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Rahier, Martine

Nom
Rahier, Martine
Affiliation principale
Fonction
Professeure ordinaire
Email
Martine.Rahier@unine.ch
Identifiants
https://libra.unine.ch/handle/123456789/99

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  • Publication
    Accès libre
    Sequestration, Maintenance, and Tissue Distribution of Pyrrolizidine Alkaloid N-Oxides in Larvae of Two Oreina Species
    (1999)
    Ehmke, Adelheid
    ;
    Rahier, Martine 
    ;
    Pasteels, Jacques M.
    ;
    Theuring, Claudine
    ;
    Hartmann, Thomas
    Oreina cacaliae and O. speciosissima are leaf beetles that, as larvae and adults, sequester pyrrolizidine alkaloid N-oxides (PAs) as defensive compounds from their host plants Adenostyles alliariae and Senecio nemorensis. As in most Oreina species, O. speciosissima is also defended by autogenously produced cardenolides (mixed defensive strategy), whereas O. cacaliae does not synthesize cardenolides and is exclusively dependent on host-plant-acquired PAs (host-derived defense). Adults of the two Oreina species were found to have the same PA storage capacity. The larvae, however, differ; larvae of O. speciosissima possess a significantly lower capability to store PAs than O. cacaliae. The ability of Oreina larvae to sequester PAs was studied by using tracer techniques with 14C-labeled senecionine N-oxide. Larvae of the two species efficiently take up [14C]senecionine N-oxide from their food plants and store the alkaloid as N-oxide. In O. cacaliae, there is a slow but continuous loss of labeled senecionine N-oxide. This effect may reflect the equilibrium between continuous PA uptake and excretion, resulting in a time-dependent tracer dilution. No noticeable loss of labeled alkaloid is associated with molting. Senecionine N-oxide is detectable in all tissues. The hemolymph is, with ca. 50–60% of total PAs, the major storage compartment, followed by the integument, with ca 30%. The alkaloid concentration in the hemolymph is approximately sixfold higher than in the solid tissues. The selectivity of PA sequestration in larvae is comparable to PA sequestration in the bodies of adult beetles.
  • Publication
    Accès libre
    Selective sequestration and metabolism of plant derived pyrrolizidine alkaloids by chrysomelid leaf beetles
    (1997)
    Hartmann, Thomas
    ;
    Witte, Ludger
    ;
    Ehmke, Adelheid
    ;
    Theuring, Claudine
    ;
    Rahier, Martine 
    ;
    Pasteels, Jacques M.
    Pyrrolizidine alkaloids (PAs) are assumed to function as plant defence compounds against herbivory. A number of adapted insects are known to sequester plant derived PAs for their own benefit. Here we summarize the chemical interactions between leaf beetles of the genus Oreina (Coleoptera, Chrysomelidae) and their host plants Adenostyles spp., Senecio nemorensis, and S. fuchsii (Asteraceae, tribe Senecioneae). Seneciphylline N-oxide and senecionine N-oxide, the main PAs of Adenostyles, are sequestered in the bodies and exocrine defensive glands of the leaf beetles. The comparison with the PA patterns of the Senecio host plant indicates a selective PA uptake. The uptake into the body (hemolymph) is less specific, whereas the translocation into the defensive glands is highly specific. Only the N-oxides of macrocyclic retronecine esters of the senecionine type are found in significant amounts in the defensive secretions. Many other PAs such as monoesters and open-chain diesters as well as PAs of other structural types (e.g. monocrotaline N-oxide and senkirkine) are not transferred into the defensive glands. Leaf beetles sequester PAs exclusively as N-oxides. A novel PA not found in the food plants was detected in the defensive secretions of Oreina elongata; it was identified as 13,19-expoxisenecionine N-oxide (oreine), the epoxidation product of seneciphylline N-oxide. Besides this transformation, leaf beetles are able to catalyse further transformations such as the O-dealkylation of heliotrine N-oxide to rinderine N-oxide and the O-deacetylation of acetylseneciphylline N-oxide to seneciphylline N-oxide. The plant-beetle interactions are discussed in the functional context of PAs as powerful plant defensive chemicals.