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Journal of General Virology (2001), 82, 3099-3106.
© 2001 Society for General Microbiology


Plant

Evidence for RNA-mediated defence effects on the accumulation of Potato leafroll virus

Hugh Barker1, Kara D. McGeachy1, Eugene V. Ryabovb,1, Uli Commandeur2, Mike A. Mayo1 and Michael Taliansky1

Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, UK1
Aachen University of Technology (RWTH), Institute for Biology VII, Molecular Biotechnology, Worringerweg 1, D-52074 Aachen, Germany2

Author for correspondence: Hugh Barker. Fax +44 1382 562 426. e-mail H.Barker{at}scri.sari.ac.uk

In plants infected with Potato leafroll virus (PLRV), or other luteoviruses, infection is very largely confined to cells in the vascular system. Even in tobacco plants transformed with PLRV full-length cDNA, in which all mesophyll cells should synthesize infectious PLRV RNA transcripts, only a minority of the mesophyll cells accumulate detectable amounts of virus. We have explored this phenomenon further by transforming a better PLRV host, Nicotiana benthamiana, with the same transgene, by superinfecting transformed plants with Potato virus Y and by producing tobacco plants in which cells contained both PLRV cDNA and DNA encoding the P1/HC-Pro genes of the potyvirus Tobacco etch virus. A greater proportion of cells in superinfected plants or in doubly transgenic plants accumulated PLRV than did in singly transgenic tobacco plants. However, most cells in these plants did not accumulate virus. To investigate restriction of the multiplication of viruses containing PLRV sequences, transgenic plants were infected with a chimeric virus that consisted of Tobacco mosaic virus (TMV) containing genes for either the coat protein (CP) of PLRV or jellyfish green fluorescent protein (GFP) in place of the TMV coat protein. The virus that encoded PLRV CP spread more slowly and accumulated less extensively than did the virus that expressed GFP. The results support the suggestion that an RNA-mediated form of resistance that resembles post-transcriptional gene silencing operates in non-vascular cells and may be part of the mechanism that restricts PLRV to vascular tissue in conventionally infected plants.




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S. Haupt, T. Stroganova, E. Ryabov, S. H. Kim, G. Fraser, G. Duncan, M. A. Mayo, H. Barker, and M. Taliansky
Nucleolar localization of potato leafroll virus capsid proteins
J. Gen. Virol., October 1, 2005; 86(10): 2891 - 2896.
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