Grant: Collaborative Research and Development Grants
University of Waterloo
$118,000.00
Developing and optimizing cell lines to study and control emerging viral diseases in farmed Atlantic Salmon: the HSMI and PRV case
FY 2016-17
Summary
Fish represent one of the most healthy sources of food in the world; yet, capture fisheries are declining. In the future, aquaculture will likely supply most fish. As a result, fish farming has become a valuable economic activity, but maintaining aquaculture is challenging. One challenge is emerging viral diseases. An example for Atlantic salmon (AS) is heart and skeletal muscle inflammation (HSMI). The causative agent is thought to be piscine reovirus (PRV). PRV reproduces only marginally in vitro and only in 1 cell line, preventing easy diagnosis, virus isolation and vaccine preparation. Therefore, this proposal has 5 interacting goals. The 1st is to develop AS cell lines from hearts and blood cell producing cultures from spleens. Viruses need cells in order to replicate but are selective as to what cells they will replicate in and reveal themselves. Two potential replication sites for PRV are cardiac cells and blood cells. Cell lines can be cryopreserved, providing stable reagents to study emerging viral diseases in the future. The 2nd is to identify the best cell cultures for studying viruses of HSMI. The cell lines will be the new ones plus existing ones from a range of fish and tissues. The test material will be samples from fish with HSMI. The 3rd is varying sample preparation and exposure conditions to improve viral detection by cell cultures. The 4th goal will be to optimize a diagnostic tool that can be used specifically in this research for goals 2 to 5 and generally to study HSMI. This is the polymerase chain reaction to quantify the amount of virus in cultures and in fish. Finally, cell lines will be used to produce PRV so that fish can be exposed and the causal relationship between PRV and HSMI tested and pathogenesis of the disease described.If PRV causes HMSI, vaccines could be developed, and these could become valuable commercial products for our partner, a pharmaceutical company.
Program
Collaborative Research and Development Grants
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
468298-2014
Name nom
Bols, Niels
Department département
Biology
Organization id
33
Institution établissement
University of Waterloo
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2016
Competition year année de concours
2014
Award amount
118000
Program id
CRDPJ
Program name en
Collaborative Research and Development Grants
Program name fr
Subventions de recherche et développement coopérative
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
96
Committee name en
RPP Internal Decision Cttee
Committee name fr
Cté de décision interne - PPR
Area of application code
106
Area of application group en
Agriculture and primary food production
Area of application group fr
Agriculture et produits alimentaires primaires
Area of application en
Aquaculture
Area of application fr
Aquiculture
Research subject code
5100
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Cell biology
Research subject fr
Biologie cellulaire
Partie
3
Nb partie
3
Application title
Developing and optimizing cell lines to study and control emerging viral diseases in farmed Atlantic Salmon: the HSMI and PRV case
Keyword
NSERC
Application summary
Fish represent one of the most healthy sources of food in the world; yet, capture fisheries are declining. In the future, aquaculture will likely supply most fish. As a result, fish farming has become a valuable economic activity, but maintaining aquaculture is challenging. One challenge is emerging viral diseases. An example for Atlantic salmon (AS) is heart and skeletal muscle inflammation (HSMI). The causative agent is thought to be piscine reovirus (PRV). PRV reproduces only marginally in vitro and only in 1 cell line, preventing easy diagnosis, virus isolation and vaccine preparation. Therefore, this proposal has 5 interacting goals. The 1st is to develop AS cell lines from hearts and blood cell producing cultures from spleens. Viruses need cells in order to replicate but are selective as to what cells they will replicate in and reveal themselves. Two potential replication sites for PRV are cardiac cells and blood cells. Cell lines can be cryopreserved, providing stable reagents to study emerging viral diseases in the future. The 2nd is to identify the best cell cultures for studying viruses of HSMI. The cell lines will be the new ones plus existing ones from a range of fish and tissues. The test material will be samples from fish with HSMI. The 3rd is varying sample preparation and exposure conditions to improve viral detection by cell cultures. The 4th goal will be to optimize a diagnostic tool that can be used specifically in this research for goals 2 to 5 and generally to study HSMI. This is the polymerase chain reaction to quantify the amount of virus in cultures and in fish. Finally, cell lines will be used to produce PRV so that fish can be exposed and the causal relationship between PRV and HSMI tested and pathogenesis of the disease described.If PRV causes HMSI, vaccines could be developed, and these could become valuable commercial products for our partner, a pharmaceutical company.