Evidence map›Paper›PMID 25360550›Full record

ArticlePloS one2014

Characterisation of pellicles formed by Acinetobacter baumannii at the air-liquid interface.

Yassine Nait Chabane, Sara Marti, Christophe Rihouey, Stéphane Alexandre, Julie Hardouin, Olivier Lesouhaitier, Jordi Vila, Jeffrey B Kaplan, Thierry Jouenne, Emmanuelle Dé

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed.

  1. Diversification of biofilm architecture among freshwaterApplied and environmental microbiology · 2026
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  7. Signaling inComputational and structural biotechnology journal · 2025
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  9. Morphogenesis and mechanical properties ofCurrent research in microbial sciences · 2025
    Article
  10. Article
  11. Pathogens (Basel, Switzerland) · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Frontiers in microbiology · 2023
    Review
  17. Article
  18. Frontiers in cellular and infection microbiology · 2022
    Review
  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

10 authors.

Yassine Nait ChabaneUnité Mixte de Recherche 6270 CNRS - Laboratory "Polymères, Biopolymères, Surfaces", University of Rouen, Mont-Saint-Aignan, France.
Sara MartiUnité Mixte de Recherche 6270 CNRS - Laboratory "Polymères, Biopolymères, Surfaces", University of Rouen, Mont-Saint-Aignan, France.
Christophe RihoueyUnité Mixte de Recherche 6270 CNRS - Laboratory "Polymères, Biopolymères, Surfaces", University of Rouen, Mont-Saint-Aignan, France.
Stéphane AlexandreUnité Mixte de Recherche 6270 CNRS - Laboratory "Polymères, Biopolymères, Surfaces", University of Rouen, Mont-Saint-Aignan, France.
Julie HardouinUnité Mixte de Recherche 6270 CNRS - Laboratory "Polymères, Biopolymères, Surfaces", University of Rouen, Mont-Saint-Aignan, France.
Olivier LesouhaitierLaboratory of "Microbiologie Signaux et Micro-Environnement" - Equipe d'Accueil 4312, University of Rouen, Evreux, France.
Jordi VilaDepartment of Microbiology, Hospital Clinic, Barcelona, Spain.
Jeffrey B KaplanDepartment of Biology, American University, Washington, District of Columbia, United States of America.
Thierry JouenneUnité Mixte de Recherche 6270 CNRS - Laboratory "Polymères, Biopolymères, Surfaces", University of Rouen, Mont-Saint-Aignan, France.
Emmanuelle DéUnité Mixte de Recherche 6270 CNRS - Laboratory "Polymères, Biopolymères, Surfaces", University of Rouen, Mont-Saint-Aignan, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical importance of Acinetobacter baumannii is partly due to its natural ability to survive in the hospital environment. This persistence may be explained by its capacity to form biofilms and, interestingly, A. baumannii can form pellicles at the air-liquid interface more readily than other less pathogenic Acinetobacter species. Pellicles from twenty-six strains were morphologically classified into three groups: I) egg-shaped (27%); II) ball-shaped (50%); and III) irregular pellicles (23%). One strain representative of each group was further analysed by Brewster's Angle Microscopy to follow pellicle development, demonstrating that their formation did not require anchoring to a solid surface. Total carbohydrate analysis of the matrix showed three main components: Glucose, GlcNAc and Kdo. Dispersin B, an enzyme that hydrolyzes poly-N-acetylglucosamine (PNAG) polysaccharide, inhibited A. baumannii pellicle formation, suggesting that this exopolysaccharide contributes to pellicle formation. Also associated with the pellicle matrix were three subunits of pili assembled by chaperon-usher systems: the major CsuA/B, A1S_1510 (presented 45% of identity with the main pilin F17-A from enterotoxigenic Escherichia coli pili) and A1S_2091. The presence of both PNAG polysaccharide and pili systems in matrix of pellicles might contribute to the virulence of this emerging pathogen.

Indexed as

AirAcinetobacter baumanniiBacterial ProteinsBiofilmsExtracellular MatrixHydrophobic and Hydrophilic InteractionsMicroscopyMonosaccharidesBacterial ProteinsMonosaccharides

Identifiers

PMID25360550
PMCPMC4216135

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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.