Hostname: page-component-848d4c4894-xfwgj Total loading time: 0 Render date: 2024-07-05T01:33:23.245Z Has data issue: false hasContentIssue false

The responses of a tropical breed of domestic rabbit, Oryctolagus cuniculus, to experimental infection with Trichostrongylus colubriformis

Published online by Cambridge University Press:  12 April 2024

G.A. Musongong
Affiliation:
Veterinary Research Laboratory, Wakwa Regional Centre for Agricultural Research for Development, PO Box 65, Ngaoundere, Cameroon
S.N. Chiejina*
Affiliation:
Department of Veterinary Parasitology and Entomology, University of Nigeria, Nsukka, Nigeria
B.B. Fakae
Affiliation:
Department of Veterinary Parasitology and Entomology, University of Nigeria, Nsukka, Nigeria
M.M. Ikeme
Affiliation:
Department of Veterinary Parasitology and Entomology, University of Nigeria, Nsukka, Nigeria
*
*Fax: +234 42 770075, Email: [email protected]

Abstract

Clinical, parasitological and pathological responses of a tropical out-bred domestic rabbit to experimental Trichostrongylus colubriformis infection were used to evaluate its suitability as a laboratory host and model for studying the host–parasite relationships of T. colubriformis. In the first experiment, three groups each of 16, predominantly juvenile male, 8- to 10-week-old rabbits were given a single pulse infection with 500, 5000 or 25000 infective larvae (L3) of T. colubriformis, to represent low, medium and high levels of infection, respectively. A fourth group of 16 rabbits of similar age formed the uninfected controls. In the second experiment, two groups of 10 juvenile (8- to 10-week-old) and 10 adult (8- to 10-month-old) rabbits were similarly infected with 20000 L3, with appropriate naïve controls. Prepatency was 14 and 16 days and peak faecal egg counts occurred on days 24 and 20 after infection in young and adult rabbits respectively. Peak worm counts occurred on day 14 in both age groups and at all levels of infection. Subsequently, parasite burdens declined in a highly significantly dose- and age-dependent manner. At low and moderate levels of infection, approximately 83–98% of worms were recovered from the first 60 cm of the small intestine. Worm fecundity was also significantly influenced by host age and larval dose. Host age also had a significant effect on worm length. Infections with T. colubriformis were associated with a highly significant loss of body weight, accompanied by anorexia, diarrhoea and 25% mortality at high dose levels during the patent period of infection. There were no significant changes in packed cell volume and eosinophil counts at all ages and levels of infection but significant lymphocytosis occurred at the high dose level between days 7 and 21. Parasite-specific serum IgG responses were not related to worm burden. Overall, data showed that this miniature, docile and relatively inexpensive breed of rabbit is a potentially valuable laboratory host for studying T. colubriformis infections. The larval dose, duration of infection and host age were major determinants of host responsiveness to primary infections in this rabbit genotype.

Type
Review Article
Copyright
Copyright © Cambridge University Press 2004

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

Arrington, L.R. & Kelly, K.C. (1976) Domestic rabbit biology and production. 203 pp. Gainsville, Florida, The University Press.Google Scholar
Baker, R.L., Mwamachi, D.M., Audho, J.O., Aduda, E.O. & Thorpe, W. (1998) Resistance of Galla and Small East African goats in the sub-humid tropics to gastrointestinal nematode infections and the peri-parturient rise in faecal egg counts. Veterinary Parasitology 79, 5364.CrossRefGoogle ScholarPubMed
Barker, I.K. (1975) Intestinal pathology associated with Trichostrongylus colubriformis infection in sheep: vascular permeability and ultrastructure of the mucosa. Parasitology 70, 173180.CrossRefGoogle ScholarPubMed
Barker, I.K. & Ford, G.E. (1975) Development and distribution of atrophic enteritis in the small intestine of rabbits infected with Trichostrongylus colubriformis . Journal of Comparative Pathology 85, 427435.CrossRefGoogle Scholar
Chiejina, S.N. (1987) Some parasitic diseases of intensively managed West African Dwarf sheep and goats in Nsukka, eastern Nigeria. British Veterinary Journal 143, 264272.CrossRefGoogle ScholarPubMed
Chiejina, S.N. (1994) The epidemiology of some helminth parasites of domesticated ruminants in the tropics with emphasis on fasciolosis and parasitic gastroenteritis, pp. 3472 in Chowdhury, N. & Tanada, I. (Eds) Helminthology. New Dehli, India, Narosa Publishing House.CrossRefGoogle Scholar
Chiejina, S.N. & Fakae, B.B. (1984) Development and survival of infective larvae of gastrointestinal nematode parasites of cattle on pasture in eastern Nigeria. Research in Veterinary Science 37, 148153.CrossRefGoogle ScholarPubMed
Chiejina, S.N. & Fakae, B.B. (1989) The ecology of infective larvae of bovine gastrointestinal trichostrongylids in dry season contaminated pastures in the Nigerian derived savannah. Journal of Helminthology 63, 127139.CrossRefGoogle Scholar
Chiejina, S.N. & Sewell, M.M.H. (1974) Worm burdens, acquired resistance and liveweight gains in lambs during prolonged daily infections with Trichostrongylus colubriformis (Giles, 1892) Loss, 1905. Parasitology 69, 315327.CrossRefGoogle Scholar
Chieng, L.Y. (1987) Enzyme linked immunosorbent assay. p. 206 in Jeyaseelem, K., Chung, M.C.M. & Kon, O.L. (Eds) Genes and proteins. A laboratory manual of selected techniques in molecular biology. National University of Singapore, ICSU Press.Google Scholar
Christensen, N.O., Nansen, P., Fagbemi, B.D. & Monrad, J. (1987) Heterologous antagonistic and synergistic interactions between helminths and protozoans in concurrent experimental infections of mammalian hosts. Parasitology Research 73, 387410.CrossRefGoogle ScholarPubMed
Dacie, J.V. & Lewis, S.M. (1995) Practical haematology. 8th edn. 609 pp. London, Churchill Livingstone.Google Scholar
Darji, J.D. (1982) The influence of genetic factors on the resistance of ruminants to gastrointestinal nematode and trypanosome infections. pp. 1751 in Owen, D.G. (Ed.) Animal models in parasitology. London, McMillan Press.Google Scholar
Dickmans, G. (1937) A note on the nematode genus, Trichostrongylus occurring in rodents and lagomorphs, with description of two new species. Journal of the Washington Academy of Science 27, 203209.Google Scholar
Fakae, B.B. (1990) The epidemiology of helminthosis in small ruminants under the traditional husbandry system in eastern Nigeria. Veterinary Research Communications 14, 381391.CrossRefGoogle ScholarPubMed
Fakae, B.B., Harrison, L.J.S., Ross, C.A. & Sewell, M.M.H. (1994) Heligmosomoides polygyrus and Trypanosoma congolense infections in mice: a laboratory model for concurrent gastrointestinal nematode and trypanosome infections. Parasitology 108, 6168.CrossRefGoogle ScholarPubMed
Fakae, B.B., Chiejina, S.N., Behnke, J.M., Ezeokonkwo, R.C., Nnadi, P.A., Onyenwe, W.I., Gilbert, F. & Wakelin, D. (1998) The response of Nigerian West African Dwarf goats to experimental infections with Haemonchus contortus . Research in Veterinary Science 66, 147158.CrossRefGoogle Scholar
Fowler, J. & Cohen, L. (1990) Practical statistics for field biology. 1st edn. 227 pp. Milton Keynes, Open University Press.Google Scholar
Gill, H.S., Husband, A.J., Watson, D.L. & Gray, G.D. (1994) Antibody containing cells in the abomasal mucosa of sheep with genetic resistance to Haemonchus contortus . Research in Veterinary Science 56, 4147.CrossRefGoogle ScholarPubMed
Gill, H.S., Altmann, K., Cross, M.L. & Husband, A.J. (2000) Induction of T helper 1 and T helper 2 immune responses during Haemonchus contortus infection in sheep. Immunology 99, 458463.CrossRefGoogle Scholar
Griffiths, G. & Pritchard, D.I. (1994) Vaccination against gastrointestinal nematodes of sheep using purified secretory acetylecholinesterase from Trichostrongylus colubriformis . Parasite Immunology 16, 507510.CrossRefGoogle Scholar
Hohenhaus, M.A., Josey, M.J., Dobson, C. & Outteridge, P.M. (1998) The eosinophil leucocyte, a phenotypic marker of resistance to nematode parasites, is associated with calm behaviour in sheep. Immunology and Cell Biology 76, 153158.CrossRefGoogle ScholarPubMed
Horak, I.G., Clark, R. & Gray, R.S. (1968) The pathological physiology of helminth infections. III. Trichostrongylus colubriformis . Onderstepoort Journal of Veterinary Research 35, 195224.Google Scholar
Karanu, F.N., McGuire, T.C., Davis, W.C., Besser, T.E. & Jasmer, D.P. (1997) CD4+T lymphocytes control protective immunity induced in sheep and goats by Haemonchus contortus gut antigens. Parasite Immunology 19, 435445.CrossRefGoogle Scholar
MAFF (1977) Manual of veterinary parasitological laboratory techniques. 2nd edn. pp. 550. Ministry of Agriculture Fisheries and Food Technical Bulletin No. 18. London, HMSO.Google Scholar
Manton, V.J.A., Peacock, R., Poynter, D., Silverman, P.H. & Terry, R.J. (1962) The influence of age on naturally acquired resistance to Haemonchus contortus in lambs. Research in Veterinary Science 3, 308314.CrossRefGoogle Scholar
McClure, S.J., Emery, D.L., Wagland, B.M. & Jones, W.O. (1992) A study of rejection of Trichostrongylus colubriformis by immune sheep. International Journal for Parasitology 22, 227234.CrossRefGoogle ScholarPubMed
Onah, D.N. & Wakelin, D. (1999) Trypanosome-induced suppression of responses to Trichinella spiralis in mice. International Journal for Parasitology 29, 10171026.CrossRefGoogle Scholar
Purvis, G.M. & Sewell, M.M.H. (1972) Trichostrongylus colubriformis. Age resistance in the rabbit, Oryctolagus cuniculus . Experimental Parasitology 32, 191195.CrossRefGoogle ScholarPubMed
Samson, K.S. (1970) Experimental infection of domestic sheep with Trichostrongylus colubriformis from natural infections in black-tailed jackrabbits. Journal of Parasitology 56, 1037.CrossRefGoogle ScholarPubMed
Schallig, H.D. (2000) Immunological responses of sheep to Haemonchus contortus . Parasitology 120, S63S72.CrossRefGoogle ScholarPubMed
Schallig, H.D. & Van Leeuwen, M.A.. (1997) Protective immunity to the blood-feeding nematode, Haemonchus contortus induced by vaccination with parasite low molecular weight antigens. Parasitology 114, 293299.CrossRefGoogle Scholar
Schallig, H.D., van der Aar, W.M., Boersema, J.M. & Cornelissen, A.W. (2000) The effect of oxfendazole terminated infections with Haemonchus contortus on the development of immunity in sheep. Veterinary Parasitology 88, 6172.CrossRefGoogle ScholarPubMed
Sileghem, M., Flynn, J.N., Darji, A., DeBaetselier, P. & Naessens, P. (1994) African trypanosomiasis. pp. 150 in Kierszenbaum, F. (Ed.) Parasitic infections and the immune system. San Diego, Academic Press.Google Scholar
Skidmore, L.V. (1932) Trichostrongylus colubriformisz (= T instabilis) in the jackrabbit (Lepus californicus melanotis) . Journal of the American Veterinary Medical Association 80, 800801.Google Scholar
Soulsby, E.J.L. (1982) Helminths, arthropods, and protozoa of domesticated animals. 7th edn. 809 pp. London, Bailliere Tindall.Google Scholar
Stear, M.J., Strain, S. & Bishop, S.C. (1999) Mechanisms underlying resistance to nematode infection. International Journal for Parasitology 29, 5156.CrossRefGoogle ScholarPubMed
Wedrychowicz, H. & Bezubik, B. (1988) Systemic and local responses in rabbits following single and multiple infections with Trichostrongylus colubriformis . Acta Parasitologica Polonica 33, 303315.Google Scholar
Wedrychowicz, H. & Bezubik, B. (1990) Influence of adjuvants on immunity in rabbits vaccinated with infective larval somatic proteins of Trichostrongylus colubriformis . Veterinary Parasitology 37, 273284.CrossRefGoogle ScholarPubMed
Wedrychowicz, H., Bezubik, B. & Trojanczuk, I. (1989) Local and systemic humoral immunity in rabbits vaccinated with adult Trichostrongylus colubriformis somatic proteins. Acta Parasitologica Polonica 34, 453458.Google Scholar
Woolaston, R.R., Manueli, P., Eady, S.J., Barger, I.A., Le Jambre, L.F., Banks, D.J.D. & Windon, R.G. (1996) The value of circulating eosinophil count as a selection criterion for resistance of sheep to trichostrongyle parasites. International Journal for Parasitology 26, 123126.CrossRefGoogle ScholarPubMed