Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-23T11:22:05.141Z Has data issue: false hasContentIssue false
  • English
  • Français

Hymenolepis diminuta: an investigation of juvenile hormone titre, degradation and supplementation in the intermediate host, Tenebrio molitor

Published online by Cambridge University Press:  06 April 2009

H. Hurd ,
C. Strambi  and
N. E. Beckage
H. Hurd
Affiliation:
Parasitology Research Laboratory, Department of Biological Sciences, University of Keele, Keele, Staffs ST5 5BG, UK
C. Strambi
Affiliation:
CNRS-Laboratoire de Neurobiologie, BP 71, 13402 Marseille Cedex 9, France
N. E. Beckage
Affiliation:
Stored Products Insect Research Unit, ARS, USDA, Wisconsin, Department of Entomology, University of Wisconsin, Madison 53706, USA
Get access Rights & Permissions [Opens in a new window]

Summary

Metacestodes of Hymenolepis diminuta cause a perturbance of vitellogenesis in the intermediate host Tenebrio molitor. The reduction in host reproductive output associated with infection may be due to this pathophysiology. Many of these events are regulated by host juvenile hormone (JH). A comparison of the titre of JH and its rate of degradation in female control and parasitized 15-day-old insects has been made. Haemolymph from female beetles contained 1·27 pMol JH equivalents/100 µl. No significant difference was associated with infection. However, topical application of a JH analogue, methoprene, at the time of infecion or 8 days post-infection reduced the significant accumulation of vitellogenin usually found in the haemolymph of females 12 days or more post-infection. These findings indicate that parasite-induced alteration of host vitellogenesis is not mediated via alteration in JH titres, although observations made after hormone supplementation suggest some form of interaction between the parasite and the host endocrine system.

Keywords

host—parasite interactionscestodeHymenolepis diminuta metacestodesTenebrio molitorhost vitellogenesishost juvenile hormonehost juvenile hormone esterase
Type
Research Article
Information
Parasitology , Volume 100 , Issue 3 , June 1990 , pp. 445 - 452
Copyright
Copyright © Cambridge University Press 1990

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

Abdel-Aal, Y. A. I. & Hammock, B. D. (1985). 3- Octylthio- 1,1,1 -trifluoro- 2-propanone, a high affinity and slow binding inhibitor of juvenile hormone esterase from Trichoplusia ni (Hubner). Insect Biochemistry 15, 111.CrossRefGoogle Scholar
Beckage, N. E. (1985). Endocrine interactions between endoparasitic insects and their hosts. Annual Review of Entomology 30, 371–413.CrossRefGoogle Scholar
Beckage, N. E. (1990). Parasitic effects on host development. In UCLA Symposia on Molecular and Cellular Biology, New Series, Vol. 112 (ed. Baker, R. & Dunn, P.). New York: Alan R. Liss. (in the Press.)Google Scholar
Beckage, N. E. & Riddiford, L. M. (1982). Effects of parasitism by Apanteles congregatus on the endocrine physiology of the Tobacco Hornworm Manduca sexta. General and Comparative Endocrinology 47, 308–22.CrossRefGoogle ScholarPubMed
Connat, J. L. (1983). Juvenile hormone esterase activity during the last larval and pupal stages of Tenebrio molitor. Journal of Insect Physiology 29, 515–21.CrossRefGoogle Scholar
Davey, K. G. & Huebner, E. (1974). The response of the follicle cells of Rhodnius prolixus to juvenile hormone and antigonadotropin. Canadian Journal of Zoology 52, 1407–12.CrossRefGoogle ScholarPubMed
De Kort, C. A. D., Koopmanschap, A. B., Strambi, C. & Strambi, A. (1985). The application and evaluation of a radioimmunoassay for measuring juvenile hormone titres in Colorado beetle haemolymph. Insect Biochemistry 15, 771–5.CrossRefGoogle Scholar
Dowell, F. H. & Jones, A. W. (1966). Establishment of Tribolium confusum populations after stress by parasitism with Hymenolepis microstoma. Experimental Parasitology 18, 99–108.CrossRefGoogle ScholarPubMed
Englemann, F. (1983). Vitellogenesis controlled by juvenile hormone. In Endocrinology of Insects (ed. Downer, R. G. H. & Laufer, H.), pp. 259–270. New York: Alan R. Liss Inc.Google Scholar
Fioravanti, C. F. & Macinnis, A. J. (1977). The identification and characterization of a prenoid constituent (fanesol) of Hymenolepis diminuta (Cestoda). Comparative Biochemistry and Physiology 57B, 227–33.Google Scholar
Goodman, W. G. & Chang, E. S. (1985). Juvenile hormone cellular binding proteins. In Comprehensive Insect Physiology, Biochemistry and Pharmacology, vol. 7 (ed. Kerkut, G. A. & Gilbert, L. I.), pp. 491–510. Oxford: Pergamon Press.Google Scholar
Hammock, B. D. & Sparks, T. C. (1977). A rapid assay for juvenile hormone esterase activity. Analytical Biochemistry 82, 573–9.CrossRefGoogle ScholarPubMed
Hurd, H. (1990). Physiological and behavioural interactions between parasites and invertebrate hosts. In Advances in Parasitology, vol. 29 (ed. Baker, J. & Muller, R.), pp. 271–318. London: Academic Press.Google Scholar
Hurd, H. & Arme, C. (1984 a). Tenebrio molitor (Coleoptera): effect of metacestodes of Hymenolepis diminuta (Cestoda) on haemolymph amino acids. Parasitology 89, 245–53.CrossRefGoogle Scholar
Hurd, H. & Arme, C. (1984 b). Pathophysiology of Hymenolepis diminuta infections in Tenebrio molitor: effect of parasitism on haemolymph proteins. Parasitology 89, 253–62.CrossRefGoogle Scholar
Hurd, H. & Arme, C. (1986 a). Hymenolepis diminuta: Effect of metacestodes on production and viability of eggs in the intermediate host, Tenebrio molitor. Journal of Invertebrate Pathology 47, 225–30.CrossRefGoogle ScholarPubMed
Hurd, H. & Arme, C. (1986 b). Hymenolepis diminuta: influence of metacestodes on synthesis and secretion of fat body protein and its ovarian sequestration in the intermediate host Tenebrio molitor. Parasitology 81, 405–21.Google Scholar
Hurd, H. & Arme, C. (1987). Hymenolepis diminuta: Effect of infection upon the patency of the follicular epithelium of Tenebrio molitor. Journal of Invertebrate Pathology 49, 227–34.CrossRefGoogle ScholarPubMed
Hurd, H. & Weaver, R. J. (1987). Evidence against the hypothesis that metacestodes of Hymenolepis diminuta inhibit corpora allata functioning in the intermediate host, Tenebrio molitor. Parasitology 95, 93–6.CrossRefGoogle ScholarPubMed
Jong-Brink, M. De. (1990). How trematode parasites interfere with reproduction of their intermediate hosts, freshwater snails. Journal of Medical and Applied Malacology. (in the Press.)Google Scholar
Jones, G., Jones, D. & Hiremath, S. (1987). An in vitro system for studying juvenile hormone induction of juvenile hormone esterase from the fat body of Trichoplusia ni (Hubner). Insect Biochemistry 17, 897–904.CrossRefGoogle Scholar
Judy, K. J., Schooley, D. A., Troelschler, R. G., Jennings, R. C., Bergot, B. J. & Hall, M. S. (1975). Juvenile Hormone production by corpora allata of Tenebrio molitor in vitro. Life Sciences 16, 1059–66.CrossRefGoogle ScholarPubMed
Keymer, A. (1980). The influence of Hymenolepis diminuta on the survival and fecundity of the intermediate host, Tribolium confusum. Parasitology 81, 405–21.CrossRefGoogle ScholarPubMed
Keymer, A. (1981). Population dynamics of Hymenolepis diminuta in the intermediate host. Journal of Animal Ecology 50, 941–50.CrossRefGoogle Scholar
Kramer, S. J. & De Kort, C. A. D. (1976). Age dependent changes in juvenile hormone esterase and general carboxylesterase activity in the haemolymph of the colorado potato beetle Leptinotarsa decemlineata. Molecular and Cellular Endocrinology 4, 43–53.CrossRefGoogle Scholar
Laemmli, U. K. (1970). Cleavage of structural proteins during the assembly of the head of Bacteriophage T4. Nature, London 227, 680—5.CrossRefGoogle ScholarPubMed
Laverdure, A.-M. (1970). Action de l'ecdysone et de l'ester méthylique du farnesol sur l'ovaire nymphal de Tenebrio molitor (Coléoptère) cultive in vitro. Annales d' Endocrinologie 31, 516–24.Google Scholar
Lawrence, P. O. (1986). Host–parasite hormonal interactions: an overview. Journal of Insect Physiology 32, 295–8.CrossRefGoogle Scholar
Peterson, G. L. (1983). Determination of total protein. Methods in Enzymology 91, 95–119.CrossRefGoogle ScholarPubMed
Reddy, G. & Kumaran, A. K. (1985). The effect of juvenile hormone and its antagonists on JH esterase activity in Tenebrio molitor. Entomology Experimental and Applied 37, 213–18.CrossRefGoogle Scholar
Renucci, M., Martin, N. & Strambi, C. (1984). Temporal variations in haemolymph esterase activity and juvenile hormone titres during ovocyte maturation in Acheta domesticus (Orthoptera). General and Comparative Endocrinology 55, 480–7.CrossRefGoogle ScholarPubMed
Rotin, D., Feyereisen, R., Koener, J. & Tobe, S. S.(1982). Haemolymph juvenile hormone esterase activity during the reproductive cycle of the viviparous cockroach Diploptera punctata. Insect Biochemistry 12, 263–8.CrossRefGoogle Scholar
Shapiro, A. B., Wheelock, G. D., Hagedorn, H. H., Baker, F. C., Tsai, L. W. & Schooley, D. A. (1986). Juvenile hormone and juvenile hormone esterase in adult females of the mosquito Aedes aegypti. Journal of Insect Physiology 32, 869–77.CrossRefGoogle Scholar
Sokal, R. R. & Rohlf, F. J. (1985). Biometry. San Francisco: W.H. Freeman & Co.Google Scholar
Strambi, A. & Girardie, A. (1973). Effet de l'implantation de corpora allata actifs de Locusta migratoria (Orthoptère) dans des femelles de Polistes gallicus L. (Hymenoptère) saines et parasitées par Xenos vesparum Rossi (Insecte, Strepsiptère). Comptes Rendus de l'Academie des Sciences 276, 3319–22.Google Scholar
Strambi, C. & Strambi, A. (1973). Influence du développment du parasite Xenos Vesparum Rossi (Insecte Strepsiptère) sur le système neuroendocrinien des femelles de Polistes (Hymenoptère, Vespide) au début de leur imaginale. Archives d'Anatomie Microscopique et de Morphologie Expérimental 62, 39–54.Google Scholar
Strambi, C., Strambi, A., De Reggi, M. L. & Delange, M. A. (1981). Radioimmunoassay of insect juvenile hormones and of their diol derivatives. European Journal of Biochemistry 118, 401–6.CrossRefGoogle ScholarPubMed
Trautmann, K. H., Masner, P., Schuler, A., Suchy, M. & Wipf, H. K. (1974). Evidence of the juvenile hormone methyl (2E, 6E)- 10,11 -epoxy-3, 7, 11,-trimethyl-2,6- dodecadienoate (JH-3) in insects of four orders. Zeitschrift für Naturforschung 29, 757–9.CrossRefGoogle Scholar
Weaver, R. J., Pratt, G. E., Hamnett, A. F. & Jennings, R. C. (1980). The influence of incubation conditions on the rates of juvenile hormone biosynthesis by corpora allata isolated from adult females of the beetle Tenebrio molitor. Insect Biochemistry 10, 245–54.CrossRefGoogle Scholar
Woodring, J. P. & Sparks, T. C. (1987). Juvenile hormone esterase activity in the plasma and body tissues during the larval development and adult stages of the house cricket. Insect Biochemstry 17, 751–8.CrossRefGoogle Scholar