Evidence map›Paper›PMID 8675322›Full record

ArticleInfection and immunity1996

In vivo cytokine response to Escherichia coli alpha-hemolysin determined with genetically engineered hemolytic and nonhemolytic E. coli variants.

A K May, R G Sawyer, T Gleason, A Whitworth, T L Pruett

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

  1. Current research in microbial sciences · 2025
    Article
  2. Microorganisms · 2022
    Review
  3. Role of pore-forming toxins in bacterial infectious diseases.Microbiology and molecular biology reviews : MMBR · 2013
    Review
  4. Role of pore-forming toxins in neonatal sepsis.Clinical & developmental immunology · 2013
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. 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

5 authors at 1 institution in 1 country.

A K MayDepartment of Surgery, Surgical Infectious Disease Laboratory, University of Virginia, Charlottesville 22908, USA.
R G Sawyer
T Gleason
A Whitworth
T L Pruett
University of Virginia · US

Funding

BACTERIAL EXPOSURE, T CELLS AND SURGICAL INFECTIONF32AI009482 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI GLEASON, THOMAS G · 1996 to 1996
–
E COLI VIRULENCE TRAITS IN INTRAABDOMINAL INFECTIONR29AI028954 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI PRUETT, TIMOTHY L · 1990 to 1994
–
NIAID NIH HHS 29 AI 28954-01NIAID NIH HHS F32 AI009482
6 · The paper itself

Abstract

Alpha-hemolysin is an Escherichia coli exotoxin that enhances bacterial virulence, has profound effects on leukocytes in vitro, and induces the release of interleukin-1 (IL-1) but not tumor necrosis factor (TNF) from human monocytes in vitro. The purpose of this study was to examine alpha-hemolysin's influence on virulence and TNF and IL-1 production in vivo. Two genetically engineered, isogeneic strains of E. coli were used; one variant produces alpha-hemolysin, and the other does not. Male BALB/c mice were injected with either of the two variants and serum TNF and IL-1 were assayed. These results were compared with those obtained from the injection of either of two serotypes of lipopolysaccharide (LPS). The nonhemolytic E. coli strain produced no mortality and no significant elevation of serum TNF or IL-1 levels. In contrast, equal inocula of the hemolytic E. coli strain produced significant mortality and elevation of serum IL-1 levels. No significant elevation of TNF levels was detected in this group despite high-level mortality. A pattern of induction of mortality and elevation of serum IL-1 levels without elevation of serum TNF levels is distinct from the pattern typical of LPS. In these experiments, both serotypes of LPS caused elevations of TNF and IL-1 levels whether or not mortality was induced. Thus, alpha-hemolysin produces a cytokine response in vivo that is similar to that previously demonstrated in vitro by Bhakdi et al. (S. Bhakdi, M. Muhly, S. Korom, and G. Schmidt, J. Clin. Invest. 85:1746-1753, 1990) and appears to induce mortality independently of serum TNF.

Indexed as

Escherichia coli ProteinsAnimalsBacterial ProteinsBacterial ToxinsEscherichia coliHemolysin ProteinsInterleukin-1LipopolysaccharidesMaleMiceMice, Inbred BALB CTumor Necrosis Factor-alphaBacterial ProteinsBacterial ToxinsEscherichia coli ProteinsHemolysin ProteinsHlya protein, E coliInterleukin-1LipopolysaccharidesTumor Necrosis Factor-alpha

Identifiers

PMID8675322
PMCPMC174051
OpenAlexW2104463631

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.