Evidence map›Paper›PMID 21708992›Full record

ArticleInfection and immunity2011

Context-dependent activation kinetics elicited by soluble versus outer membrane vesicle-associated heat-labile enterotoxin.

Halima Chutkan, Meta J Kuehn

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 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.5field-weighted citation impact, top 11% 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, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Outer Membrane Vesicles: Biogenesis, Functions, and Issues.Microbiology and molecular biology reviews : MMBR · 2022
    Review
  6. Article
  7. Article
  8. Review
  9. Outer Membrane Vesicle Production byInternational journal of molecular sciences · 2021
    Article
  10. Article
  11. Article
  12. [Research progress on the role of extracellular vesicles in bacterial pathogenesis].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2018
    Review
  13. Review
  14. EnterotoxigenicBioscience of microbiota, food and health · 2017
    Review
  15. Pathogenic Lifestyles ofFrontiers in cellular and infection microbiology · 2016
    Article
  16. Article
  17. Review
  18. Article
  19. Functional advantages conferred by extracellular prokaryotic membrane vesicles.Journal of molecular microbiology and biotechnology · 2013
    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

2 authors at 1 institution in 1 country.

Halima ChutkanDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Meta J Kuehn
Duke University Hospital · US

Funding

Enterotoxin targeting and delivery mechanismsR01AI064464 · NIAID · DUKE UNIVERSITY · PI KUEHN, META J · 2006 to 2010
$1.5M
NIAID NIH HHS R01 AI064464NIAID NIH HHS R01AI064464
6 · The paper itself

Abstract

Enterotoxigenic Escherichia coli (ETEC) is the leading cause of traveler's diarrhea and children's diarrhea worldwide. Among its virulence factors, ETEC produces heat-labile enterotoxin (LT). Most secreted LT is associated with outer membrane vesicles that are rich in lipopolysaccharide. The majority of prior studies have focused on soluble LT purified from ETEC periplasm. We investigated the hypothesis that the extracellular vesicle context of toxin presentation might be important in eliciting immune responses. We compared the polarized epithelial cell responses to apically applied soluble LT and LT-containing vesicles (LT(+) vesicles) as well as controls using a catalytically inactive mutant of LT and vesicles lacking LT. Although vesicle treatments with no or catalytically inactive LT induced a modest amount of interleukin-6 (IL-6), samples containing catalytically active LT elicited higher levels. A combination of soluble LT and LT-deficient vesicles induced significantly higher IL-6 levels than either LT or LT(+) vesicles alone. The responses to LT(+) vesicles were found to be independent of the canonical LT pathway, because the inhibition of cyclic AMP response element (CRE)-binding protein (CREB) phosphorylation did not lead to a decrease in cytokine gene expression levels. Furthermore, soluble LT caused earlier phosphorylation of CREB and activation of CRE compared with LT(+) vesicles. Soluble LT also led to the activation of activator protein 1, whereas LT(+) vesicle IL-6 responses appeared to be mediated by NF-κB. In summary, the results demonstrate that soluble LT and vesicle-bound LT elicit ultimately similar cytokine responses through distinct different activation pathways.

Indexed as

Bacterial Outer Membrane ProteinsBacterial ToxinsCell LineCyclic AMP Response Element-Binding ProteinCytokinesEnterotoxigenic Escherichia coliEnterotoxinsEpithelial CellsEscherichia coli ProteinsHEK293 CellsHumansImmunoblottingInterleukin-6Intestinal MucosaLipopolysaccharidesMutationBacterial Outer Membrane ProteinsBacterial ToxinsCyclic AMP Response Element-Binding ProteinCytokinesEnterotoxinsEscherichia coli Proteinsheat-labile enterotoxin, E coliInterleukin-6LipopolysaccharidesNF-kappa BTranscription Factor AP-1Tumor Necrosis Factor-alphaVirulence Factors

Identifiers

PMID21708992
PMCPMC3165487
OpenAlexW2162959497

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.