Evidence map›Paper›PMID 17630833›Full record

ArticlePLoS pathogens2007

Integrin-mediated host cell invasion by type 1-piliated uropathogenic Escherichia coli.

Danelle S Eto, Tiffani A Jones, Jamie L Sundsbak, Matthew A Mulvey

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 171 papers.

0numbers the graph read from it
0cells of the map it votes in
171citing papers in PubMed
9.2field-weighted citation impact, top 2% 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

171 citing papers in PubMed, 298 citations in OpenAlex.

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  16. Metabolic cross-talk promotes persistence ofbioRxiv : the preprint server for biology · 2025
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111 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

4 authors at 1 institution in 1 country.

Danelle S EtoDivision of Cell Biology and Immunology, Pathology Department, University of Utah, Salt Lake City, Utah, United States of America.
Tiffani A Jones
Jamie L Sundsbak
Matthew A Mulvey
University of Utah · US

Funding

Training Program in Microbial PathogenesisT32AI055434 · NIAID · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI MULVEY, MATTHEW A, PLANELLES, VICENTE · 2004 to 2025
$6.0M
Bacterial Invasion and Trafficking within the BladderR01DK068585 · NIDDK · UNIVERSITY OF UTAH · PI MULVEY, MATTHEW A · 2004 to 2010
$2.4M
Control of bladder infections by NF-kappaBR21DK069526 · NIDDK · UNIVERSITY OF UTAH · PI MULVEY, MATTHEW A · 2004 to 2005
$336k
NIAID NIH HHS T32 AI055434NIAID NIH HHS T32 AI055434-01A1NIDDK NIH HHS DK068585NIDDK NIH HHS DK069526NIDDK NIH HHS R01 DK068585NIDDK NIH HHS R21 DK069526
6 · The paper itself

Abstract

Uropathogenic Escherichia coli (UPEC), the primary causative agent of urinary tract infections, typically express filamentous adhesive organelles called type 1 pili that mediate both bacterial attachment to and invasion of bladder urothelial cells. Several host proteins have previously been identified as receptors for type 1 pili, but none have been conclusively shown to promote UPEC entry into host bladder cells. Using overlay assays with FimH, the purified type 1 pilus adhesin, and mass spectroscopy, we have identified beta1 and alpha3 integrins as key host receptors for UPEC. FimH recognizes N-linked oligosaccharides on these receptors, which are expressed throughout the urothelium. In a bladder cell culture system, beta1 and alpha3 integrin receptors co-localize with invading type 1-piliated bacteria and F-actin. FimH-mediated bacterial invasion of host bladder cells is inhibited by beta1 and alpha3 integrin-specific antibodies and by disruption of the beta1 integrin gene in the GD25 fibroblast cell line. Phosphorylation site mutations within the cytoplasmic tail of beta1 integrin that alter integrin signaling also variably affect UPEC entry into host cells, by either attenuating or boosting invasion frequencies. Furthermore, focal adhesion and Src family kinases, which propagate integrin-linked signaling and downstream cytoskeletal rearrangements, are shown to be required for FimH-dependent bacterial invasion of target host cells. Cumulatively, these results indicate that beta1 and alpha3 integrins are functionally important receptors for type 1 pili-expressing bacteria within the urinary tract and possibly at other sites within the host.

Indexed as

Adhesins, Escherichia coliFimbriae, BacterialHost-Pathogen InteractionsActinsBase SequenceCell LineEscherichia coliEscherichia coli InfectionsFimbriae ProteinsHumansIntegrin alpha3Integrin beta1Mass SpectrometryMolecular Sequence DataMutationPhosphorylationActinsAdhesins, Escherichia coliFimbriae ProteinsIntegrin alpha3Integrin beta1

Identifiers

PMID17630833
PMCPMC1914067
OpenAlexW2088566842

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.