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Obligatory multiparasitism in the tussock moth, Orgyia leucostigma

Published online by Cambridge University Press:  06 April 2009

D. Guzo
Affiliation:
Department of Microbiology, Dalhousie University, Halifax, Nova Scotia
D. B. Stoltz
Affiliation:
Department of Microbiology, Dalhousie University, Halifax, Nova Scotia

Extract

Orgyia leucostigma haemocytes were able to encapsulate and destroy eggs of Hyposoter species, thereby preventing successful parasitism. When host larvae had previously been parasitized by Cotesia melanoscela, however, this response was not observed, and 3 different Hyposoter species could be reared to maturity in the normally non-permissive host. Appropriate injection experiments established that C. melanoscela virus and venom were both required in order for successful parasitism by Hyposoter to occur. Covalent cross-linking of C. melanoscela viral DNA led to an immune response against Hyposoter larvae, but not eggs, suggesting that an active viral genome may be required for complete development of Hyposoter species in tussock moth larvae.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1985

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References

REFERENCES

Askew, R. R. (1971). Parasitic Insects. New York: Elsevier.Google Scholar
Beckage, N. E. & Riddiford, L. M. (1982). Effects of parasitism by Apanteles congregatus on the endocrine physiology of the tobacco hornworm Manduca sexta. General and Comparative Endocrinology 47, 308–22.CrossRefGoogle ScholarPubMed
Boman, H. G. & Steiner, H. (1981). Humoral immunity in Cecropia pupae. Current Topics in Microbiology and Immunology 94/95, 7591.CrossRefGoogle ScholarPubMed
Burgess, A. F. & Crossman, S. S. (1929). Imported insect enemies of the gypsy moth and the brown-tail moth. USDA Technical Bulletin 86.Google Scholar
Cook, D. I., Stoltz, D. B. & Vinson, S. B. (1984). Induction of a new haemolymph glycoprotein in larvae of permissive hosts parasitized by Campoletis sonorensis. Insect Biochemistry 14, 4550.CrossRefGoogle Scholar
Dahlman, D. L. (1975). Trehalose and glucose levels in hemolymph of diet-reared, tobacco leaf-reared and parasitized tobacco hornworm larvae. Comparative Biochemical Physiology 50A, 165–7.CrossRefGoogle ScholarPubMed
Dahlsten, D. L., Luck, R. F., Schlinger, E. I., Wenz, J. M. & Copper, W. A. (1977). Parasitoids and predators of the Douglas-fir tussock moth, Orgyia pseudotsugata (Lepidoptera: Lymantriidae), in low to moderate populations in central California. Canadian Entomologist 109, 727–46.CrossRefGoogle Scholar
Dulbecco, R. & Voot, M. (1954). Plaque formation and isolation of pure lines of Poliomyelitis viruses. Journal of Experimental Medicine 99, 167–82.CrossRefGoogle ScholarPubMed
Edson, K. M., Vinson, S. B., Stoltz, D. B. & Summers, M. D. (1981). Virus in a parasitoid wasp: suppression of the cellular immune response in the parasitoid's host. Science 211, 582–3.CrossRefGoogle Scholar
Fleming, J. G. W., Blissard, G. W., Summers, M. D. & Vinson, S. B. (1983). Expression of Campoletis sonorensis virus in the parasitized host, Heliothis virescens. Journal of Virology 48, 74–8.CrossRefGoogle ScholarPubMed
Hanson, C. V., Riggs, J. L. & Lennette, E. H. (1978). Photochemical inactivation of DNA and RNA viruses by psoralen derivatives. Journal of General Virology 40, 345–58.CrossRefGoogle ScholarPubMed
Hulme, M. A. (1982). Biological control in the Canadian Forestry Service. CFS Report # DPC-X-11.Google Scholar
Kitano, H. (1982). Effect of the venom of the gregarious parasitoid Apanteles glomeratus on its hemocytic encapsulation by the host, Pieris. Journal of Invertebrate Pathology 40, 61–7.CrossRefGoogle Scholar
Krell, P. J. & Stoltz, D. B. (1979). Unusual baculovirus of the parasitoid wasp Apanteles melanoscelus: isolation and preliminary characterization. Journal of Virology 29, 1118–30.CrossRefGoogle ScholarPubMed
Krell, P. J. & Stoltz, D. B. (1980). Virus-like particles in the ovary of an ichneumonid wasp: purification and preliminary characterization. Virology 101, 408–18.CrossRefGoogle ScholarPubMed
Krombein, K. V., Hurd, P. E. Jr., Smith, D. R. & Burks, B. D. (1979). Catalogue of Hymenoptera north of Mexico, vol. 1. Washington: Smithsonian Institution Press.CrossRefGoogle Scholar
Pemberton, C. E. & Willard, H. F. (1918). A contribution to the biology of fruit-fly parasites in Hawaii. Journal of Agricultural Research 15, 419–66.Google Scholar
Pschorn-Walcher, H. (1977). Biological control of forest insects. Annual Review of Entomology 22, 122.CrossRefGoogle Scholar
Ratcliffe, N. A. & Rowley, A. F. (1979). Insect Hemocytes (ed. Gupta, A. P.). Cambridge: Cambridge University Press.Google Scholar
Salt, G. (1968). The defense reactions of insects to metazoan parasites. Parasitology 53, 527642.CrossRefGoogle Scholar
Salt, G. (1970). The Cellular Defence Reactions of Insects. Cambridge: Cambridge University Press.CrossRefGoogle Scholar
Stoltz, D. B. & Cook, D. I. (1983). Inhibition of host phenoloxidase activity by parasitoid hymenoptera. Experientia 39, 1022–4.CrossRefGoogle Scholar
Stoltz, D. B. & Faulkner, G. (1978). Apparent replication of an unusual virus-like particle in both a parasitoid wasp and its host. Canadian Journal of Microbiology 24, 1509–14.CrossRefGoogle ScholarPubMed
Stoltz, D. B., Krell, P. J. & Vinson, S. B. (1981). Polydisperse viral DNA's in ichneumonid ovaries: a survey. Canadian Journal of Microbiology 27, 123–30.CrossRefGoogle ScholarPubMed
Stoltz, D. B. & Vinson, S. B. (1977). Baculovirus-like particles in the reproductive tracts of female parasitoid wasps. II. The genus Apanteles. Canadian Journal of Microbiology 23, 2837.CrossRefGoogle Scholar
Stoltz, D. B. & Vinson, S. B. (1979). Viruses and parasitism in insects. Advances in Virus Research 24, 125–71.CrossRefGoogle ScholarPubMed
Streams, F. A. & Greenberg, L. (1969). Inhibition of the defense reaction of Drosophila melanogaster parasitized simultaneously by the wasps Pseudeucoila bochei and Pseudeucoila mellipes. Journal of Invertebrate Pathology 13, 371–7.CrossRefGoogle Scholar
Van Den Bosch, R. & Dietrich, E. J. (1959). The interrelationships of Hypera brunneipennis (Coleoptera: Curculionidae) and Bathyplectes curculionis (Hymenoptera: Ichneumonidae) in Southern California. Annals of the Entomological Society of America 52, 609–16.CrossRefGoogle Scholar
Veronese, F. M., Schiavon, O., Bevilacqua, R., Bordin, F. & Rodighiero, G. (1981). The effects of psoralens and angelicins on proteins in the presence of UV-A irradiation. Photochemistry and Photobiology 34, 351–4.CrossRefGoogle ScholarPubMed