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Transmission of microsporidia, especially Orthosoma operophterae (Canning, 1960) between generations of winter moth Operophtera brumata (L) (Lepidoptera: Geometridae)

Published online by Cambridge University Press:  06 April 2009

Elizabeth U. Canning
Affiliation:
Department of Pure and Applied Biology, Imperial College, London SW7 2BB
Rosalind J. Barker
Affiliation:
Department of Pure and Applied Biology, Imperial College, London SW7 2BB
A. M. Page
Affiliation:
Department of Pure and Applied Biology, Imperial College, London SW7 2BB
J. P. Nicholas
Affiliation:
Department of Pure and Applied Biology, Imperial College, London SW7 2BB

Extract

The transmission mechanisms of microsporidia between generations of Operophtera brumata, a geometrid moth with an univoltine life-cycle, have been investigated. The parasites, Orthosoma operophterae, Pleistophora operophterae and Nosema wistmansi were present in moths collected from Wistman's Wood on Dartmoor. An infection rate of 100% was found in eggs laid by moderately or heavily infected female moths. Thus, 100% infection was found in eggs laid by 78 out of 90 infected females. Lower prevalences were found in eggs laid by the remaining 12 and these moths were subsequently shown to have very light infections. Male moths do not pass on this infection to progeny. The development of O. operophterae was followed during embryonation. The microsporidia do not invade the cells of the developing larva but are restricted to the yolk, where spores accumulate in abundance after earlier merogonies. When the larva is mature and ready to hatch, spores are ingested with the remains of the yolk, as the larva eats its way through the egg-shell. Spores are then found in the meconium in the lumen of the gut. These spores are infective and, once the gut of the larva has become functional, are responsible for infecting the tissues of the larvae which harbour them, as well as healthy larvae reared with them. Spores of O. operophterae held in the natural environment for 7 months from winter until mid-summer still retained infectivity and those contaminating the environment from the bodies of one generation must contribute to transmission between generations.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1985

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References

REFERENCES

Brooks, W. M. & Cranford, J. D. (1978). Host parasite relationships of Nosema heliothidis Lutz and Splendore. Miscellaneous Publications of the Entomological Society of America 11, 5163.Google Scholar
Canning, E. U. (1960). Two new microsporidian parasites of the winter moth, Operophtera brumata (L.) Journal of Parasitology 46, 755–63.CrossRefGoogle ScholarPubMed
Canning, E. U., Barker, R. J., Page, A. M. & Nicholas, J. P. (1982). Speculation on the transmission mechanisms of microsporidia and a trypanosomatine flagellate of winter moths, Operophtera brumata (L.) Journal of Protozoology 29, 635.Google Scholar
Canning, E. U., Wigley, P. J. & Barker, R. J. (1983). The taxonomy of three species of microsporidia (Protozoa: Microspora) from an oakwood population of winter moths Operophtera brumata (L.) (Lepidoptera, Geometridae). Systematic Parasitology 5, 147–59.CrossRefGoogle Scholar
Hunter, F., Crook, N. & Entwhistle, P. F. (1984). Viruses as pathogens for the control of insects. In Microbial Methods for Environmental Biotechnology, (ed. Grainger, J. M. and Lynch, J. M.). New York and London: Academic Press (in the Press).Google Scholar
Kaya, H. K. (1977). Survival of spores of Vairmorpha (= Nosema) necatrix (Microsporidia: Nosematidae) exposed to sunlight, ultra-violet radiation and high temperature. Journal of Invertebrate Pathology 30, 192–8.CrossRefGoogle Scholar
Maddox, J. V. (1973). The persistence of microsporidia in the environment. Miscellaneous Publications of the Entomological Society of America 9, 99104.Google Scholar
Milner, R. J. & Lutton, G. G. (1980). Interactions between Oncopera alboguttata (Lepidoptera: Hepialidae) and its microsporidian pathogen, Pleistophora oncoperae (Protozoa: Microsporida). Journal of Invertebrate Pathology 36, 198202.CrossRefGoogle Scholar
Sikorowski, P. P. & Lashomb, J. H. (1977). Effect of sunlight on the infectivity of Nosema heliothidis spores isolated from Heliothis zea. Journal of Invertebrate Pathology 30, 95–6.CrossRefGoogle ScholarPubMed
Teetor, G. E. & Kramer, J. P. (1977). Effect of ultraviolet radiation on the microsporidian Octosporea muscaedomesticae with reference to protectants provided by the host Phormia regina. Journal of Invertebrate Pathology 30, 348–53.CrossRefGoogle ScholarPubMed
Thomson, H. M. (1958). Some aspects of the epidemiology of a microsporidian parasite of the spruce budworm, Choristoneura fumiferana (Clem). Canadian Journal of Zoology 36, 309–16.CrossRefGoogle Scholar
Varley, G. C., Gradwell, G. R. & Hassell, M. P. (1973). Insect Population Ecology: an Analytical Approach. Oxford: Blackwell Scientific Publications.Google Scholar
Wigley, P. J. (1976). The epizootiology of a nuclear polyhedrosis virus disease of the winter moth, Operophtera brumata L. at Wistman's Wood Dartmoor. D.Phill thesis, University of Oxford.Google Scholar