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Molecular Mechanisms Underpinning the Circulation and Cellular Uptake of Mycobacterium ulcerans Toxin Mycolactone

Authors :
Bruno Tello Rubio
Florence Bugault
Blandine Baudon
Bertrand Raynal
Sébastien Brûlé
Jean-David Morel
Sarah Saint-Auret
Nicolas Blanchard
Caroline Demangel
Laure Guenin-Macé
Immunobiologie de l'Infection - Immunobiology of Infection
Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité)
Biophysique Moléculaire (plateforme) - Molecular Biophysics (platform)
Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité)
Laboratoire d'innovation moléculaire et applications (LIMA)
Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
This work was supported by the Fondation Raoul Follereau.
Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)
Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS)
Source :
Frontiers in Pharmacology, Frontiers in Pharmacology, 2021, 12, pp.733496. ⟨10.3389/fphar.2021.733496⟩, Frontiers in Pharmacology, Frontiers, 2021, 12, pp.733496. ⟨10.3389/fphar.2021.733496⟩, Frontiers in Pharmacology, Vol 12 (2021)
Publication Year :
2021
Publisher :
HAL CCSD, 2021.

Abstract

International audience; Mycolactone is a diffusible lipid toxin produced by Mycobacterium ulcerans, the causative agent of Buruli ulcer disease. Altough bacterially derived mycolactone has been shown to traffic from cutaneous foci of infection to the bloodstream, the mechanisms underpinning its access to systemic circulation and import by host cells remain largely unknown. Using biophysical and cell-based approaches, we demonstrate that mycolactone specific association to serum albumin and lipoproteins is necessary for its solubilization and is a major mechanism to regulate its bioavailability. We also demonstrate that Scavenger Receptor (SR)-B1 contributes to the cellular uptake of mycolactone. Overall, we suggest a new mechanism of transport and cell entry, challenging the dogma that the toxin enters host cells via passive diffusion.

Details

Language :
English
ISSN :
16639812
Database :
OpenAIRE
Journal :
Frontiers in Pharmacology, Frontiers in Pharmacology, 2021, 12, pp.733496. ⟨10.3389/fphar.2021.733496⟩, Frontiers in Pharmacology, Frontiers, 2021, 12, pp.733496. ⟨10.3389/fphar.2021.733496⟩, Frontiers in Pharmacology, Vol 12 (2021)
Accession number :
edsair.pmid.dedup....baaa792727464b0d5dc2ee17d3690f9b
Full Text :
https://doi.org/10.3389/fphar.2021.733496⟩