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SESSION THIRTY – ROLE AND EXPRESSION OF NEMATODE<br />

PARASITISM GENES<br />

CONVENORS: ERIC DAVIS & ANN BURNELL<br />

Hookworm Genes and the Infectious Process<br />

Datu, B. (1), R. Gasser (2), A. Hofmann (3), J. Mulvenna (1) & A. Loukas (1)<br />

(1) Queensland Institute of Medical Research, Brisbane, Australia; (2) University of Melbourne, Melbourne,<br />

Australia; (3) Griffith University, Brisbane, Australia<br />

Third-stage larvae (L3) of the canine hookworm, Ancylostoma caninum, undergo arrested<br />

development preceding transmission to a host. Many of the mRNAs up-regulated at this stage<br />

are likely to encode proteins that facilitate the transition from a free-living to a parasitic larva.<br />

The initial phase of mammalian host invasion by A. caninum L3 (herein termed ‘activation’)<br />

can be mimicked in vitro by culturing L3 in serum-containing medium. The mRNAs<br />

differentially transcribed between activated and non-activated L3 were identified by<br />

suppression subtractive hybridisation (SSH). The analysis of these mRNAs on a custom<br />

oligonucleotide microarray printed with the SSH expressed sequence tags (ESTs) and<br />

publicly available A. caninum ESTs (non-subtracted) yielded 602 differentially expressed<br />

mRNAs, of which the most highly represented sequences encoded members of the<br />

pathogenesis-related protein (PRP) superfamily and proteases. Comparison of these A.<br />

caninum mRNAs with those of Caenorhabditis elegans larvae exiting from developmental<br />

(dauer) arrest demonstrated unexpectedly large differences in gene ontology profiles. C.<br />

elegans dauer exiting L3 up-regulated expression of mostly intracellular molecules involved<br />

in growth and development. Such mRNAs are virtually absent from activated hookworm<br />

larvae, and instead are over-represented by mRNAs encoding extracellular proteins with<br />

putative roles in host-parasite interactions. One family of proteins inparticular, the<br />

Ancylostoma Secreted Proteins (ASPs), has undergone enormous expansion in the hookworm<br />

genome and seventeen of the thirty most highly upregulated genes encoded for ASPs. The<br />

functions of ASPs are mostly unknown, but structural and modelling studies show a large<br />

peptide-binding groove which likely accommodates host-derived ligands. Although the data<br />

presented here should not invalidate C. elegans dauer exit as a model for hookworm<br />

activation, it highlights the limitations of this free-living nematode as a model organism for<br />

the transition of nematode larvae from a free-living to a parasitic state.<br />

5 th International Congress of Nematology, 2008 108

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