Deletion of both Dectin-1 and Dectin-2 affects the bacterial but not fungal gut microbiota and susceptibility to colitis in mice

• Published in: Microbiome 2022-06, Vol.10 (1), p.91-91, Article 91
• Main Authors: Wang, Yazhou, Spatz, Madeleine, Da Costa, Gregory, Michaudel, Chloé, Lapiere, Alexia, Danne, Camille, Agus, Allison, Michel, Marie-Laure, Netea, Mihai G, Langella, Philippe, Sokol, Harry, Richard, Mathias L
• Format: Article
• Language: English
• Subjects: Animals; Antifungal agents; Bacteria; Bacteria - genetics; Cell walls; Colitis; Crohn's disease; Dectin-1; Dectin-2; Dextran; Dextran Sulfate - adverse effects; Digestive system; Disease Models, Animal; Feces; Fungi; Gastrointestinal Microbiome; Gastrointestinal tract; Glucans; Gut inflammation; Immune response; Inflammation; Inflammatory bowel disease; Inflammatory bowel diseases; Innate immunity; Intestinal microflora; Intestine; Lachnospiraceae; Lectins, C-Type; Life Sciences; Mice; Mice, Inbred C57BL; Microbiota; Mycobiome; Opportunist infection; Phenotypes; Polyethylene glycol; Sodium sulfate; Susceptibility; β-Glucan
• ISSN: 2049-2618; 2049-2618
• DOI: 10.1186/s40168-022-01273-4

Innate immunity genes have been reported to affect susceptibility to inflammatory bowel diseases (IBDs) and colitis in mice. Dectin-1, a receptor for fungal cell wall β-glucans, has been clearly implicated in gut microbiota modulation and modification of the susceptibility to gut inflammation. Here, we explored the role of Dectin-1 and Dectin-2 (another receptor for fungal cell wall molecules) deficiency in intestinal inflammation. Susceptibility to dextran sodium sulfate (DSS)-induced colitis was assessed in wild-type, Dectin-1 knockout (KO), Dectin-2KO, and double Dectin-1KO and Dectin-2KO (D-1/2KO) mice. Inflammation severity, as well as bacterial and fungal microbiota compositions, was monitored. While deletion of Dectin-1 or Dectin-2 did not have a strong effect on DSS-induced colitis, double deletion of Dectin-1 and Dectin-2 significantly protected the mice from colitis. The protection was largely mediated by the gut microbiota, as demonstrated by fecal transfer experiments. Treatment of D-1/2KO mice with opportunistic fungal pathogens or antifungal agents did not affect the protection against gut inflammation, suggesting that the fungal microbiota had no role in the protective phenotype. Amplicon-based microbiota analysis of the fecal bacterial and fungal microbiota of D-1/2KO mice confirmed the absence of changes in the mycobiota but strong modification of the bacterial microbiota. We showed that bacteria from the Lachnospiraceae family were at least partly involved in this protection and that treatment with Blautia hansenii was enough to recapitulate the protection. Deletion of both the Dectin-1 and Dectin-2 receptors triggered a global shift in the microbial gut environment, affecting, surprisingly, mainly the bacterial population and driving protective effects in colitis. Members of the Lachnospiraceae family seem to play a central role in this protection. These findings provide new insights into the role of the Dectin receptors, which have been described to date as affecting only the fungal population, in intestinal physiopathology and in IBD. Video Abstract.