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The effect of inulin and sugar beet fibre on Oesophagostomum dentatum infection in pigs

Published online by Cambridge University Press:  09 October 2003

S. PETKEVIČIUS
Affiliation:
Danish Centre for Experimental Parasitology, Department of Veterinary Microbiology, Royal Veterinary and Agricultural University, Dyrlægevej 100, Frederiksberg C, DK-1870 Copenhagen, Denmark Veterinary Institute of Lithuanian Veterinary Academy, Instituto 2, LT-4230 Kaišiadorys, Lithuania
K. E. BACH KNUDSEN
Affiliation:
Department of Animal Nutrition and Physiology, Danish Institute of Agricultural Sciences, Research Centre Foulum, P.O. Box 50, DK-8830 Tjele, Denmark
K. D. MURRELL
Affiliation:
Danish Centre for Experimental Parasitology, Department of Veterinary Microbiology, Royal Veterinary and Agricultural University, Dyrlægevej 100, Frederiksberg C, DK-1870 Copenhagen, Denmark
H. WACHMANN
Affiliation:
Veterinary and Food Advisory Service, Danish Bacon and Meat Council, Axeltorv 3, DK-1609 Copenhagen V, Denmark

Abstract

The present study was designed to assess the role of inulin and sugar beet fibres (SBF) on adult O. dentatum in growing pigs. Four experimental diets were formulated based on barley flour with added insoluble fibre from oat husk (Diet 1), a pure carbohydrate source inulin (Diet 2), soluble fibre from sugar beet fibre (SBF) with a high proportion of soluble fibre components (Diet 3) or inulin plus SBF (Diet 4). Thirty-two 10-week-old pigs were divided randomly into 4 groups each of 8 pigs. After 3 weeks adaptation on Diet 1 all pigs were infected with a single dose of 6000 L3O. dentatum. At week 7 p.i. one group was switched to Diet 2, another group to Diet 3 and another group to Diet 4. The remaining 8 pigs continued on Diet 1 until the end of the experiment and served as controls. At week 13, all pigs were necropsied and their worm burdens determined. The worm recoveries from the pigs on the inulin supplemented diet (Diet 2) were reduced by 97% compared to the controls (Diet 1). Further, the inulin-fed pigs exhibited markedly reduced faecal egg counts. The pigs on inulin plus SBF diet (Diet 4) and on SBF diet (Diet 3) had 86% and 70% adult worm reductions compared with the controls, respectively. The results from this study indicate that highly degradable and rapidly fermentable carbohydrates such as dietary inulin have a profound deworming effect on O. dentatum infection.

Type
Research Article
Copyright
2003 Cambridge University Press

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References

REFERENCES

ASSOCIATION OF OFFICIAL ANALYTICAL CHEMISTS (1990). Official methods of analysis. In Association of Official Analytical Chemists. Washington D.C.
BACH KNUDSEN, K. E. (1997). Carbohydrates and lignin of plant materials used in animal production. Animal Feed Science and Technology 67, 319338.CrossRefGoogle Scholar
BACH KNUDSEN, K. E. (2001). Development of antibiotic resistance and options to replace antimicrobials in animal diets. Proceedings of the Nutrition Society 60, 291299.Google Scholar
BACH KNUDSEN, K. E. & HESSOV, I. (1995). Recovery of inulin from Jerusalem artichoke (Helianthus tuberosus L.) in the small intestine of man. British Journal of Nutrition 74, 101113.Google Scholar
BACH KNUDSEN, K. E., JENSEN, B. B. & HANSEN, I. (1993). Digestion of polysaccharides and other major components in the small and large intestine of pigs fed diets consisting of oat fractions rich in β-D-glucan. British Journal of Nutrition 70, 537556.CrossRefGoogle Scholar
BACH KNUDSEN, K. E. & JØRGENSEN, H. (2001). Intestinal degradation of carbohydrates from birth to maturity. In Digestive Physiology in Pigs (ed. Lindberg, J. E. & Ogle, E.), pp. 109120. Wallingford, Oxon, CAB International.CrossRef
BACH KNUDSEN, K. E., JØRGENSEN, H. & CANIBE, N. (2000). Quantification of the absorption of nutrients derived from carbohydrate assimilation: model experiment with catheterized pigs fed on wheat- or oat based rolls. British Journal of Nutrition 84, 449458.Google Scholar
BJØRN, H., ROEPSTORFF, A. & NANSEN, P. (1996). A possible influence of diet composition on the establishment of nematodes in the pig. Veterinary Parasitology 63, 167171.CrossRefGoogle Scholar
BOISEN, S. & FERNANDEZ, J. A. (1998). Prediction of the total tract digestibility of energy in feedstuffs and pig diets by in vitro analyses. Animal Feed Science and Technology 68, 277286.Google Scholar
BRUNSGAARD, G. (1998). Effects of cereal type and feed particle size on morphological characteristics, epithelial cell proliferation, and lectin binding patterns in the large intestine of pigs. Journal of Animal Science 76, 27872798.CrossRefGoogle Scholar
COOP, R. L. & KYRIAZAKIS, I. (1999). Nutrition–parasite interaction. Veterinary Parasitology 84, 187204.CrossRefGoogle Scholar
COOP, R. L. & KYRIAZAKIS, I. (2001). Influence of host nutrition on the development and consequences of nematode parasitism in ruminants. Trends in Parasitology 17, 325330.CrossRefGoogle Scholar
CUMMINGS, J. H., ROBERTFROID, M. B., ANDERSON, H., BARTH, C. A.et al. (1997). A new look at dietary carbohydrate: chemistry, physiology and health. European Journal of Clinical Nutrition 51, 417423.CrossRefGoogle Scholar
GOODEY, T. (1926). Some stages in the development of Oesophagostomum dentatum from the pig. Journal of Helminthology 4, 191198.CrossRefGoogle Scholar
HAMMOND, J. A., FIELDING, D. & BISHOP, S. C. (1997). Prospects for plant anthelmintics in tropical veterinary medicine. Veterinary Research Communication 21, 1328.Google Scholar
JENSEN, M. T., COX, R. P. & JENSEN, B. B. (1995). Microbial production of skatole in the hind gut of pigs given different diets and its relation to skatole deposition in the back fat. Animal Science 61, 293304.CrossRefGoogle Scholar
JENSEN, T. K. & JØRGENSEN, C. M. (1994). Effect of dietary fiber on microbial activity and microbial gas production in various regions of the gastrointestinal tract of pigs. Applied and Environmental Microbiology 60, 18971904.Google Scholar
JIN, L., REYNOLDS, L. P., REDMER, D. A., CATON, J. S. & CRENSHAW, J. D. (1994). Effects of dietary fiber on intestinal growth, cell proliferation, and morphology in growing pigs. Journal of Animal Science 72, 22702278.CrossRefGoogle Scholar
JØRGENSEN, H., ZHAO, X.-Q. & EGGUM, B. O. (1996). The influence of dietary fibre and environmental temperature on the development of the gastrointestinal tract, digestibility, degree of fermentation in the hind-gut and energy metabolism in pigs. British Journal of Nutrition 75, 365378.CrossRefGoogle Scholar
KELLY-QUAGLIANA, K. A., BUDDINGTON, R. K., VAN LOO, J. & NELSON, P. D. (1998). Immunomodulation by oligofructose and inulin. In Nutritional and Health Benefits of Inulin and Oligofructose. NIH, Bethesda.
KEULS, M. (1952). The use of the studentized range in connection with an analysis of variance. Euphytica 1, 112122.CrossRefGoogle Scholar
KEUSCH, G. T. & FARTHING, M. J. (1995). Global impact of intestinal helminth infection. In Enteric Infection 2. Intestinal Helminths (ed. Farthing, M. J. G., Keusch, G. T. & Wakelin, D.), pp. 13. Chapman and Hall Medical, London.
KNOX, D. P. & SMITH, W. D. (2001). Vaccination against gastrointestinal nematode parasites of ruminants using gut-expressed antigens. Veterinary Parasitology 100, 2132.CrossRefGoogle Scholar
LARSEN, M. (2000). Prospects for controling animal parasitic nematodes by predacious micro fungi. Parasitology 120, S121S131.Google Scholar
LOW, A. G. (1989). Secretory response of the pig gut to non-starch polysaccharides. Animal Feed Science and Technology 23, 5565.CrossRefGoogle Scholar
McCORKIE, C. M. (1995). Back to the future: lessons from ethnoveterinary RD and E for studying and applying local knowledge. Agriculture and Human Values 12, 5281.CrossRefGoogle Scholar
MILLER, E. R. & ULLREY, D. E. (1987). The pig as a model for human nutrition. Annual Review of Nutrition 7, 361382.CrossRefGoogle Scholar
PETKEVIČIUS, S., BACH KNUDSEN, K. E., NANSEN, P. & MURRELL, K. D. (2001). The effect of dietary carbohydrates with different digestibility on the populations of Oesophagostomum dentatum in the intestinal tract of pigs. Parasitology 123, 315324.CrossRefGoogle Scholar
PETKEVIČIUS, S., BACH KNUDSEN, K. E., NANSEN, P., ROEPSTORFF, A., SKJØTH, F. & JENSEN, K. (1997). The impact of diets varying in carbohydrates resistant to endogenous enzymes and lignin on populations of Ascaris suum and Oesophagostomum dentatum in pigs. Parasitology 114, 555568.Google Scholar
PETKEVIČIUS, S., BJØRN, H., ROEPSTORFF, A., NANSEN, P., BACH KNUDSEN, K. E., BARNES, E. H. & JENSEN, K. (1995). The effect of two types of diet on populations of Ascaris suum and Oesophagostomum dentatum in experimentally infected pigs. Parasitology 111, 395402.CrossRefGoogle Scholar
PETKEVIČIUS, S., NANSEN, P., BACH KNUDSEN, K. E. & SKJØTH, F. (1999). The effect of increasing levels of insoluble dietary fibre on the establishment and persistence of Oesophagostomum dentatum in pigs. Parasite 6, 1726.CrossRefGoogle Scholar
POLDERMAN, A. M. & BLOTKAMP, J. (1995). Oesophagostomum infection in humans. Parasitology Today 11, 451456.CrossRefGoogle Scholar
PRATT, V. C., TAPPENDEN, K. A., McBURNEY, M. I. & FIEDL, C. J. (1996). Short-chain fatty acid supplemented total parenteral nutrition improves nonspecific immunity after intestinal resection in rats. Journal of Parenteral and Enteral Nutrition 20, 264271.CrossRefGoogle Scholar
ROEPSTORFF, A. & NANSEN, P. (1994). Epidemiology and control of helminth infections in pigs under intensive and non-intensive production systems. Veterinary Parasitology 54, 6985.CrossRefGoogle Scholar
ROEPSTORFF, A. & NANSEN, P. (1998). Epidemiology, diagnosis and control of helminth parasites of swine. FAO Animal Health Manual No 3.FAO, Rome, Italy.
SCHÜRCH, A. F., LOYD, L. E. & CRAMPTON, E. W. (1950). The use of chromic oxide as an index for determination the digestibility of a diet. Journal of Nutrition 50, 629636.Google Scholar
SLOTVED, H.-C., BARNES, E. H., BJØRN, H., CHRISTENSEN, C. M., ERIKSEN, L., ROEPSTORFF, A. & NANSEN, P. (1996). Recovery of Oesophagostomum dentatum from pigs by isolation of parasites migrating from large intestinal contents embedded in agar-gel. Veterinary Parasitology 63, 237245.CrossRefGoogle Scholar
STEAR, M. J. & MURRAY, M. (1994). Genetic resistance to parasitic disease. Veterinary Parasitology 54, 161176.CrossRefGoogle Scholar
STEWART, T. B. & GASBARRE, L. C. (1989). The veterinary importance of nodular worms (Oesophagostomum spp.). Parasitology Today 5, 209213.CrossRefGoogle Scholar
STOLDT, W. (1952). Vorschlag zur Vereinheitlichung der Fettbestimmung in Lebensmitteln. Fette, Seifen, Anstrichmittel 54, 206207.CrossRefGoogle Scholar
THEODOROPOULOS, G., HICKS, S. J., CORFIELD, A. P., MILLER, B. G. & CARRINGTON, S. D. (2001). The role of mucins in host–parasite interactions: Part II-helminth parasites. Trends in Parasitology 17, 130135.CrossRefGoogle Scholar
WALLER, P. J. (1993). Control strategies to prevent resistance. Veterinary Parasitology 46, 133142.CrossRefGoogle Scholar