Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-24T11:55:56.771Z Has data issue: false hasContentIssue false

Ultrastructure and cytochemistry of the tegument of Orthocoelium scoliocoelium and Paramphistomum cervi (Trematoda: Digenea)

Published online by Cambridge University Press:  05 June 2009

P. N. Sharma
Affiliation:
Department of Zoology, Queen's University, Belfast BT7 INN, Northern Ireland
R. E. B. Hanna
Affiliation:
Department of Zoology, Queen's University, Belfast BT7 INN, Northern Ireland

Abstract

The tegument of Orthocoelium scoliocoelium and Paramphistomum cervi was examined using histochemical techniques and electron microscopy. On the basis of the distribution of acid and alkaline phosphatase (E.C. 3.1.3.2, E.C. 3.1.3.1), non-specific esterase (E.C. 3.1.1.1), cholinesterase (E.C. 3.1.1.7) and succinate dehydrogenase (E.C. 1.3.99.1) at light microscope level two distinct regions were recognized, an outer and an inner zone. Electron microscopy revealed that the tegument comprises an outer surface syncytium underlain by a thick subsyncytial zone and musculature. Deeper still occur the nucleated “tegumental cells”. The latter are in cytoplasmic continuity with the surface syncytium via vacuolated cytoplasmic trabeculae which traverse the muscle layers and the subsyncytial zone. Three types of tegumental cells each lacking mitochondria were observed. The T1 cells synthesize discoid and electron dense T1 bodies while T2 cells produce oval and electron lucent T2 bodies. The third type of tegumental cells apparently produce no secretory bodies and may represent an embryonic cell type. The surface syncytium contains T1 and T2 secretory bodies and is bounded apically by a plasma membrane invested externally by a fuzzy and filamentous glycocalyx. The surface syncytium lacks mitochondria and is traversed by infoldings of the basal plasma membrane. Beneath the surface syncytium the subsyncytial zone is largely comprised of fibrous interstitial material. This zone, which is particularly thick in the amphistomes, is traversed by trabeculae and extensions of underlying parenchymal cells which usually contain mitochondria and lysosomes. The subsyncytial zone overlies numerous circular and longitudinal muscle fibres. The absence of mitochondria and enzymes associated with active transport suggests that the amphistome tegument may be mainly specialized for protection of the worm against mechanical and chemical conditions prevailing in the rumen. Active uptake of nutrients is probably not a primary function.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 1988

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bjorkman, N. & Thorsell, W. (1964) On the fine structure and resorptive function of the cuticle of the liver fluke, Fasciola hepatica L. Experimental Cell Research, 33, 319329.CrossRefGoogle Scholar
Bogitsh, B. J. (1968) Cytochemical and ultrastructural observations on the tegument of the trematode, Megalodiscus temperatus. Transactions of the American Microscopical Society, 87, 477486.CrossRefGoogle ScholarPubMed
Choubisa, S. L., Agrawal, M. P. & Sharma, P. N. (1982) Histochemical distribution and functional significance of acetyl and butyrylcholinesterases in the amphistone Gastrothylax crumenifer. Proceedings of the Indian Academy of Parasitology, 3, 6975.Google Scholar
Dunn, T. S., Hanna, R. E. B. & Nizami, W. A. (1987) Ultrastructural and cytochemical observations on the tegument of three species of paramphistomes (Platyhelminthes: Digenea) from the Indian water buffalo, Bubalus bubalis. International Journal for Parasitology, 17, 11531161.CrossRefGoogle ScholarPubMed
Dutta, S. C. (1980) Paramphistomes and paramphistomiasis of domestic ruminants in India. Punjab Agricultural University, Ludhiana, India.Google Scholar
Erasmus, D. A. & Ohman, C. (1963) The structure and function of the adhesive organ in strigeid trematodes. Annals of the New York Academy of Sciences, 113, 735.CrossRefGoogle ScholarPubMed
Fripp, P. J. (1967) The histochemical localization of esterase activity in schistosomes. Experimental Parasitology, 19, 254263.Google Scholar
Gomori, G. (1952) Microscopic histochemistry. University Press, Chicago.Google Scholar
Halton, D. W. (1967) Histochemical studies of carboxylic esterase activity in Fasciola hepatica. Journal of Parasitology, 53, 12101216.CrossRefGoogle ScholarPubMed
Hanna, R. E. B. (1980) Fasciola hepatica: glycocalyx replacement in the juvenile as a possible mechanism for protection against host immunity. Experimental Parasitology, 50, 103114.Google Scholar
Hayat, M. A. (1973) Electron microscopy of enzymes. Vol. 1. Van Nostrand Reinhold Company Ltd., New York.Google Scholar
Hayat, M. A. (1974) Electron microscopy of enzymes. Vol. 2. Van Nostrand Reinhold Company Ltd., New York.Google Scholar
Hayat, M. A. (1975) Electron microscopy of enzymes. Vol. 3. Van Nostrand Reinhold Company Ltd., New York.Google Scholar
Hockley, D. J. (1973) Ultrastructure of the tegument of Schistosoma. Advances in Parasitology, 11, 233305.CrossRefGoogle ScholarPubMed
Holt, S. J. & Withers, R. F. J. (1952) Cytochemical localization of esterases using indoxy derivatives. Nature, 170, 1012.Google Scholar
Karnovsky, M. J. & Roots, L. (1964) A direct colouring method for cholinesterases. Journal of Histochemistry and Cytochemistry, 12, 219221.CrossRefGoogle ScholarPubMed
Lee, D. J. (1972) The structure of the helminth cuticle. Advances in Parasitology, 4, 347379.Google Scholar
Lumsden, R. D. (1975) Surface ultrastructure and cytochemistry of parasitic platyhelminths. Experimental Parasitology, 37, 267339.Google Scholar
Madge, D. S. (1975) The mammalian alimentary system: A functional approach. Edward Arnold, London.Google Scholar
Nachlas, M., Tsou, K. C., Desouza, E., Cheng, C. S. & Seligman, A. M. (1957) Cytochemical demonstration of succinic dehydrogenase by the use of new P-nitrophenyl substituted ditetrazole. Journal of Histochemistry and Cytochemistry, 5, 420436.Google Scholar
Nollen, P. N., Pyne, J. L. & Bajt, J. F. (1974) Megalodiscus temperatus: Absorption and incorporation of tritiated tyrosine, thymidine and adenosine. Experimental Parasitology, 35, 132140.CrossRefGoogle ScholarPubMed
Pearse, E. A. G. (1968) Histochemistry. Theoretical and Applied. 2nd ed. Churchill Limited, London.Google Scholar
Shannon, W. Jr & Bogitsh, B. J. (1971) Megalodiscus temperatus: Comparative radioautography of glucose-3H and galactose-3H incorporation. Experimental Parasitology, 29, 309319.Google Scholar
Sharma, P. N. (1978) Histochemical localization of succinate dehydrogenase in the lymphatic system of a trematode Ceylonocotyle scoliocoelium.Journal of Helminthology, 52, 159162.CrossRefGoogle Scholar
Sharma, P. N. (1979) Histochemical localization of succinate dehydrogenase in certain tissues of a digenetic trematode Ceylonocotyle scoliocoelium. Indian Journal of Experimental Biology, 17, 515520.Google Scholar
Sharma, P. N. & Mandawat, S. (1979) Histochemical distribution of acid mucopolysaccharide in the tissues of Paramphistomum cervi (Trematoda: Digenea). Indian Journal of Parasitology, 3, 181182.Google Scholar
Sharma, P. N. & Sharma, A. N. (1981) Cytochemical characteristics of neurosecretory cells of Ceylonocotyle scoliocoelium (Trematoda: Digenea). Journal of Helminthology, 55, 223229.CrossRefGoogle ScholarPubMed
Sharma, P. N. & Ratnu, L. S. (1982) Morphology, histochemistry and the biological significance of the lymphatic system of the trematode Orthocoelium scoliocoelium. Journal of Helminthology, 56, 5967.Google Scholar
Sharma, P. N. & Hora, C. (1983) Role of oesophageal glands in the digestive physiology of two rumen amphistomes, Orthocoelium scoliocoelium and Paramphistomum cervi. Journal of Helminthology, 56, 1120.Google Scholar
Silk, M. H., Spence, I. M. & Gear, J. H. S. (1969) Ultrastructural studies of the blood fluke—Schistosoma mansoni. I The Integument. South African Journal of Medical Sciences, 34, 110.Google Scholar
Threadgold, L. T. (1984) Parasitic platyhelminths. In: Biology of the Integument. (editors, Bereiter-Hahn, A., Matoltsy, A. G. & Richards, K. S.), Springer-Verlag: Berlin, Heidelberg, 132185.Google Scholar