Grant: Project Grant
University of Toronto
$802,725.00
The role of the ClpP protease in bacterial pathogenesis
EF 2015-16
Résumé
With the emergence of new forms of drug-resistant bacteria, it becomes essential that new classes of antibiotics be discovered and developed. The proposed project brings together a team of four researchers interested in the development of a new class of antibiotics that we identified targeting a highly conserved self-compartmentalizing serine protease termed ClpP using a novel mode of action. Recently, we found that the infectivity of the pathogenic bacteria Neisseria meningitidis is abolished if the clpP gene is disrupted and that Neisseria meningitidis and Neisseria gonorrhoeae are very sensitive to the new class of compounds. Hence, we are interested in determining the mechanism of action of these compounds in Neisseria. We are also interested investigating the cellular function of ClpP in these bacteria under normal growth as well as during infection. These studies will provide important insights into the development of new strategies to combat bacterial infections.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
343305
Name
Houry Walid A
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
The role of the ClpP protease in bacterial pathogenesis
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$802,725
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cell Stress Response; Clpp; Clpx; Molecular Chaperones; Neisseria Gonorrhoeae; Neisseria Meningitidis; Protein Degradation; Protein Folding; Protein Homeostasis; Protein Translation
Abstract
With the emergence of new forms of drug-resistant bacteria, it becomes essential that new classes of antibiotics be discovered and developed. The proposed project brings together a team of four researchers interested in the development of a new class of antibiotics that we identified targeting a highly conserved self-compartmentalizing serine protease termed ClpP using a novel mode of action. Recently, we found that the infectivity of the pathogenic bacteria Neisseria meningitidis is abolished if the clpP gene is disrupted and that Neisseria meningitidis and Neisseria gonorrhoeae are very sensitive to the new class of compounds. Hence, we are interested in determining the mechanism of action of these compounds in Neisseria. We are also interested investigating the cellular function of ClpP in these bacteria under normal growth as well as during infection. These studies will provide important insights into the development of new strategies to combat bacterial infections.
Competitiondate
201603
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Houry, Walid A
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $802,725~ $0~