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Grant: Proof of Principle Program - Phase I

University of British Columbia

$160,000.00

Anti-Biofilm Therapy

FY 2012-13

Summary
The current therapy for infectious diseases is facing twin threats. On the one hand antibiotic and antiviral resistance is rising rapidly; on the other there are relatively few novel compounds or strategies under development or entering the clinic. The frequent growth of bacteria as biofilms, which are surface-associated bacterial communities that grow in a protective matrix, is of great concern. Biofilm infections are especially difficult to treat with conventional antibiotics, and are a major problem in trauma patients with major injuries and individuals with an implanted medical device, causing 60% or more of all clinical infections. Based on our breakthrough observation that a human peptide LL-37 is able to inhibit biofilm formation and dissolve existing biofilms, we screened for and obtained small, protease-resistant peptides that have potent broad-spectrum anti-biofilm properties. Here we propose to perform pre-clinical investigations on these peptides as a novel treatment for biofilm infections, preparatory to commercialization.
Program
Proof of Principle Program - Phase I
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
268527
Name
Hancock Robert Ernest W
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Proof of Principle
Projecttitle
Anti-Biofilm Therapy
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$160,000
Cihrequipment2
$0
Programname2
Proof of Principle Program - Phase I
Keyworddelim
Animal Models; Antibiotic Resistance; Antibiotics; Antimicrobial Peptides; Biofilms; Drug Formulation; Innate Defence Regulator Peptides; Medical Implants; Pseudomonas Aeruginosa; Staphylococcus Aureus
Abstract
The current therapy for infectious diseases is facing twin threats. On the one hand antibiotic and antiviral resistance is rising rapidly; on the other there are relatively few novel compounds or strategies under development or entering the clinic. The frequent growth of bacteria as biofilms, which are surface-associated bacterial communities that grow in a protective matrix, is of great concern. Biofilm infections are especially difficult to treat with conventional antibiotics, and are a major problem in trauma patients with major injuries and individuals with an implanted medical device, causing 60% or more of all clinical infections. Based on our breakthrough observation that a human peptide LL-37 is able to inhibit biofilm formation and dissolve existing biofilms, we screened for and obtained small, protease-resistant peptides that have potent broad-spectrum anti-biofilm properties. Here we propose to perform pre-clinical investigations on these peptides as a novel treatment for biofilm infections, preparatory to commercialization.
Competitiondate
201209
Approvedterm2
1 yr 0 mth
Pinamesdelim
Hancock, Robert Ernest W
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $160,000~ $0~
University of British Columbia - $160,000 Grant (2012… | Canada Spends