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The life-cycle, ultrastructure and mode of feeding of the locust amoeba Malpighamoeba locustae

Published online by Cambridge University Press:  06 April 2009

Owen G. Harry
Affiliation:
Department of Zoology and Comparative Physiology, The University of Birmingham, Edgbaston, Birmingham
L. H. Finlayson
Affiliation:
Department of Zoology and Comparative Physiology, The University of Birmingham, Edgbaston, Birmingham

Extract

The primary trophozoites of Malpighamoeba locustae excyst in the crop and midgut of the Desert Locust (Schistocerca gregaria) and then penetrate the epithelial cells of the midgut and caeca where they grow and multiply slowly. After about 10–12 days they leave the gut epithelium passively when the cells in which they have grown degenerate and are extruded. From the lumen of the gut they make their way into the lumen of the Malpighian tubules where they feed upon the brush border as extracellular parasites. No primary or secondary trophozoites were found in the haemocoele of the host.

During the first few days in the Malpighian tubules the secondary trophozoites undergo a rapid series of divisions which enables them to double their numbers every 24 h so that by day 20–22 the lumen of the tubules is packed with cysts and trophozoites. The trophozoites phagocy-tose small pieces of brush border and numerous food vacuoles are present in their cytoplasm. The cytoplasm of the primary trophozoite contains the normal complement of cell organelles, a notable feature of which are the large, numerous mitochondria with their tubular cristae. When the trophozoites are ready to encyst they round up and begin to lay down a series of membranes which totally cover the trophozoite. Numerous storage granules are found in mature trophozoites which are about to encyst and these may be utilized in cyst wall production.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1976

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References

Dudley, B. A. C. (1964). The effects of temperature and humidity upon certain morphometry and color characters of the Desert Locust (Schistocerca gregaria Forskal) reared under controlled conditions. Transactions of the Royal entomological Society, London 116, 115–29.Google Scholar
Evans, W. A. & Elias, R. (1970). The life cycle of Malamoeba locustar (King and Taylor) in Locusta migratoria migratoides (R. et F.). Acta Protozoological 7, 229–41.Google Scholar
Gray, P. (1954). The Microtomists Formulary and Guide. London: Constable and Co.Google Scholar
Harry, O. G. (1965). Studies on the early development of the eugregarine Gregarina garnhami. Journal of Protozoology 12, 296305.CrossRefGoogle ScholarPubMed
Hoyle, G. (1955). The effects of some common cations on neuromuscular transmission in insects. Journal of general Physiology 127, 90103.Google ScholarPubMed
King, R. L. & Taylor, A. B. (1936). Malpighamoeba locustae n.sp. (Amoebidae) a protozoan parasite in the malpighian tubule of grasshoppers. Transactions of the American microscopical Society 55, 610.Google Scholar
Manton, I. (1964). The possible significance of some details of flagellar bases in plants. Journal of the microscopical Society 82, 279–85.Google Scholar
Osborne, M. P. (1972). Helical filaments in the glial cells of the locust Schistocerca gregaria. Journal of Cell Science 11, 295303.Google Scholar
Proctor, E. M. & Gregory, M. A. (1973 a). Ultrastructure of cysts of E. histolytica. International Journal of Parasitology 3, 455–6.Google Scholar
Proctor, E. M. & Gregory, M. A. (1973). Ultrastructure of Entamoeba histolytica strain NTH 200. International Journal of Parasitology 3 (4), 457–60.CrossRefGoogle Scholar
Salt, G. (1970). The Cellular Defence Reactions of Insects. Cambridge University Press.Google Scholar
Taylor, A. B. & King, R. L. (1937). Further studies on the parasitic amoeba found in grasshoppers. Transactions of the American microscopical Society 56, 172–6.Google Scholar
Vickerman, K. (1962). Patterns of cellular organisation in limax amoebae. Experimental Cell Research 26, 497519.Google Scholar
Wigglesworth, V. B. (1942). The significance of ‘chromatic droplets’ in the growth of insects. Quarterly Journal of microscopical Science 83, 141–52.Google Scholar
Wigglesworth, V. B. (1959). A simple method for cutting sections in the 0−5−1 μm range and for sections of chitin. Quarterly Journal of microscopical Science 100, 315–20.Google Scholar
Yao-Nan, (1927). Sur un fixative cytologique particulièrement adapte aux tissues des insects. Bulletin d'Histologie appliquie a la Physiologie et á la Pathologie et de Technique micro-scopique 4, 71–2.Google Scholar
Zaman, V. (1972). Ultrastructure of lodamoeba butschlii cysts. Annals of tropical Medicine and Parasitology 66, 251–3.Google Scholar