Evidence map›Paper›PMID 25847961›Full record

ArticleInfection and immunity2015

Transcriptional analysis of the MrpJ network: modulation of diverse virulence-associated genes and direct regulation of mrp fimbrial and flhDC flagellar operons in Proteus mirabilis.

Nadine J Bode, Irina Debnath, Lisa Kuan, Anjelique Schulfer, Maureen Ty, Melanie M Pearson

Abstract read
In one paragraph

Article in Infection and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Article
  2. Functional loss ofFrontiers in microbiology · 2025
    Article
  3. Unveiling the hidden arsenal: new insights intoFrontiers in cellular and infection microbiology · 2024
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Pathogenesis ofEcoSal Plus · 2018
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Proteus mirabilis fimbriae- and urease-dependent clusters assemble in an extracellular niche to initiate bladder stone formation.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  20. The Versatile Type VI Secretion System.Microbiology spectrum · 2016
    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

6 authors.

Nadine J BodeDepartment of Microbiology, New York University Medical Center, New York, New York, USA.
Irina DebnathDepartment of Microbiology, New York University Medical Center, New York, New York, USA.
Lisa KuanDepartment of Microbiology, New York University Medical Center, New York, New York, USA.
Anjelique SchulferDepartment of Microbiology, New York University Medical Center, New York, New York, USA.
Maureen TyDepartment of Microbiology, New York University Medical Center, New York, New York, USA.
Melanie M PearsonDepartment of Microbiology, New York University Medical Center, New York, New York, USA Melanie.Pearson@nyumc.org.

Funding

Contribution of Novel Frimbriae to Proteus Mirabilis VirulenceK22AI083743 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PEARSON, MELANIE M. · 2011 to 2013
$359k
NIAID NIH HHS AI083743NIAID NIH HHS K22 AI083743
6 · The paper itself

Abstract

The enteric bacterium Proteus mirabilis is associated with a significant number of catheter-associated urinary tract infections (UTIs). Strict regulation of the antagonistic processes of adhesion and motility, mediated by fimbriae and flagella, respectively, is essential for disease progression. Previously, the transcriptional regulator MrpJ, which is encoded by the mrp fimbrial operon, has been shown to repress both swimming and swarming motility. Here we show that MrpJ affects an array of cellular processes beyond adherence and motility. Microarray analysis found that expression of mrpJ mimicking levels observed during UTIs leads to differential expression of 217 genes related to, among other functions, bacterial virulence, type VI secretion, and metabolism. We probed the molecular mechanism of transcriptional regulation by MrpJ using transcriptional reporters and chromatin immunoprecipitation (ChIP). Binding of MrpJ to two virulence-associated target gene promoters, the promoters of the flagellar master regulator flhDC and mrp itself, appears to be affected by the condensation state of the native chromosome, although both targets share a direct MrpJ binding site proximal to the transcriptional start. Furthermore, an mrpJ deletion mutant colonized the bladders of mice at significantly lower levels in a transurethral model of infection. Additionally, we observed that mrpJ is widely conserved in a collection of recent clinical isolates. Altogether, these findings support a role of MrpJ as a global regulator of P. mirabilis virulence.

Indexed as

AnimalsBacterial ProteinsChromosomes, BacterialFlagellaGene Expression Regulation, BacterialMiceMutationOperonProteus mirabilisRepressor ProteinsTranscription, GeneticUrinary Tract InfectionsVirulenceBacterial ProteinsMrpJ protein, Proteus mirabilisRepressor Proteins

Identifiers

PMID25847961
PMCPMC4432738

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.