Hostname: page-component-78c5997874-m6dg7 Total loading time: 0 Render date: 2024-11-08T07:29:32.881Z Has data issue: false hasContentIssue false

The effects of pregnancy and treatment with progesterone on the host–parasite relationship of Amplicaecum robertsi Sprent & Mines, 1960, in the mouse

Published online by Cambridge University Press:  06 April 2009

Colin Dobson
Affiliation:
Department of Parasitology, University of Queensland, St Lucia, Brisbane, Queensland, Australia

Extract

Male mice harboured more third-stage larvae of Amplicaecum robertsi than females; these larvae also grew longer than did those in female mice. Gonadectomy removed the differences, evident between the sexes, in both the numbers recovered and the growth of the third-stage larva, between male and female mice. The worms recovered from the gonadectomized hosts were smaller than those from the intact male and female host.

Pregnant female mice harboured more worms than either the male or the non-pregnant female mouse. These worms were also smaller than those from the male and non-pregnant females. There was no difference in the growth of the larvae from gonadectomized and pregnant hosts.

The treatment of spayed female mice with progesterone resulted in an increase in the size of worm population as compared with the numbers of worms recovered from intact female mice. The worms from the progesterone-treated spayed females were also longer than those from the spayed female hosts.

Treatment of normal female mice with progesterone resulted in an increased recovery of worms compared with the numbers of worms recovered from normal female animals. The worms were stunted but they were of a size comparable to those recovered from pregnant female mice.

It is suggested that the increase in the size of worm populations and the stunting of the worms recovered from pregnant female mice is associated with the effects of progesterone in relation to the hormone balance associated with the ovary at the time of pregnancy.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1966

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

addis, C. J. Jr (1946). Experiments on the relation between sex hormones and the growth of tapeworms (Hymenolepis diminuta) in rats. J. Parasit. 32, 574–80.CrossRefGoogle ScholarPubMed
Asboe-Hansen, G. (1958). Hormonal effects on connective tissue. Physiol. Rev. 38, 446–62.CrossRefGoogle ScholarPubMed
Bondareff, W. (1957). Submicroscopic morphology of connective tissue ground substance with particular regard to fibrillo-genesis and aging. Gerontologia 1, 222–33.CrossRefGoogle Scholar
Bull, P. C. (1959). A seasonal sex difference in the infestation of rabbits with the nematode Trichostrongylus retortaeformis (Zeder, 1800). Nature, Lond. 184, 281–2.CrossRefGoogle Scholar
Dennis, J. B. (1959). Effects of various factors on the distribution of ferricyanide in ground-substance. A.M.A. Archs Path. 67, 533–49.Google Scholar
Dobson, C. (1960). An investigation of the host–parasite relations of Nematospiroides dubius, Baylis, 1926, Heligmosomidae, a mouse nematode in its normal and an abnormal host. Thesis, University Library, Sheffield.Google Scholar
Dobson, C. (1961 a). Certain aspects of the host–parasite relationship of Nematospiroides dubius (Baylis). I. Resistance of male and female mice to experimental infections. Parasitology 51, 173–9.CrossRefGoogle ScholarPubMed
Dobson, C. (1961 b). Certain aspects of the host–parasite relationship of Nematospiroides dubius (Baylis). II. The effect of sex on experimental infections in the rat (an abnormal host). Parasitology 51, 499510.CrossRefGoogle ScholarPubMed
Dobson, C. (1961 c). Certain aspects of the host–parasite relationship of Nematospiroides dubuis (Baylis). III. The effect of a milk diet on experimental infections in the adult male mouse. Parasitology 51, 511–14.CrossRefGoogle Scholar
Dobson, C. (1962 a). Certain aspects of the host–parasite relationship of Nematospiroides dubuis (Baylis). IV. The effect of the host's age on experimental infections in the mouse and rat. Parasitology 52, 3140.CrossRefGoogle Scholar
Dobson, C. (1962 b). Certain aspects of the host–parasite relationship of Nematospiroides dubuis (Baylis). V. Host specificity. Parasitology 52, 41–8.CrossRefGoogle Scholar
Dobson, C. (1964). Host endocrine interactions with nematode infections. I. Effects of sex, gonadectomy, and thyroidectomy on experimental infections in lambs. Expl Parasit. 15, 200–12.CrossRefGoogle ScholarPubMed
Dobson, C. (1966). The age and sex of the host as factors affecting the host–parasite relationship of the third-stage larva of Amplicaecum robertsi Sprent & Mines, 1960, in the laboratory mouse. Parasitology 56, 399406.CrossRefGoogle ScholarPubMed
Dudzinski, M. L. & Mykytowycz, R. (1963). Relationship between sex and age of rabbits (Oryctolagus cuniculus L.) and infections with nematodes Trichostrongylus retortaeformis and Graphidium strigosum. J. Parasit. 49, 55–9.CrossRefGoogle Scholar
Gersh, I. (1952). Ground substance and the plasticity of connective tissue. The Harvey Lectures, pp. 24241. The Harvey Society of New York. Springfield, Illinois: Charles C. Thomas.Google Scholar
Gersh, I. & Catchpole, H. R. (1949). The organization of ground substance and basement membrane and its significance in tissue injury, disease and growth. Am. J. Anat. 85, 457522.CrossRefGoogle ScholarPubMed
Herlich, H. & Porter, D. A. (1953). Prenatal infection of a calf with the nematode Neoascaris vitulorum. J. Parasit. 39, sect. 2, Suppl., pp. 33–4. (Abstr.)Google Scholar
Kao, K. Y. T. & McGavack, T. H. (1959). Connective tissue. I. Age and sex influence on protein composition of rat tissues. Proc. Soc. exp. Biol. Med. 101, 153–7.CrossRefGoogle Scholar
Lees, E. (1962). The incidence of helminth parasites in a particular frog population. Parasitology 52, 95102.CrossRefGoogle Scholar
Lewert, R. M. (1958). Invasiveness of helminth larvae. Rice Inst. Pamph. 45, 97113.Google Scholar
Lewert, R. M. & Mandlowitz, S. (1963). Innate immunity to Schistosoma mansoni relative to the state of connective tissue. Ann. N.Y. Acad. Sci. 113, 5462.CrossRefGoogle Scholar
Lurie, M. B. (1950). Mechanism affecting spread in tuberculosis. Ann. N.Y. Acad. Sci. 52, 1074.CrossRefGoogle ScholarPubMed
Nelson, G. S., Heisch, R. B. & Furlong, M. (1962). Studies on filariasis in East Africa. II. Filarial infections in man, animals and mosquitoes on the Kenya coast. Trans. R. Soc. trop. Med. Hyg. 56, 202–17.CrossRefGoogle ScholarPubMed
Oshima, T. (1961). Influence of pregnancy and lactation on migration of the larvae of Toxocara canis in mice. J. Parasit. 47, 657–60.CrossRefGoogle ScholarPubMed
Roman, E. (1951). Étude ecologique et morphologique sur les acanthocephales et les nematodes parasites des rats de la région Lyonnaise. Mem. Mus. Hist. not. Paris, 2A, 49270.Google Scholar
Sprent, J. F. A. (1961). Post-parturient infection of the bitch with Toxocara canis. J. Parasit. 47, 284.CrossRefGoogle Scholar
Sprent, J. F. A. (1963). The life history and development of Amplicaecum robertsi, an ascaridoid nematode of the python (Morelia spilotes variegatus). I. Morphological and functional significance of larval stages. Parasitology 53, 738.CrossRefGoogle Scholar
Sprunt, D. H. (1950). The ground substance in infection. Ann. N.Y. Acad. Sci. 52, 1052.CrossRefGoogle ScholarPubMed
Thomas, J. D. (1964). A comparison between the helminth burdens of male and female brown trout, Salmo trutta L., from a natural population in the River Teify, West Wales. Parasitology 54, 263–72.CrossRefGoogle Scholar
Velardo, J. T. (1958). The anatomy and endocrine physiology of the female reproductive system. In The Endocrinology of Reproduction (ed. Velardo, J. T.), pp. 101212. New York: Oxford University Press.Google Scholar