Evidence map›Paper›PMID 19273646›Full record

ArticleJournal of medical microbiology2009

Neutrophil enhancement of Pseudomonas aeruginosa biofilm development: human F-actin and DNA as targets for therapy.

Quinn M Parks, Robert L Young, Katie R Poch, Kenneth C Malcolm, Michael L Vasil, Jerry A Nick

Open access · greenAbstract read
In one paragraph

Article in Journal of medical microbiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.6field-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

55 citing papers in PubMed, 113 citations in OpenAlex.

  1. Article
  2. Review
  3. Bidirectional effects of neutrophils onJournal of oral microbiology · 2025
    Article
  4. What Is a Biofilm? Lessons Learned from Interactions with Immune Cells.International journal of molecular sciences · 2024
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Immunometabolism in biofilm infection: lessons from cancer.Molecular medicine (Cambridge, Mass.) · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. Immune Responses toFrontiers in immunology · 2021
    Review
  14. Review
  15. Review
  16. Article
  17. Specific Disruption of EstablishedLangmuir : the ACS journal of surfaces and colloids · 2020
    Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Quinn M ParksDepartment of Medicine, National Jewish Health, 1400 Jackson, Denver, CO, USA.
Robert L YoungDivision of Pulmonary Science and Critical Care Medicine, University of Colorado, 4200 E. 9th Ave, Denver, CO, USA.
Katie R PochDepartment of Medicine, National Jewish Health, 1400 Jackson, Denver, CO, USA.
Kenneth C MalcolmDepartment of Medicine, National Jewish Health, 1400 Jackson, Denver, CO, USA.
Michael L VasilDepartment of Microbiology, University of Colorado Denver Anschutz Medical Campus, 12800 E. 19th Ave, Aurora, CO, USA.
Jerry A NickDivision of Pulmonary Science and Critical Care Medicine, University of Colorado, 4200 E. 9th Ave, Denver, CO, USA.
University of Colorado Denver · USNational Jewish Health · US

Funding

TRANSLOCATION AND TRANSCELLULAR BIOSYNTHESISP01HL034303 · NHLBI · NATIONAL JEWISH HEALTH · PI BRATTON, DONNA L · 1985 to 2015
$25.0M
Viral-induced Adaptation of Neutrophil Response in ARDSR01HL090991 · NHLBI · NATIONAL JEWISH HEALTH · PI NICK, JERRY A · 2007 to 2010
$1.7M
NHLBI NIH HHS HL090991NHLBI NIH HHS HL34303NHLBI NIH HHS P01 HL034303NHLBI NIH HHS R01 HL090991
6 · The paper itself

Abstract

In the cystic fibrosis (CF) airway, chronic infection by Pseudomonas aeruginosa results from biofilm formation in a neutrophil-rich environment. We tested the capacity of human neutrophils to modify early biofilm formation of P. aeruginosa strain PAO1, and an isogenic CF strain isolated early and years later in infection. In a static reactor, P. aeruginosa biofilm density of all strains was enhanced at 24 h in the presence of neutrophils, with the greatest relative increase associated with the lowest inoculum of P. aeruginosa tested. Previously, neutrophil-induced biofilm enhancement was shown to largely result from the incorporation of F-actin and DNA polymers into the bacterial biofilm. This finding was advanced by the comparison of biofilm enhancement from intact unstimulated neutrophils and from lysed or apoptotic neutrophils. Apoptotic neutrophils, with an intact cell membrane, were unable to contribute to biofilm enhancement, while lysed neutrophils evoked a similar response to that of intact cells. Using F-actin and DNA as targets, the capacity of negatively charged poly(amino acids) to disrupt, or prevent, early biofilm formation was tested. Anionic poly(aspartic acid) effectively prevented or disrupted biofilm formation. Combination of poly(aspartic acid) with DNase resulted in a synergistic increase in biofilm disruption. These results demonstrate that the presence of dying neutrophils can facilitate the initial stages of biofilm development by low inocula of P. aeruginosa. Neutrophil F-actin represents a potential new therapeutic target for disruption of pathogenic biofilms.

Indexed as

ActinsAnti-Bacterial AgentsBiofilmsCiprofloxacinDeoxyribonucleasesDNAHumansNeutrophilsPeptidesPseudomonas aeruginosaTobramycinActinsAnti-Bacterial AgentsCiprofloxacinDeoxyribonucleasesDNAPeptidespolyaspartateTobramycin

Identifiers

PMID19273646
PMCPMC2677169
OpenAlexW2050204173

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.