conference schedule and program with abstracts - Horticulture ...
conference schedule and program with abstracts - Horticulture ...
conference schedule and program with abstracts - Horticulture ...
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O-41<br />
Gene silencing as strategy to induce grapevine fan leaf virus (GFLV) resistance in<br />
grapevine rootstocks<br />
E. Torres, A. Cadavid, C. Santibáñez, F. Godoy, C. Medina, P. Arce-Johnson*<br />
P. Universidad Catholica de Chile, Fac. de Ciencias Biologicas, Santiago, Chile<br />
*Corresponding author: parce@bio.puc.cl<br />
Viral infections in grapevines cause physiological disorders that lead to foliar deformations,<br />
alterations in the berry color <strong>and</strong> finally reductions in productivity. Most viral infections in<br />
grapevine are disseminated by biological vectors <strong>and</strong> then by the vegetative propagation of<br />
infected material. More than ten viruses commonly infect the grapevine, <strong>and</strong> it is not rare to find<br />
two or three different viruses in one infected plant. There are not efficient chemical treatments<br />
against virus infections. A molecular strategy to induce virus resistance in plants is gene<br />
silencing. This strategy requires the transformation of plants <strong>with</strong> a short sequence of the<br />
pathogen in a way that a double-str<strong>and</strong> RNA structure is formed during transcription, initiating<br />
gene silencing in the host. The objective of this work is the induction of virus silencing in<br />
grapevine rootstocks plants in order to use it for grafting. It is hoped that the mobile silencing<br />
signal induces virus silencing in the scion. We have transformed rootstocks plants (110 Richter<br />
<strong>and</strong> Harmony) by co-culture of embryogenic <strong>and</strong> organogenic tissues <strong>with</strong> Agrobacterium<br />
tumefaciens carrying a silencing vector containing a sequence of the coat protein of grapevine<br />
fanleaf virus (GFLV). Twenty-three transgenic plants of the 110 Richter rootstock have been<br />
recovered, analyzed by PCR against the GFLV sequence, <strong>and</strong> propagated to obtain several plants<br />
of each line. The transgenic rootstocks have been grafted <strong>with</strong> GFLV infected plants that were<br />
positive for virus presence by RT-PCR analysis. Once the grafts were set, the RT-PCR analysis<br />
was repeated in the scion. After one month the detection of the virus has been abolished in the<br />
scion, in four of ten analyzed rootstocks lines <strong>and</strong> the same result was maintained after six<br />
months.<br />
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