Evidence map›Paper›PMID 15385508›Full record

ArticleInfection and immunity2004

Bacterial overgrowth in the cystic fibrosis transmembrane conductance regulator null mouse small intestine.

Oxana Norkina, Tim G Burnett, Robert C De Lisle

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 2 pooled it
6.3field-weighted citation impact, top 3% 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

82 citing papers in PubMed, 2 syntheses or guidelines pooled it, 177 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Trial
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. CFTR and Gastrointestinal Cancers: An Update.Journal of personalized medicine · 2022
    Review
  15. Goblet cell hyperplasia is not epithelial-autonomous in the Cftr knockout intestine.American journal of physiology. Gastrointestinal and liver physiology · 2022
    Article
  16. Article
  17. Review
  18. Review
  19. Lung and Gut Microbiota Changes Associated withInternational journal of molecular sciences · 2021
    Article
  20. Article

22 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.

Oxana NorkinaAnatomy and Cell Biology, University of Kansas School of Medicine, Kansas City, Kansas 66160, USA. rdelisle@kumc.edu
Tim G Burnett
Robert C De Lisle
University of Kansas · USEmporia State University · US

Funding

PATHOGENEISIS OF CYSTIC FIBROSIS IN THE GI SYSTEMR01DK056791 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI DE LISLE, ROBERT C · 2000 to 2003
$835k
NIDDK NIH HHS DK56791NIDDK NIH HHS R01 DK056791
6 · The paper itself

Abstract

We recently reported the inflammation of the cystic fibrosis (CF) mouse small intestine, and we hypothesized bacterial overgrowth as a possible cause. Quantitative PCR of bacterial 16S genomic DNA in the CF mouse small intestine revealed an increase of greater than 40-fold compared to controls. Sequencing of 16S PCR products and Gram staining showed that the majority of bacteria in the CF mouse intestine were gram negative. Bacteria were observed to colonize the mucus that accumulates in the intestinal lumen of mice with CF. Impaired Paneth cell defenses were suggested by observation of partially dispersed Paneth granules in the mucus plugs of CF mouse intestinal crypts, and this mucus was strongly immunoreactive for Paneth cell bactericidal products. The role of bacterial overgrowth in intestinal inflammation in CF was tested by treating mice with oral antibiotics (ciprofloxacin and metronidazole) for 3 weeks, which reduced bacterial load in the CF mouse small intestine over 400-fold. Antibiotic treatment decreased the expression of the inflammation-related genes mast cell protease 2, leucine-rich alpha2 glycoprotein/leucine-rich high endothelial venule glycoprotein, suppressor of cytokine signaling 3, hematopoietic cell transcript 1, and resistin-like molecule beta/found in inflammatory zone 2, all of which were no longer expressed at levels significantly different from control levels. The reduction of intestinal bacteria also significantly improved the growth of CF mice but had no effect on the growth of wild-type mice. These data suggest that bacterial overgrowth in the CF mouse small intestine has a role in inflammation and contributes to the failure to thrive in this mouse model of CF.

Indexed as

AnimalsAnti-Bacterial AgentsBacteriaBody WeightCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorFemaleGene DeletionInflammationIntestine, SmallMaleMiceMice, Inbred C57BLMice, KnockoutNeutrophilsAnti-Bacterial AgentsCystic Fibrosis Transmembrane Conductance Regulator

Identifiers

PMID15385508
PMCPMC517588
OpenAlexW2130824853

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.