Evidence map›Paper›PMID 25712925›Full record

ArticleInfection and immunity2015

The CpxRA two-component system is essential for Citrobacter rodentium virulence.

Jenny-Lee Thomassin, Natalia Giannakopoulou, Lei Zhu, Jeremy Gross, Kristiana Salmon, Jean-Mathieu Leclerc, France Daigle, Hervé Le Moual, Samantha Gruenheid

Open access · bronzeAbstract 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 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 37 citations in OpenAlex.

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  12. Simulated Colonic Fluid Replicates theInfection and immunity · 2022
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  18. Review
  19. Successful Host Adaptation of IncK2 Plasmids.Frontiers in microbiology · 2019
    Article
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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.

Jenny-Lee ThomassinDepartment of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.
Natalia GiannakopoulouDepartment of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.
Lei ZhuDepartment of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.
Jeremy GrossDepartment of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.
Kristiana SalmonDepartment of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.
Jean-Mathieu LeclercDepartment of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.
France DaigleDépartement de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Montréal, Québec, Canada.
Hervé Le MoualDepartment of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada Microbiome and Disease Tolerance Centre, McGill University, Montreal, Quebec, Canada Faculty of Dentistry, McGill University, Montreal, Quebec, Canada.
Samantha GruenheidDepartment of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada Microbiome and Disease Tolerance Centre, McGill University, Montreal, Quebec, Canada samantha.gruenheid@mcgill.ca.
McGill University · CAUniversité de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Citrobacter rodentium is a murine intestinal pathogen used as a model for the foodborne human pathogens enterohemorrhagic Escherichia coli and enteropathogenic E. coli. During infection, these pathogens use two-component signal transduction systems to detect and adapt to changing environmental conditions. In E. coli, the CpxRA two-component signal transduction system responds to envelope stress by modulating the expression of a myriad of genes. Quantitative real-time PCR showed that cpxRA was expressed in the colon of C57BL/6J mice infected with C. rodentium. To determine whether CpxRA plays a role during C. rodentium infection, a cpxRA deletion strain was generated and found to have a colonization defect during infection. This defect was independent of an altered growth rate or a defective type III secretion system, and single-copy chromosomal complementation of cpxRA restored virulence. The C. rodentium strains were then tested in C3H/HeJ mice, a lethal intestinal infection model. Mice infected with the ΔcpxRA strain survived infection, whereas mice infected with the wild-type or complemented strains succumbed to infection. Furthermore, we found that the cpxRA expression level was higher during early infection than at a later time point. Taken together, these data demonstrate that the CpxRA two-component signal transduction system is essential for the in vivo virulence of C. rodentium. In addition, these data suggest that fine-tuned cpxRA expression is important for infection. This is the first study that identifies a C. rodentium two-component transduction system required for pathogenesis. This study further indicates that CpxRA is an interesting target for therapeutics against enteric pathogens.

Indexed as

AnimalsBacterial ProteinsCitrobacter rodentiumColonEnteritisGene DeletionGenetic Complementation TestMice, Inbred C3HMice, Inbred C57BLProtein KinasesSurvival AnalysisVirulence FactorsBacterial ProteinsCpxA protein, bacteriaCpxR protein, BacteriaProtein KinasesVirulence Factors

Identifiers

PMID25712925
PMCPMC4399039
OpenAlexW2156908798

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.