Evidence map›Paper›PMID 39358320›Full record

ArticleNature communications2024

Aquatic environment drives the emergence of cell wall-deficient dormant forms in Listeria.

Filipe Carvalho, Alexis Carreaux, Anna Sartori-Rupp, Stéphane Tachon, Anastasia D Gazi, Pascal Courtin, Pierre Nicolas, Florence Dubois-Brissonnet, Aurélien Barbotin, Emma Desgranges and 8 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Quantitative Risk Assessment ofFoods (Basel, Switzerland) · 2025
    Article
  6. Microbiology spectrum · 2025
    Article
  7. Article
  8. Article
  9. Article
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

18 authors.

Filipe CarvalhoINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.ORCID 0000-0002-6828-1772
Alexis CarreauxINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Anna Sartori-RuppNanoImaging Core Facility, Institut Pasteur, Paris, France.ORCID 0000-0001-8540-9910
Stéphane TachonNanoImaging Core Facility, Institut Pasteur, Paris, France.
Anastasia D GaziUltrastructural Bioimaging Facility, Institut Pasteur, Paris, France.ORCID 0000-0002-2922-3625
Pascal CourtinINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Pierre NicolasINRAE, Université Paris-Saclay, MaIAGE, Jouy-en-Josas, France.ORCID 0000-0002-1133-0609
Florence Dubois-BrissonnetINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Aurélien BarbotinINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.ORCID 0000-0001-8561-5191
Emma DesgrangesINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Matthieu BertrandINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Karine GlouxINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.ORCID 0000-0002-8880-6628
Catherine SchoulerINRAE, Université de Tours, ISP, Nouzilly, France.ORCID 0000-0002-3480-6278
Rut Carballido-LópezINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.ORCID 0000-0001-9383-8811
Marie-Pierre Chapot-ChartierINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Eliane MilohanicINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.ORCID 0009-0002-8812-3023
Hélène BierneINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Alessandro PagliusoINRAE, Université Paris-Saclay, AgroParisTech, Micalis Institute, Jouy-en-Josas, France. alessandro.pagliuso@inrae.fr.

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-20-CE15-0008-01
6 · The paper itself

Abstract

Stressed bacteria can enter a dormant viable but non-culturable (VBNC) state. VBNC pathogens pose an increased health risk as they are undetectable by growth-based techniques and can wake up back into a virulent state. Although widespread in bacteria, the mechanisms governing this phenotypic switch remain elusive. Here, we investigate the VBNC state transition in the human pathogen Listeria monocytogenes. We show that bacteria starved in mineral water become VBNC by converting into osmotically stable cell wall-deficient coccoid forms, a phenomenon that occurs in other Listeria species. We reveal the bacterial stress response regulator SigB and the autolysin NamA as major actors of VBNC state transition. We lastly show that VBNC Listeria revert to a walled and virulent state after passage in chicken embryos. Our study provides more detail on the VBNC state transition mechanisms, revealing wall-free bacteria naturally arising in aquatic environments as a potential survival strategy in hypoosmotic and oligotrophic conditions.

Indexed as

Cell WallListeria monocytogenesAnimalsBacterial ProteinsChick EmbryoHumansListeriaListeriosisMicrobial ViabilityVirulenceBacterial Proteins

Identifiers

PMID39358320
PMCPMC11447242

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.