Intitulé du projet
Decoding Dormancy: Uncovering the VBNC state and its role in pathogenesis
Nature du financement
ANR
État du projet
Soumis
Année de soumission
2025
Programme / appel + année
PRC 2026
Programme / appel + année
Axe H.03 - Maladies infectieuses et environnement - CE35
Equipe(s) impliquée(s) dans le projet
StatInfOmics
Coordinateur·trice (nom et prénom)
NICOLAS Pierre
Rôle de MaIAGE dans le projet
Partenaire (projet multipartenaires)
Nom(s) du(des) participant(s) - MaIAGE
Sandra Dérozier, Guillaume Kon Kam King, Pierre Nicolas
Nom(s) du(des) partenaire(s) (nom, labo et localisation) - Hors MaIAGE
Alessandro PAGLIUSO - MICALIS (INRAE Jouy-en-Josas), Marc LECUIT "Unité de Biologie des Infections" (Institut Pasteur, Paris)
Date de fin du projet
Résumé
Listeria monocytogenes is a ubiquitous opportunistic pathogen that can cope with stress by entering a
hibernation-like state called viable but non-culturable (VBNC) state. VBNC cells escape routine detection
methods posing a risk for human and animal health. We recently discovered that during the transition to
the VBNC state in an aquatic environment, Listeria paradoxically sheds its cell wall to generate cell wall-
deficient forms. The role of these atypical variants in pathogen dissemination and pathogenesis remains
obscure. The aim of the DormaList project is to integrate genome-wide forward genetic screens with omics
approaches and in vivo infection models to uncover the molecular mechanisms behind VBNC state entry
and reversal, and to understand how these dormant forms contribute to Listeria survival and virulence. By
deepening our understanding of bacterial dormancy, this project will promote new strategies to detect and
eradicate persistent pathogens. It will also reveal novel transmission mechanisms of a major foodborne
zoonotic agent, thus fostering human and animal health surveillance.
hibernation-like state called viable but non-culturable (VBNC) state. VBNC cells escape routine detection
methods posing a risk for human and animal health. We recently discovered that during the transition to
the VBNC state in an aquatic environment, Listeria paradoxically sheds its cell wall to generate cell wall-
deficient forms. The role of these atypical variants in pathogen dissemination and pathogenesis remains
obscure. The aim of the DormaList project is to integrate genome-wide forward genetic screens with omics
approaches and in vivo infection models to uncover the molecular mechanisms behind VBNC state entry
and reversal, and to understand how these dormant forms contribute to Listeria survival and virulence. By
deepening our understanding of bacterial dormancy, this project will promote new strategies to detect and
eradicate persistent pathogens. It will also reveal novel transmission mechanisms of a major foodborne
zoonotic agent, thus fostering human and animal health surveillance.