Grant: DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
University of British Columbia
$120,000.00
Modeling Microbe-Host Interactions in Patients with Crohn's Disease
EF 2025-26
Résumé
Trillions of microorganisms including bacteria and fungi reside within and on the human body and together are known as the microbiota. The gut microbiota in the gastrointestinal (GI) tract contains a majority of these microorganisms which aid in digestion through breaking down components of food and providing important vitamins and metabolites for us to use. The GI tract and the gut microbiota interact at the mucus layer consisting of a gel-like substance that protects the host and provides a niche and nutrients for the gut microbiota. The mucus layer is also very low in oxygen making the interaction between microbes and the gut lining difficult to study in the lab.
In Canada over 300,000 Canadians are diagnosed with inflammatory bowel disease (IBD) a form of chronic inflammation in the GI tract where the mucus layer is disrupted. IBD is thought to be result of a disrupted microbiota-host interaction leading to an exaggerated inflammatory response. Furthermore, patients with IBD tend to have changes in their microbiota with the loss of certain beneficial bacteria and lack of vital metabolites and this is referred to as dysbiosis.
Utilizing a novel system we have developed to culture microbes and patient derived cells in a low oxygen environment we will investigate how mucin degradation metabolites contribute to normal gut function. Additionally, we will determine whether the abnormal mucus produced by patients with IBD leads to aberrant interactions with the gut microbiota. Lastly, we will determine whether introducing dietary fibre that feeds beneficial bacteria can restore healthy metabolite production. Ultimately this work will lead to a deeper understanding of how the gut microbiota interacts with dysfunctional mucus and leads to dysbiosis in patients with IBD. Furthermore, our research can be used to help identify therapeutics and preventative strategies targeting the gut mucus layer in IBD.
Programme
DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
560065
Name
Sousa James A
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
DT1 (Biomedical and/or Clinical Research) CGRS Doctoral
Projecttitle
Modeling Microbe-Host Interactions in Patients with Crohn's Disease
Programtype2
Studentship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$120,000
Cihrequipment2
$0
Programname2
DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Keyworddelim
Inflammatory Bowel Disease; Microbiome; Mucus; Organoid
Abstract
Trillions of microorganisms including bacteria and fungi reside within and on the human body and together are known as the microbiota. The gut microbiota in the gastrointestinal (GI) tract contains a majority of these microorganisms which aid in digestion through breaking down components of food and providing important vitamins and metabolites for us to use. The GI tract and the gut microbiota interact at the mucus layer consisting of a gel-like substance that protects the host and provides a niche and nutrients for the gut microbiota. The mucus layer is also very low in oxygen making the interaction between microbes and the gut lining difficult to study in the lab.
In Canada over 300,000 Canadians are diagnosed with inflammatory bowel disease (IBD) a form of chronic inflammation in the GI tract where the mucus layer is disrupted. IBD is thought to be result of a disrupted microbiota-host interaction leading to an exaggerated inflammatory response. Furthermore, patients with IBD tend to have changes in their microbiota with the loss of certain beneficial bacteria and lack of vital metabolites and this is referred to as dysbiosis.
Utilizing a novel system we have developed to culture microbes and patient derived cells in a low oxygen environment we will investigate how mucin degradation metabolites contribute to normal gut function. Additionally, we will determine whether the abnormal mucus produced by patients with IBD leads to aberrant interactions with the gut microbiota. Lastly, we will determine whether introducing dietary fibre that feeds beneficial bacteria can restore healthy metabolite production. Ultimately this work will lead to a deeper understanding of how the gut microbiota interacts with dysfunctional mucus and leads to dysbiosis in patients with IBD. Furthermore, our research can be used to help identify therapeutics and preventative strategies targeting the gut mucus layer in IBD.
Competitiondate
202511
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Sousa, James A
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $120,000~ $0~