Evidence map›Paper›PMID 17277217›Full record

ArticleApplied and environmental microbiology2007

Erosion from Staphylococcus aureus biofilms grown under physiologically relevant fluid shear forces yields bacterial cells with reduced avidity to collagen.

Patrick Ymele-Leki, Julia M Ross

Open access · greenAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 58 citations in OpenAlex.

  1. A Predictive Computational Framework forPathogens (Basel, Switzerland) · 2026
    Article
  2. Simulation and Modeling of the Adhesion ofPathogens (Basel, Switzerland) · 2024
    Article
  3. Review
  4. Polymicrobial Biofilm Organization ofInternational journal of molecular sciences · 2022
    Article
  5. Article
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  7. Review
  8. Article
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  11. Article
  12. Article
  13. Bacterial fight-and-flight responses enhance virulence in a polymicrobial infection.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  14. Article
  15. Biofilms' role in planktonic cell proliferation.International journal of molecular sciences · 2013
    Article
  16. Article
  17. Article
  18. Article
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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

2 authors at 1 institution in 1 country.

Patrick Ymele-LekiDepartment of Chemical and Biochemical Engineering, University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA.
Julia M Ross
University of Maryland, Baltimore County · US

Funding

Characterizing the Phenotype of Staphylococcal BiofilmsR01AI059369 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI ROSS, JULIA M · 2005 to 2008
$1.4M
NIAID NIH HHS R01 AI059369
6 · The paper itself

Abstract

An estimated 65% of infective diseases are associated with the presence of bacterial biofilms. Biofilm-issued planktonic cells promote blood-borne, secondary sites of infection by the inoculation of the infected sites with bacteria from the intravascular space. To investigate the potential role of early detachment events in initiating secondary infections, we studied the phenotypic attributes of Staphylococcus aureus planktonic cells eroding from biofilms with respect to expression of the collagen adhesin, CNA. The collagen-binding abilities of S. aureus have been correlated to the development of osteomyelitis and septic arthritis. In this study, we focused on the impact of CNA expression on S. aureus adhesion to immobilized collagen in vitro under physiologically relevant shear forces. In contrast to the growth phase-dependent adhesion properties characteristic of S. aureus cells grown in suspension, eroding planktonic cells expressed invariant and lower effective adhesion rates regardless of the age of the biofilm from which they originated. These results correlated directly with the surface expression level of CNA. However, subsequent analysis revealed no qualitative differences between biofilms initiated with suspension cells and secondary biofilms initiated with biofilm-shed planktonic cells. Taken together, our findings suggest that, despite their low levels of CNA expression, S. aureus planktonic cells shed from biofilms retain the capacity for metastatic spread and the initiation of secondary infection. These findings demonstrate the need for a better understanding of the phenotypic properties of eroding planktonic cells, which could lead to new therapeutic strategies to target secondary infections.

Indexed as

Bacterial AdhesionBiofilmsAdhesins, BacterialCollagenFlow CytometryStaphylococcus aureusAdhesins, Bacterialadhesin, Staphylococcus aureusCollagen

Identifiers

PMID17277217
PMCPMC1828840
OpenAlexW2006709588

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.