Evidence map›Paper›PMID 39841841›Full record

ArticleScience advances2025

Elucidating assembly and function of VirB8 cell wall subunits refines the DNA translocation model in Gram-positive T4SSs.

Robine Maffo-Woulefack, Abbas Mohamad Ali, Haifa Laroussi, Julien Cappèle, Felipe Romero-Saavedra, Nancy Ramia, Emilie Robert, Sandrine Mathiot, Nicolas Soler, Yvonne Roussel and 6 more

Abstract read
In one paragraph

Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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  3. 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

16 authors.

Robine Maffo-WoulefackUniversité de Lorraine, INRAE, DynAMic, F-54000 Nancy, France.ORCID 0000-0003-2746-0229
Abbas Mohamad AliUniversité de Lorraine, INRAE, DynAMic, F-54000 Nancy, France.
Haifa LaroussiUniversité de Lorraine, INRAE, DynAMic, F-54000 Nancy, France.
Julien CappèleUniversité de Lorraine, CNRS, CRM2, F-54000 Nancy, France.
Felipe Romero-SaavedraDivision of Pediatric Infectious Diseases, Dr. von Hauner Children's Hospital, Ludwig-Maximillians University, Munich, Germany.ORCID 0000-0003-3134-7018
Nancy RamiaUniversité de Lorraine, INRAE, DynAMic, F-54000 Nancy, France.
Emilie RobertUniversité de Lorraine, INRAE, DynAMic, F-54000 Nancy, France.
Sandrine MathiotUniversité de Lorraine, CNRS, CRM2, F-54000 Nancy, France.
Nicolas SolerUniversité de Lorraine, INRAE, DynAMic, F-54000 Nancy, France.ORCID 0000-0002-4292-4020
Yvonne RousselUniversité de Lorraine, INRAE, DynAMic, F-54000 Nancy, France.ORCID 0000-0003-3191-043X
Rémi FronzesInstitut Européen de Chimie et Biologie, University of Bordeaux, Pessac, France.
Johannes HuebnerDivision of Pediatric Infectious Diseases, Dr. von Hauner Children's Hospital, Ludwig-Maximillians University, Munich, Germany.ORCID 0000-0003-1232-4646
Claude DidierjeanUniversité de Lorraine, CNRS, CRM2, F-54000 Nancy, France.ORCID 0000-0002-3176-8974
Frédérique FavierUniversité de Lorraine, CNRS, CRM2, F-54000 Nancy, France.ORCID 0000-0003-3249-997X
Nathalie Leblond-BourgetUniversité de Lorraine, INRAE, DynAMic, F-54000 Nancy, France.ORCID 0000-0001-5739-1370
Badreddine DouziUniversité de Lorraine, INRAE, DynAMic, F-54000 Nancy, France.ORCID 0000-0003-3140-4713

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial type IV secretion systems (T4SSs) are widespread nanomachines specialized in the transport across the cell envelope of various types of molecules including mobile genetic elements during conjugation. Despite their prevalence in Gram-positive bacteria, including relevant pathogens, their assembly and functioning remain unknown. This study addresses these gaps by investigating VirB8 proteins, known to be central components of conjugative T4SSs in Gram-positive bacteria. However, the functional packing and precise role of VirB8 in T4SSs biology remain undefined. Our findings elucidate the nature of VirB8 proteins as cell wall components, where they multimerize and exhibit a conserved assembly pattern, distinct from VirB8 in Gram-negative bacteria. We also demonstrate that VirB8 proteins interact with other T4SS subunits and DNA, indicating their pivotal role in the building of the DNA translocation channel across the cell wall. We lastly propose a distinct architecture for conjugative T4SSs in Gram-positive bacteria compared to their Gram-negative counterparts, possibly attributed to the differences in the cell wall structure.

Indexed as

Bacterial ProteinsCell WallDNA, BacterialGram-Positive BacteriaType IV Secretion SystemsProtein BindingProtein MultimerizationBacterial ProteinsDNA, BacterialType IV Secretion Systems

Identifiers

PMID39841841
PMCPMC11753425

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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.