Inulin Prebiotic Protects against Lethal Pseudomonas aeruginosa Acute Infection via γδ T Cell Activation.
Emilie BoucherCaroline PlazyAudrey Le GouëllecBertrand ToussaintDalil HannaniPublished in: Nutrients (2023)
Pseudomonas aeruginosa ( P. aeruginosa ) causes harmful lung infections, especially in immunocompromised patients. The immune system and Interleukin (IL)-17-producing γδ T cells (γδ T) are critical in controlling these infections in mice. The gut microbiota modulates host immunity in both cancer and infection contexts. Nutritional intervention is a powerful means of modulating both microbiota composition and functions, and subsequently the host's immune status. We have recently shown that inulin prebiotic supplementation triggers systemic γδ T activation in a cancer context. We hypothesized that prophylactic supplementation with inulin might protect mice from lethal P. aeruginosa acute lung infection in a γδ T-dependent manner. C57Bl/6 mice were supplemented with inulin for 15 days before the lethal P. aeruginosa lung infection, administered intranasally. We demonstrate that prophylactic inulin supplementation triggers a higher proportion of γδ T in the blood, accompanied by a higher infiltration of IL-17-producing γδ T within the lungs, and protects 33% of infected mice from death. This observation relies on γδ T, as in vivo γδ TcR blocking using a monoclonal antibody completely abrogates inulin-mediated protection. Overall, our data indicate that inulin supplementation triggers systemic γδ T activation, and could help resolve lung P. aeruginosa infections. Moreover, our data suggest that nutritional intervention might be a powerful way to prevent/reduce infection-related mortality, by reinforcing the microbiota-dependent immune system.
Keyphrases
- pseudomonas aeruginosa
- high fat diet induced
- randomized controlled trial
- end stage renal disease
- monoclonal antibody
- liver failure
- cystic fibrosis
- chronic kidney disease
- drug induced
- electronic health record
- escherichia coli
- intensive care unit
- risk factors
- biofilm formation
- squamous cell
- peritoneal dialysis
- young adults
- insulin resistance
- multidrug resistant
- data analysis
- mechanical ventilation