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SESSION FORTY-EIGHT – EXPLOITING RNA INTERFERENCE IN<br />

PLANTS AND NEMATODES<br />

CONVENORS: CARLA DE GIORGI & ROSANE CURTIS<br />

Host Delivered RNAi: An Effective Strategy to Control Plant Parasitic<br />

Nematodes<br />

Fairbairn, D.J., A.S. Cavallaro, M. Bernard, J. Mahalinga-Iyer, M.W. Graham<br />

& J.R. Botella<br />

Plant Genetic Engineering Laboratory, Department of Botany, School of Integrative Biology, University of<br />

Queensland, Brisbane 4072, Australia.<br />

Root-knot nematodes (Meloidogyne spp.) are obligate, sedentary endoparasites that infect<br />

many plant species causing large economic losses worldwide. They have the ability to infect<br />

hundreds of plant species, which often lack natural resistance. Available nematicides are<br />

being banned due to their toxicity or ozone-depleting properties and alternative control<br />

strategies are urgently required. We have produced transgenic tobacco (Nicotiana tabacum)<br />

plants expressing different dsRNA hairpin structures targeting a root-knot nematode<br />

(Meloidogyne javanica) putative transcription factor, MjTis11. We provide evidence that<br />

MjTis11 was consistently silenced in nematodes feeding on the roots of transgenic plants. The<br />

observed silencing was specific for MjTis11, with other sequence-unrelated genes being<br />

unaffected in the nematodes. Those transgenic plants able to induce silencing of MjTis11,<br />

also showed the presence of small interfering RNAs. Even though down-regulation of<br />

MjTis11 did not result in a lethal phenotype, this study demonstrates the feasibility of<br />

silencing root-knot nematode genes by expressing dsRNA in the host plant. Host Delivered<br />

RNA Interference-triggered (HD-RNAi) silencing of parasite genes provides a novel disease<br />

resistance strategy with wide biotechnological applications. The potential of HD-RNAi is not<br />

restricted to parasitic nematodes but could be adapted to control other plant-feeding pests.<br />

Transcriptome Analysis of Syncytia Induced by the Cyst Nematode<br />

Heterodera schachtii in Arabidopsis and Role of Myo-Inositol Oxygenase<br />

Genes for its Induction and Maintenance<br />

Siddique, S. (1), S. Endreas (2), D. Szakasits (1), K. Wieczorek (1), J. Hofmann (1), F.M.W.<br />

Grundler (1), R. Tenhaken (2) & H. Bohlmann (1)<br />

(1) Institute of Plant Protection, Department of Applied Plant Sciences and Plant Biotechnology, University of<br />

Natural Resources and Applied Life Sciences, Vienna, Austria; (1) University of Salzburg, Plant Physiology,<br />

Hellbrunnerstr. 34, A-5020 Salzburg, Austria<br />

Arabidopsis thaliana is a host for the sugar beet cyst nematode Heterodera schachtii.<br />

Juvenile nematodes invade the roots and induce the development of a syncytium which<br />

functions as a feeding site for the nematode. We report here the transcriptome of syncytia<br />

induced in the roots of Arabidopsis. Microaspiration was employed to harvest pure syncytium<br />

material which was then used to prepare RNA for hybridization to Affymetrix GeneChips.<br />

Initial data analysis showed that gene expression in syncytia at 5 and 15 days after infection<br />

was not much different and both time points were therefore compared together to control<br />

roots. Out of a total of 21,138 genes, 18.4% (3,893) had a higher expression level and 15.8%<br />

5 th International Congress of Nematology, 2008 176

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