Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-26T21:11:26.088Z Has data issue: false hasContentIssue false

Breakdown of immunity to Nippostrongylus brasiliensis in lactating rats

Published online by Cambridge University Press:  09 March 2007

Jos G. M. Houdijk*
Affiliation:
Animal Nutrition and Health Department, Scottish Agricultural College, West Mains Road, Edinburgh EH9 3JG, UK
Neil S. Jessop
Affiliation:
Institute of Ecology and Resource Management, The University of Edinburgh, West Mains Road, Edinburgh EH9 3JG, UK
David P. Knox
Affiliation:
Moredun Research Institute, Pentland Science Park, Bush Loan, Penicuik EH26 0PZ, UK
Ilias Kyriazakis
Affiliation:
Animal Nutrition and Health Department, Scottish Agricultural College, West Mains Road, Edinburgh EH9 3JG, UK
*
*Corresponding author: Dr Jos Houdijk, fax +44 131 5353121, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The nutritional basis of breakdown of immunity to parasites may be addressed in a rodent model. We hypothesized that lactating rats would show a breakdown of immunity to Nippostrongylus brasiliensis, and that this breakdown of immunity would be sensitive to protein supply. Rats were immunized with 1600 infective N. brasiliensis larvae and subsequently mated. During lactation, these rats were offered foods with 90 (low protein; LP) or 210 (high protein, HP) g crude protein (N X 6.25)/kg and re-infected with 400, 800 or 1600 larvae on day 2 post-parturition. Immunized non-reproducing rats were offered a food containing 60 g crude protein/kg and re-infected with 1600 larvae. Seven days after secondary infection, lactating rats had more adult nematodes in their small intestine and nematode eggs in their colon contents than the non-reproducing rats. Protein supply did not affect worm or egg counts, although LP rats carried relatively more female nematodes than the HP rats. All lactating rats had lower intakes than expected from previous studies using similar nutritional protocols. This may have resulted in insufficient protein supply, even for the HP rats, and this could explain the absence of effects of protein supply on egg and worm counts. We conclude that a breakdown of immunity to N. brasiliensis can occur in lactating rats; this strongly suggests that the lactating rat is a suitable model for elucidating a possible nutritional basis of breakdown of immunity to parasites. However, sufficient protein intake must be achieved to address the hypothesis that breakdown of immunity to N. brasiliensis is sensitive to protein supply.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2003

References

Africa, CM (1931) Studies on the host relations of Nippostrongylus muris. J Parasitol 18, 113.CrossRefGoogle Scholar
Berghen, P, Dorny, P, Hilderson, H, Vercruysse, J & Hollanders, W (1990) Observations on parasitic gastroenteritis and parasitic bronchitis in calves over two grazing seasons. Vet Rec 127, 426430.Google ScholarPubMed
Brown, PJ, Charleypoulin, J & Pery, P (1981) Nippostrongylus brasiliensis infection in the rat. 2. A comparison of production of antibodies in bile and serum by baby rats, lactating rats and adult rats. Vet Immunol Immunopathol 2, 475482.CrossRefGoogle Scholar
Chandra, RK (1989) Nutritional regulation of immunity and risk of infection in old age. Immunology 67, 141147.Google ScholarPubMed
Chemical Rubber Company (2001) Handbook of Chemistry and Physics, 82nd ed. London: CRC Press.Google Scholar
Connan, RM (1970) The effect of host lactation on the self-cure of Nippostrongylus brasiliensis in rats. Parasitology 61, 2733.CrossRefGoogle Scholar
Connan, RM (1972) The effect of host lactation on a second infection of Nippostrongylus brasiliensis in rats. Parasitology 64, 229233.CrossRefGoogle ScholarPubMed
Coop, RL & Kyriazakis, I (1999) Nutrition–parasite interaction. Vet Parasitol 84, 187204.CrossRefGoogle ScholarPubMed
Dineen, JK & Kelly, JD (1972) The suppression of rejection of Nippostrongylus brasiliensis in lactating rats: the nature of the immunological defect. Immunology 22, 112.Google ScholarPubMed
Gray, GD & Gill, HS (1993) Host genes, parasites and parasitic infections. Int J Parasitol 23, 485494.CrossRefGoogle ScholarPubMed
Houdijk, JGM, Jessop, NS & Kyriazakis, I (2001) Nutrient partitioning between reproductive and immune functions in animals. Proc Nutr Soc 60, 515525.CrossRefGoogle ScholarPubMed
Houdijk, JGM, Kyriazakis, I, Jackson, F, Huntley, JF & Coop, RL (2003) Is the allocation of metabolisable protein prioritised to milk production rather than to immune functions in Teladorsagia circumcincta infected lactating ewes? Int J Parasitol 33, 327338.CrossRefGoogle Scholar
James, PJ (1999) Do sheep regulate the size of their mallophagan louse populations? Int J Parasitol 29, 869875.CrossRefGoogle Scholar
Jarrett, EEE, Jarrett, WFH & Urquhart, GM (1968) Quantitative studies on the kinetics of establishment and expulsion of intestinal nematode populations in susceptible and immune hosts. Nippostrongylus brasiliensis in the rat. Parasitology 58, 625639.CrossRefGoogle ScholarPubMed
Jessop, NS (1997) Protein metabolism during lactation. Proc Nutr Soc 56, 169175.CrossRefGoogle ScholarPubMed
Johnson, NL, Kotz, S & Balakrishnan, N (1988) Continuous Univariate Distributions, Vol. 1, 2nd ed. Boston, MA: PWS-KENT.Google Scholar
Kassai, T (1982) Handbook of Nippostrongylus brasiliensis (nematode). Budapest: Commonwealth Agricultural Bureaux.Google Scholar
Littel, RC, Henry, PR & Ammerman, CB (1998) Statistical analysis of repeated measures data using SAS procedures. J Anim Sci 76, 12161231.CrossRefGoogle Scholar
Lloyd, S, Amerasinghe, PH & Soulsby, EJL (1983) Periparturient immunosuppression in the bitch and its influence on infection with Toxocara canis. J Small Anim Pract 24, 237247.CrossRefGoogle Scholar
National Research Council (1995) Nutrient Requirements of Laboratory Animals, 4th ed. Washington, DC: National Academy Press.Google Scholar
Nawa, Y, Ishikawa, N, Tsuchiya, K, et al. (1994) Selective effector mechanisms for the expulsion of intestinal helminths. Parasite Immunol 16, 333338.CrossRefGoogle ScholarPubMed
Ogilvie, BM (1965) Role of adult worms in immunity of rats to Nippostrongylus brasiliensis. Parasitology 55, 325335.CrossRefGoogle ScholarPubMed
Pine, AP, Jessop, NS & Oldham, JD (1994) Maternal protein reserves and their influence on lactational performance in rats. Br J Nutr 71, 1327.CrossRefGoogle ScholarPubMed
Rothwell, TLW (1989) Immune expulsion of parasitic nematodes from the alimentary tract. Int J Parasitol 19, 139168.CrossRefGoogle ScholarPubMed
Stear, MJ, Strain, S & Bishop, SC (1999) How lambs control infection with Ostertagia circumcincta. Vet Immunol Immunopathol 72, 213218.CrossRefGoogle ScholarPubMed
Taylor, EL (1935) Seasonal fluctuation in the number of eggs of trichostrongylid worms in the faeces of ewes. J Parasitol 21, 175179.CrossRefGoogle Scholar
Woodbury, RG, Miller, HRP, Huntley, JF, Newlands, GFJ, Palliser, AC & Wakelin, D (1984) Mucosal mast cells are functionally active during spontaneous expulsion of intestinal nematode infections in rat. Nature 312, 450452.CrossRefGoogle ScholarPubMed
Xiao, L & Herd, RP (1994) Epidemiology of equine Cryptosporidium and Giardia infections. Equine Vet J 26, 1417.CrossRefGoogle ScholarPubMed