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Grant: Catalyst Grant: Pandemic Preparedness

Université de Sherbrooke

$100,000.00

Development of a SOFA-ribozyme-based strategy to control the propagation of the influenza virus.

FY 2009-10

Summary
The ability of ribozymes, RNA molecules that possess enzymatic activities, to specifically recognize and subsequently catalyze the cleavage of RNA substrates makes them attractive as therapeutic tools for the inactivation of viruses. Our goal is to use ribozymes to specifically cleave influenza RNA transcripts thereby inhibiting the replication of the virus. During the past year, we have designed various ribozymes aimed at inhibiting the replication of the virus, performed the basic in vitro experiments demonstrating the efficiency of influenza-specific ribozymes, developed a system to monitor the efficiency of ribozymes in human cells, and finally, initiated experiments in animal models to identify the most suitable system to deliver the selected ribozymes to target cells in the lungs. We now feel confident that we have all the necessary tools to assess the efficacy of our gene-inactivation approach against influenza. In the current proposal, we want to complete the screen our collection of ribozymes and ultimately monitor the ability of selected ribozymes to inhibit the replication of the virus in animals.
Program
Catalyst Grant: Pandemic Preparedness
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
183301
Name
Bisaillon Martin
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Pandemic Preparedness
Projecttitle
Development of a SOFA-ribozyme-based strategy to control the propagation of the influenza virus.
Programtype2
Operating Grants
Orgnameinp2
Université de Sherbrooke
Cihramount2
$100,000
Cihrequipment2
$0
Programname2
Catalyst Grant: Pandemic Preparedness
Keyworddelim
Influenza Virus; Ribozymes
Abstract
The ability of ribozymes, RNA molecules that possess enzymatic activities, to specifically recognize and subsequently catalyze the cleavage of RNA substrates makes them attractive as therapeutic tools for the inactivation of viruses. Our goal is to use ribozymes to specifically cleave influenza RNA transcripts thereby inhibiting the replication of the virus. During the past year, we have designed various ribozymes aimed at inhibiting the replication of the virus, performed the basic in vitro experiments demonstrating the efficiency of influenza-specific ribozymes, developed a system to monitor the efficiency of ribozymes in human cells, and finally, initiated experiments in animal models to identify the most suitable system to deliver the selected ribozymes to target cells in the lungs. We now feel confident that we have all the necessary tools to assess the efficacy of our gene-inactivation approach against influenza. In the current proposal, we want to complete the screen our collection of ribozymes and ultimately monitor the ability of selected ribozymes to inhibit the replication of the virus in animals.
Competitiondate
200904
Approvedterm2
1 yr 0 mth
Pinamesdelim
Bisaillon, Martin
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $100,000~ $0~