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Grant: Foundation Grant

University of Toronto

$4,122,983.00

Leveraging Essential Genes and Genetic Networks to Cripple Human Fungal Pathogens

EF 2016-17

Résumé
The impact of fungal pathogens on human health is devastating. They infect billions of people around the globe, and kill more than 1.5 million each year. The most vulnerable are people with reduced immune function, such as those with HIV or those undergoing immune suppressing treatments for cancer or organ transplants. One of the leading fungal pathogens of humans is Candida albicans. It kills ~40% of people suffering from bloodstream infections. Treating these infections is extremely difficult, as fungi are closely related to humans and there are very few drugs that kill the fungus but not the host. With the emergence of drug resistance, it is now critical to develop new therapeutic strategies. To address this important clinical need, it is critical to uncover the genes and genetic networks that are required for the pathogen to survive and cause disease. We are one of the first academic labs to obtain a powerful resource that will allow us to test the function of almost every gene in the C. albicans genome. Through collaboration with a pharmaceutical company, we now have access to the largest library of C. albicans mutants, which enables genetic depletion of ~40% of genes in the genome. We will use sophisticated computational approaches to predict essential genes, and will expand this resource to cover them all. This resource provides an unprecedented opportunity to identify which genes are essential for the pathogen, and to determine their molecular function and interactions. We will use this platform to characterize the impact of reducing the dosage of each gene on growth, cellular physiology, and traits associated with the capacity to cause disease. We will perform state-of-the-art screens to identify new molecules that target essential genes, and will evaluate their therapeutic potential. This research will reveal new approaches to cripple the pathogen, and enable development of novel therapeutic strategies to improve clinical outcome for millions of people.
Programme
Foundation Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
354227
Name
Cowen Leah E
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Foundation Grant
Projecttitle
Leveraging Essential Genes and Genetic Networks to Cripple Human Fungal Pathogens
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$4,122,983
Cihrequipment2
$0
Programname2
Foundation Grant
Keyworddelim
Antifungal Drug Target Identification; Candida Albicans; Chemical Genomics; Emerging Pathogen; Essential Gene Function; Functional Genomics; Fungal Pathogenesis; Haploinsufficiency Profiling; Microbial Genomics; Next Generation Sequencing
Abstract
The impact of fungal pathogens on human health is devastating. They infect billions of people around the globe, and kill more than 1.5 million each year. The most vulnerable are people with reduced immune function, such as those with HIV or those undergoing immune suppressing treatments for cancer or organ transplants. One of the leading fungal pathogens of humans is Candida albicans. It kills ~40% of people suffering from bloodstream infections. Treating these infections is extremely difficult, as fungi are closely related to humans and there are very few drugs that kill the fungus but not the host. With the emergence of drug resistance, it is now critical to develop new therapeutic strategies. To address this important clinical need, it is critical to uncover the genes and genetic networks that are required for the pathogen to survive and cause disease. We are one of the first academic labs to obtain a powerful resource that will allow us to test the function of almost every gene in the C. albicans genome. Through collaboration with a pharmaceutical company, we now have access to the largest library of C. albicans mutants, which enables genetic depletion of ~40% of genes in the genome. We will use sophisticated computational approaches to predict essential genes, and will expand this resource to cover them all. This resource provides an unprecedented opportunity to identify which genes are essential for the pathogen, and to determine their molecular function and interactions. We will use this platform to characterize the impact of reducing the dosage of each gene on growth, cellular physiology, and traits associated with the capacity to cause disease. We will perform state-of-the-art screens to identify new molecules that target essential genes, and will evaluate their therapeutic potential. This research will reveal new approaches to cripple the pathogen, and enable development of novel therapeutic strategies to improve clinical outcome for millions of people.
Competitiondate
201610
Approvedterm2
7 yrs 0 mth
Pinamesdelim
Cowen, Leah E
Approvedterm
7 ans 0 mois
Cihrcontribution2
~ $4,122,983~ $0~