Evidence map›Paper›PMID 20605984›Full record

ArticleInfection and immunity2010

Naturally produced outer membrane vesicles from Pseudomonas aeruginosa elicit a potent innate immune response via combined sensing of both lipopolysaccharide and protein components.

Terri N Ellis, Sara A Leiman, Meta J Kuehn

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 154 papers.

0numbers the graph read from it
0cells of the map it votes in
154citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

154 citing papers in PubMed, 241 citations in OpenAlex.

  1. Review
  2. Review
  3. Targeting Outer Membrane Vesicles ofJournal of microbiology and biotechnology · 2026
    Review
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94 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Terri N EllisDuke University Medical Center, Department of Biochemistry, Box 3711, Durham, NC 27710, USA.
Sara A Leiman
Meta J Kuehn
Duke University Hospital · USDuke University · US

Funding

Biogenesis and Function of Bacterial Outer Membrane VesiclesR01AI079068 · NIAID · DUKE UNIVERSITY · PI KUEHN, META J · 2009 to 2010
$750k
NIAID NIH HHS R01 AI079068
6 · The paper itself

Abstract

Pseudomonas aeruginosa is a prevalent opportunistic human pathogen that, like other Gram-negative pathogens, secretes outer membrane vesicles. Vesicles are complex entities composed of a subset of envelope lipid and protein components that have been observed to interact with and be internalized by host cells. This study characterized the inflammatory responses to naturally produced P. aeruginosa vesicles and determined the contribution of vesicle Toll-like receptor (TLR) ligands and vesicle proteins to that response. Analysis of macrophage responses to purified vesicles by real-time PCR and enzyme-linked immunosorbent assay identified proinflammatory cytokines upregulated by vesicles. Intact vesicles were shown to elicit a profoundly greater inflammatory response than the response to purified lipopolysaccharide (LPS). Both TLR ligands LPS and flagellin contributed to specific vesicle cytokine responses, whereas the CpG DNA content of vesicles did not. Neutralization of LPS sensing demonstrated that macrophage responses to the protein composition of vesicles required the adjuvantlike activity of LPS to elicit strain specific responses. Protease treatment to remove proteins from the vesicle surface resulted in decreased interleukin-6 and tumor necrosis factor alpha production, indicating that the production of these specific cytokines may be linked to macrophage recognition of vesicle proteins. Confocal microscopy of vesicle uptake by macrophages revealed that vesicle LPS allows for binding to macrophage surfaces, whereas vesicle protein content is required for internalization. These data demonstrate that macrophage sensing of both LPS and protein components of outer membrane vesicles combine to produce a bacterial strain-specific response that is distinct from those triggered by individual, purified vesicle components.

Indexed as

AnimalsBacterial Outer Membrane ProteinsCells, CulturedChemokine CXCL2DNA, BacterialFlagellinImmunity, InnateInterleukin-6LipopolysaccharidesMacrophagesMicePseudomonas aeruginosaSpecies SpecificityToll-Like Receptor 9Tumor Necrosis Factor-alphaBacterial Outer Membrane ProteinsChemokine CXCL2Cxcl2 protein, mouseDNA, BacterialFlagellinInterleukin-6LipopolysaccharidesTlr9 protein, mouseToll-Like Receptor 9Tumor Necrosis Factor-alpha

Identifiers

PMID20605984
PMCPMC2937433
OpenAlexW2056506612

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.