Title of article
The N protein of Tomato spotted wilt virus (TSWV) is associated with the induction of programmed cell death (PCD) in Capsicum chinense plants, a hypersensitive host to TSWV infection
Author/Authors
Fernanda Antinolfi Lovato، نويسنده , , Alice Kazuko Inoue-Nagata، نويسنده , , Tatsuya Nagata، نويسنده , , Antônio Carlos de ?vila، نويسنده , , Luiz Alfredo Rodrigues Pereira، نويسنده , , Renato Oliveira Resende، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2008
Pages
8
From page
245
To page
252
Abstract
In sweet pepper, the Tsw gene, originally described in Capsicum chinense, has been widely used as an efficient gene for inducing a hypersensitivity response (HR) derived Tomato spotted wilt virus (TSWV) resistance. Since previously reported studies suggested that the TSWV-S RNA mutation(s) are associated with the breakdown of Tsw mediated TSWV resistance in peppers, the TSWV genes N (structural nucleocapsid protein) and NSS (non-structural silencing suppressor protein) were cloned into a Potato virus X (PVX)-based expression vector, and inoculated into the TSWV-resistant C. chinense genotype, PI 159236, to identify the Tsw-HR viral elicitor. Typical HR-like chlorotic and necrotic lesions followed by leaf abscission were observed only in C. chinense plants inoculated with the PVX-N construct. Cytopathological analyses of these plants identified fragmented genomic DNA, indicative of programmed cell death (PCD), in mesophyll cell nuclei surrounding PVX-N-induced necrotic lesions. The other constructs induced only PVX-like symptoms without HR-like lesions and there were no microscopic signs of PCD. The mechanism of TSWV N-gene HR induction is apparently species specific as the N gene of a related tospovirus, Tomato chlorotic spot virus, was not a HR elicitor and did not cause PCD in infected cells.
Keywords
TospovirusVirus resistanceNucleocapsid proteinHypersensitive responseCapsicum chinenseProgrammed cell death
Journal title
Virus Research
Serial Year
2008
Journal title
Virus Research
Record number
786927
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