scholarly journals A Sobemovirus coat protein gene complements long-distance movement of a coat protein-null Dianthovirus

Virology ◽  
2004 ◽  
Vol 330 (1) ◽  
pp. 186-195 ◽  
Author(s):  
Anton S. Callaway ◽  
Carol G. George ◽  
Steven A. Lommel

1989 ◽  
Vol 17 (4) ◽  
pp. 1768-1768 ◽  
Author(s):  
B. Prill ◽  
E. Maiss ◽  
U. Timpe ◽  
R. Casper


2009 ◽  
Vol 22 (10) ◽  
pp. 1302-1311 ◽  
Author(s):  
V. Decroocq ◽  
B. Salvador ◽  
O. Sicard ◽  
M. Glasa ◽  
P. Cosson ◽  
...  

In Arabidopsis thaliana Columbia (Col-0) plants, the restriction of Tobacco etch virus (TEV) long-distance movement involves at least three dominant RTM (restricted TEV movement) genes named RTM1, RTM2, and RTM3. Previous work has established that, while the RTM-mediated resistance is also effective against other potyviruses, such as Plum pox virus (PPV) and Lettuce mosaic virus (LMV), some isolates of these viruses are able to overcome the RTM mechanism. In order to identify the viral determinant of this RTM-resistance breaking, the biological properties of recombinants between PPV-R, which systemically infects Col-0, and PPV-PSes, restricted by the RTM resistance, were evaluated. Recombinants that contain the PPV-R coat protein (CP) sequence in an RTM-restricted background are able to systemically infect Col-0. The use of recombinants carrying chimeric CP genes indicated that one or more PPV resistance-breaking determinants map to the 5′ half of the CP gene. In the case of LMV, sequencing of independent RTM-breaking variants recovered after serial passages of the LMV AF199 isolate on Col-0 plants revealed, in each case, amino acid changes in the CP N-terminal region, close to the DAG motif. Taken together, these findings demonstrate that the potyvirus CP N-terminal region determines the outcome of the interaction with the RTM-mediated resistance.



2011 ◽  
Vol 36 (2) ◽  
pp. 121-124 ◽  
Author(s):  
José Evando A. Beserra Jr. ◽  
Eduardo C. Andrade ◽  
Rosa F.R. Araújo Camarço ◽  
Aline K.Q. Nascimento ◽  
José Albérsio A. Lima


2002 ◽  
Vol 27 (3) ◽  
pp. 279-284 ◽  
Author(s):  
OSMAR NICKEL ◽  
THOR V. M. FAJARDO ◽  
FRANCISCO J. L. ARAGÃO ◽  
CÉSAR M. CHAGAS ◽  
GILMAR B. KUHN

An isolate of Grapevine virus B (GVB), obtained by indexing Vitis labrusca and V. vinifera grapevines on the indicator LN33, was transmitted mechanically to several Nicotiana species. The virus was partially purified from N. cavicola and the coat protein estimated at 23 kDa by SDS-PAGE. In negatively stained leaf extracts of experimentally inoculated N. cavicola and N. occidentalis, flexuous particles with cross banding were observed, predominantly measuring 750-770 x 12 nm, with a modal length of 760 nm. Decoration indicated a clear, positive reaction against AS-GVB. In DAS-ELISA, GVB was detected in N. cavicola and grapevine extracts, and Western blots showed homologous and cross reaction of GVB and GVA antisera with GVB coat protein. Using specific primers for GVB, a fragment of 594 bp, comprising the coat protein gene coding for 197 amino acids, was amplified by RT-PCR with viral RNA extracted from GVB-infected N. occidentalis. The nucleotide and the deduced amino acid sequences of the coat protein gene showed high identities with Italian and Japanese isolates of GVB.



1991 ◽  
Vol 117 (3-4) ◽  
pp. 297-304 ◽  
Author(s):  
M. A. Serghini ◽  
M. Pinck ◽  
L. Pinck


2004 ◽  
Vol 37 (3) ◽  
pp. 439-448 ◽  
Author(s):  
Ja Choon Koo ◽  
Sebastian Asurmendi ◽  
Jennifer Bick ◽  
Terry Woodford‐Thomas ◽  
Roger N. Beachy


1997 ◽  
Vol 3 (1) ◽  
pp. 75-86 ◽  
Author(s):  
Sylvie Dinant ◽  
Brigitte Maisonneuve ◽  
Josette Albouy ◽  
Yves Chupeau ◽  
Marie-Christine Chupeau ◽  
...  


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