Evidence map›Paper›PMID 24001788›Full record

ArticleGastroenterology2013

Altered expression and localization of ion transporters contribute to diarrhea in mice with Salmonella-induced enteritis.

Ronald R Marchelletta, Melanie G Gareau, Declan F McCole, Sharon Okamoto, Elise Roel, Rachel Klinkenberg, Donald G Guiney, Joshua Fierer, Kim E Barrett

Open access · bronzeAbstract read
In one paragraph

Article in Gastroenterology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
  2. Review
  3. Milk andAmerican journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  4. SLC26A3 (DRA) is stimulated in a synergistic, intracellular CaAmerican journal of physiology. Cell physiology · 2023
    Article
  5. Review
  6. Article
  7. Cross-Talk Between the Intestinal Epithelium andFrontiers in microbiology · 2022
    Review
  8. Article
  9. Epithelial transport in digestive diseases: mice, monolayers, and mechanisms.American journal of physiology. Cell physiology · 2020
    Review
  10. Article
  11. NHERF3 is necessary forAmerican journal of physiology. Cell physiology · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. The Role of Ion Transporters in the Pathophysiology of Infectious Diarrhea.Cellular and molecular gastroenterology and hepatology · 2018
    Review
  19. Article
  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

9 authors at 2 institutions in 1 country.

Ronald R MarchellettaDepartment of Medicine, School of Medicine, University of California, San Diego, La Jolla, California.
Melanie G Gareau
Declan F McCole
Sharon Okamoto
Elise Roel
Rachel Klinkenberg
Donald G Guiney
Joshua Fierer
Kim E Barrett
University of California, San Diego · USUniversity of California San Diego Medical Center · US

Funding

Training Grant in GastroenterologyT32DK007202 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GHOSH, PRADIPTA · 1985 to 2022
$7.7M
A NOVEL ROLE FOR PTPN2 IN INTESTINAL EPITHELIAL BARRIER REGULATIONR01DK091281 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Declan McCole · 2012 to 2026
$5.5M
The UCSD Digestive Diseases Research Development CenterR24DK080506 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ECKMANN, LARS · 2008 to 2012
$2.7M
Intestinal Physiology in the Host Response to Enteric Salmonella InfectionsR01AI077661 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GUINEY, DONALD G. · 2009 to 2013
$2.5M
NIAID NIH HHS 1R01 AI077661-01A1NIAID NIH HHS R01 AI077661NIDDK NIH HHS DK080506NIDDK NIH HHS R01 DK091281NIDDK NIH HHS R24 DK080506NIDDK NIH HHS T32 DK007202NIDDK NIH HHS T32 DK07202
6 · The paper itself

Abstract

BACKGROUND &

aimsSalmonella enterica serovar Typhimurium is an enteropathogen that causes self-limiting diarrhea in healthy individuals, but poses a significant health threat to vulnerable populations. Our understanding of the pathogenesis of Salmonella-induced diarrhea has been hampered by the lack of a suitable mouse model. After a dose of oral kanamycin, Salmonella-infected congenic BALB/c.D2(NrampG169) mice, which carry a wild-type Nramp1 gene, develop clear manifestations of diarrhea. We used this model to elucidate the pathophysiology of Salmonella-induced diarrhea.

methodsBALB /c.D2(NrampG169) mice were treated with kanamycin and then infected with wild-type or mutant Salmonella by oral gavage. Colon tissues were isolated and Ussing chambers, quantitative polymerase chain reaction, immunoblot, and confocal microscopy analyses were used to study function and expression of ion transporters and cell proliferation.

resultsStudies with Ussing chambers demonstrated reduced basal and/or adenosine 3',5'-cyclic monophosphate-mediated electrogenic ion transport in infected colonic tissues, attributable to changes in chloride or sodium transport, depending on the segment studied. The effects of infection were mediated, at least in part, by effector proteins secreted by the bacterial Salmonella pathogenicity island 1- and Salmonella pathogenicity island-2-encoded virulence systems. Infected tissue showed reduced expression of the chloride-bicarbonate exchanger down-regulated in adenoma in surface colonic epithelial cells. Cystic fibrosis transmembrane conductance regulator was internalized in colonic crypt epithelial cells without a change in overall expression levels. Confocal analyses, densitometry, and quantitative polymerase chain reaction revealed that expression of epithelial sodium channel β was reduced in distal colons of Salmonella-infected mice. The changes in transporter expression, localization, and/or function were accompanied by crypt hyperplasia in Salmonella-infected mice.

conclusionsSalmonella infection induces diarrhea by altering expression and/or function of transporters that mediate water absorption in the colon, likely reflecting the fact that epithelial cells have less time to differentiate into surface cells when proliferation rates are increased by infection.

Indexed as

AnimalsCation Transport ProteinsCell DifferentiationCell ProliferationColonCystic Fibrosis Transmembrane Conductance RegulatorDiarrheaDisease Models, AnimalEnteritisEpithelial Sodium ChannelsFemaleHyperplasiaIntestinal MucosaIon TransportMaleMiceCation Transport ProteinsCystic Fibrosis Transmembrane Conductance RegulatorEpithelial Sodium ChannelsNatural Resistance-associated Macrophage Protein 1CFTRColoncystic fibrosis transmembrane conductance regulatordown-regulated in adenomaDRAENaCepithelial sodium channelforskolinFSKKanakanamycinmessenger RNAmRNAqPCRquantitative polymerase chain reactionSalmonellaSalmonella pathogenicity islandSPIT3SStype-3 protein secretion systemwild-typewt

Identifiers

PMID24001788
PMCPMC3899031
OpenAlexW2084716544

What OpenQuestion holds

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Registered trials

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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.