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The effect of a zinc, cobalt and selenium soluble glass bolus on the trace element status of extensively grazed sheep over winter

Published online by Cambridge University Press:  18 August 2016

N. R. Kendall*
Affiliation:
Centre for Animal Sciences, Leeds Institute of Biotechnology and Agriculture, School of Biology, University of Leeds, Leeds LS2 9JT, UK
D. W. Jackson
Affiliation:
Centre for Animal Sciences, Leeds Institute of Biotechnology and Agriculture, School of Biology, University of Leeds, Leeds LS2 9JT, UK
A. M. Mackenzie
Affiliation:
School of Agriculture, Harper Adams University College, Newport, Shropshire TF10 8NB, UK
D. V. Illingworth
Affiliation:
Centre for Animal Sciences, Leeds Institute of Biotechnology and Agriculture, School of Biology, University of Leeds, Leeds LS2 9JT, UK
I. M. Gill
Affiliation:
Thrums Veterinary Group, 1 Morrison Street, Kirriemuir, Angus DD8 5DB, UK
S. B. Telfer
Affiliation:
Centre for Animal Sciences, Leeds Institute of Biotechnology and Agriculture, School of Biology, University of Leeds, Leeds LS2 9JT, UK
*
Present address: Academic Division of Reproductive Medicine, School of Human Development, Floor D, East Block, Queens Medical Centre, Nottingham, NG7 2UH. E-mail [email protected]
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Abstract

The effects of trace element deficiencies in lambs, particularly zinc, copper, cobalt and selenium, include decreased growth rates and increased mortality. However, trace element supplementation of sheep reared under extensive conditions has several logistical problems.

Two trials were designed to investigate the effect of a zinc, cobalt and selenium soluble glass bolus on the trace element status of out-wintered ewe lambs. In trial 1 600 8-month-old ewe lambs (500 Scottish Blackface and 100 North Country Cheviots) were allocated to two treatment groups; 300 were treated with a zinc, cobalt and selenium soluble glass bolus (zinc) and 300 were untreated (control). In trial 2, 315 8-month-old Scottish Blackface ewe lambs were allocated to three treatments: 105 were treated with the zinc, cobalt and selenium soluble glass bolus (zinc), 105 were treated with a copper, cobalt and selenium soluble glass bolus (copper) and the remaining 105 were untreated (control). Blood samples were collected immediately prior to giving boluses and again after approximately 4 months. These were assessed for zinc (plasma zinc concentration), cobalt (serum vitamin B12 concentration), selenium (erythrocyte glutathione peroxidase activity) and copper status (plasma copper concentration, caeruloplasmin, amine oxidase and superoxide dismutase activity and calculation of the ratio between the caeruloplasmin and plasma copper).

The zinc bolus in both trials significantly increased the plasma zinc concentrations (P < 0·001 and P < 0·01 respectively), erythrocyte glutathione peroxidase activities (P < 0·001) and serum vitamin B12 concentrations (P < 0·001). The copper bolus also significantly increased the erythrocyte glutathione peroxidase activities (P < 0·001) and serum vitamin B12 concentrations (P < 0·001) when compared with the controls but were not significantly different from the zinc group. The copper bolus significantly increased all of the copper status indicators (P < 0·01) when compared with the control and zinc groups. However, in trial 1 when only the zinc and control groups were compared, the zinc bolus significantly increased the ratio (P < 0·001) and serum caeruloplasmin (P < 0·001) and erythrocyte superoxide dismutase (P < 0·01) activities. These responses were not observed in trial 2 with the erythrocyte superoxide dismutase being significantly reduced in the zinc group when compared with the control group (P < 0·001).

The zinc, cobalt and selenium soluble glass bolus increased the status of all three trace elements consistently for a period of at least 100 days. The increases of cobalt and selenium status were similar to those achieved using the copper, cobalt and selenium bolus, which also increased the copper status of the sheep.

Type
Ruminant nutrition, behaviour and production
Copyright
Copyright © British Society of Animal Science 2001

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References

Bremner, I., Young, B. W. and Mills, C. F. 1976. Protective effect of zinc supplementation against copper toxicosis in sheep. British Journal of Nutrition 36: 551561.Google Scholar
Chen, X. C., Yin, T. A., He, J. S., Ma, Q. Y., Han, Z. M. and Li, L. X. 1985. Low levels of zinc in hair and blood, pica, anorexia, and poor growth in Chinese preschool children. The American Journal of Clinical Nutrition 42: 694700.Google Scholar
Demertzis, P. N., Spais, A. G. and Papsteriadis, A. A. 1978. Zinc therapy in control of footrot in sheep. Veterinary Medical Review 1: 101106.Google Scholar
Gershwin, M. E., Keen, C. L., Fletcher, M. P. and Hurley, L. S. 1987. Trace element deficiencies and immune responsiveness. In Trace elements in man and animals — 6 (ed. Hurley, L.S. Keen, C. L. Fletcher, M. P. and Rucker, R. B.), proceedings of the sixth international symposium on trace elements in man and animals, pp. 8591. Plenum Press, New York.Google Scholar
Hambridge, K. M., Casey, C. E. and Krebs, N. F. 1986. Zinc. In Trace elements in human and animal nutrition, volume 2 (ed. Mertz, W. D.), pp. 1138. Academic Press Inc., Orlando, Florida.Google Scholar
Henry, R. J., Cannon, D. C. and Winkleman, J. W. 1974. Clinical chemistry: principles and techniques, second edition. Harper and Row Publishers, Maryland.Google Scholar
Jelinek, P. D., Ellis, T., Wroth, R. H., Sutherland, S. S., Masters, H. G. and Petterson, D. S. 1988. The effect of selenium supplementation on immunity, and the establishment of an experimental Haemonchus contortus infection in weaner Merino sheep fed a low selenium diet. Australian Veterinary Journal 65: 214217.Google Scholar
Jones, D. G. and Suttle, N. F. 1981. Some effects of copper deficiency on leukocyte function in sheep and cattle. Research in Veterinary Science 31: 151156.Google Scholar
Kendall, P. T. 1977. Studies in the use of feedblocks for ruminants. Ph.D. thesis, University of Glasgow.Google Scholar
Kendall, N. R., Farrar, N. C., Illingworth, D. V., Jackson, D. W. and Telfer, S. B. 1999. The use of a soluble glass copper, cobalt and selenium bolus to supply selenium to sheep. Proceedings of the British Society of Animal Science, 1999, p. 99.Google Scholar
Kendall, N. R., Mackenzie, A. M. and Telfer, S. B. 1997. Effect of a soluble cobalt, selenium and zinc glass bolus on humoral immune response and trace element status in lambs. In Trace elements in man and animals-9 (ed. Fischer, P. W. F., Abbé, M. R., Cockell, K. A. and Gibson, R. S.), proceedings of the ninth international symposium on trace elements in man and animals, pp. 442444. NRC Research Press, Ottawa, Canada.Google Scholar
Kendall, N. R., Mackenzie, A. M. and Telfer, S. B. 2001. The effect of a copper, cobalt and selenium soluble glass bolus given to grazing sheep. Livestock Production Science 68: 3139.Google Scholar
Kendall, N. R., Middlemas, C., Maxwell, H., Birch, F., Illingworth, D. V., Jackson, D. W. and Telfer, S. B. 2000. A comparison of the efficacy of proprietary products in the treatment of molybdenum induced copper deficiency. In Trace elements in man and animals — 10 (ed. Roussel, A. M., Anderson, R. A. and Favier, A. E.), proceedings of the tenth international symposium on trace elements in man and animals, pp. 741748. Plenum Press, New York.Google Scholar
Kendall, N. R. and Telfer, S. B. 2000. Induction of zinc deficiency in sheep and its correction with a bolus of soluble glass containing zinc. Veterinary Record 146: 634637.Google Scholar
McDowell, L. R. 1992. Minerals in animal and human nutrition. Academic Press Ltd, London.Google Scholar
Mackenzie, A. M., Illingworth, D. V., Jackson, D. W. and Telfer, S. B. 1997. The use of caeruloplasmin activities and plasma copper concentrations as an indicator of copper status in ruminants. In Trace elements in man and animals-9 (ed. Fischer, P. W. F., Abbé, M. R., Cockell, K. A. and Gibson, R. S.), proceedings of the ninth international symposium on trace elements in man and animals, pp. 137138. NRC Research Press, Ottawa, Canada.Google Scholar
Martin, R. M., Gonzalez, M. J. V. and Gomez, A. M. 1996. Use of zinc-methionine in milking cows. Proceedings of the XIX world buiatrics congress pp. 259260.Google Scholar
Miller, J. K. 1991. The significance of trace-element nutrition in broken-mouth periodontitis. Proceedings of the Sheep Veterinary Society, vol. 15, pp. 4348.Google Scholar
Misra, H. P. and Fridovich, I. 1977. Superoxide dismutase: a photochemical augmentation assay. Archives of Biochemistry and Biophysiology 181: 308312.Google Scholar
Moeini, M. M., Mackenzie, A. M. and Telfer, S. B. 1997. Effect of Cosecure® on the fertility and trace element status of dairy cattle. Proceedings of the British Society of Animal Science, 1997, p. 192.Google Scholar
Mulryan, G. and Mason, J. 1992. Assessment of liver copper status in cattle from plasma copper and plasma copper enzymes. Annales de Recherches Veterinaires 23: 233238.Google Scholar
Nicholson, J. W. G., Bush, R. S. and Allen, J. G. 1993. Antibody-responses of growing beef-cattle fed silage diets with and without selenium supplementation. Canadian Journal of Animal Science 73: 355365.Google Scholar
O’Dell, B. L. 1989. Mineral interactions relevant to nutrient requirements. Journal of Nutrition 119: 18321838.Google Scholar
Paglia, D. E. and Valentine, W. N. 1967. Studies on quantitative and qualitative characterisation of erythrocyte glutathione peroxidase. Journal of Laboratory Clinical Medicine 70: 158169.Google Scholar
Reddy, P. G. and Frey, R. A. 1990. Nutritional modulation of immunity. In Immunomodulation in domestic food animals (ed. Blecha, F. and Charley, B.), pp. 255281. Academic Press Ltd, London.Google Scholar
Spallholz, J. E. 1981. Anti-inflammatory, immunologic and carcinostatic attributes of selenium in experimental animals. Advances in Experimental and Medical Biology 135: 4365.Google Scholar
Towers, N. R., Wright, D. E., Aitken, B. I., Smith, B. L., Sim, A. L. and Sinclair, D. P. 1976. Zinc and facial eczema. Proceedings of Ruakura farmer’s conference, vol. 28, pp. 6568.Google Scholar
Underwood, E. J. 1981. The mineral nutrition of livestock. Commonwealth Agricultural Bureaux, London.Google Scholar
Vellema, P., Rutten, V. P. M. G., Hoek, A., Moll, A. and Wentink, G. H. 1996. The effect of cobalt supplementation on the immune response in vitamin B12 deficient Texel lambs. Veterinary Immunology and Immunopathology 55: 151161.Google Scholar
Wacker, W. E. C. 1976. Role of zinc in wound healing: a critical review. In Trace elements in human health and disease, vol. 1 (ed. Prasad, A. S.), pp. 107113. Academic Press, New York.Google Scholar
Whitaker, D. A., Eayres, H. F., Aithison, K. and Kelly, J. M. 1996. No effect of a dietary zinc proteinate on clinical mastitis, infection rate, recovery rate and somatic cell count in dairy cows. Proceedings of the XIX world buiatrics congress, pp. 291292.Google Scholar