Evidence map›Paper›PMID 20093500›Full record

ArticleThe American journal of pathology2010

Epithelial cell apoptosis facilitates Entamoeba histolytica infection in the gut.

Stephen M Becker, Kyou-Nam Cho, Xiaoti Guo, Kirsten Fendig, Mohammed N Oosman, Robert Whitehead, Steven M Cohn, Eric R Houpt

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
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  3. Gasdermins in Innate Host Defense AgainstFrontiers in immunology · 2022
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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

8 authors at 2 institutions in 1 country.

Stephen M BeckerDivision of Infectious Diseases and International Health, Department of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Kyou-Nam Cho
Xiaoti Guo
Kirsten Fendig
Mohammed N Oosman
Robert Whitehead
Steven M Cohn
Eric R Houpt
University of Virginia · USVanderbilt University · US

Funding

Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
UVA Digestive Health Research CenterP30DK067629 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI COMINELLI, FABIO · 2004 to 2008
$5.6M
Mouse Strain dependent innate resistance to intestinal amebiasisR01AI071373 · NIAID · UNIVERSITY OF VIRGINIA · PI HOUPT, ERIC R · 2006 to 2009
$1.5M
Biodefense Short-Term Training for Minority StudentT35AI060528 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI HALME, ADRIAN J, PETRI, WILLIAM A · 2004 to 2024
$1.3M
NIAID NIH HHS AI071373NIAID NIH HHS R01 AI071373NIAID NIH HHS T35 AI060528NIDDK NIH HHS DK058404NIDDK NIH HHS DK067629NIDDK NIH HHS P30 DK058404NIDDK NIH HHS P30 DK067629
6 · The paper itself

Abstract

Entamoeba histolytica is the protozoan parasite that causes amebic colitis. The parasite triggers apoptosis on contact with host cells; however, the biological significance of this event during intestinal infection is unclear. We examined the role of apoptosis in a mouse model of intestinal amebiasis. Histopathology revealed that abundant epithelial cell apoptosis occurred in the vicinity of amoeba in histological specimens. Epithelial cell apoptosis occurred rapidly on co-culture with amoeba in vitro as measured by annexin positivity, DNA degradation, and mitochondrial dysfunction. Administration of the pan caspase inhibitor ZVAD decreased the rate and severity of amebic infection in CBA mice by all measures (cecal culture positivity, parasite enzyme-linked immunosorbent assay, and histological scores). Similarly, caspase 3 knockout mice on the resistant C57BL/6 background exhibited even lower cecal parasite antigen burden and culture positive rates than wild type mice. The permissive effect of apoptosis on infection could be tracked to the epithelium, in that transgenic mice that overexpressed Bcl-2 in epithelial cells were more resistant to infection as measured by cecal parasite enzyme-linked immunosorbent assay and histological scores. We concluded that epithelial cell apoptosis in the intestine facilitates amebic infection in this mouse model. The parasite's strategy for inducing apoptosis may point to key virulence factors, and therapeutic maneuvers to diminish epithelial apoptosis may be useful in amebic colitis.

Indexed as

ApoptosisAnimalsCaspase 3Caspase InhibitorsCecumDisease Models, AnimalDysentery, AmebicEntamoeba histolyticaEpithelial CellsGastrointestinal TractMaleMiceMice, TransgenicProto-Oncogene Proteins c-bcl-2Caspase 3Caspase InhibitorsProto-Oncogene Proteins c-bcl-2

Identifiers

PMID20093500
PMCPMC2832152
OpenAlexW2086913566

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.