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A stilbonematid nematode EST project

A stilbonematid nematode EST project

Jörg Ott (ORCID: 0000-0003-2274-5989)
  • Grant DOI 10.55776/P17710
  • Funding program Principal Investigator Projects
  • Status ended
  • Start January 1, 2005
  • End August 31, 2007
  • Funding amount € 167,177
  • Project website

Disciplines

Biology (100%)

Keywords

    Stilbonematid nematodes, Symbiosis, Immune defense, Expressed sequence tag dataset, Gene discovery

Abstract Final report

In the last years it became clear that the study of biological systems in which invertebrates and procaryotes succeed to beneficially interact with each other could enlarge our understanding of how chronic pathogenic infections develop and persist. Among the very few known non-pathogenic nematode-bacteria associations, the most spectacular ones are those involving the Stilbonematinae (Desmodoridae, Chromadoria). Chemoautotrophic sulfur- oxidizing bacteria arranged in a genus- or even species-specific pattern cover the cuticle of these marine nematodes, irrespectively of their age. The association of stilbonematids of the genus Laxus could be specifically disrupted by incubation in D-mannose and a worm cDNA predicted to encode for a secreted mannose-binding C- type lectin (provisionally called STIL-1) was identified. STIL-1, which shares significant identity with mammalians dendritic cell immunoreceptors, is supposedly only one of a whole battery of proteins encoded by symbiosis- specific genes. Here we propose to carry out a stilbonematid expressed sequence tag (EST) project to identify other molecular key players belonging to this battery. The potential of a stilbonematid EST-based gene discovery approach goes beyond that of identifying adaptations requisite for bacterial association at the molecular level. Indeed, the availability of the full genome sequence of three Caenorhabditis species and of Brugia malayi, as well as EST datasets of many parasitic nematodes, yields an exceptional opportunity to compare free-living, parasitic and symbiotic gene sequences and structures. Finally, from a phylogenetic point of view, the acquisition from stilbonematid sequence data will help rooting the main radiation of the Secernentea and resolving the trichotomy at the base of the Nematoda.

In the last years it became clear that the study of biological systems in which invertebrates and procaryotes succeed to beneficially interact with each other could enlarge our understanding of how chronic pathogenic infections develop and persist. Among the very few known non-pathogenic nematode-bacteria associations, the most spectacular ones are those involving the Stilbonematinae (Desmodoridae, Chromadoria). Chemoautotrophic sulfur- oxidizing bacteria arranged in a genus- or even species-specific pattern cover the cuticle of these marine nematodes, irrespectively of their age. The association of stilbonematids of the genus Laxus could be specifically disrupted by incubation in D-mannose and a worm cDNA predicted to encode for a secreted mannose-binding C- type lectin (provisionally called STIL-1) was identified. STIL-1, which shares significant identity with mammalians dendritic cell immunoreceptors, is supposedly only one of a whole battery of proteins encoded by symbiosis- specific genes. Here we propose to carry out a stilbonematid expressed sequence tag (EST) project to identify other molecular key players belonging to this battery. The potential of a stilbonematid EST-based gene discovery approach goes beyond that of identifying adaptations requisite for bacterial association at the molecular level. Indeed, the availability of the full genome sequence of three Caenorhabditis species and of Brugia malayi, as well as EST datasets of many parasitic nematodes, yields an exceptional opportunity to compare free-living, parasitic and symbiotic gene sequences and structures. Finally, from a phylogenetic point of view, the acquisition from stilbonematid sequence data will help rooting the main radiation of the Secernentea and resolving the trichotomy at the base of the Nematoda.

Research institution(s)
  • Universität Wien - 100%
International project participants
  • Jonathan Ewbank, Université de la Méditerranée - France
  • Mark Blaxter, Wellcome Sanger Institute

Research Output

  • 142 Citations
  • 4 Publications
Publications
  • 2009
    Title Molecular characterization of the symbionts associated with marine nematodes of the genus Robbea‡
    DOI 10.1111/j.1758-2229.2009.00019.x
    Type Journal Article
    Author Bayer C
    Journal Environmental Microbiology Reports
    Pages 136-144
    Link Publication
  • 2008
    Title C-type lectin Mermaid inhibits dendritic cell mediated HIV-1 transmission to CD4+ T cells
    DOI 10.1016/j.virol.2008.05.025
    Type Journal Article
    Author Nabatov A
    Journal Virology
    Pages 323-328
  • 2011
    Title First detection of thiotrophic symbiont phylotypes in the pelagic marine environment
    DOI 10.1111/j.1574-6941.2011.01096.x
    Type Journal Article
    Author Heindl N
    Journal FEMS Microbiology Ecology
    Pages 223-227
    Link Publication
  • 2011
    Title Paracatenula, an ancient symbiosis between thiotrophic Alphaproteobacteria and catenulid flatworms
    DOI 10.1073/pnas.1105347108
    Type Journal Article
    Author Gruber-Vodicka H
    Journal Proceedings of the National Academy of Sciences
    Pages 12078-12083
    Link Publication

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