Jump to ContentJump to Main Navigation
Show Summary Details
More options …

Acta Parasitologica

4 Issues per year


IMPACT FACTOR 2016: 1.160
5-year IMPACT FACTOR: 1.185

CiteScore 2017: 1.17

SCImago Journal Rank (SJR) 2017: 0.641
Source Normalized Impact per Paper (SNIP) 2017: 0.738

Online
ISSN
1896-1851
See all formats and pricing
More options …
Volume 51, Issue 2

Issues

Accumulation and utilization of lipids during the development of Hymenolepis diminuta cysticercoids

Tadeusz Moczoń
  • W. Stefański Institute of Parasitology, Polish Academy of Sciences, 51/55 Twarda Street, 00-818, Warszawa, Poland
  • Email
  • Other articles by this author:
  • De Gruyter OnlineGoogle Scholar
Published Online: 2006-06-01 | DOI: https://doi.org/10.2478/s11686-006-0023-7

Abstract

The accumulation of neutral lipids in the cells predetermined to evolve into the cyst cavity lining in Hymenolepis diminuta cysticercoids is presented. The differentiation of these cells from the mesenchyma cells and the accompanying systhesis of lipids began in very young, blastula-shaped larvae. Both the number of the cells and the amount of their lipids increased gradually during further development of the parasites. In the pre-encystment stage of the cysticercoids the cells concentrated around the cavity of the prospective cyst. Following encystment, the scolex and the inverted neck became surrounded by a compact mass of the cells, which started using the stored lipids as a source of energy indispensable for the formation of the cyst tissues and of the definitive multilayer lining of the cyst cavity. No neutral lipids were detected in the mature 23-day-old cysticercoids as well as in the experimentally excysted scoleces. Beside a low level of uniformly distributed phospholipids apparently associated with cell membranes, no local accumulations of these substances were observed at any step of the development of the larvae. The utilization of neutral lipids proves both the presence of a lipase-type enzyme(s) and an operative β-oxidation pathway in the cells of the cysticercoids, the latter feature being highly indicative of oxidative metabolism of these larvae.

Keywords: Cestoda; Hymenolepis diminuta; cysticercoids; histochemistry; lipids

  • [1] Adams C.W.M. 1959. A histochemical methods for the simultaneous demonstration of normal and degenerated myelin. Journal of Pathology and Bacteriology, 77, 648–650. http://dx.doi.org/10.1002/path.1700770240CrossrefGoogle Scholar

  • [2] Allison V.F., Ubelaker J.E., Cooper N.B. 1972. The fine structure of the cysticercoid of Hymenolepis diminuta. II. The inner wall of the capsule. Zeitschrift für Parasitenkunde, 39, 137–147. http://dx.doi.org/10.1007/BF00329641CrossrefGoogle Scholar

  • [3] Baron J.P. 1971. On the histology, histochemistry and ultrastructure of the cysticercoid of Raillietina cesticillus (Molin, 1958) Fuhrmann, 1920 (Cestoda, Cyclophyllidea). Parasitology, 62, 233–245. http://dx.doi.org/10.1017/S003118200007147XCrossrefGoogle Scholar

  • [4] Butler M.S., Fried B. 1977. Histochemical and thin layer chromatographic analyses of neutral lipids in Echinostoma revolutum metacercariae cultured in vitro. Journal of Parasitology, 63, 1041–1045. http://dx.doi.org/10.2307/3279840CrossrefGoogle Scholar

  • [5] Caley J. 1974. The functional significance of scolex retraction and subsequent cyst formation in the cysticercoid larva of Hymenolepis microstoma. Parasitology, 68, 207–227. PubMedGoogle Scholar

  • [6] Caley J. 1976. Ultrastructural studies of the cysticercoid of Moniezia expansa (Anoplocephalidae) with special reference to the development of the cyst. Zeitschrift für Parasitenkunde, 48, 251–262. http://dx.doi.org/10.1007/BF00380399CrossrefGoogle Scholar

  • [7] Collin W.K. 1970. Electron microscopy of postembryonic stages of the tapeworm, Hymenolepis citelli. Journal of Parasitology, 56, 1159–1170. http://dx.doi.org/10.2307/3277562CrossrefGoogle Scholar

  • [8] Fairbairn D.G., Wertheim R., Harpur R., Schiller E. 1961. Biochemistry of normal and irradiated strains of Hymenolepis diminuta. Experimental Parasitology, 11, 248–263. http://dx.doi.org/10.1016/0014-4894(61)90031-5CrossrefGoogle Scholar

  • [9] Fried B., Appel A.J. 1977. Excretion of lipids by Echinostoma revolutum (Trematoda) adults. Journal of Parasitology, 63, 447. http://dx.doi.org/10.2307/3279998CrossrefGoogle Scholar

  • [10] Fried B., Butler M.S. 1977. Histochemical and thin layer chromatographic analyses of neutral lipids in metacercarial and adult Cotylurus sp. (Trematoda: Strigeidae). Journal of Parasitology, 63, 831–834. http://dx.doi.org/10.2307/3279887CrossrefGoogle Scholar

  • [11] Fried B., Shapiro I.L. 1975. Accumulation and secretion of neutral lipids in the metacercaria of Leucochloridiomorpha constantiae (Trematoda) maintained in vitro. Journal of Parasitology, 61, 906–909. http://dx.doi.org/10.2307/3279233CrossrefGoogle Scholar

  • [12] Ginger C., Fairbairn D. 1966. Lipid metabolism in helminth parasites. II. The major origins of the lipids of Hymenolepis diminuta (Cestoda). Journal of Parasitology, 52, 1097–1107. http://dx.doi.org/10.2307/3276353CrossrefGoogle Scholar

  • [13] Jacobsen N., Fairbairn D. 1967. Lipid metabolism in helminth parasites. II. Biosynthesis and interconversion of fatty acids by Hymenolepis diminuta (Cestoda). Journal of Parasitology, 53, 355–361. http://dx.doi.org/10.2307/3276590CrossrefGoogle Scholar

  • [14] King J.W., Lumsden R.D. 1969. Cytological aspects of lipid assimilation by cestodes. Incorporation of linoleic acid into the parenchyma and eggs of Hymenolepis diminuta. Journal of Parasitology, 55, 250–260. http://dx.doi.org/10.2307/3277385CrossrefGoogle Scholar

  • [15] Lumsden R.D., Harrington G.W. 1966. Incorporation of linoleic acid by the cestode Hymenolepis diminuta (Rudolphi, 1819). Journal of Parasitology, 52, 695–700. http://dx.doi.org/10.2307/3276433CrossrefGoogle Scholar

  • [16] Moczoń T. 1973. Histochemical studies on the enzymes of Hymenolepis diminuta (Rud., 1819). I. Some oxidoreductases in oncospheres and cysticercoids. Acta Parasitologica Polonica, 21, 85–97. Google Scholar

  • [17] Moczoń T., Świetlikowska A. 2006. Distribution of acetylcholinesterase activity during the development of cysticercoids of Hymenolepis diminuta (Cestoda). Acta Parasitologica, 51, 143–151. http://dx.doi.org/10.2478/s11686-006-0022-8CrossrefGoogle Scholar

  • [18] Romeis B. 1948. Mikroskopische Technik. Leibnitz Verlag, München. Google Scholar

  • [19] Ward C.W., Fairbairn D. 1970. Enzymes of beta-oxidation and the tricarboxylic acid cycle in adult Hymenolepis diminuta (Cestoda) and Ascaris lumbricoides (Nematoda). Journal of Parasitology, 56, 1009–1012. http://dx.doi.org/10.2307/3277526CrossrefGoogle Scholar

  • [20] Voge M. 1960. Studies in cysticercoid histology. IV. Observations on histogenesis in the cysticercoid of Hymenolepis diminuta. Journal of Parasitology, 46, 717–725. http://dx.doi.org/10.2307/3275517CrossrefGoogle Scholar

  • [21] Voge M., Heyneman D. 1957. Development of Hymenolepis nana and Hymenolepis diminuta (Cestoda: Hymenolepididae) in the intermediate host Tribolium confusum. University of California Publications in Zoology, 59, 549–580. Google Scholar

About the article

Published Online: 2006-06-01

Published in Print: 2006-06-01


Citation Information: Acta Parasitologica, Volume 51, Issue 2, Pages 152–155, ISSN (Online) 1896-1851, ISSN (Print) 1230-2821, DOI: https://doi.org/10.2478/s11686-006-0023-7.

Export Citation

© 2006 W. Stefański Institute of Parasitology, PAS. This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License. BY-NC-ND 3.0

Citing Articles

Here you can find all Crossref-listed publications in which this article is cited. If you would like to receive automatic email messages as soon as this article is cited in other publications, simply activate the “Citation Alert” on the top of this page.

[2]
Madhumita Mondal, Debalina Mukhopadhyay, Debasree Ghosh, C. Dey, and K. K. Misra
Proceedings of the Zoological Society, 2009, Volume 62, Number 2, Page 131

Comments (0)

Please log in or register to comment.
Log in