O., Richter, A. M., & Hengge, R. (2013) · Journal of Bacteriology · doi:10.1128/jb.00946-13 · Cited by 379
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Metadata
- Authors
- Serra, D. O., Richter, A. M., Klauck, G., Mika, F., & Hengge, R.
- Venue
- mBio
- Publisher
- American Society for Microbiology
- Published
- 2013-05
- Volume
- 4
- Issue
- 2
- Pages
- e00103-13
- ISSN
- 2150-7511 (ISSN-L)
- 2161-2129
- OpenAlex
- W2006823831
- Cited by
- 355
- References
- 7
- FWCI
- 13.72
- Type
- journal article
- Language
- en
- Open access
- gold
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