Evidence map›Paper›PMID 25418293›Full record

ArticleBiophysical journal2014

Molecular determinants of mechanical properties of V. cholerae biofilms at the air-liquid interface.

Emily C Hollenbeck, Jiunn C N Fong, Ji Youn Lim, Fitnat H Yildiz, Gerald G Fuller, Lynette Cegelski

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2014. 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
4.3field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 68 citations in OpenAlex.

  1. Diversification of biofilm architecture among freshwaterApplied and environmental microbiology · 2026
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  3. Geometric ordering in bacterial communities.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  4. Article
  5. Article
  6. Antibacterial and Antibiofilm Activities of Bluestem (International journal of microbiology · 2026
    Article
  7. Thermodynamics of Surfactant-Enriched Binary-Fluid Systems.Langmuir : the ACS journal of surfaces and colloids · 2025
    Article
  8. Article
  9. Article
  10. Microstructural and Rheological Transitions in Bacterial Biofilms.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Biophysical methods to quantify bacterial behaviors at oil-water interfaces.Journal of industrial microbiology & biotechnology · 2020
    Review
  16. AnApplied and environmental microbiology · 2020
    Article
  17. Article
  18. Article
  19. Review
  20. 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

6 authors at 3 institutions in 1 country.

Emily C HollenbeckDepartment of Chemical Engineering, Stanford University, Stanford, California.
Jiunn C N FongDepartment of Microbiology and Environmental Toxicology, UC Santa Cruz, Santa Cruz, California.
Ji Youn LimDepartment of Chemistry, Stanford University, Stanford, California.
Fitnat H YildizDepartment of Microbiology and Environmental Toxicology, UC Santa Cruz, Santa Cruz, California.
Gerald G FullerDepartment of Chemical Engineering, Stanford University, Stanford, California.
Lynette CegelskiDepartment of Chemistry, Stanford University, Stanford, California. Electronic address: cegelski@stanford.edu.
Stanford University · USUniversity of California, Santa Cruz · USStanford Medicine · US

Funding

Smooth to Rugose phase variation in Vibrio choleraeR01AI055987 · NIAID · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI YILDIZ, HAVVA FITNAT · 2003 to 2019
$4.4M
Structure, Function, and Disruption of Microbial Amyloid Assembly and Biofilm ForDP2OD007488 · OD · STANFORD UNIVERSITY · PI CEGELSKI, LYNETTE S · 2010 to 2010
$2.4M
NIAID NIH HHS R01 AI055987NIAID NIH HHS R01AI055987NIH HHS DP2 OD007488NIH HHS DP2OD007488
6 · The paper itself

Abstract

Biofilm formation increases both the survival and infectivity of Vibrio cholerae, the causative agent of cholera. V. cholerae is capable of forming biofilms on solid surfaces and at the air-liquid interface, termed pellicles. Known components of the extracellular matrix include the matrix proteins Bap1, RbmA, and RbmC, an exopolysaccharide termed Vibrio polysaccharide, and DNA. In this work, we examined a rugose strain of V. cholerae and its mutants unable to produce matrix proteins by interfacial rheology to compare the evolution of pellicle elasticity in real time to understand the molecular basis of matrix protein contributions to pellicle integrity and elasticity. Together with electron micrographs, visual inspection, and contact angle measurements of the pellicles, we defined distinct contributions of the matrix proteins to pellicle morphology, microscale architecture, and mechanical properties. Furthermore, we discovered that Bap1 is uniquely required for the maintenance of the mechanical strength of the pellicle over time and contributes to the hydrophobicity of the pellicle. Thus, Bap1 presents an important matrix component to target in the prevention and dispersal of V. cholerae biofilms.

Indexed as

AirBiofilmsMechanical PhenomenaBacterial ProteinsBiomechanical PhenomenaElasticityHydrophobic and Hydrophilic InteractionsMicroscopy, ElectronRheologyVibrio choleraeBacterial Proteins

Identifiers

PMID25418293
PMCPMC4241461
OpenAlexW2050340502

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.