The role of JAK/STAT signaling in the cellular immune response of Drosophila is not well understood. Here, we show that parasitoid wasp infection activates JAK/STAT signaling in somatic muscles of the Drosophila larva, triggered by secretion of the cytokines Upd2 and Upd3 from circulating hemocytes. Deletion of upd2 or upd3, but not the related os (upd1) gene, reduced the cellular immune respon...

developmental periodsof thegrapevine aphid, aphis illinoisensis shimer (hemiptera: aphididae) on the grape, vitis vinifera l., and its two parasitoid species, lysiphlebus testaceipes (cresson) (exotic) (hymenoptera: braconidae: aphidiinae) and aphelinus albipodus hayat and fatima (indigenous) (hymenoptera: aphelinidae) were studied at two constant temperatures (20 and 25 ± 2 oc), 70 ± 5 % r.h. ...

Banker plants with Aphidius colemani Viereck were tested in greenhouses in Massachusetts and New York for control of cotton aphid Aphis gossypii Glover, and green peach aphid Myzus persicae (Sulzer) on 2 spring flower crops, pansies ( Viola tricolor hortensis ) and Marguerite daisies ( Argyranthemum hybrid). Banker plants consisted of pots of barley plants infested with the bird cherry-oat aphi...

Drosophila is an extremely useful model organism for understanding how innate immune mechanisms defend against microbes and parasitoids. Large foreign objects trigger a potent cellular immune response in Drosophila larva. In the case of endoparasitoid wasp eggs, this response includes hemocyte proliferation, lamellocyte differentiation and eventual encapsulation of the egg. The encapsulation re...

Parasitoid wasps are taxonomically and biologically extremely diverse. A conceptual framework has recently been developed for understanding life-history evolution and diversification in these animals, and it has confirmed that each of two linked life-history traits - the mode of larval development and the temporal pattern of egg maturation - acts as an organiser of life-history. The framework h...

The interactions between Drosophila melanogaster and the parasitoid wasps that infect species provide an important model for understanding host–parasite relationships. Following infection, D. larvae mount a response in which immune cells (hemocytes) form capsule around wasp egg, then melanizes, leading to death of parasitoid. Previous studies have found host hemocyte load; number hemocytes avai...

The maternally transmitted bacterium Wolbachia pipientis is well known for spreading and persisting in insect populations through manipulation of the fitness of its host. Here, we identify three new Wolbachia pipientis strains, wHho, wHho2 and wHho3, infecting Hyposoter horticola, a specialist wasp parasitoid of the Glanville fritillary butterfly. The wHho strain (ST435) infects about 50% of th...

Symbionts are widespread and might have a substantial effect on the outcome of interactions between species, such as in host-parasitoid systems. Here, we studied the effects of symbionts on the outcome of host-parasitoid interactions in a four-partner system, consisting of the parasitoid wasp Leptopilina boulardi, its two hosts Drosophila melanogaster and D. simulans, the wasp virus LbFV, and t...

Some bees and wasps that host mites have peculiar pocket-like structures called acarinaria. These have long been considered as morphological adaptations to securely transfer beneficial mites into nests, and thus are thought to be the product of a mutualistic relationship. However, there has been little compelling evidence to support this hypothesis. We demonstrated that the parasitic mite Ensli...

Theory predicts that intraguild consumers such as predators or parasitoids may displace more specialized heterospecific competitors and thereby actually increase the population densities of a shared host or prey. We tested this idea with a native primary parasitoid, Eretmocerus eremicus, and an exotic autoparasitoid Encarsia sophia, both attacking the sweetpotato whitefly Bemisia tabaci. Autopa...