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Título

The coat protein of tobamovirus acts as elicitor of both L2 and L4 gene-mediated resistance in Capsicum

AutorGilardi, Patricia CSIC; García-Luque, Isabel CSIC ; Serra, María Teresa CSIC
Fecha de publicación2004
EditorSociety for General Microbiology
CitaciónJournal of General Virology 85(7): 2077-2085(2004)
ResumenIn Capsicum, the resistance conferred by the L2 gene is effective against all of the pepper-infecting tobamoviruses except Pepper mild mottle virus (PMMoV), whereas that conferred by the L4 gene is effective against them all. These resistances are expressed by a hypersensitive response, manifested through the formation of necrotic local lesions (NLLs) at the primary site of infection. The Capsicum L2 gene confers resistance to Paprika mild mottle virus (PaMMV), while the L4 gene is effective against both PaMMV and PMMoV. The PaMMV and PMMoV coat proteins (CPs) were expressed in Capsicum frutescens (L2L2) and Capsicum chacoense (L4L4) plants using the heterologous Potato virus X (PVX)-based expression system. In C. frutescens (L2L2) plants, the chimeric PVX virus containing the PaMMV CP was localized in the inoculated leaves and produced NLLs, whereas the chimeric PVX containing the PMMoV CP infected the plants systemically. Thus, the data indicated that the PaMMV CP is the only tobamovirus factor required for the induction of the host response mediated by the Capsicum L2 resistance gene. In C. chacoense (L4L4) plants, both chimeric viruses were localized to the inoculated leaves and produced NLLs, indicating that either PaMMV or PMMoV CPs are required to elicit the L4 gene-mediated host response. In addition, transient expression of PaMMV CP into C. frutescens (L2L2) leaves and PMMoV CP into C. chacoense (L4L4) leaves by biolistic co-bombardment with a β-glucuronidase reporter gene led to the induction of cell death and the expression of host defence genes in both hosts. Thus, the tobamovirus CP is the elicitor of the Capsicum L2 and L4 gene-mediated hypersensitive response. © 2004 SGM.
URIhttp://hdl.handle.net/10261/73709
DOI10.1099/vir.0.80017-0
Identificadoresdoi: 10.1099/vir.0.80017-0
issn: 0022-1317
e-issn: 1465-2099
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