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Grant: Operating Grant

University of Toronto

$826,540.00

Amino acid starvation pathways in the host response to bacterial infection

EF 2011-12

Résumé
We study how our cells respond to infection by bacteria. In preliminary work, we have identified a critical new aspect of this response to the infection: we have observed that the entry of these micro-organisms into our cells induces a very rapid metabolic starvation. Indeed, approximately 1 hour after invasion, our cells respond as if they were missing amino acids, which are key building blocks of our molecules. Not only did we observe that the infected cells are starved, but we also showed that this has critical consequences for the way we respond to these intruders: by mounting a starvation response, our cells promote a "self-eating" (also known as autophagy) process, which replenishes amino acids, but also favors the destruction of the bacteria. The discovery of this cellular process triggered after infection might prove to be important for the development of new therapeutic strategies against bacteria that cause diseases in humans, such as listeriosis, salmonellosis or tuberculosis.
Programme
Operating Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
252633
Name
Girardin Stephen E
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Microbiology & Infectious Diseases
Projecttitle
Amino acid starvation pathways in the host response to bacterial infection
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$826,540
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Autophagy; Bacterial Infection; Cell Signaling; Cellular Stress; Host-Pathogen Interaction; Mtor
Abstract
We study how our cells respond to infection by bacteria. In preliminary work, we have identified a critical new aspect of this response to the infection: we have observed that the entry of these micro-organisms into our cells induces a very rapid metabolic starvation. Indeed, approximately 1 hour after invasion, our cells respond as if they were missing amino acids, which are key building blocks of our molecules. Not only did we observe that the infected cells are starved, but we also showed that this has critical consequences for the way we respond to these intruders: by mounting a starvation response, our cells promote a "self-eating" (also known as autophagy) process, which replenishes amino acids, but also favors the destruction of the bacteria. The discovery of this cellular process triggered after infection might prove to be important for the development of new therapeutic strategies against bacteria that cause diseases in humans, such as listeriosis, salmonellosis or tuberculosis.
Competitiondate
201203
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Girardin, Stephen E
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $826,540~ $0~