Evidence map›Paper›PMID 35197500›Full record

ArticleScientific reports2022

The fliR gene contributes to the virulence of S. marcescens in a Drosophila intestinal infection model.

Bechara Sina Rahme, Matthieu Lestradet, Gisela Di Venanzio, Arshad Ayyaz, Miriam Wennida Yamba, Martina Lazzaro, Samuel Liégeois, Eleonora Garcia Véscovi, Dominique Ferrandon

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Innate immunity inPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Review
  7. 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

9 authors at 6 institutions in 4 countries.

Bechara Sina RahmeUniversité de Strasbourg, Strasbourg, France.
Matthieu LestradetUniversité de Strasbourg, Strasbourg, France.
Gisela Di VenanzioInstituto de Biología Molecular y Cellular de Rosario, Consejo Nacional de Investigaciones Cientificas y Tecnológicas, Universidad Nacional de Rosario, Rosario, Argentina.
Arshad AyyazUniversité de Strasbourg, Strasbourg, France.
Miriam Wennida YambaUniversité de Strasbourg, Strasbourg, France.
Martina LazzaroInstituto de Biología Molecular y Cellular de Rosario, Consejo Nacional de Investigaciones Cientificas y Tecnológicas, Universidad Nacional de Rosario, Rosario, Argentina.
Samuel LiégeoisUniversité de Strasbourg, Strasbourg, France.
Eleonora Garcia VéscoviInstituto de Biología Molecular y Cellular de Rosario, Consejo Nacional de Investigaciones Cientificas y Tecnológicas, Universidad Nacional de Rosario, Rosario, Argentina.
Dominique FerrandonUniversité de Strasbourg, Strasbourg, France. D.Ferrandon@ibmc-cnrs.unistra.fr.
Université de Strasbourg · FRNational University of Rosario · ARCentre National de la Recherche Scientifique · FRModèles Insectes de l'Immunité Innée · FRUniversity of Calgary · CAWashington University in St. Louis · US

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
NIH HHS P40 OD018537
6 · The paper itself

Abstract

Serratia marcescens is an opportunistic bacterium that infects a wide range of hosts including humans. It is a potent pathogen in a septic injury model of Drosophila melanogaster since a few bacteria directly injected in the body cavity kill the insect within a day. In contrast, flies do not succumb to ingested bacteria for days even though some bacteria cross the intestinal barrier into the hemolymph within hours. The mechanisms by which S. marcescens attacks enterocytes and damages the intestinal epithelium remain uncharacterized. To better understand intestinal infections, we performed a genetic screen for loss of virulence of ingested S. marcescens and identified FliR, a structural component of the flagellum, as a virulence factor. Next, we compared the virulence of two flagellum mutants fliR and flhD in two distinct S. marcescens strains. Both genes are required for S. marcescens to escape the gut lumen into the hemocoel, indicating that the flagellum plays an important role for the passage of bacteria through the intestinal barrier. Unexpectedly, fliR but not flhD is involved in S. marcescens-mediated damages of the intestinal epithelium that ultimately contribute to the demise of the host. Our results therefore suggest a flagellum-independent role for fliR in bacterial virulence.

Indexed as

Serratia InfectionsAnimalsBacterial ProteinsDisease Models, AnimalDrosophila melanogasterFlagellaGastroenteritisIntestinal MucosaMembrane ProteinsMutationSerratia marcescensVirulenceBacterial ProteinsFliR protein, BacteriaMembrane Proteins

Identifiers

PMID35197500
PMCPMC8866479
OpenAlexW4220998771

What OpenQuestion holds

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LicenceCC BY
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.