Evidence map›Paper›PMID 26272750›Full record

ArticleScientific reports2015

Artificial biofilms establish the role of matrix interactions in staphylococcal biofilm assembly and disassembly.

Elizabeth J Stewart, Mahesh Ganesan, John G Younger, Michael J Solomon

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. PslG-Mediated Disruption ofInternational journal of molecular sciences · 2026
    Article
  2. Temperature-dependent reprogramming of virulence traits duringbioRxiv : the preprint server for biology · 2026
    Article
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  10. The structural role of bacterial eDNA in the formation of biofilm streamers.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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  12. Review
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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

4 authors.

Elizabeth J StewartDepartment of Chemical Engineering, University of Michigan, 3074 H.H. Dow, 2300 Hayward Street, Ann Arbor, MI 48109.
Mahesh GanesanDepartment of Chemical Engineering, University of Michigan, 3074 H.H. Dow, 2300 Hayward Street, Ann Arbor, MI 48109.
John G YoungerDepartment of Emergency Medicine, University of Michigan, North Campus Research Complex, 2800 Plymouth Road, Ann Arbor, MI 48109.
Michael J SolomonDepartment of Chemical Engineering, University of Michigan, 3074 H.H. Dow, 2300 Hayward Street, Ann Arbor, MI 48109.

Funding

Biomechanics of Blood Stream InfectionsR01GM081702 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SOLOMON, MICHAEL J · 2009 to 2017
$3.2M
Complement C5A in Human SepsisR01GM069438 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YOUNGER, JOHN G · 2004 to 2014
$3.2M
NIGMS NIH HHS GM-069438NIGMS NIH HHS GM-081702NIGMS NIH HHS R01 GM069438NIGMS NIH HHS R01 GM081702
6 · The paper itself

Abstract

We demonstrate that the microstructural and mechanical properties of bacterial biofilms can be created through colloidal self-assembly of cells and polymers, and thereby link the complex material properties of biofilms to well understood colloidal and polymeric behaviors. This finding is applied to soften and disassemble staphylococcal biofilms through pH changes. Bacterial biofilms are viscoelastic, structured communities of cells encapsulated in an extracellular polymeric substance (EPS) comprised of polysaccharides, proteins, and DNA. Although the identity and abundance of EPS macromolecules are known, how these matrix materials interact with themselves and bacterial cells to generate biofilm morphology and mechanics is not understood. Here, we find that the colloidal self-assembly of Staphylococcus epidermidis RP62A cells and polysaccharides into viscoelastic biofilms is driven by thermodynamic phase instability of EPS. pH conditions that induce phase instability of chitosan produce artificial S. epidermidis biofilms whose mechanics match natural S. epidermidis biofilms. Furthermore, pH-induced solubilization of the matrix triggers disassembly in both artificial and natural S. epidermidis biofilms. This pH-induced disassembly occurs in biofilms formed by five additional staphylococcal strains, including three clinical isolates. Our findings suggest that colloidal self-assembly of cells and matrix polymers produces biofilm viscoelasticity and that biofilm control strategies can exploit this mechanism.

Indexed as

BiofilmsBiomimetic MaterialsCell MovementElastic ModulusExtracellular MatrixHydrogen-Ion ConcentrationPolysaccharides, BacterialStaphylococcus epidermidisViscosityPolysaccharides, Bacterial

Identifiers

PMID26272750
PMCPMC4536489

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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.