Nematodes from terrestrial, freshwater and brackish water habitats in Belgium: an updated list with special emphasis on compost nematodes.

A study of nematodes from a semi-artificial and controlled composting process in Eastern Flanders revealed 35 taxa, 21 of which were new records for Belgium. An updated checklist of free-living, plant-parasitic and entomopathogenic nematodes from terrestrial, freshwater and brackish water habitats in Belgium is presented. The Belgian non-marine nematofauna comprises 418 taxa, representing 4 subclasses, 14 orders, and 76 families. In total 127 new records were added: i.e. 21 from the newly explored compost habitat, 7 from freshwater samples and 99 from published data in literature.

The embryonic cell lineage of the nematode Rhabditophanes sp.

One of the unique features of the model organism Caenorhabditis elegans is its invariant development, where a stereotyped cell lineage generates a fixed number of cells with a fixed cell type. It remains unclear how embryonic development evolved within the nematodes to give rise to the complex, invariant cell lineage of C. elegans. Therefore, we determined the embryonic cell lineage of the nematode, Rhabditophanes sp. (family Alloionematidae) and made detailed cell-by-cell comparison with the known cell lineages of C. elegans, Pellioditis marina and Halicephalobus gingivalis. This gave us a unique data set of four embryonic cell lineages, which allowed a detailed comparison between these cell lineages at the level of each individual cell. This lineage comparison revealed a similar complex polyclonal fate distribution in all four nematode species (85% of the cells have the same fate). It is striking that there is a conservation of a 'C. elegans' like polyclonal cell lineage with strong left-right asymmetry. We propose that an early symmetry-breaking event in nematodes of clade IV-V is a major developmental constraint which shapes their asymmetric cell lineage.

An SXP/RAL-2 protein produced by the subventral pharyngeal glands in the plant parasitic root-knot nematode Meloidogyne incognita.

Meloidogyne incognita is a major parasite of numerous plant families, including many crop species. Upon infection of the plant root, it induces several multinucleate giant cells by the injection of pharyngeal gland secretions into the root cells. In order to obtain a better understanding of the nematode-plant interaction, characterization of the pharyngeal gland secretions is a necessity. By differential display, a nematode gene was identified that encodes a new member of the SXP/RAL-2 protein family. The gene is specifically expressed in the subventral pharyngeal glands and the protein is most likely secreted.

A new class of ubiquitin extension proteins secreted by the dorsal pharyngeal gland in plant parasitic cyst nematodes.

By performing cDNA AFLP on pre- and early parasitic juveniles, we identified genes encoding a novel type of ubiquitin extension proteins secreted by the dorsal pharyngeal gland in the cyst nematode Heterodera schachtii. The proteins consist of three domains, a signal peptide for secretion, a mono-ubiquitin domain, and a short C-terminal positively charged domain. A gfp-fusion of this protein is targeted to the nucleolus in tobacco BY-2 cells. We hypothesize that the C-terminal peptide might have a regulatory function during syncytium formation in plant roots.

Secretions of plant-parasitic nematodes: a molecular update.

The interaction between sedentary endoparasitic nematodes and plants is fascinating, because these animals have developed an ingenious way to manipulate the plant's gene regulation and metabolism to their own advantage. They are able to form highly specialized feeding structures in the plant root to satisfy their nutritional demands for development and reproduction. This ability makes them extremely successful parasites with severe consequences for agriculture. Triggered by these economical losses, detailed studies of the parasitic interaction have been performed, which resulted in an extensive descriptive knowledge. However, the underlying biochemical and molecular events of this intimate relationship have still not been elucidated. It is generally accepted that secretions produced by the nematode are responsible for the dramatic alteration of specific cells in the host plant. In the past few years, the identification of genes coding for secreted proteins was a breakthrough in plant nematode research. However, the available information is still too limited to allow the formulation of a comprehensive model, mainly because the sequences of many of these genes are novel with no similar sequence found in the existing databases. A new challenge in the coming years will be the functional analysis of these putative parasitism genes.

Embryonic cell lineage of the marine nematode Pellioditis marina.

We describe the complete embryonic cell lineage of the marine nematode Pellioditis marina (Rhabditidae) up to somatic muscle contraction, resulting in the formation of 638 cells, of which 67 undergo programmed cell death. In comparison with Caenorhabditis elegans, the overall lineage homology is 95.5%; fate homology, however, is only 76.4%. The majority of the differences in fate homology concern nervous, epidermal, and pharyngeal tissues. Gut and, remarkably, somatic muscle is highly conserved in number and position. Partial lineage data from the slower developing Halicephalobus sp. (Panagrolaimidae) reveal a lineage largely, but not exclusively, built up of monoclonal sublineage blocs with identical fates, unlike the polyclonal fate distribution in C. elegans and P. marina. The fate distribution pattern in a cell lineage could be a compromise between minimizing the number of specification events by monoclonal specification and minimizing the need for migrations by forming the cells close at their final position. The latter could contribute to a faster embryonic development. These results reveal that there is more than one way to build a nematode.

Use of the Verrucomicrobia-specific probe EUB338-III and fluorescent in situ hybridization for detection of "Candidatus Xiphinematobacter" cells in nematode hosts.

Fluorescent in situ hybridization with a 16S rRNA probe specific for Verrucomicrobia was used to (i) confirm the division-level identity of and (ii) study the behavior of the obligate intracellular verrucomicrobium "Candidatus Xiphinematobacter" in its nematode hosts. Endosymbionts in the egg move to the pole where the gut primordium arises; hence, they populate the intestinal epithelia of juvenile worms. During the host's molt to adult female, the endosymbionts concentrate around the developing ovaries to occupy the ovarian wall. Some bacteria are enclosed in the ripening oocytes for vertical transmission. Verrucomicrobia in males stay outside the testes because the tiny spermatozoids are not suitable for transmission of cytoplasmic bacteria.

A simplified whole mount in situ hybridization protocol using DIG-labelled DNA probes to visualize gene activity in Heterodera schachtii.

Information concerning gene expression during the nematode's life cycle is rapidly accumulating as a result of different screening approaches. In the majority of the cases, the initial characterization of these genes involves determination of their temporal and tissue-specific expression patterns. This preliminary insight into the characteristics of newly isolated genes allows the formulation of a hypothesis and sets the course for further research. Here, we present an optimised method to visualize gene expression in the beet cyst nematode Heterodera schachtii by means of whole mount in situ hybridization. Two different probes for targets with known expression pattern in other nematode species were used to optimise the protocol. It was experimentally observed that the use of vacuum-infiltration during fixation resulted in a fast and complete penetration of the fixative, which was essential to preserve the morphological constitution of the nematode tissue. Some other modifications were introduced that significantly reduced the experimental time without loss of efficiency. As such, we were able to localize the expression pattern of some novel genes with a possible function in the pathogenesis of this nematode.