Evidence map›Paper›PMID 41290585›Full record

ArticleNature communications2025

Meningococci drive host membrane tubulation to recruit their signaling receptors.

Audrey Laurent-Granger, Kévin Sollier, Bruno Saubamea, Virginie Mignon, Nicolas Goudin, Yaëlle Wormser, Morgane Wuckelt, Mahmoud Rifai, Thomas Heng, Lya L'hermitte and 11 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Audrey Laurent-Granger *Université Paris Cité, INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Paris, France.ORCID http://orcid.org/0009-0001-0291-1532
Kévin Sollier *Université Paris Cité, INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Paris, France.
Bruno SaubameaPlateforme d'Imagerie Cellulaire et MOléculaire PICMO, Université Paris Cité, US25 Inserm, UAR3612 CNRS, Faculté de Pharmacie de Paris, Paris, France.ORCID http://orcid.org/0000-0002-6218-0460
Virginie MignonPlateforme d'Imagerie Cellulaire et MOléculaire PICMO, Université Paris Cité, US25 Inserm, UAR3612 CNRS, Faculté de Pharmacie de Paris, Paris, France.
Nicolas GoudinPlatform for Image Analysis Center, SFR Necker, INSERM US 24, Paris, France.ORCID http://orcid.org/0000-0002-3967-4016
Yaëlle WormserUniversité Paris Cité, INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Paris, France.ORCID http://orcid.org/0009-0003-7997-9425
Morgane WuckeltUniversité Paris Cité, INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Paris, France.
Mahmoud RifaiUniversité Paris Cité, INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Paris, France.ORCID http://orcid.org/0009-0008-6012-2890
Thomas HengUniversité Paris Cité, INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Paris, France.
Lya L'hermitteUniversité Paris Cité, INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Paris, France.
Marta ConflittiUniversity of Padova, Padova, Italy.ORCID http://orcid.org/0009-0006-0250-2065
Julie MeyerUniversité Paris Cité, INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Paris, France.ORCID http://orcid.org/0000-0002-6144-927X
Hervé LecuyerLaboratoire de microbiologie clinique, AP-HP, Hôpital Necker Enfants Malades, Malades, France.
Anne JametUniversité Paris Cité, INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Paris, France.ORCID http://orcid.org/0000-0002-1902-6943
Nicolas BorghiUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.ORCID http://orcid.org/0000-0002-1558-5246
Philippe GirardUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
Emmanuelle BilleUniversité Paris Cité, INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Paris, France.ORCID http://orcid.org/0000-0001-9172-0510
Grégory LavieuUniversité Paris Cité, INSERM U1334, CNRS UMR8175, Department of Biomedical and Fundamental Sciences, Campus Saints-Germain-des-Prés, Paris, France.ORCID http://orcid.org/0000-0001-9852-4977
Eric RubinsteinSorbonne Université, Inserm, CNRS, Centre d'Immunologie et des Maladies Infectieuses, CIMI-Paris, Paris, France.ORCID http://orcid.org/0000-0001-7623-9665
Stefano MarulloUniversité Paris Cité, INSERM U1016, CNRS UMR8104, Institut Cochin, Paris, France. stefano.marullo@inserm.fr.ORCID http://orcid.org/0000-0001-9604-9973
Mathieu CoureuilUniversité Paris Cité, INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Paris, France. mathieu.coureuil@inserm.fr.ORCID http://orcid.org/0000-0001-7655-9685

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-19-CE14-0045-002
6 · The paper itself

Abstract

Once passed into the bloodstream, bacterial pathogens have a limited time to interact with permissive receptors at the surface of host cells. Neisseria meningitidis has developed an extremely effective strategy allowing it to find its receptors in a few seconds. Here, we report that N. meningitidis type IV pili exploit the physical properties of host cells' plasma membranes to promote the formation of early tubular membrane structures essential for initial bacterial adhesion. These tubular structures, which form before any signaling events in host cells, concentrate and trap multiple plasma membrane-associated proteins in the vicinity of bacteria, thereby facilitating the selection, interaction and activation of specific adhesion and signaling receptors by bacterial ligands present on type IV pili. Our results define an additional paradigm for the recruitment of specific receptors by pathogenic bacteria, which depends on the physical property of bacterial pili to induce the formation of tubular plasma membrane structures enriched in integral plasma membrane receptors.

Indexed as

Cell MembraneFimbriae, BacterialNeisseria meningitidisReceptors, Cell SurfaceBacterial AdhesionHeLa CellsHost-Pathogen InteractionsHumansSignal TransductionReceptors, Cell Surface

Identifiers

PMID41290585
PMCPMC12647851

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.