The Systemic Infection by Tobacco Mosaic Virus of Tobacco Plants Coutaining the N Gene at Temperatures Below 28°C

1996 ◽  
Vol 144 (3) ◽  
pp. 139-142 ◽  
Author(s):  
R. F. White ◽  
J. M. Sugars
1977 ◽  
Vol 83 (2) ◽  
pp. 41-59 ◽  
Author(s):  
Jeanne Dijkstra ◽  
G. C. A. Bruin ◽  
Ankie C. Burgers ◽  
L. C. Loon ◽  
Christien Ritter ◽  
...  

Virology ◽  
1989 ◽  
Vol 173 (1) ◽  
pp. 11-20 ◽  
Author(s):  
Tetsuichiro Saito ◽  
Kimiko Yamanaka ◽  
Yuichiro Watanabe ◽  
Nobuhiko Takamatsu ◽  
Tetsuo Meshi ◽  
...  

2003 ◽  
Vol 16 (6) ◽  
pp. 485-494 ◽  
Author(s):  
Olga del Pozo ◽  
Eric Lam

The p35 protein from baculovirus is a broad-range caspase inhibitor and suppresses programmed cell death in animals. We report here the effects of transgenic expression in tobacco of the p35 protein during the hypersensitive response (HR). Expression of p35 causes partial inhibition of nonhost HR triggered by bacteria and gene-for-gene HR triggered by virus. Infection of p35-expressing tobacco plants with Tobacco mosaic virus (TMV) disrupts N-mediated disease resistance, causing systemic spreading of the virus within a resistant background. Mutant variants altered in aspartate residues within the loop region of p35 are inefficient substrates for caspases in vitro, and they do not suppress caspase proteolytic activity in animal systems. Tobacco plants expressing these mutant variants of the p35 protein do not show inhibition of HR cell death or enhanced virus systemic movement. Thus, HR inhibition and TMV systemic spreading phenotype in p35-expressing plants correlate with the ability of the p35 protein to suppress caspase activity in animal systems. In addition, a C-terminal truncated variant of p35 is unable to suppress cell death in animals as well as HR cell death in transgenic tobacco. Our results provide evidence for the participation of caspase-like proteases during the HR. In addition, they suggest that timely activation of cell death is necessary for effective TMV containment within the primary infection site.


2002 ◽  
Vol 76 (24) ◽  
pp. 12908-12916 ◽  
Author(s):  
Tomas Canto ◽  
Peter Palukaitis

ABSTRACT The N gene conditions for resistance to Tobacco mosaic virus (TMV) but only below 28°C. However, a TMV-based vector expressing green fluorescent protein (TMV-GFP) showed only limited movement at 33°C in tobacco plants harboring the N gene and other genes cointrogressed from Nicotiana glutinosa. TMV-GFP moved efficiently in tobacco plants that either lacked these genes or that contained the N gene but were transgenic for RNA1 of Cucumber mosaic virus. These findings identified novel temperature-independent resistance to the movement of TMV-GFP which could be neutralized by a different viral transgene. Using the N gene and nahG gene-transgenic tobacco, we show that this novel resistance is manifested specifically by the N gene itself and operates via a pathway independent of salicylic acid.


1998 ◽  
Vol 72 (1) ◽  
pp. 731-738 ◽  
Author(s):  
X. Ares ◽  
G. Calamante ◽  
S. Cabral ◽  
J. Lodge ◽  
P. Hemenway ◽  
...  

ABSTRACT The p24 protein, one of the three proteins implicated in local movement of potato virus X (PVX), was expressed in transgenic tobacco plants (Nicotiana tabacum Xanthi D8 NN). Plants with the highest level of p24 accumulation exhibited a stunted and slightly chlorotic phenotype. These transgenic plants facilitate the cell-to-cell movement of a mutant of PVX that contained a frameshift mutation in p24. Upon inoculation with tobacco mosaic virus (TMV), the size of necrotic local lesions was significantly smaller in p24+ plants than in nontransgenic, control plants. Systemic resistance to tobamoviruses was also evidenced after inoculation of p24+ plants with Ob, a virus that evades the hypersensitive response provided by the N gene. In the latter case, no systemic symptoms were observed, and virus accumulation remained low or undetectable by Western immunoblot analysis and back-inoculation assays. In contrast, no differences were observed in virus accumulation after inoculation with PVX, although more severe symptoms were evident on p24-expressing plants than on control plants. Similarly, infection assays conducted with potato virus Y showed no differences between control and transgenic plants. On the other hand, a considerable delay in virus accumulation and symptom development was observed when transgenic tobacco plants containing the movement protein (MP) of TMV were inoculated with PVX. Finally, a movement defective mutant of TMV was inoculated on p24+ plants or in mixed infections with PVX on nontransgenic plants. Both types of assays failed to produce TMV infections, implying that TMV MP is not interchangeable with the PVX MPs.


Author(s):  
K. W. Mundry ◽  
W. Schaible ◽  
M. Ellwart-Tschürtz ◽  
H. Nitschko ◽  
C. Hapke

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