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Manganese Superoxide Dismutase in Meloidogyne incognita Isolates<br />

Selected for Virulence on Tomato<br />

Molinari, S. (1), L. Rosso (1) & C. Ornat Longaron (2)<br />

(1) Institute of Plant Protection, National Council of Research (C.N.R.), Via G. Amendola 122/D – 70126 Bari,<br />

Italy; (2) Departament d'Enginyeria Agroalimentària i Biotecnologia, Universitat Politecnica de Catalunya,<br />

08860 Castelldefels – Barcelona, Spain<br />

Root knot nematodes (Meloidogyne spp.) are important pests of a wide range of crops,<br />

including tomato. Resistance of tomato to root-knot nematodes is conferred by the single<br />

dominant gene Mi-1, which is present in all commercially available resistant tomato cultivars,<br />

at present. However, several resistance-breaking populations are being collected world-wide.<br />

Two isolates coming from the same standard population of Meloidogyne incognita, one<br />

selected for virulence against Mi-1 and the other left avirulent, have been used in this study.<br />

Manganese superoxide dismutase activity (Mn-SOD) was higher in virulent infective<br />

juveniles compared with avirulent counterparts. m-RNA was extracted from those two<br />

isolates and converted into cDNA. Species-specific primers of Mn-SOD were used for PCR<br />

and one single PCR product was generated from each isolate (EMBL accessions nos.<br />

AM285679 and AM285680). Such products were sequenced and the deduced amino-acid<br />

sequence recognized as a mitochondrial dimeric manganese SOD. The amount of transcripts<br />

was quantified by realtime-PCR. The virulent isolate showed an amount of transcripts 4-fold<br />

higher than that present in the avirulent isolate. The up-regulation of manganese SOD gene,<br />

which was associated with a high activity of the enzyme, has been found to be a characteristic<br />

of pre-parasitic juveniles of M. incognita isolates selected for virulence on tomato.<br />

Expression Analysis of Plant Defensin Genes in Nematode Induced Feeding<br />

Sites<br />

Siddique, S., D. Szakasits, K. Wieczorek, F.M.W. Grundler & H. Bohlmann<br />

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

Natural Resources and Applied Life Sciences, Vienna, 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. Transcriptome analysis of syncytia induced in<br />

the roots of Arabidopsis by Heterodera schachtii was performed with Affymetrix GeneChips<br />

using microaspiration to isolate pure syncytium material. Initial data analysis has shown that<br />

defense gene expression is repressed similar to the results obtained for galls induced by the<br />

root knot nematode Meloidogyne incognita in Arabidopsis roots (Jammes et al., 2005).<br />

However, an exception is the expression of a group of plant defensin genes. Pdf2.2 and<br />

Pdf2.3 were strongly expressed both in control root sections and in syncytia, and Pdf2.1 was<br />

among the most strongly upregulated genes in syncytia. The expression pattern of these genes<br />

in Arabidopsis plants and their response to infection by H. schachtii, H. glycines and M.<br />

incognita has been studied using GUS-lines, in situ RT-PCR and RT-PCR.<br />

5 th International Congress of Nematology, 2008 248

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