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Minimal prophylactic concentration of dietary zinc compounds in a mouse model of swine dysentery

Published online by Cambridge University Press:  28 February 2007

Peng Zhang
Affiliation:
Department of Veterinary and Biomedical Sciences, University of Nebraska, Lincoln, USA
Michael P. Carlson
Affiliation:
Department of Veterinary and Biomedical Sciences, University of Nebraska, Lincoln, USA
Norman R. Schneider
Affiliation:
Department of Veterinary and Biomedical Sciences, University of Nebraska, Lincoln, USA
Gerald E. Duhamel*
Affiliation:
Department of Veterinary and Biomedical Sciences, University of Nebraska, Lincoln, USA
*
*Rm 147, Veterinary Basic Science Building, Department of Veterinary & Biomedical Sciences, University of Nebraska-Lincoln, Lincoln, NE 68583–0905, USA. E-mail: [email protected]

Abstract

Dietary supplementation with 6000 mg of Zn2+/kg of feed has been shown to modify the clinicopathologic expression of Brachyspira hyodysenteriaeinfection in a laboratory mouse model of swine dysentery. However, this concentration impaired the body weight gain of the mice. The purpose of the present study was to determine a minimal prophylactic concentration of feed-grade zinc compounds that would not affect the growth of mice challenge-exposed with B. hyodysenteriae. A total of 440, 6- to 8-week-old, C3H/HeN mice were allocated randomly to groups and fed either a defined diet or a defined diet containing either 1000, 2000 or 4000 mg/kg ZnO, ZnSO4 or zinc-methionine for 7 days before intra- gastric inoculation with B. hyodysenteriae. From days 7 to 35 after inoculation, mice in each group were necropsied at weekly intervals for determination of body weight, presence of B. hyodysenteriae in the cecum, and histological assessment of cecal lesions. Only ZnO fed at 2000 mg/kg had a prophylactic effect against B. hyodysenteriaeinfection without affecting the body weight gain of the mice. The prophylactic effect of Zn2+ against infection with B. hyodysenteriae was also affected by the relative concentration of Fe2+ and Zn2+/Fe2+ratio of the diet.

Type
Research Article
Copyright
Copyright © CAB International 2001

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References

Ananda, SP (1993). Zinc and enzymes. In: Frieden, E (ed.), Biochemistry of Zinc. New York: Plenum Press, pp.1754.Google Scholar
Bland, AP, Frost, AJ and Lysons, RJ (1995). Susceptibility of porcine ileal enterocytes to the cytotoxin of Serpulina hyodysenteriae and the resolution of the epithelial lesions: An electron microscopic study. Veterinary Pathology 32: 2435.CrossRefGoogle Scholar
Cohen, I, Bitan, R and Nitzan, Y (1991). The effect of zinc and cadmium ions on Escherichia coli B. Microbios 68: 157168.Google ScholarPubMed
Committee on Animal Nutrition, Subcommittee on Mineral Toxicity in Animals (1980). Zinc. In: Mineral Tolerance of Domestic Animals. Washington, DC: National Academy of Sciences, pp.553577.Google Scholar
Cox, CD (1989). Importance of iron in bacterial virulence. In: Beveridge, TJ, Doyle, RJ (eds), Metal Ions and Bacteria. New York: John Wiley & Sons, pp.207246.Google Scholar
Dupont, DP, Duhamel, GE, Carlson, MP and Mathiesen, MR (1994). Effect of divalent cations on hemolysin synthesis by Serpulina (Treponema) hyodysenteriae: Inhibition induced by zinc and copper. Veterinary Microbiology 41: 6373.CrossRefGoogle ScholarPubMed
Elder, RO, Duhamel, GE, Schafer, RW, Mathiesen, MR and Ramanathan, M (1994). Rapid detection of Serpulina hyo-dysenteriae in diagnostic specimens by PCR. Journal of Clinical Microbiology 32: 14971502.CrossRefGoogle ScholarPubMed
Hahn, JD and Baker, DH (1993). Growth and plasma zinc responses of young pigs fed pharmacologic levels of zinc. Journal of Animal Science 71: 30203024.CrossRefGoogle ScholarPubMed
Hambidge, KM, Krebs, NF, Jacobs, MA, Favier, A, Guyette, L and Ikle, DN (1983). Zinc nutritional status during pregnancy: A longitudinal study. American Journal of Clinical Nutrition 37: 429442.CrossRefGoogle ScholarPubMed
Harris, DL, Glock, RD, Christensen, CR and Kinyon, JM (1972). Swine dysentery – I. Inoculation of pigs with Treponema hyodysenteriae (new species) and reproduction of the disease. Veterinary Medicine and Small Animal Clinician 67: 6164.Google Scholar
Harris, DL, Alexander, TJL, Whipp, SC, Robinson, IM, Glock, RD and Matthews, PJ (1978). Swine dysentery: Studies of gno-tobiotic pigs inoculated with Treponema hyodysenteriae, Bacteroides vulgatus, and Fusobacterium necrophorum . Journal of the American Veterinary Medical Association 172: 468471.Google ScholarPubMed
Harris, DL, Hampson, DJ and Glock, RD (1999). Swine dysentery. In: Straw, BE, D'Allaire, S, Mengeling, WL and Taylor, DJ (eds), Diseases of Swine. Ames: Iowa State University Press, pp.579600.Google Scholar
Holm, A and Poulsen, HD (1996). Zinc oxide in treating E. coli diarrhea in pigs after weaning. Compendium of Continuing Education 18: S26–S48.Google Scholar
Hutto, DL and Wannemuhler, MJ (1999). A comparison of the morphologic effects of Serpulina hyodysenteriae or its beta-hemolysin on the murine cecal mucosa. Veterinary Pathology 36: 412422.CrossRefGoogle ScholarPubMed
Hyatt, DR, ter Huurne, AAHM, van der Zeijst, BAM and Joens, LA (1994). Reduced virulence of Serpulina hyodysenteriae hemolysin-negative mutants in pigs and their potential to protect pigs against challenge with virulent strain. Infection and Immunity 62: 22442248.CrossRefGoogle ScholarPubMed
Jensen-Waern, M, Melin, L, Lindberg, R, Johannisson, A and Wallgren, PP (1998). Dietary zinc oxide in weaned pigs –effects on performance, tissue concentrations, morphol-ogy, neutrophil functions and faecal microflora. Research in Veterinary Science 64: 225231.CrossRefGoogle ScholarPubMed
Joens, LA, Robinson, IM, Glock, RD and Matthews, PJ (1981). Production of lesions in gnotobiotic mice by inoculation with Treponema hyodysenteriae . Infection and Immunity 31: 504506.CrossRefGoogle ScholarPubMed
Katouli, M, Melin, L, Jensen-Waern, M, Wallgren, P and Möllby, R (1999). The effect of zinc oxide supplementation on the stability of the intestinal flora with special reference to composition of coliforms in weaned pigs. Journal of Applied Microbiology 87: 564573.CrossRefGoogle ScholarPubMed
Kent, KA, Lemcke, RM and Lysons, RJ (1988). Production, purifi-cation and molecular weight determination of the haemolysin of Treponema hyodysenteriae . Journal of Medical Microbiology 27: 215224.CrossRefGoogle Scholar
Kreuzer, M and Kirchgessner, M (1994). Effect of oral and i.v. iron on tissue retention and excretion of copper and zinc in growing rats. Journal of Animal Physiology and Animal Nutrition 72: 242251.CrossRefGoogle Scholar
Kunkle, RA and Kinyon, JM (1988). Improved selective medium for the isolation of Treponema hyodysenteriae . Journal of Clinical Microbiology 26: 23572360.CrossRefGoogle ScholarPubMed
Lysons, RJ, Kent, KA, Bland, AP, Sellwood, R, Robinson, WF and Frost, AJ (1991). A cytotoxic haemolysin from Treponema hyodysenteriae – a probable virulence determinant in swine dysentery. Journal of Medical Microbiology 34: 97102.CrossRefGoogle ScholarPubMed
Mølbak, K, Baggesen, DL, Aarestrup, FM, Ebbesen, JM, Engberg, J, Frydendahl, K, Gerner-Smidt, P, Petersen, AM and Wegener, HC (1999). An outbreak of multidrug-resistant, quinolone-resistant Salmonella enterica serotype typhimurium DT104. New England Journal of Medicine 341: 14201425.CrossRefGoogle ScholarPubMed
Mysore, JV and Duhamel, GE (1994). Morphometric analysis of enteric lesions in C3H/HeN mice inoculated with Serpulina hyodysenteriae serotypes 2 and 4 with or without oral streptomycin pretreatment. Canadian Journal of Veterinary Research 58: 281286.Google ScholarPubMed
Ochiai, S, Adachi, Y and Mori, K (1997). Unification of the genera Serpulina and Brachyspira, and proposals of Brachyspira hyodysenteriae comb. nov., Brachyspira innocens comb. nov. and Brachyspira pilosicoli comb. nov. Microbiology Immunology 41: 445452.CrossRefGoogle ScholarPubMed
Puls, R (1988). Mineral Levels in Animal Health. Clearbrook, British Columbia, Canada: Sherpa International.Google Scholar
Sandstrom, B, Davidsson, L, Cederblad, A and Lonnerdal, B (1985). Oral iron, dietary ligands and zinc absorption. Journal of Nutrition 115: 411414.CrossRefGoogle ScholarPubMed
SAS Institute (1985). SAS User's Guide, Statistics. Cary: SAS Institute Inc., pp.433506.Google Scholar
Stanton, TB and Cornell, CP (1987). Erythrocytes as a source of essential lipids for Treponema hyodysenteriae . Infection and Immunity 55: 304308.CrossRefGoogle ScholarPubMed
Taylor, DJ and Alexander, TJL (1971). The production of dysentery in swine by feeding cultures containing a spirochaete. British Veterinary Journal 127: 5861.CrossRefGoogle ScholarPubMed
ter Huurne, AAHM, van Houten, M, Muir, S, Kusters, JG, vander Zeijst, BAM and Gaastra, W (1992). Inactivation of a Serpula (Treponema) hyodysenteriae hemolysin gene by homologous recombination: importance of this hemolysin in pathogenesis of S. hyodysenteriae in mice. FEMS Microbiology Letters 92: 109114.Google Scholar
Van Asbeck, BS, Verbrugh, HA, van Oost, BA, Marx, JJ, Imhof, HW and Verhoef, J (1982). Listeria monocytogenes meningitis and decreased phagocytosis associated with iron overload. British Medical Journal 284: 542544.CrossRefGoogle ScholarPubMed
Van Asbeck, BS, Marx, JJM, Struyvenberg, A, van Kats, JH and Verhoef, J (1984). Effect of iron (III) in the presence of various ligands on the phagocytic and metabolic activity of human polymophonuclear leukocytes. Journal of Immunology 132: 851856.CrossRefGoogle Scholar
Whipp, SC, Robinson, IM, Harris, DL, Glock, RD, Matthews, PJ and Alexander, TJL (1979). Pathogenic synergism between Treponema hyodysenteriae and other anaerobes in gnotobiotic pigs. Infection and Immunity 26: 10421047.CrossRefGoogle ScholarPubMed
Witters, NA and Duhamel, GE (1996). Cell membrane permeability- and mitochondrial dysfunction-inducing activities in cell free supernatants from Serpulina hyodysenteriae serotypes 1 and 2. Comparative Immunology Microbiology and Infectious Diseases 19: 233244, 1996.CrossRefGoogle Scholar
Zhang, P, Duhamel, GE, Mysore, JV, Carlson, MP and Schneider, NR (1995). Prophylactic effect of dietary zinc in a laboratory mouse model of swine dysentery. American Journal of Veterinary Research 56: 334339.CrossRefGoogle Scholar