Grant: Discovery Grants Program - Individual
University of Western Ontario
$33,000.00
Towards a better understanding of molecular virus-plant interactions: componenets and intracellular trafficking of viral genome translation/replication complexes
FY 2013-14
Summary
Plant viruses are obligate intracellular parasites that infect many major crops and cause yearly losses over multibillion dollars in the world. Potyviruses constitute the largest group of plant viruses, including approximately 30% of all known plant viruses. Some of the most agriculturally important potyviruses include Turnip mosaic virus (TuMV), Clover yellow vein virus (ClYVV), Plum pox virus (PPV), Soybean mosaic virus (SMV), Potato virus Y (PVY), and Tobacco etch virus (TEV). One of the common properties shared by plant potyviruses and other plant viruses is their relatively small genome with a very limited protein-coding capacity. Thus, these viral pathogens must interact with host cells to recruit an array of host proteins (host factors) and metabolites to fulfill their life cycles. Recent studies on virus-plant interactions have identified several host factors. It has been shown that some of them can be manipulated to generate genetic resistance against target viruses. Thus, a better understanding of molecular potyvirus-host interactions may result in new strategies to control plant potyviruses as well as other plant viruses. In search for host factors, in the previous funding cycle, we have screened out approximately 4000 host factor gene candidates using diverse tools such as microarray, yeast two-hybrid system, and expressed sequence tags. These candidate genes include genes coding for translation initiation factors that may be required for viral genome translation, RNA helicase proteins that may participate in viral RNA replication, assembly and transport, and vesicular transport proteins that may be essential for the intracellular trafficking of virus replication complexes. This proposal will enable the identification of genes in these three important gene groups required in potyviral infection, and further characterization of their roles in the formation, function and trafficking of the virus replication complex. Therefore, this proposal will advance our knowledge of the virus replication mechanism. It is anticipated that the new knowledge generated in this study will contribute to the development of novel antiviral strategies.
Program
Discovery Grants Program - Individual
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
312251-2010
Name nom
Wang, Aiming
Department département
Biology
Organization id
36
Institution établissement
University of Western Ontario
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2013
Competition year année de concours
2010
Award amount
33000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
100
Area of application group en
Agriculture and primary food production
Area of application group fr
Agriculture et produits alimentaires primaires
Area of application en
Agriculture and primary food production
Area of application fr
Agriculture et produits alimentaires primaires
Research subject code
4906
Research subject group en
Plant and treebiology
Research subject group fr
Biologie végétale et des arbres
Research subject en
Plant pathology
Research subject fr
Phytopathologie
Partie
4
Nb partie
5
Application title
Towards a better understanding of molecular virus-plant interactions: componenets and intracellular trafficking of viral genome translation/replication complexes
Keyword
NSERC
Application summary
Plant viruses are obligate intracellular parasites that infect many major crops and cause yearly losses over multibillion dollars in the world. Potyviruses constitute the largest group of plant viruses, including approximately 30% of all known plant viruses. Some of the most agriculturally important potyviruses include Turnip mosaic virus (TuMV), Clover yellow vein virus (ClYVV), Plum pox virus (PPV), Soybean mosaic virus (SMV), Potato virus Y (PVY), and Tobacco etch virus (TEV). One of the common properties shared by plant potyviruses and other plant viruses is their relatively small genome with a very limited protein-coding capacity. Thus, these viral pathogens must interact with host cells to recruit an array of host proteins (host factors) and metabolites to fulfill their life cycles. Recent studies on virus-plant interactions have identified several host factors. It has been shown that some of them can be manipulated to generate genetic resistance against target viruses. Thus, a better understanding of molecular potyvirus-host interactions may result in new strategies to control plant potyviruses as well as other plant viruses. In search for host factors, in the previous funding cycle, we have screened out approximately 4000 host factor gene candidates using diverse tools such as microarray, yeast two-hybrid system, and expressed sequence tags. These candidate genes include genes coding for translation initiation factors that may be required for viral genome translation, RNA helicase proteins that may participate in viral RNA replication, assembly and transport, and vesicular transport proteins that may be essential for the intracellular trafficking of virus replication complexes. This proposal will enable the identification of genes in these three important gene groups required in potyviral infection, and further characterization of their roles in the formation, function and trafficking of the virus replication complex. Therefore, this proposal will advance our knowledge of the virus replication mechanism. It is anticipated that the new knowledge generated in this study will contribute to the development of novel antiviral strategies.