Antihyperalgesic properties of gut microbiota: Parabacteroides distasonis as a new probiotic strategy to alleviate chronic abdominal pain

Author:

Gervason Sandie1,Meleine Mathieu1,Lolignier Stéphane1,Meynier Maëva12,Daugey Valentine1,Birer Aurélien23,Aissouni Youssef1,Berthon Jean-Yves4,Ardid Denis1,Filaire Edith5,Carvalho Frédéric Antonio1ORCID

Affiliation:

1. NeuroDol, UMR 1107 INSERM, University of Clermont Auvergne, Clermont-Ferrand, France

2. M2iSH, UMR 1071 INSERM, University of Clermont Auvergne, Clermont-Ferrand, France

3. Centre National de Référence de la Résisitance aux Antibiotiques, Service de Bactériologie, Clermont-Ferrand, France

4. GREENTECH SA, Saint-Beauzire, France

5. ECREIN Team, Human Nutrition Unit (UNH), UMR 1019 INRAE-UCA, University of Clermont-Auvergne, Clermont-Ferrand, France

Abstract

Abstract The potential role of gut microbiota in pain modulation is arousing an emerging interest since recent years. This study investigated neuromodulatory properties of gut microbiota to identify next-generation probiotics to propose alternative therapies for visceral pain management. Neuromodulation ability of 10 bacterial strains isolated from a healthy donor was assessed both on ND7/23 immortalized cell line and primary neuronal cells from rat dorsal root ganglia. This screening highlighted the neuroinhibitory property of Parabacteroides distasonis (F1-2) strain, supported both by its intracellular content and membrane fraction, which was further investigated in visceral pain mouse models. Oral administration of F1-2 resulted in a significant decrease of colonic hypersensitivity (CHS) in dextran sulfate sodium (0.5%) model associated with low-grade inflammation and a significant decrease of CHS in Citrobacter rodentium postinfectious models. No effect of F1-2 oral administration on CHS was observed in a neonatal maternal separation stress model. Antihyperalgesic effect unlikely involved modulation of inflammatory processes or restoration of intestinal barrier. Exploration of direct dialogue mechanisms between this strain and nervous system, assessed by calcium imaging experiments, revealed that F1-2 interacts directly with nociceptors by reducing activation level on capsaicin, inflammatory soup, and bradykinin stimulations. Our study provides new insights about bacteria–host interaction and places P distasonis as a potential therapeutic strategy in the treatment of visceral pain observed in leaky gut–associated pathologies.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine,Neurology (clinical),Neurology

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