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Pigs experimentally infected with Serpulina hyodysenteriae can be protected from developing swine dysentery by feeding them a highly digestible diet

Published online by Cambridge University Press:  15 May 2009

P. M. Siba
Affiliation:
School of Veterinary Studies, Murdoch University, Murdoch, Western Australia 6150, Australia
D. W. Pethick
Affiliation:
School of Veterinary Studies, Murdoch University, Murdoch, Western Australia 6150, Australia
D. J. Hampson*
Affiliation:
School of Veterinary Studies, Murdoch University, Murdoch, Western Australia 6150, Australia
*
* Corresponding author.
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Weaner pigs (n = 72) were fed 1 of 4 diets. These were based on either cooked rice and animal protein, cooked rice and lupin, wheat and lupin, or wheat and animal protein. Twenty-six of the pigs were slaughtered after 1 month. Those fed the highly digestible cooked rice and animal protein diet had drier colonic contents and faeces, lighter large intestines, and the contents of their large intestines had increased pH values and decreased total VFA concentrations. The other 46 pigs were orally challenged with broth cultures of Serpulina hyodysenteriae, and were monitored for faecal excretion of the spirochaetes, and for the development of swine dysentery (SD). None of 18 pigs fed the cooked rice and animal protein diet developed colonic changes or disease, whereas most pigs on the other diets developed mucohaemorrhagic colitis and dysentery. The reduced fermentation that occurred in the large intestines of pigs fed cooked rice and animal protein was associated with a subsequent failure of colonization by S. hyodysenteriae, and resultant protection against SD.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1996

References

1.Roncalli, RA, Leaning, WHD. Geographical distribution of swine dysentery. Proc Int Pig Vet Soc Cong, Ames, Iowa, 1977; 17.Google Scholar
2.Harris, DL, Glock, RD, Christensen, CR, Kinyon, JM. Swine dysentery. I. Inoculation of pigs with Treponema hyodysenteriae (new species) and reproduction of the disease. Vet Med Sm Anim Clin 1972; 67: 61–4.Google Scholar
3.Stanton, TB, Jensen, NS, Casey, TA, Tordoff, LA, Dewhirst, FE, Paster, BJ. Reclassification of Treponema hyodysenteriae and Treponema innocens in a new genus, Serpula gen. nov., as Serpula hyodysenteriae comb. nov. and Serpula innocens comb. nov. Int J Syst Bacteriol 1991; 41: 50–8.CrossRefGoogle Scholar
4.Stanton, TB. Proposal to change the genus designation Serpula to Serpulina gen. nov. containing species Serpulina hyodysenteriae comb. nov. and Serpulina innocens comb. nov. Int J Syst Bacteriol 1991; 42: 189–92.CrossRefGoogle Scholar
5.Hughes, R, Olander, HJ, Williams, CB. Swine dysentery: pathogenicity of Treponema hyodysenteriae. Am J Vet Res 1975; 36: 971–7.Google ScholarPubMed
6.Trowell, H, Southgate, DAT, Wolever, TMS, Leeds, AR, Gassull, MA, Jenkins, DJA. Dietary fibre redefined. Lancet 1976; 1: 967.CrossRefGoogle ScholarPubMed
7.Knudsen, KEB, Jensen, BB, Andersen, JO, Hansen, I. Gastrointestinal implications in pigs of wheat and oat fractions. II. Microbial activity in the gastrointestinal tract. Br J Nutr 1991; 65: 233–48.CrossRefGoogle Scholar
8.Radecki, SV, Yokoyama, MT. Intestinal bacteria and their influence on swine nutrition. In: Miller, ER, Ullrey, DE, Lewis, AJ, eds. Swine nutrition. Boston: Butterworth Heinemann, 1991: 439–47.CrossRefGoogle Scholar
9.Varel, VH. Activity of fiber-degrading microorganisms in the pig large intestine. J Anim Sci 1987; 65: 488–96.CrossRefGoogle ScholarPubMed
10.Jensen, BB, Jorgensen, H. Effect of dietary fiber on microbial activity and microbial gas production in various regions of the gastrointestinal tract of pigs. J Appl Environ Sci 1994; 60: 1897–904.Google ScholarPubMed
11.Argenzio, RA, Southworth, M. Sites of organic acid production and absorption in the gastrointestinal tract of the pig. Am J Physiol 1974; 228: 454–60.CrossRefGoogle Scholar
12.Clemens, ET, Stevens, CE, Southworth, M. Sites of organic acid production and pattern of digesta movement in the gastrointestinal tract of swine. J Nutr 1975; 105: 759–68.CrossRefGoogle ScholarPubMed
13.Kass, ML, Van Soest, PJ, Pond, WG. Utilization of dietary fibre from alfalfa by growing swine: volatile fatty acid concentrations in and disappearance from the gastrointestinal tract. J Anim Sci 1980; 50: 192–7.CrossRefGoogle Scholar
14.Imoto, S, Namioka, S. VFA production in the pigs large intestine. J Anim Sci 1978; 47: 467–78.CrossRefGoogle ScholarPubMed
15.Prohaszka, L, Baron, F. Studies on E. coli enteropathy in weanling rabbits. Zbl Vet Med B 1991; 28: 102–10.CrossRefGoogle Scholar
16.Prohaszka, L, Lukacs, K. Influence of the diet on the antibacterial effect of volatile fatty acids and on the development of swine dysentery. Zbl Vet Med B 1984; 31: 779–85.CrossRefGoogle ScholarPubMed
17.Prohaszka, L. Comparative studies on the antibacterial defence mechanism of volatile fatty acids in five animal species. Acta Vet Hungarica 1988; 36: 165–71.Google ScholarPubMed
18.Hampson, DJ, Cutler, R, Lee, BJ. Isolation of virulent Serpulina hyodysenteriae from a pig in a herd free from clinical dysentery. Vet Rec 1992; 131: 318–9.CrossRefGoogle Scholar
19.Mhoma, JRL, Hampson, DJ, Robertson, ID. A serological survey to determine the prevalence of infection with Treponema hyodysenteriae in Western Australia. Aust Vet J 1992; 69: 81–4.CrossRefGoogle ScholarPubMed
20.Kunkle, RA, Harris, DL, Kinyon, JM. Autoclaved liquid medium for propagation of Treponema hyodysenteriae. J Clin Microbiol 1986; 24: 669–71.CrossRefGoogle ScholarPubMed
21.Jenkinson, SR, Winger, CR. Selective medium for the isolation of Treponema hyodysenteriae. Vet Rec 1981; 109: 384–5.CrossRefGoogle ScholarPubMed
22.Hampson, DJ. Slide agglutination for rapid serological typing of Treponema hyodysenteriae. Epidemiol Infect 1991; 106: 541–7.CrossRefGoogle ScholarPubMed
23.Pethick, DW, Lindsay, DB, Barker, PJ, Northrop, AJ. Acetate supply and utilisation by the tissues of sheep. Br J Nutr 1981; 46: 97110.CrossRefGoogle ScholarPubMed
24.Stephen, AM. Whole grains-impact of consuming whole grains on physiological effects of dietary fiber and starch. Crit Rev Food Sci Nutr 1994; 34: 499511.CrossRefGoogle ScholarPubMed
25.Marsono, Y, Topping, DL. Complex carbohydrates in Australian rice products: influence of microwave cooking and food processing. Lebensm-Wiss u-Technol 1993; 26: 364–70.CrossRefGoogle Scholar
26.Coffman, WR, Juliano, BO. Rice. In: Nutritional qualities of cereal grains, Olson, WR, Frey, KJ, ed. Madison: American Society of Agronomy, 1987: 101–31.Google Scholar
27.Knudsen, KEB. Carbohydrates and lignin in feedstuffs. 44th Ann Meet E.A.A.P. 1993: 18.Google Scholar
28.Evans, AJ, Cheung, CKP. The carbohydrate composition of cotyledons and hull of cultivars of Lupinus angustifolius from Western Australia. J Sci Food Agric 1993; 61: 189–94.CrossRefGoogle Scholar
29.Kennelly, JJ, Aherne, FX, Sauer, WC. Volatile fatty acid production in the hindgut of swine. Can J Anim Sci 1981; 61: 349–61.CrossRefGoogle Scholar
30.Cranwell, PD. Microbial fermentation in the alimentary tract of the pig. Nutr Abst Rev 1968; 38: 721–30.Google ScholarPubMed
31.Russell, PL, Berry, CS, Greenwell, P. Characterisation of resistant starch from wheat and maize. J Cereal Sci 1989; 9: 115.CrossRefGoogle Scholar
32.Knudsen, KEB, Jensen, BB, Hansen, I. Oat bran but not a β-glucan-enriched oat fraction enhances butyrate production in the large intestine of pigs. J Nutr 1993; 123: 1235–47.CrossRefGoogle Scholar
33.Low, AG. Role of dietary fibre in pig diets. In: Recent advances in animal nutrition, Cole, DJA, Haresighn, W. eds. London: Butterworths, 1985: 87112.CrossRefGoogle Scholar
34.Topping, DL, Illman, RJ, Clarke, JM, Trimble, RP, Jackson, KA, Marsono, Y. Effects of dietary wheat bran, baked beans and oat bran on plasma lipids and large bowel volatile fatty acids in the pig. J Nutr 1992; 12: 3133–43.Google Scholar
35.Kidder, DE, Manners, MJ. Digestion in the pig. Bristol: Scientechnica, 1978: 96149.Google Scholar
36.Whipp, SC, Robinson, IM, Harris, DL, Glock, RD, Mathews, PJ, Alexander, TJL. Pathogenic synergism between Treponema hyodysenteriae and other selected anaerobes in gnotobiotic pigs. Infect Immun 1979; 26: 1042–7.CrossRefGoogle ScholarPubMed
37.Harris, DLT, Alexander, JL, Whipps, SC, Robinson, IM, Glock, RD, Mathews, PJ. Swine dysentery: studies of gnotobiotic pigs inoculated with Treponema hyodysenteriae, Bacteroides vulgatus, and Fusobacterium necrophorum. J Am Vet Med Assoc 1978; 172: 468–71.Google ScholarPubMed
38.Meyer, RC, Simon, J, Byerly, CS. The etiology of swine dysentery. III. The role of selected gram-negative obligate anaerobes. Vet Pathol 1975; 12: 4654.CrossRefGoogle ScholarPubMed
39.Suenaga, I, Yamazaki, T. Eliminating organisms against Treponema hyodysenteriae in the gut of mice. Zentralbl Bakteriol Mikrobiol Hyg Orig Reine A 1986; 261: 322–9.Google ScholarPubMed
40.Meyer, RC. Swine dysentery: a perspective. Adv Vet Sci Comp Med 1978; 22: 133–58.Google ScholarPubMed
41.Sharma, R, Schumacher, U, Ronaasen, V, Coates, M. Rat intestinal mucosal response to a microbial flora and different diets. Gut 1995; 36: 209–14.CrossRefGoogle ScholarPubMed
42.Milner, JA, Sellwood, R. Chemotactic response to mucin by Serpulina hyodysenteriae and other porcine spirochetes: a potential role in intestinal colonization. Infect Immun 1994; 62: 4095–9.CrossRefGoogle ScholarPubMed