Evidence map›Paper›PMID 42447168›Full record

ArticlePLoS pathogens2026

Unveiling a missing component of the atypical type IV secretion system required for natural transformation of Helicobacter pylori.

J Francisco Villa, Sumedha Kondekar, Yoann Fauconnet, Mérick Machouri, Céline Lacrouts, Xavier Veaute, Raphaël Guérois, Eduardo P C Rocha, Jessica Andreani, J Pablo Radicella

Abstract read
In one paragraph

Article in PLoS pathogens, 2026. 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
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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

5 · Who and what money

Authors and funding

10 authors.

J Francisco VillaUniversité Paris-Saclay, Université Paris Cité, CEA, Stabilité Génétique Cellules Souches et Radiations, DRCM, Institut de Biologie François Jacob, Fontenay aux Roses, France.
Sumedha KondekarUniversité Paris-Saclay, Université Paris Cité, CEA, Stabilité Génétique Cellules Souches et Radiations, DRCM, Institut de Biologie François Jacob, Fontenay aux Roses, France.
Yoann FauconnetUniversité Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), Gif-sur-Yvette, France.
Mérick MachouriUniversité Paris-Saclay, Université Paris Cité, CEA, Stabilité Génétique Cellules Souches et Radiations, DRCM, Institut de Biologie François Jacob, Fontenay aux Roses, France.
Céline LacroutsUniversité Paris-Saclay, Université Paris Cité, CEA, Stabilité Génétique Cellules Souches et Radiations, DRCM, Institut de Biologie François Jacob, Fontenay aux Roses, France.
Xavier VeauteUniversité Paris-Saclay, Université Paris Cité, CEA, INSERM, Stabilité Génétique Cellules Souches et Radiations, DRCM, Institut de Biologie François Jacob, Fontenay aux Roses, France.
Raphaël GuéroisUniversité Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), Gif-sur-Yvette, France.
Eduardo P C RochaInstitut Pasteur, Université de Paris Cité, CNRS UMR3525, Microbial Evolutionary Genomics, Paris, France.
Jessica AndreaniUniversité Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), Gif-sur-Yvette, France.
J Pablo RadicellaUniversité Paris-Saclay, Université Paris Cité, CEA, Stabilité Génétique Cellules Souches et Radiations, DRCM, Institut de Biologie François Jacob, Fontenay aux Roses, France.ORCID 0000-0002-8807-7226

Funding

Agence Nationale de la RechercheCommissariat à l’Energie Atomique (JPR)Grand équipement national de calcul intensif (GENCI)
6 · The paper itself

Abstract

Exchange of genetic information by natural transformation shapes bacterial evolution. In Helicobacter pylori it is thought to drive its unusually high recombination rate, which has a crucial role in the evolution of virulence and the propagation of antibiotics resistance genes. While in most cases uptake of the incoming DNA into the periplasm is mediated by type IV pili, in H. pylori this initial step of natural transformation requires ComB, a unique competence-specific type IV secretion system (T4SS). The mechanisms by which ComB mediates DNA uptake are still poorly understood, since T4SS are usually involved in an opposite process of DNA export. Here, we identify a gene (hp1421) that is absolutely required for uptake of the transforming DNA into the periplasm, although distant from the comB operons. We show that hp1421 codes for a hexameric ATPase from the VirB11 family. HP1421 is present in the cytoplasm and interacts with ComB4, another ATPase of the T4SS inner membrane subcomplex. The structural modelling and functional analysis of HP1421 and its interaction with ComB4 indicate that HP1421 is a missing component of the ComB inner-membrane subcomplex that we propose to name ComB11. Phylogenetic analyses show that comB11 is a H. pylori core gene and suggest that the competence-dedicated ComB T4SS was a recent acquisition within Helicobacteraceae. Hence, co-option of the T4SS for DNA transformation requires nearly all the proteins that were previously essential for DNA conjugation.

Indexed as

Bacterial ProteinsHelicobacter pyloriTransformation, BacterialType IV Secretion SystemsAdenosine TriphosphatasesDNA, BacterialPhylogenyAdenosine TriphosphatasesBacterial ProteinsDNA, BacterialType IV Secretion Systems

Identifiers

PMID42447168
PMCPMC13395361

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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.