Evidence map›Paper›PMID 28039436›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Cell morphology drives spatial patterning in microbial communities.

William P J Smith, Yohan Davit, James M Osborne, Wook Kim, Kevin R Foster, Joe M Pitt-Francis

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
–field-weighted citation impact
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

89 citing papers in PubMed.

  1. Mesolens imaging in microbiology.Essays in biochemistry · 2026
    Review
  2. Article
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  4. Article
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  6. Article
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  9. Dissecting the physics of bacterial biofilms with agent-based simulations.Current opinion in solid state & materials science · 2025
    Article
  10. Article
  11. Review
  12. Spatial population dynamics of bacterial colonies with social antibiotic resistance.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. Multiplicity of type 6 secretion system toxins limits the evolution of resistance.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article

29 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

6 authors.

William P J SmithDepartment of Computer Science, University of Oxford, Oxford OX1 3QD, United Kingdom.
Yohan DavitInstitut de Mécanique des Fluides de Toulouse (IMFT), Université de Toulouse, Centre National de la Recherche Scientifique (CNRS), Institut National Polytechnique de Toulouse (INPT), Université Paul Sabatier (UPS), F-31400 Toulouse, France.
James M OsborneSchool of Mathematics and Statistics, University of Melbourne, VIC 3010, Australia.
Wook KimDepartment of Zoology, University of Oxford, Oxford OX1 3PS, United Kingdom.
Kevin R FosterDepartment of Zoology, University of Oxford, Oxford OX1 3PS, United Kingdom kevin.foster@zoo.ox.ac.uk joe.pitt-francis@cs.ox.ac.uk.ORCID 0000-0003-4687-6633
Joe M Pitt-FrancisDepartment of Computer Science, University of Oxford, Oxford OX1 3QD, United Kingdom; kevin.foster@zoo.ox.ac.uk joe.pitt-francis@cs.ox.ac.uk.

Funding

European Research Council 242670
6 · The paper itself

Abstract

The clearest phenotypic characteristic of microbial cells is their shape, but we do not understand how cell shape affects the dense communities, known as biofilms, where many microbes live. Here, we use individual-based modeling to systematically vary cell shape and study its impact in simulated communities. We compete cells with different cell morphologies under a range of conditions and ask how shape affects the patterning and evolutionary fitness of cells within a community. Our models predict that cell shape will strongly influence the fate of a cell lineage: we describe a mechanism through which coccal (round) cells rise to the upper surface of a community, leading to a strong spatial structuring that can be critical for fitness. We test our predictions experimentally using strains of Escherichia coli that grow at a similar rate but differ in cell shape due to single amino acid changes in the actin homolog MreB. As predicted by our model, cell types strongly sort by shape, with round cells at the top of the colony and rod cells dominating the basal surface and edges. Our work suggests that cell morphology has a strong impact within microbial communities and may offer new ways to engineer the structure of synthetic communities.

Indexed as

Microbial ConsortiaModels, BiologicalBioengineeringBiofilmsBiophysical PhenomenaComputer SimulationEscherichia coliEscherichia coli ProteinsMutationPhenotypeSynthetic BiologyEscherichia coli ProteinsMreB protein, E colibiofilmsbiophysicscell morphologyself-organizationsynthetic biology

Identifiers

PMID28039436
PMCPMC5255625

What OpenQuestion holds

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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.