The colibactin-producing Escherichia coli alters the tumor microenvironment to immunosuppressive lipid overload facilitating colorectal cancer progression and chemoresistance
Nilmara de Oliveira Alves,
Guillaume Dalmasso,
Darja Nikitina,
Amaury Vaysse,
Richard Ruez,
Lea Ledoux,
Thierry Pedron,
Emma Bergsten,
Olivier Boulard,
Lora Autier,
Sofian Allam,
Laurence Motreff,
Pierre Sauvanet,
Diane Letourneur,
Pragya Kashyap,
Johan Gagnière,
Denis Pezet,
Catherine Godfraind,
Michel Salzet,
Emmanuel Lemichez,
Mathilde Bonnet,
Imène Najjar,
Christophe Malabat,
Marc Monot,
Denis Mestivier,
Nicolas Barnich,
Pankaj Yadav,
Isabelle Fournier,
Sean Kennedy,
Amel Mettouchi,
Richard Bonnet,
Iradj Sobhani,
Mathias Chamaillard
Affiliations
Nilmara de Oliveira Alves
ONCOLille, INSERM, Phycell, University of Lille, Lille, France
Guillaume Dalmasso
Microbes, Intestin, Inflammation et Susceptibilité de l’Hôte (M2iSH), Centre de Recherche en Nutrition Humaine Auvergne, Université Clermont Auvergne, Clermont-Ferrand, France
Darja Nikitina
CNRS, Institute Pasteur, Paris, France
Amaury Vaysse
Institut Pasteur, Université Paris Cité, Bioinformatics and Biostatistics Hub, Plate-Forme Technologique Biomics, Paris, France
Richard Ruez
ONCOLille, INSERM, Phycell, University of Lille, Lille, France
Lea Ledoux
Réponse Inflammatoire et Spectrométrie de Masse-PRISM, University of Lille, Lille, France
Thierry Pedron
Institut Pasteur, Inserm, Paris, France
Emma Bergsten
Institut Pasteur, Université Paris Cité, Paris, France
Olivier Boulard
ONCOLille, INSERM, Phycell, University of Lille, Lille, France
Lora Autier
ONCOLille, INSERM, Phycell, University of Lille, Lille, France
Sofian Allam
ONCOLille, INSERM, Phycell, University of Lille, Lille, France
Laurence Motreff
Institut Pasteur, Université Paris Cité, Bioinformatics and Biostatistics Hub, Plate-Forme Technologique Biomics, Paris, France
Pierre Sauvanet
Microbes, Intestin, Inflammation et Susceptibilité de l’Hôte (M2iSH), Centre de Recherche en Nutrition Humaine Auvergne, Université Clermont Auvergne, Clermont-Ferrand, France
Diane Letourneur
Institut Pasteur, Université Paris Cité, Paris, France
Pragya Kashyap
Department of Bioscience & Bioengineering, Indian Institute of Technology, Jodhpur, Rajasthan, India
Johan Gagnière
Microbes, Intestin, Inflammation et Susceptibilité de l’Hôte (M2iSH), Centre de Recherche en Nutrition Humaine Auvergne, Université Clermont Auvergne, Clermont-Ferrand, France
Denis Pezet
Microbes, Intestin, Inflammation et Susceptibilité de l’Hôte (M2iSH), Centre de Recherche en Nutrition Humaine Auvergne, Université Clermont Auvergne, Clermont-Ferrand, France
Catherine Godfraind
Microbes, Intestin, Inflammation et Susceptibilité de l’Hôte (M2iSH), Centre de Recherche en Nutrition Humaine Auvergne, Université Clermont Auvergne, Clermont-Ferrand, France
Michel Salzet
Réponse Inflammatoire et Spectrométrie de Masse-PRISM, University of Lille, Lille, France
Emmanuel Lemichez
Institut Pasteur, Université Paris Cité, Paris, France
Mathilde Bonnet
Microbes, Intestin, Inflammation et Susceptibilité de l’Hôte (M2iSH), Centre de Recherche en Nutrition Humaine Auvergne, Université Clermont Auvergne, Clermont-Ferrand, France
Imène Najjar
Institut Pasteur, Université Paris Cité, Bioinformatics and Biostatistics Hub, Plate-Forme Technologique Biomics, Paris, France
Christophe Malabat
Institut Pasteur, Université Paris Cité, Bioinformatics and Biostatistics Hub, Plate-Forme Technologique Biomics, Paris, France
Marc Monot
Institut Pasteur, Université Paris Cité, Bioinformatics and Biostatistics Hub, Plate-Forme Technologique Biomics, Paris, France
Denis Mestivier
Université Paris Est Créteil, Créteil, France
Nicolas Barnich
Microbes, Intestin, Inflammation et Susceptibilité de l’Hôte (M2iSH), Centre de Recherche en Nutrition Humaine Auvergne, Université Clermont Auvergne, Clermont-Ferrand, France
Pankaj Yadav
Department of Bioscience & Bioengineering, Indian Institute of Technology, Jodhpur, Rajasthan, India
Isabelle Fournier
Réponse Inflammatoire et Spectrométrie de Masse-PRISM, University of Lille, Lille, France
Sean Kennedy
CNRS, Institute Pasteur, Paris, France
Amel Mettouchi
Institut Pasteur, Université Paris Cité, Paris, France
Richard Bonnet
Microbes, Intestin, Inflammation et Susceptibilité de l’Hôte (M2iSH), Centre de Recherche en Nutrition Humaine Auvergne, Université Clermont Auvergne, Clermont-Ferrand, France
Iradj Sobhani
Université Paris Est Créteil, Créteil, France
Mathias Chamaillard
ONCOLille, INSERM, Phycell, University of Lille, Lille, France
ABSTRACTIntratumoral bacteria flexibly contribute to cellular and molecular tumor heterogeneity for supporting cancer recurrence through poorly understood mechanisms. Using spatial metabolomic profiling technologies and 16SrRNA sequencing, we herein report that right-sided colorectal tumors are predominantly populated with Colibactin-producing Escherichia coli (CoPEC) that are locally establishing a high-glycerophospholipid microenvironment with lowered immunogenicity. It coincided with a reduced infiltration of CD8+ T lymphocytes that produce the cytotoxic cytokines IFN-γ where invading bacteria have been geolocated. Mechanistically, the accumulation of lipid droplets in infected cancer cells relied on the production of colibactin as a measure to limit genotoxic stress to some extent. Such heightened phosphatidylcholine remodeling by the enzyme of the Land’s cycle supplied CoPEC-infected cancer cells with sufficient energy for sustaining cell survival in response to chemotherapies. This accords with the lowered overall survival of colorectal patients at stage III-IV who were colonized by CoPEC when compared to patients at stage I-II. Accordingly, the sensitivity of CoPEC-infected cancer cells to chemotherapies was restored upon treatment with an acyl-CoA synthetase inhibitor. By contrast, such metabolic dysregulation leading to chemoresistance was not observed in human colon cancer cells that were infected with the mutant strain that did not produce colibactin (11G5∆ClbQ). This work revealed that CoPEC locally supports an energy trade-off lipid overload within tumors for lowering tumor immunogenicity. This may pave the way for improving chemoresistance and subsequently outcome of CRC patients who are colonized by CoPEC.