Evidence map›Paper›PMID 23798445›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Self-organization of bacterial biofilms is facilitated by extracellular DNA.

Erin S Gloag, Lynne Turnbull, Alan Huang, Pascal Vallotton, Huabin Wang, Laura M Nolan, Lisa Mililli, Cameron Hunt, Jing Lu, Sarah R Osvath and 7 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed
12.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

130 citing papers in PubMed, 285 citations in OpenAlex.

  1. Imaging nucleic acids in biofilms.Essays in biochemistry · 2026
    Review
  2. Intercalated bacterial biofilms are intrinsic internal components of calcium-based kidney stones.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Single-cell lysis patterns morphogenesis of eDNA in the matrix ofProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. The Effects ofMicroorganisms · 2025
    Article
  8. Article
  9. Carbapenem-ResistantAntibiotics (Basel, Switzerland) · 2025
    Review
  10. Article
  11. Article
  12. Biofilm formation byProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Review
  14. Antibiotics (Basel, Switzerland) · 2024
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

70 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

Erin S GloagThe ithree institute, University of Technology Sydney, Ultimo, NSW 2007, Australia.
Lynne Turnbull
Alan Huang
Pascal Vallotton
Huabin Wang
Laura M Nolan
Lisa Mililli
Cameron Hunt
Jing Lu
Sarah R Osvath
Leigh G Monahan
Rosalia Cavaliere
Ian G Charles
Matt P Wand
Michelle L Gee
Ranganathan Prabhakar
Cynthia B Whitchurch
Monash University · AUUniversity of Melbourne · AUUniversity of Technology Sydney · AUHealth Sciences and Nutrition · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Twitching motility-mediated biofilm expansion is a complex, multicellular behavior that enables the active colonization of surfaces by many species of bacteria. In this study we have explored the emergence of intricate network patterns of interconnected trails that form in actively expanding biofilms of Pseudomonas aeruginosa. We have used high-resolution, phase-contrast time-lapse microscopy and developed sophisticated computer vision algorithms to track and analyze individual cell movements during expansion of P. aeruginosa biofilms. We have also used atomic force microscopy to examine the topography of the substrate underneath the expanding biofilm. Our analyses reveal that at the leading edge of the biofilm, highly coherent groups of bacteria migrate across the surface of the semisolid media and in doing so create furrows along which following cells preferentially migrate. This leads to the emergence of a network of trails that guide mass transit toward the leading edges of the biofilm. We have also determined that extracellular DNA (eDNA) facilitates efficient traffic flow throughout the furrow network by maintaining coherent cell alignments, thereby avoiding traffic jams and ensuring an efficient supply of cells to the migrating front. Our analyses reveal that eDNA also coordinates the movements of cells in the leading edge vanguard rafts and is required for the assembly of cells into the "bulldozer" aggregates that forge the interconnecting furrows. Our observations have revealed that large-scale self-organization of cells in actively expanding biofilms of P. aeruginosa occurs through construction of an intricate network of furrows that is facilitated by eDNA.

Indexed as

BiofilmsDNA, BacterialPseudomonas aeruginosaDNA, Bacterialcollective behaviorswarmingt4ptfptype IV pili

Identifiers

PMID23798445
PMCPMC3710876
OpenAlexW1976778204

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.