Evidence map›Paper›PMID 39055904›Full record

ArticleNature physics2023

Biofilms as self-shaping growing nematics.

Japinder Nijjer, Changhao Li, Mrityunjay Kothari, Thomas Henzel, Qiuting Zhang, Jung-Shen B Tai, Shuang Zhou, Tal Cohen, Sulin Zhang, Jing Yan

Abstract read
In one paragraph

Article in Nature physics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Physical encounters impose a consistency-amount trade-off on bacterial group formation in marine environments.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Dissecting the physics of bacterial biofilms with agent-based simulations.Current opinion in solid state & materials science · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
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

10 authors.

Japinder NijjerDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA.
Changhao LiDepartment of Engineering Science and Mechanics, Pennsylvania State University, University Park, PA, USA.
Mrityunjay KothariDepartment of Civil and Environmental Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Thomas HenzelDepartment of Civil and Environmental Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Qiuting ZhangDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA.
Jung-Shen B TaiDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA.
Shuang ZhouDepartment of Physics, University of Massachusetts Amherst, Amherst, MA, USA.
Tal CohenDepartment of Civil and Environmental Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Sulin ZhangDepartment of Engineering Science and Mechanics, Pennsylvania State University, University Park, PA, USA.
Jing YanDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA.

Funding

Tracking single-cell gene expression heterogeneity and its consequences in bacterial biofilmsDP2GM146253 · NIGMS · YALE UNIVERSITY · PI YAN, JING · 2021 to 2024
$2.5M
NIGMS NIH HHS DP2 GM146253
6 · The paper itself

Abstract

Active nematics are the nonequilibrium analogue of passive liquid crystals. They consist of anisotropic units that consume free energy to drive emergent behaviour. Like liquid crystal molecules in displays, ordering and dynamics in active nematics are sensitive to boundary conditions. However, unlike passive liquid crystals, active nematics have the potential to regulate their boundaries through self-generated stresses. Here, we show how a three-dimensional, living nematic can actively shape itself and its boundary to regulate its internal architecture through growth-induced stresses, using bacterial biofilms confined by a hydrogel as a model system. We show that biofilms exhibit a sharp transition in shape from domes to lenses upon changing environmental stiffness or cell-substrate friction, which is explained by a theoretical model that considers the competition between confinement and interfacial forces. The growth mode defines the progression of the boundary, which in turn determines the trajectories and spatial distribution of cell lineages. We further demonstrate that the evolving boundary and corresponding stress anisotropy define the orientational ordering of cells and the emergence of topological defects in the biofilm interior. Our findings may provide strategies for the development of programmed microbial consortia with emergent material properties.

Identifiers

PMID39055904
PMCPMC11271743

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Registered trials

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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.