Evidence map›Paper›PMID 31761719›Full record

ArticleCell host & microbe2019

An RNA-Binding Protein Secreted by a Bacterial Pathogen Modulates RIG-I Signaling.

Alessandro Pagliuso, To Nam Tham, Eric Allemand, Stevens Robertin, Bruno Dupuy, Quentin Bertrand, Christophe Bécavin, Mikael Koutero, Valérie Najburg, Marie-Anne Nahori and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Cell host & microbe, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

38 citing papers in PubMed, 65 citations in OpenAlex.

  1. bioRxiv : the preprint server for biology · 2026
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  8. Frontiers in immunology · 2025
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  12. TheProceedings of the National Academy of Sciences of the United States of America · 2023
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  13. Inactivation ofFrontiers in microbiology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 6 institutions in 3 countries.

Alessandro PagliusoUnité des Interactions Bactéries-Cellules, Institut Pasteur, Paris, France; U604 Inserm, Paris, France; USC2020 INRA, Paris, France. Electronic address: alessandro.pagliuso@inra.fr.
To Nam ThamUnité des Interactions Bactéries-Cellules, Institut Pasteur, Paris, France; U604 Inserm, Paris, France; USC2020 INRA, Paris, France.
Eric AllemandUnité de régulation épigénétique, Institut Pasteur, UMR3738 CNRS, Paris, France.
Stevens RobertinUnité des Interactions Bactéries-Cellules, Institut Pasteur, Paris, France; U604 Inserm, Paris, France; USC2020 INRA, Paris, France.
Bruno DupuyLaboratoire Pathogenèse des Bactéries Anaérobies, Institut Pasteur, Paris, Université de Paris, Paris, France.
Quentin BertrandUniversité Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale (IBS), Bacterial Pathogenesis Group, Grenoble, France.
Christophe BécavinHub de bioinformatique et biostatistique - Centre de Bioinformatique, Biostatistique et Biologie Intégrative, Unité mixte de Service et Recherche 3756 Institut Pasteur - Centre National de la Recherche Scientifique, Paris 75015, France.
Mikael KouteroUnité des Interactions Bactéries-Cellules, Institut Pasteur, Paris, France; U604 Inserm, Paris, France; USC2020 INRA, Paris, France.
Valérie NajburgUnité de Génomique Virale et Vaccination, Institut Pasteur, Paris 75015, France; CNRS UMR-3569, Paris, France.
Marie-Anne NahoriUnité des Interactions Bactéries-Cellules, Institut Pasteur, Paris, France; U604 Inserm, Paris, France; USC2020 INRA, Paris, France.
Frédéric TangyUnité de Génomique Virale et Vaccination, Institut Pasteur, Paris 75015, France; CNRS UMR-3569, Paris, France.
Fabrizia StavruUnité des Interactions Bactéries-Cellules, Institut Pasteur, Paris, France; U604 Inserm, Paris, France; USC2020 INRA, Paris, France.
Sergey BessonovDepartment I of Internal Medicine, University Hospital Cologne, Cologne, Germany; Cologne Excellence Cluster on Cellular Stress Response in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany; Department of Translational Epigenetics and Tumor Genetics, University Hospital Cologne, Cologne, Germany.
Andréa DessenUniversité Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale (IBS), Bacterial Pathogenesis Group, Grenoble, France; Brazilian Biosciences National Laboratory (LNBio), CNPEM, Campinas, SP, Brazil.
Christian MuchardtUnité de régulation épigénétique, Institut Pasteur, UMR3738 CNRS, Paris, France.
Alice LebretonÉquipe Infection et Devenir de l'ARN, Institut de biologie de l'Ecole normale supérieure (IBENS), Ecole normale supérieure, CNRS, Inserm, PSL Université Paris, Paris 75005, France; INRA, IBENS, 75005 Paris, France.
Anastassia V KomarovaUnité de Génomique Virale et Vaccination, Institut Pasteur, Paris 75015, France; CNRS UMR-3569, Paris, France.
Pascale CossartUnité des Interactions Bactéries-Cellules, Institut Pasteur, Paris, France; U604 Inserm, Paris, France; USC2020 INRA, Paris, France. Electronic address: pcossart@pasteur.fr.
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FRInserm · FRBrazilian Center for Research in Energy and Materials · BRCologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEUniversité Paris Cité · FR

Funding

European Research Council 670823
6 · The paper itself

Abstract

RNA-binding proteins (RBPs) perform key cellular activities by controlling the function of bound RNAs. The widely held assumption that RBPs are strictly intracellular has been challenged by the discovery of secreted RBPs. However, extracellular RBPs have been described in eukaryotes, while secreted bacterial RBPs have not been reported. Here, we show that the bacterial pathogen Listeria monocytogenes secretes a small RBP that we named Zea. We show that Zea binds a subset of L. monocytogenes RNAs, causing their accumulation in the extracellular medium. Furthermore, during L. monocytogenes infection, Zea binds RIG-I, the non-self-RNA innate immunity sensor, potentiating interferon-β production. Mouse infection studies reveal that Zea affects L. monocytogenes virulence. Together, our results unveil that bacterial RNAs can be present extracellularly in association with RBPs, acting as "social RNAs" to trigger a host response during infection.

Indexed as

AnimalsBacterial ProteinsDEAD Box Protein 58HEK293 CellsHost Microbial InteractionsHumansImmunity, InnateInterferon-betaListeria monocytogenesMiceRNA, BacterialRNA-Binding ProteinsSignal TransductionVirulenceBacterial ProteinsDdx58 protein, mouseDEAD Box Protein 58Interferon-betaRNA, BacterialRNA-Binding Proteinsbacteriophage A118extracellular RNAtype I IFN

Identifiers

PMID31761719
PMCPMC6907008
OpenAlexW2991013360

What OpenQuestion holds

Textmetadata
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.