Hostname: page-component-cd9895bd7-jkksz Total loading time: 0 Render date: 2024-12-28T13:22:05.805Z Has data issue: false hasContentIssue false
  • English
  • Français

The role of dissolved carbon dioxide and whole bile in the in vitro activation of Taenia taeniaeformis oncospheres

Published online by Cambridge University Press:  05 June 2009

K. Ishiwata ,
Y. Oku  and
M. Kamiya
K. Ishiwata
Affiliation:
Department of Parasitology, Faculty of Veterinary Medicine, Hokkaido University, Sapporo 060, Japan
Y. Oku
Affiliation:
Department of Parasitology, Faculty of Veterinary Medicine, Hokkaido University, Sapporo 060, Japan
M. Kamiya
Affiliation:
Department of Parasitology, Faculty of Veterinary Medicine, Hokkaido University, Sapporo 060, Japan
Get access Rights & Permissions [Opens in a new window]

Abstract

Dissolved carbon dioxide was deemed not to be an important factor in the activation of Taenia taeniaeformis oncospheres. Rabbit bile was found to provide the most appropriate whole bile for in vitro activation of oncospheres

Keywords

CestodaTaenia taeniaeformisoncospherscarbon dioxidewhole bile
Type
Research Note
Information
Journal of Helminthology , Volume 67 , Issue 4 , December 1993 , pp. 325 - 328
Copyright
Copyright © Cambridge University Press 1993

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

REFERENCES

Brandt, J. R. A. & Sewell, M. M. H. (1981) In vitro hatching and activation of Taenia taeniaeformis oncospheres. Veterinary Research Communications, 5, 193–199.Google Scholar
Bullock, F. D., Dunning, W. F. & Curtis, M. R. (1934) Observations on the digestion of the shells of the eggs of Taenia taeniaeformis. American Journal of Cancer, 20, 390–397.Google Scholar
Davis, S. W. & Hammerberg, B. (1988) Activation of the alternative pathway of complement by larval Taenia taeniaeformis in resistant and susceptible strains of mice. International Journal for Parasitology, 18, 591–597.CrossRefGoogle ScholarPubMed
Fried, B. & Stableford, L. T. (1991) Cultivation of helminths in chick embryos. Advances in Parasitology, 30, 107–165.CrossRefGoogle ScholarPubMed
Gallie, G. J. & Sewell, M. M. H. (1970) A technique for hatching Taenia saginata eggs. Veterinary Record, 20, 749.CrossRefGoogle Scholar
Heath, D. D. (1982) In vitro culture of cysticerci: An aid to investigations of morphological development and host-parasite relationships. In: Cysticercosis: Present State of Knowledge and Perspectives (editors: Flisser, A., Willms, K., Laclette, J. P., Larralde, C., Ridaura, C. & Beltran, F.), pp. 477–494. Academic Press: London.Google Scholar
Heath, D. D. & Elsdon-Dew, R. (1972) The in vitro culture of Taenia saginata and Taenia taeniaeformis larvae from the oncosphere, with observations on the role of serum for in vitro culture of larval cestodes. International Journal for Parasitology, 2, 119–130.Google Scholar
Heath, D. D. & Smyth, J. D. (1970) In vitro cultivation of Echinococcus granulosus, Taenia hydatigena, T. ovis, T. pisiformis and T. serialis from oncosphere to cystic larva. Parasitology, 61, 329–343.Google Scholar
Huffman, J. L. & Jones, A. W. (1962) Hatchability, viability, and infectivity of Hydatigera taeniaeformis eggs. Experimental Parasitology, 12, 120–124.Google Scholar
Ishiwata, K., Oku, Y., Ito, M. & Kamiya, M. (1992) Responses to larval Taenia taeniaeformis in mice with severe combined immunodeficiency (scid). Parasitology, 104, 363–369.Google Scholar
Perry, R. N. (1989) Dormancy and hatching of nematode eggs. Parasitology Today, 5, 377–383.Google Scholar
Rickard, M. D. & Bell, K. J. (1971) Immunity produced against Taenia ovis and T. taeniaeformis infection in lambs and rats following in vivo growth of their larvae in filtration membrane diffusion chambers. Journal of Parasitology, 57, 571–575.Google Scholar
Salazar, P. M., Haro, I. & Voge, M. (1984) Hatching in vitro of oncospheres of Taenia solium. Journal of Parasitology, 70, 161–162.Google Scholar
Silverman, P. H. (1954) Studies of the biology of some tapeworms of the genus Taenia I. Factors affecting hatching and activation of taeniid ova, and some criteria of their viability. Annals of Tropical Medicine and Parasitology, 48, 207–215.Google Scholar
Smyth, J. D. & Haslewood, G. A. D. (1963) The biochemistry of bile as a factor in determining host specificity in intestinal parasites, with particular reference to Echinococcus granulosus. Annals of the New York Academy of Sciences, 113, 234–260.CrossRefGoogle Scholar
Smyth, J. D. & McManus, D. P. (1989a) The biology of the egg. In: The Physiology and Biochemistry of Cestodes (editors Smyth, J. D. & McManus, D. P.), pp. 156–194. Cambridge University Press: Cambridge.Google Scholar
Smyth, J. D. & McManus, D. P. (1989b) The adult cestode in its environment. In: The Physiology and Biochemistry of Cestodes (editors Smyth, J. D. & McManus, D. P.), pp. 35–52. Cambridge University Press: Cambridge.Google Scholar
Stevenson, P. (1983) Observations on the hatching and activation of fresh Taenia saginata eggs. Annals of Tropical Medicine and Parasitology, 77, 399–404.Google Scholar
Taylor, A. E. R. & Baker, J. R. (1987) In vitro Methods for Parasite Cultivation. 465 pp. Academic Press: London.Google Scholar