Evidence map›Paper›PMID 21115716›Full record

ArticleInfection and immunity2011

Role of defensins in corneal epithelial barrier function against Pseudomonas aeruginosa traversal.

Danielle K Augustin, Susan R Heimer, Connie Tam, Wing Y Li, Jeff M Le Due, David J Evans, Suzanne M J Fleiszig

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

56 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. ThemBio · 2025
    Article
  5. Article
  6. Contact Lens Wear Alters Transcriptional Responses tobioRxiv : the preprint server for biology · 2024
    Article
  7. Increased tolerance to commonly used antibiotics in aMicrobiology (Reading, England) · 2024
    Article
  8. Mechanisms and regulation of defensins in host defense.Signal transduction and targeted therapy · 2023
    Review
  9. Comparative Evaluation ofVision (Basel, Switzerland) · 2023
    Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Nerve-associated transient receptor potential ion channels can contribute to intrinsic resistance to bacterial adhesion in vivo.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  16. Review
  17. Review
  18. Article
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  20. Review
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

7 authors at 2 institutions in 1 country.

Danielle K AugustinGraduate Group in Microbiology, Department of Plant and Microbial Biology, University of California, Berkeley, California, USA.
Susan R Heimer
Connie Tam
Wing Y Li
Jeff M Le Due
David J Evans
Suzanne M J Fleiszig
University of California, Berkeley · USTouro University California · US

Funding

SIGNIFICANCE OF CORNEAL CELL INVASION BY BACTERIAR01EY011221 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI Suzanne MJ FLEISZIG · 1995 to 2026
$8.4M
Identifying mechanisms of translocation of epithelial cells by P. aeruginosa.F31EY019456 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI AUGUSTIN, DANIELLE KRISTY · 2009 to 2010
$65k
NEI NIH HHS EY011221NEI NIH HHS EY019456NEI NIH HHS F31 EY019456NEI NIH HHS R01 EY011221
6 · The paper itself

Abstract

Studies have shown that epithelium-expressed antimicrobial peptides (AMPs), e.g., β-defensins, play a role in clearing bacteria from mouse corneas already infected with Pseudomonas aeruginosa. Less is known about the role of AMPs in allowing the cornea to resist infection when healthy. We previously reported that contact lens exposure, a major cause of P. aeruginosa keratitis, can inhibit the upregulation of human β-defensin 2 (hBD-2) by corneal epithelial cells in response to P. aeruginosa antigens in vitro. Here, we studied the role of AMPs in maintaining the corneal epithelial barrier to P. aeruginosa penetration using both in vitro (human) and in vivo (mouse) experiments. Results showed that preexposing human corneal epithelial multilayers to bacterial antigens in a culture supernatant (known to upregulate AMP expression) reduced epithelial susceptibility to P. aeruginosa traversal up to 6-fold (P < 0.001). Accordingly, small interfering RNA (siRNA) knockdown of any one of four AMPs expressed by human epithelia promoted P. aeruginosa traversal by more than 3-fold (P < 0.001). The combination knockdown of AMPs further enhanced susceptibility to bacterial traversal by ∼8-fold (P < 0.001). In vivo experiments showed that the loss of murine β-defensin 3 (mBD-3), a murine ortholog of hBD-2, enhanced corneal susceptibility to P. aeruginosa. The uninjured ocular surface of mBD-3(-/-) mice showed a reduced capacity to clear P. aeruginosa, and their corneal epithelia were more susceptible to bacterial colonization, even when inoculated ex vivo to exclude tear fluid effects. Together, these in vitro and in vivo data show functional roles for AMPs in normal corneal epithelial cell barrier function against P. aeruginosa.

Indexed as

Animalsbeta-DefensinsCell LineDefensinsEpithelium, CornealGene Expression RegulationHumansMiceMice, Inbred C57BLMice, KnockoutPseudomonas aeruginosabeta-defensin 3, mousebeta-DefensinsDefensins

Identifiers

PMID21115716
PMCPMC3028852
OpenAlexW2166813768

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.