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Grant: DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)

University of British Columbia

$120,000.00

Microbial modulation of stress hormones in inflammatory bowel disease

FY 2025-26

Summary
Inflammatory Bowel Disease (IBD) is a lifelong condition affecting over 7 million people worldwide with no cure. In Canada, nearly 1% of the population is expected to be diagnosed by 2030, of which 25% are children. Pediatric IBD patients experience more severe symptoms and problems beyond the gut, including changes in hormone levels, mood disorders, and delayed puberty. One explanation for these effects may lie in the gut microbiota - the community of bacteria in the gut. In IBD, the microbiota differs markedly from healthy people. Research suggests that these microbes influence hormone levels by producing, modifying, or breaking down chemical signals, altering the stress response. Our recent work has shown that even without obvious inflammation, mice colonized with IBD microbiotas have higher stress hormone levels, delayed puberty, and reduced reproductive success. These results point toward a powerful but poorly understood connection between gut microbes, stress, and endocrine development. My research aims to uncover not just correlations, but causal links between gut bacteria in IBD and changes in stress hormones . First, I will use mice colonized with gut bacteria from IBD (hIBD) or healthy patients to examine how they affect hormone regulation and stress responses during development. To test causality, I will introduce specific protective microbes into hIBD mice and assess whether they can reverse stress hormone and developmental changes. Secondly, I will engineer a "living sensor" - a probiotic bacterium that detects and reports stress and inflammation signals in real time. This tool will enable quick, non-invasive monitoring of hormone and inflammation shifts, directly linking microbial changes with endocrine outcomes. Ultimately, my research seeks to clarify how stress and the microbiota interact to shape hormone regulation in pediatric IBD, paving the way for microbiota-based tools and therapies that can improve lifelong health for affected children .
Program
DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
560017
Name
Sie Claire
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
Microbial modulation of stress hormones in inflammatory bowel 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
Endocrine Disorders; Gnotobiotic Mouse Models; Inflammatory Bowel Disease; Microbial Therapeutics; Microbiome; Puberty; Stress
Abstract
Inflammatory Bowel Disease (IBD) is a lifelong condition affecting over 7 million people worldwide with no cure. In Canada, nearly 1% of the population is expected to be diagnosed by 2030, of which 25% are children. Pediatric IBD patients experience more severe symptoms and problems beyond the gut, including changes in hormone levels, mood disorders, and delayed puberty. One explanation for these effects may lie in the gut microbiota - the community of bacteria in the gut. In IBD, the microbiota differs markedly from healthy people. Research suggests that these microbes influence hormone levels by producing, modifying, or breaking down chemical signals, altering the stress response. Our recent work has shown that even without obvious inflammation, mice colonized with IBD microbiotas have higher stress hormone levels, delayed puberty, and reduced reproductive success. These results point toward a powerful but poorly understood connection between gut microbes, stress, and endocrine development. My research aims to uncover not just correlations, but causal links between gut bacteria in IBD and changes in stress hormones . First, I will use mice colonized with gut bacteria from IBD (hIBD) or healthy patients to examine how they affect hormone regulation and stress responses during development. To test causality, I will introduce specific protective microbes into hIBD mice and assess whether they can reverse stress hormone and developmental changes. Secondly, I will engineer a "living sensor" - a probiotic bacterium that detects and reports stress and inflammation signals in real time. This tool will enable quick, non-invasive monitoring of hormone and inflammation shifts, directly linking microbial changes with endocrine outcomes. Ultimately, my research seeks to clarify how stress and the microbiota interact to shape hormone regulation in pediatric IBD, paving the way for microbiota-based tools and therapies that can improve lifelong health for affected children .
Competitiondate
202511
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Sie, Claire
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $120,000~ $0~
University of British Columbia - $120,000 Grant (2025… | Canada Spends