An official website of the United States government.

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Contribution of phytochemicals to gut symbiont colonization and synthesis of immunomodulatory sphingolipids

Investigators
Oh, Sungwhan F
Institutions
Brigham and Women's Hospital
Start date
2019
End date
2023
Objective
Project summaryRecent findings in studies of the human microbiome have added a layer of complexity to research on the impactof the diet on health. While the health benefits of certain classes of diet-derived molecules are well appreciated,the molecular mechanisms underlying these benefits have been only partially elucidated. The diet providesnutrients not only to the host but also to the microorganisms that make up the gut microbiota. The commensalmetagenome, which numerically exceeds the host genome by >100-fold, contributes enormous chemicaldiversity to nutrient metabolism. Dietary metabolites attributable to specific gut commensals, have been identifiedas key effector molecules of host health and disease in several studies.At the tripartite juncture of host, diet, and microbiota, we have been investigating a unique class of sphingolipidsof the gut commensal Bacteroides fragilis (BfaGCs) and their host immunomodulatory functions. BfaGCsregulate the proliferation of invariant natural killer T (NKT) cells in the host's colon, which determines diseasesusceptibility in the NKT cell?mediated murine model of inflammatory bowel disease. This colonic NKT-cellregulation by B. fragilis occurs only when colonization takes place during the first few days of life in mice. Thisobservation indicates that early postnatal exposure of the gut immune system to the microbiota is crucial inestablishing the number of gut NKT cells throughout life. Further studies have shown that terminal branching inthe glycosphingolipid structure is crucial in directing either agonism or antagonism of NKT cells functions. It is ofconsiderable interest that dietary branched-chain amino acids (BCAAs) can dictate the lipid structure of BfaGCs.This observation suggests a novel concept in symbiotic mediator synthesis: direct incorporation of dietary factorsinto bacterial biochemical pathways, where they are further converted into bioactive mediators.BCAAs are essential amino acids for humans and are primarily produced by plants. Many BCAA-rich diets ofplant origin are also rich in plant oligosaccharides (POs), some of which are metabolized exclusively by B. fragilisand confer this a survival advantage to this organism in the competitive environment of the gut. We hypothesizethat these phytochemicals (BCAAs and POs) act synergistically to help induce colonization by B. fragilis andpromote the production of NKT cell?regulatory BfaGCs that protect the host from NKT cell?mediated colitis.Using multi-pronged approaches (bacterial genetics, gnotobiotic mouse models, and high-sensitivity analyticalplatforms), we propose (1) to characterize critical genes in the BCAA-derived sphingolipid biosynthetic pathwayin B. fragilis and investigate their colonic NKT cell modulatory functions and (2) to determine the impact ofphytochemicals on immunomodulatory BfaGC production, postnatal NKT cell development, and colitis resistancein adulthood. We expect to acquire molecular-level information on how dietary factors can synergize growth ofbeneficial bacteria and bacterial production of symbiotic factors.
Funding Source
Nat'l. Center for Complementary and Integrative Health
Project source
View this project
Project number
1R01AT010268-01
Accession number
10268
Categories
Sanitation and Quality Standards