DROP: Molecular voucher database for identification of Drosophila parasitoids.

Molecular identification is increasingly used to speed up biodiversity surveys and laboratory experiments. However, many groups of organisms cannot be reliably identified using standard databases such as GenBank or BOLD due to lack of sequenced voucher specimens identified by experts. Sometimes a large number of sequences are available, but with too many errors to allow identification.

Virulence strategies in parasitoid Hymenoptera as an example of adaptive diversity.

Parasitoids are mostly insects that develop at the expense of other arthropods, which will die as a result of the interaction. Their reproductive success thus totally depends on their ability to successfully infest their host whose reproductive success relies on its own ability to avoid or overcome parasitism. Such intense selective pressures have resulted in extremely diverse adaptations in parasitoid strategies that ensure parasitism success.

Variation of success of Leptopilina boulardi in Drosophila yakuba: the mechanisms explored.

Despite an increasing knowledge of insect immune defences and virulence strategies used by parasitoids to escape them, the mechanisms underlying variation of success between parasitoid strains are still poorly understood. We have investigated this point using two lines of the parasitoid wasp Leptopilina boulardi that differ in virulence towards Drosophila yakuba. By injecting oil drops in D.

Parasite suppression of the oxidations of eumelanin precursors in Drosophila melanogaster.

In insects, eukaryotic endoparasites encounter a series of innate immune effector responses mediated in large part by circulating blood cells (hemocytes) that rapidly form multilayer capsules around foreign organisms. Critical components of the encapsulation response are chemical and enzyme-catalyzed oxidations involving phenolic and catecholic substrates that lead to synthesis of eumelanin. These responses are initiated immediately upon infection and are very site-specific, provoking no undesirable systemic responses in the host.

Dexamethasone inhibition of the cellular immune response of Drosophila melanogaster against a parasitoid.

Host larvae of Drosophila melanogaster injected with the eicosanoid biosynthesis inhibitor, dexamethasone, prior to parasitization by the wasp Leptopilina boulardi, exhibited significantly reduced rates of melanotic encapsulation in comparison with control and saline-injected larvae. The results of this investigation suggest that prostaglandins and other eicosanoids are involved as cell-signaling molecules in the hemocytic encapsulation reaction of D. melanogaster larvae.

Cellular immune response to parasite infection in the Drosophila lymph gland is developmentally regulated.

The mechanisms by which an organism becomes immune competent during its development are largely unknown. When infected by eggs of parasitic wasps, Drosophila larvae mount a complex cellular immune reaction in which specialized host blood cells, lamellocytes and crystal cells, are activated and recruited to build a capsule around the parasite egg to block its development. Here, we report that parasitization by the wasp Leptopilina boulardi leads to a dramatic increase in the number of both lamellocytes and crystal cells in the Drosophila larval lymph gland.