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Grant: Project Grant

University of British Columbia

$879,750.00

The how and and why of cholesterol catabolism in Mycobacterium tuberculosis.

EF 2017-18

Résumé
More people die of tuberculosis (TB) each year than any other infectious disease. The bacterium that causes the disease, Mycobacterium tuberculosis (Mtb), infects one third of all people world-wide. With the rise of drug resistant strains and co-infection with HIV, TB remains a global health emergency and, in Canada, is of particular concern in the First Nations. The treatment of even drug-sensitive TB is arduous, with patients taking a cocktail of toxic chemotherapeutics for six months. Novel therapies are urgently needed to decrease the length, and improve the efficacy, of treatment. We discovered a pathway in Mtb that enables the pathogen to grow on cholesterol during infection. This pathway has become a target for novel drugs to treat TB. Nevertheless, there are many aspect of Mtb's cholesterol degradation that are not yet known. The overall objective of this project is to better understand Mtb's cholesterol degradation pathway, including how this pathway works and how it contributes to the disease. Improved understanding of the pathway will facilitate the development of novel drugs urgently needed to combat this global emergency.
Programme
Project Grant
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
380100
Name
Eltis Lindsay D
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Microbiology & Infectious Diseases
Projecttitle
The how and and why of cholesterol catabolism in Mycobacterium tuberculosis.
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$879,750
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Beta-Oxidation; Catabolism; Cholesterol; Coenzyme A (Coash); Enzymology; Metabolomics; Mycobacterium Tuberculosis; Protein Structure And Function; Transcriptional Regulation
Abstract
More people die of tuberculosis (TB) each year than any other infectious disease. The bacterium that causes the disease, Mycobacterium tuberculosis (Mtb), infects one third of all people world-wide. With the rise of drug resistant strains and co-infection with HIV, TB remains a global health emergency and, in Canada, is of particular concern in the First Nations. The treatment of even drug-sensitive TB is arduous, with patients taking a cocktail of toxic chemotherapeutics for six months. Novel therapies are urgently needed to decrease the length, and improve the efficacy, of treatment. We discovered a pathway in Mtb that enables the pathogen to grow on cholesterol during infection. This pathway has become a target for novel drugs to treat TB. Nevertheless, there are many aspect of Mtb's cholesterol degradation that are not yet known. The overall objective of this project is to better understand Mtb's cholesterol degradation pathway, including how this pathway works and how it contributes to the disease. Improved understanding of the pathway will facilitate the development of novel drugs urgently needed to combat this global emergency.
Competitiondate
201803
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Eltis, Lindsay D
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $879,750~ $0~