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Uncovering the Parasitic Interaction between Meloiodgyne hapla and<br />

Pasteuria penetrans<br />

Deighton, N. (1), N.J. Glassbrook (1), J.E. Schaff (1), M. Burke (2), C.H. Opperman (2) &<br />

K.G. Davies (3)<br />

(1) Genomic Sciences Laboratory, NC State University, Raleigh, NC 27606; (2) Centre for the Biology of<br />

Nematode Parasitism, NC State University, Raleigh, NC, 27606; (3) Rothamsted Research, Harpenden, Herts.,<br />

UK AL5 2JQ<br />

Pasteuria penetrans is an endospore producing, Gram-positive bacterium that is an obligate<br />

parasite of root-knot nematodes (Meloidogyne spp.), which are themselves obligate parasites<br />

of plants. This bacterium has been associated with nematode suppressive soils and also<br />

shown to have tremendous potential for the biological control of root-knot nematodes.<br />

However, the fastidious nature of the organism and the lack of ability to perform forward<br />

genetic experiments have hindered our ability to make progress on culturing, host range<br />

expansion, and mass production techniques. With the completion of the genome sequences<br />

of both organisms, Pasteuria penetrans (Davies et al, 2008) and Meloidogyne hapla<br />

(Opperman et al, 2008) experiments investigating global gene expression, proteomics and<br />

indeed metabolomics studies of this parasitic interaction have become possible. Here we<br />

describe our experimental approach to studying these difficult organisms and present<br />

preliminary results from our studies.<br />

Interactions between Nematodes and Rhizobia: from Proteomics to Plant<br />

Distribution<br />

Costa, S.R. (1,2), Freitas, H. (1) & Mathesius, U. (2)<br />

(1) Centre for Functional Ecology, University of Coimbra, 3000-345 Coimbra, Portugal; (2) School of<br />

Biochemistry and Molecular Biology, Australian National University, Canberra, ACT 0200, Australia<br />

The establishment of legumes depends on mutualistic interactions with rhizobial bacteria, but<br />

plant performance can be affected by plant-parasitic nematodes (PPN). Previous studies<br />

indicate that PPN may reduce nodule formation and that rhizobial strains can induce plant<br />

resistance against PPN. Nematodes and rhizobia share biochemical pathways of infection and<br />

interact in the rhizosphere, but the outcomes of their interactions for plant performance and<br />

distribution are still not clear. We aim to assess the role of these interactions in the<br />

distribution of legumes in their native and exotic habitats. The model legume Medicago<br />

truncatula and laboratory cultures of the root-knot nematode Meloidogyne javanica and the<br />

rhizobial bacteria Sinorhizobium melioti were used in controlled experiments. The axenically<br />

grown legumes were inoculated with PPN and rhizobia, alone or in combination, at distinct<br />

time lags (0, 1 and 3 days). Root and shoot fresh weight, nodulation and gall formation were<br />

determined after 3 weeks. The nematodes significantly stimulated nodulation and rhizobia<br />

significantly reduced nematode infection (p

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