Grant: Catalyst Grant: Catalyzing Innovation in Preterm Birth Research
University of British Columbia
$200,000.00
Development of a genetic system for a pioneering member of the infant microbiota
EF 2016-17
Résumé
Worldwide, prematurity is the leading cause of death for all infants, with almost one million deaths per year. Babies born before 32 weeks face the worst odds. These babies are only 2% of births, but they account for over 1/3 of all infant deaths. For these infants, a disease called necrotizing enterocolitis (NEC) can be one of the most deadly complications of prematurity after the first week of life. NEC is an acquired condition in which intestinal tissue suddenly becomes inflamed and then begins to die off. NEC has a high mortality rate, and, even if the baby survives NEC, they are subject to considerable life-long health problems, resulting in tremendous costs to the health care system. With rising rates of prematurity, NEC poses a significant health and financial burden on Canada.
Humans are populated by an enormous number of microorganisms, called the "microbiome." The microbiome can play a critical role in helping to digest food and prevent infection. Interestingly, infants and adults have very different microbiomes, due in part to the different diets between the two generations. For instance, bacteria that commonly populate the infant gut have developed the ability to survive by digesting unique carbohydrates present only in human breast milk, the major diet for infants, giving these bacteria a selective advantage over other gut bacteria that cannot digest such carbohydrates. Recent research suggests that these infant-associated bacteria can also protect babies from diseases, including protecting the premature infant gut from developing NEC. In this grant, we will employ approaches from biochemistry, microbiology, and chemistry to identify the factors produced by beneficial bacteria found in the infant microbiome that protect against NEC. Altogether, our work will provide essential information for the development of novel therapeutics and preventatives for this costly disease.
Programme
Catalyst Grant: Catalyzing Innovation in Preterm Birth Research
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
351119
Name
Ryan Katherine S
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Human Development, Child and Youth Health
Theme2
Biomedical
Prcname2
Catalyst Grant: Catalyzing Innovation in Preterm Birth Research
Projecttitle
Development of a genetic system for a pioneering member of the infant microbiota
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$200,000
Cihrequipment2
$0
Programname2
Catalyst Grant: Catalyzing Innovation in Preterm Birth Research
Keyworddelim
Bifidobacteria; Deletion Mutagenesis; Fucose; Gut Microbiota; Human Milk Oligosaccharides; Inflammation; Natural Product Isolation; Necrotizing Enterocolitis; Premature Neonate; Rna Sequencing
Abstract
Worldwide, prematurity is the leading cause of death for all infants, with almost one million deaths per year. Babies born before 32 weeks face the worst odds. These babies are only 2% of births, but they account for over 1/3 of all infant deaths. For these infants, a disease called necrotizing enterocolitis (NEC) can be one of the most deadly complications of prematurity after the first week of life. NEC is an acquired condition in which intestinal tissue suddenly becomes inflamed and then begins to die off. NEC has a high mortality rate, and, even if the baby survives NEC, they are subject to considerable life-long health problems, resulting in tremendous costs to the health care system. With rising rates of prematurity, NEC poses a significant health and financial burden on Canada.
Humans are populated by an enormous number of microorganisms, called the "microbiome." The microbiome can play a critical role in helping to digest food and prevent infection. Interestingly, infants and adults have very different microbiomes, due in part to the different diets between the two generations. For instance, bacteria that commonly populate the infant gut have developed the ability to survive by digesting unique carbohydrates present only in human breast milk, the major diet for infants, giving these bacteria a selective advantage over other gut bacteria that cannot digest such carbohydrates. Recent research suggests that these infant-associated bacteria can also protect babies from diseases, including protecting the premature infant gut from developing NEC. In this grant, we will employ approaches from biochemistry, microbiology, and chemistry to identify the factors produced by beneficial bacteria found in the infant microbiome that protect against NEC. Altogether, our work will provide essential information for the development of novel therapeutics and preventatives for this costly disease.
Competitiondate
201608
Approvedterm2
2 yrs 0 mth
Pinamesdelim
Ryan, Katherine S
Approvedterm
2 ans 0 mois
Cihrcontribution2
~ $200,000~ $0~