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Grant: Doctoral: Vanier Canada Graduate Scholarships

University of British Columbia

$150,000.00

Metabolites in the mammalian small intestine: understanding host-bacterial interactions during child malnutrition and enteric dysfunction

EF 2015-16

Résumé
Child malnutrition is a serious global health issue, responsible for nearly half of the deaths in young children each year. Surprisingly, even when malnourished children are fed nutrient-rich therapeutic foods, they often do not regain normal height and weight. An intestinal disorder known as environmental enteropathy, which interferes with nutrient absorption, may be preventing malnourished children from benefiting from healthy feeding programs. This intestinal disorder is believed to result from continuous exposure to fecal bacteria in regions of poor sanitation. The human intestine harbours trillions of bacteria, collectively termed the microbiota, which help to digest foods, absorb nutrients and prevent infection. As the host and the microbiota interact with one another and digest food, they produce countless small molecules ('metabolites') with biological function in health and disease. I propose that these metabolites play an important role in environmental enteropathy. My project aims to uncover metabolites which are associated with environmental enteropathy in mice and humans, and to study their effect on cells of the mammalian intestine. I will also test whether certain metabolites can help treat the disease in a mouse model. These experiments will help us understand the molecular basis of environmental enteropathy, and may reveal molecules that would be useful in the treatment of this disease. To pursue this research in human samples, our lab is involved in a large-scale international collaboration studying environmental enteropathy in malnourished children from Madagascar and the Central African Republic. This project is extremely relevant to the unsolved problem of child malnutrition. Developing a treatment for environmental enteropathy would be a crucial advancement in the field of children's health, with the potential to reduce mortality rates and improve the development of millions of malnourished children.
Programme
Doctoral: Vanier Canada Graduate Scholarships
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
339642
Name
Huus Kelsey E
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Vanier Canada Graduate Scholarships CIHR
Projecttitle
Metabolites in the mammalian small intestine: understanding host-bacterial interactions during child malnutrition and enteric dysfunction
Programtype2
Studentship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
Doctoral: Vanier Canada Graduate Scholarships
Keyworddelim
Children'S Health; Enteric Dysfunction; Environmental Enteropathy; Malnutrition; Metabolomics; Microbiota
Abstract
Child malnutrition is a serious global health issue, responsible for nearly half of the deaths in young children each year. Surprisingly, even when malnourished children are fed nutrient-rich therapeutic foods, they often do not regain normal height and weight. An intestinal disorder known as environmental enteropathy, which interferes with nutrient absorption, may be preventing malnourished children from benefiting from healthy feeding programs. This intestinal disorder is believed to result from continuous exposure to fecal bacteria in regions of poor sanitation. The human intestine harbours trillions of bacteria, collectively termed the microbiota, which help to digest foods, absorb nutrients and prevent infection. As the host and the microbiota interact with one another and digest food, they produce countless small molecules ('metabolites') with biological function in health and disease. I propose that these metabolites play an important role in environmental enteropathy. My project aims to uncover metabolites which are associated with environmental enteropathy in mice and humans, and to study their effect on cells of the mammalian intestine. I will also test whether certain metabolites can help treat the disease in a mouse model. These experiments will help us understand the molecular basis of environmental enteropathy, and may reveal molecules that would be useful in the treatment of this disease. To pursue this research in human samples, our lab is involved in a large-scale international collaboration studying environmental enteropathy in malnourished children from Madagascar and the Central African Republic. This project is extremely relevant to the unsolved problem of child malnutrition. Developing a treatment for environmental enteropathy would be a crucial advancement in the field of children's health, with the potential to reduce mortality rates and improve the development of millions of malnourished children.
Competitiondate
201511
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Huus, Kelsey E
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $150,000~ $0~