Evidence map›Paper›PMID 25673765›Full record

ArticleMolecular & cellular proteomics : MCP2015

A metaproteomics approach to elucidate host and pathogen protein expression during catheter-associated urinary tract infections (CAUTIs).

Christian Lassek, Melanie Burghartz, Diego Chaves-Moreno, Andreas Otto, Christian Hentschker, Stephan Fuchs, Jörg Bernhardt, Ruy Jauregui, Rüdiger Neubauer, Dörte Becher and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Insights on pathoadaptation of sequentialMicrobiology spectrum · 2025
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  5. A Standardized Extract ofFrontiers in microbiology · 2022
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  6. Review
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  11. Review
  12. Article
  13. Article
  14. Full Transcriptomic Response ofFrontiers in microbiology · 2020
    Article
  15. Virulence Factors Produced byMolecular & cellular proteomics : MCP · 2019
    Article
  16. Recent progress in experimental and human disease-associated multi-species biofilms.Computational and structural biotechnology journal · 2019
    Review
  17. Environmental proteomic studies: closer step to understand bacterial biofilms.World journal of microbiology & biotechnology · 2018
    Review
  18. Article
  19. Iron Regulation inFrontiers in microbiology · 2018
    Article
  20. 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

14 authors at 3 institutions in 1 country.

Christian LassekFrom the ‡Institute of Microbiology, University of Greifswald, 17489 Greifswald, Friedrich-Ludwig-Jahn-Strasse 15, Germany; §Institute of Microbiology, Technische Universität Braunschweig, 38106 Braunschweig, Spielmannstrasse 7, Germany;
Melanie Burghartz§Institute of Microbiology, Technische Universität Braunschweig, 38106 Braunschweig, Spielmannstrasse 7, Germany;
Diego Chaves-Moreno¶Microbial Interactions and Processes Research Group, Helmholtz Centre for Infection Research, 38124 Braunschweig, Inhoffenstrasse 7, Germany;
Andreas OttoFrom the ‡Institute of Microbiology, University of Greifswald, 17489 Greifswald, Friedrich-Ludwig-Jahn-Strasse 15, Germany;
Christian HentschkerFrom the ‡Institute of Microbiology, University of Greifswald, 17489 Greifswald, Friedrich-Ludwig-Jahn-Strasse 15, Germany;
Stephan FuchsFrom the ‡Institute of Microbiology, University of Greifswald, 17489 Greifswald, Friedrich-Ludwig-Jahn-Strasse 15, Germany;
Jörg BernhardtFrom the ‡Institute of Microbiology, University of Greifswald, 17489 Greifswald, Friedrich-Ludwig-Jahn-Strasse 15, Germany;
Ruy Jauregui¶Microbial Interactions and Processes Research Group, Helmholtz Centre for Infection Research, 38124 Braunschweig, Inhoffenstrasse 7, Germany;
Rüdiger Neubauer‖Urologist's Practice, Kassel, Germany.
Dörte BecherFrom the ‡Institute of Microbiology, University of Greifswald, 17489 Greifswald, Friedrich-Ludwig-Jahn-Strasse 15, Germany;
Dietmar H Pieper¶Microbial Interactions and Processes Research Group, Helmholtz Centre for Infection Research, 38124 Braunschweig, Inhoffenstrasse 7, Germany;
Martina Jahn§Institute of Microbiology, Technische Universität Braunschweig, 38106 Braunschweig, Spielmannstrasse 7, Germany;
Dieter Jahn§Institute of Microbiology, Technische Universität Braunschweig, 38106 Braunschweig, Spielmannstrasse 7, Germany;
Katharina RiedelFrom the ‡Institute of Microbiology, University of Greifswald, 17489 Greifswald, Friedrich-Ludwig-Jahn-Strasse 15, Germany; ¶Microbial Interactions and Processes Research Group, Helmholtz Centre for Infection Research, 38124 Braunschweig, Inhoffenstrasse 7, Germany; riedela@uni-greifswald.de.
Universität Greifswald · DEHelmholtz Centre for Infection Research · DETechnische Universität Braunschweig · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-term catheterization inevitably leads to a catheter-associated bacteriuria caused by multispecies bacterial biofilms growing on and in the catheters. The overall goal of the presented study was (1) to unravel bacterial community structure and function of such a uropathogenic biofilm and (2) to elucidate the interplay between bacterial virulence and the human immune system within the urine. To this end, a metaproteomics approach combined with in vitro proteomics analyses was employed to investigate both, the pro- and eukaryotic protein inventory. Our proteome analyses demonstrated that the biofilm of the investigated catheter is dominated by three bacterial species, that is, Pseudomonas aeruginosa, Morganella morganii, and Bacteroides sp., and identified iron limitation as one of the major challenges in the bladder environment. In vitro proteome analysis of P. aeruginosa and M. morganii isolated from the biofilm revealed that these opportunistic pathogens are able to overcome iron restriction via the production of siderophores and high expression of corresponding receptors. Notably, a comparison of in vivo and in vitro protein profiles of P. aeruginosa and M. morganii also indicated that the bacteria employ different strategies to adapt to the urinary tract. Although P. aeruginosa seems to express secreted and surface-exposed proteases to escape the human innate immune system and metabolizes amino acids, M. morganii is able to take up sugars and to degrade urea. Most interestingly, a comparison of urine protein profiles of three long-term catheterized patients and three healthy control persons demonstrated the elevated level of proteins associated with neutrophils, macrophages, and the complement system in the patient's urine, which might point to a specific activation of the innate immune system in response to biofilm-associated urinary tract infections. We thus hypothesize that the often asymptomatic nature of catheter-associated urinary tract infections might be based on a fine-tuned balance between the expression of bacterial virulence factors and the human immune system.

Indexed as

Host-Pathogen InteractionsAdaptation, PhysiologicalBacterial ProteinsBiofilmsCatheter-Related InfectionsCell-Free SystemHumansImmunity, InnateMorganella morganiiPhenotypeProteomicsPseudomonas aeruginosaSpecies SpecificityUrinary TractUrinary Tract InfectionsUrineBacterial Proteins

Identifiers

PMID25673765
PMCPMC4390275
OpenAlexW1982148579

What OpenQuestion holds

Textmetadata
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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.