Grant: Project Grant
McMaster University
$956,250.00
Antibiotic resistance: Discovery, distribution, mechanisms, and inhibition
EF 2021-22
Résumé
Antibiotic resistance is a process where disease-causing bacteria acquire or evolve strategies to evade the drug's killing activity. Interventions ranging from the treatment of pneumonia to cancer chemotherapy rely on antibiotics to overcome and prevent infection. Antibiotic resistance is a pandemic; it is a global infectious disease threat that kills 5,400 Canadians and drains over $2 B in lost wealth to our economy per year. The COVID-19 pandemic has shown how important it is to control infectious diseases and what the consequences are when we cannot. Work in my lab focuses on understanding mechanisms of antibiotic resistance, where resistance comes from, how it spreads between bacteria and across the globe, and how we can overcome it. In this project, we propose to build on the extensive experience and unique resources developed over many years in my group. Examples include a library of antibiotic resistance gene-expressing bacteria, clinical isolates of multi-drug resistant bacteria, and a unique collection of bacteria and fungi that produce compounds that can block antibiotic resistance. We will use these resources to explore new mechanisms of resistance emerging both in the clinic and in the environment, the source of most resistance genes. By understanding the molecular details of resistance, we are better prepared to overcome it. A second complementary element of this project is the testing and discovery of molecules that can block resistance. The pairing of existing antibiotics threatened by resistance with such inhibitory molecules can extend the life of our 'old' antibiotics that have proven to be so vital to our health and economy. Outcomes of this work include new knowledge of resistance, new candidate molecules that can block resistance, the training of scientists and clinicians with a profound understanding of the antibiotic resistance crisis, and ultimately new drug candidates to address this existential threat to modern medicine.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
461872
Name
Wright Gerard D
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Microbiology & Infectious Diseases
Projecttitle
Antibiotic resistance: Discovery, distribution, mechanisms, and inhibition
Programtype2
Operating Grants
Orgnameinp2
McMaster University
Cihramount2
$956,250
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Antibiotic Resistance; Enzymes; High Throughput Screening; Horizontal Gene Transfer; Inhibitor; Natural Products; Resistome
Abstract
Antibiotic resistance is a process where disease-causing bacteria acquire or evolve strategies to evade the drug's killing activity. Interventions ranging from the treatment of pneumonia to cancer chemotherapy rely on antibiotics to overcome and prevent infection. Antibiotic resistance is a pandemic; it is a global infectious disease threat that kills 5,400 Canadians and drains over $2 B in lost wealth to our economy per year. The COVID-19 pandemic has shown how important it is to control infectious diseases and what the consequences are when we cannot. Work in my lab focuses on understanding mechanisms of antibiotic resistance, where resistance comes from, how it spreads between bacteria and across the globe, and how we can overcome it. In this project, we propose to build on the extensive experience and unique resources developed over many years in my group. Examples include a library of antibiotic resistance gene-expressing bacteria, clinical isolates of multi-drug resistant bacteria, and a unique collection of bacteria and fungi that produce compounds that can block antibiotic resistance. We will use these resources to explore new mechanisms of resistance emerging both in the clinic and in the environment, the source of most resistance genes. By understanding the molecular details of resistance, we are better prepared to overcome it. A second complementary element of this project is the testing and discovery of molecules that can block resistance. The pairing of existing antibiotics threatened by resistance with such inhibitory molecules can extend the life of our 'old' antibiotics that have proven to be so vital to our health and economy. Outcomes of this work include new knowledge of resistance, new candidate molecules that can block resistance, the training of scientists and clinicians with a profound understanding of the antibiotic resistance crisis, and ultimately new drug candidates to address this existential threat to modern medicine.
Competitiondate
202203
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Wright, Gerard D
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $956,250~ $0~