Fasting increases microbiome-based colonization resistance and reduces host inflammatory responses during an enteric bacterial infection

Author:

Graef Franziska A.ORCID,Celiberto Larissa S.ORCID,Allaire Joannie M.ORCID,Kuan Mimi T. Y.ORCID,Bosman Else S.ORCID,Crowley Shauna M.ORCID,Yang Hyungjun,Chan Justin H.ORCID,Stahl Martin,Yu Hongbing,Quin Candice,Gibson Deanna L.,Verdu Elena F.,Jacobson KevanORCID,Vallance Bruce A.ORCID

Abstract

Reducing food intake is a common host response to infection, yet it remains unclear whether fasting is detrimental or beneficial to an infected host. Despite the gastrointestinal tract being the primary site of nutrient uptake and a common route for infection, studies have yet to examine how fasting alters the host’s response to an enteric infection. To test this, mice were fasted before and during oral infection with the invasive bacterium Salmonella enterica serovar Typhimurium. Fasting dramatically interrupted infection and subsequent gastroenteritis by suppressing Salmonella’s SPI-1 virulence program, preventing invasion of the gut epithelium. Virulence suppression depended on the gut microbiota, as Salmonella’s invasion of the epithelium proceeded in fasting gnotobiotic mice. Despite Salmonella’s restored virulence within the intestines of gnotobiotic mice, fasting downregulated pro-inflammatory signaling, greatly reducing intestinal pathology. Our study highlights how food intake controls the complex relationship between host, pathogen and gut microbiota during an enteric infection.

Funder

Canadian Institutes of Health Research

Crohn's and Colitis Canada

Michael Smith Foundation for Health Research

The University of British Columbia

BC Children's Hospital Research Institute

Canada Research Chairs

Children with Intestinal and Liver Disorders (CHILD) Foundation

Publisher

Public Library of Science (PLoS)

Subject

Virology,Genetics,Molecular Biology,Immunology,Microbiology,Parasitology

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