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Grant: Canada-UK Partnership on Antibiotic Resistance

University of Guelph

$2,000,000.00

Novel antibacterial targets, assays, probes and opportunities in bacterial cell wall biogenesis

EF 2010-11

Résumé
Millions of people die each year from bacterial infections and tens of millions suffer from the consequences of these infections. The discovery of the antibiotic penicillin once opened the door to treat these infections by stopping bacteria making the polymer in the cell wall that holds them together. This polymer, called peptidoglycan, is made up of an interlocking network of sugars and strings of amino acids (peptides). Specialised proteins (called PBPs), with the ability to stitch together these sugars and peptides are the targets inhibited by penicillin, stopping cell wall synthesis and killing the bacterium. Many important bacteria are no longer killed by penicillin and other antibiotics that attack other stages in the production of peptidoglycan. Bacteria have changed, evading the action of these antibiotics. We need to fight back. Our progress until recently has been hampered by our inability to routinely synthesise the key chemical components that make this polymer. We can now do this. This is exciting, as we develop the capability to explore important unanswered questions about how bacteria grow and control the production of peptidoglycan. As leading researchers in peptidoglycan metabolism in Canada and the UK with complementary facilities and expertise, Team CanUK proposes to consolidate established collaborations and further the development of a research network to increase our understanding of the fundamental biology of this process. All of this will open fundamentally new biological insights, and opportunities to use these for the future development of new antibiotics that will work against multiply antibiotic resistant bacteria like MRSA and TB.
Programme
Canada-UK Partnership on Antibiotic Resistance
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
223643
Name
Clarke Anthony J
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Medical Research Council (UK)
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Canada-UK Joint Health Research Program on Antibiotic Resistance
Projecttitle
Novel antibacterial targets, assays, probes and opportunities in bacterial cell wall biogenesis
Programtype2
Operating Grants
Orgnameinp2
University of Guelph
Cihramount2
$2,000,000
Cihrequipment2
$0
Programname2
Canada-UK Partnership on Antibiotic Resistance
Keyworddelim
Antibacterial Peptides; Bacterial Cell Walls; Biosynthesis; Enzyme Substrates & Assays; High Throughput Screening; Inhibitors; Maturation; Peptidoglycan; Synthesis
Abstract
Millions of people die each year from bacterial infections and tens of millions suffer from the consequences of these infections. The discovery of the antibiotic penicillin once opened the door to treat these infections by stopping bacteria making the polymer in the cell wall that holds them together. This polymer, called peptidoglycan, is made up of an interlocking network of sugars and strings of amino acids (peptides). Specialised proteins (called PBPs), with the ability to stitch together these sugars and peptides are the targets inhibited by penicillin, stopping cell wall synthesis and killing the bacterium. Many important bacteria are no longer killed by penicillin and other antibiotics that attack other stages in the production of peptidoglycan. Bacteria have changed, evading the action of these antibiotics. We need to fight back. Our progress until recently has been hampered by our inability to routinely synthesise the key chemical components that make this polymer. We can now do this. This is exciting, as we develop the capability to explore important unanswered questions about how bacteria grow and control the production of peptidoglycan. As leading researchers in peptidoglycan metabolism in Canada and the UK with complementary facilities and expertise, Team CanUK proposes to consolidate established collaborations and further the development of a research network to increase our understanding of the fundamental biology of this process. All of this will open fundamentally new biological insights, and opportunities to use these for the future development of new antibiotics that will work against multiply antibiotic resistant bacteria like MRSA and TB.
Competitiondate
201101
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Clarke, Anthony J; Brown, Eric D; Burrows, Lori L; Levesque, Roger C; Strynadka, Natalie C
Approvedterm
4 ans 0 mois
Cihrcontribution2
Inst of Infection & Immunity~ $2,000,000~ $0~