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The effect of dietary laminarin and fucoidan in the diet of the weanling piglet on performance, selected faecal microbial populations and volatile fatty acid concentrations

Published online by Cambridge University Press:  16 November 2009

P. McDonnell
Affiliation:
UCD School of Agriculture, Food Science and Veterinary Medicine, University College Dublin, Lyons Research Farm, Newcastle, Dublin, Ireland
S. Figat
Affiliation:
UCD School of Agriculture, Food Science and Veterinary Medicine, University College Dublin, Lyons Research Farm, Newcastle, Dublin, Ireland
J. V. O’Doherty*
Affiliation:
UCD School of Agriculture, Food Science and Veterinary Medicine, University College Dublin, Lyons Research Farm, Newcastle, Dublin, Ireland
*
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Abstract

A 2 × 2 factorial experiment (n = 12 replicates per treatment, 4 pigs per replicate) was performed to investigate the effects of seaweed extracts, laminarin (derived ß-glucans) and fucoidan (sulphated polysaccharides), independently or in combination on post-weaning piglet performance and selected microbial populations. At weaning, the piglets (24 days of age, 6.4 kg live weight) were assigned to one of the four dietary treatments: (T1) basal diet, (T2) basal diet with 300 p.p.m. laminarin, (T3) basal diet with 240 p.p.m. fucoidan, (T4) basal diet with 300 p.p.m. laminarin and 240 p.p.m. fucoidan. Pigs offered diets supplemented with laminarin had an increased daily gain (P < 0.01), and gain-to-feed ratio (P < 0.05) compared to pigs offered diets without laminarin supplementation during the experimental period (days 0 to 21). Pigs offered laminarin-supplemented diets had an increased faecal dry matter and reduced diarrhoea (P < 0.05) during the critical 7 to 14 day period. Pigs offered diets containing laminarin had reduced faecal Escherichia coli populations. There was a significant interaction (P < 0.01) on faecal Lactobacilli populations between laminarin and fucoidan. Pigs offered the fucoidan diet had an increased Lactobacilli population compared to pigs offered the basal diet. However, there was no effect of fucoidan on faecal Lactobacilli populations when laminarin was added. Overall, the reduction in E. coli population and the increase in daily gain suggest that laminarin may provide a dietary means to improve gut health after weaning.

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Copyright
Copyright © The Animal Consortium 2009

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References

Berteau, O, Mulloy, B 2003. Sulfated fucans, fresh perspectives: structures, functions, and biological properties of sulfated fucans and an overview of enzymes active toward this class of polysaccharide. Glycobiology 13, 2940.CrossRefGoogle Scholar
Brown, GD, Gordon, S 2005. Immune recognition of fungal β-glucans. Cellular Microbiology 7, 471479.CrossRefGoogle ScholarPubMed
Close, WH 1994. Feeding new genotypes: establishing amino acid/energy requirements. In Principles of pig science (ed. DJA Cole, J Wiseman and MA Varley), pp. 123140. Nottingham University Press, London.Google Scholar
Dillon, S, Sweeney, T, Callan, JJ, O’ Doherty, JV 2009. The effects of lactose inclusion and seaweed extract on performance, nutrient digestibility and microbial populations in newly weaned piglets. 11th International Symposium on Digestive Physiology of Pigs, Hotel Termes de Montbrió, Montbrió del Camp, Costa Daurada, Spain, 20–22 May 2009, abstract 5.30, p. 151.Google Scholar
Drew, MD, Van Kessel, AG, Estrada, AE, Ekpe, ED, Zijlstra, RT 2002. Effect of dietary cereal on intestinal bacterial populations in weaned pigs. Canadian Journal of Animal Science 82, 607609.CrossRefGoogle Scholar
Estrada, A, Drew, MD, Van Kessel, A 2000. Effect of the dietary supplementation of fructooligosaccharides and Bifidobacterium longum to early-weaned pigs on performance and fecal bacterial populations. Canadian Journal of Animal Science 81, 141148.CrossRefGoogle Scholar
Gahan, DA, Lynch, MB, Callan, JJ, Julka, A, O’Doherty, JV 2009. Performance of weanling piglets offered low, medium or high lactose diets supplemented with a seaweed extract from Laminaria Hyperborea. Animal 3, 2431.CrossRefGoogle ScholarPubMed
Gardiner, GE, Campbell, AJ, O’Doherty, JV, Pierce, E, Lynch, PB, Leonard, FC, Stanton, C, Ross, RP, Lawlor, PG 2008. Effect of Ascophyllum nodosum extract on growth performance, digestibility, carcass characteristics and selected intestinal microflora populations of grower-finisher pigs. Animal Feed Science and Technology 141, 259273.CrossRefGoogle Scholar
Huisman, J, Tolman, GH 1992. Antinutritional factors in plant proteins of diets for non ruminants. In Recent advances in animal nutrition (ed. PC Garnsworthy, W Haresign and DJA Cole), pp. 331. Butterworth-Heinemann Ltd, Oxford.CrossRefGoogle Scholar
Kogan, G, Kocher, A 2007. Role of yeast cell wall polysaccharides in pig nutrition and health protection. Livestock Science 10th International Symposium on Digestive Physiology in Pigs, Denmark 2006, Part 2, 109, pp. 161–165.CrossRefGoogle Scholar
Lee, JB, Hayashi, K, Hashimoto, M, Nakano, T, Hayashi, T 2004. Novel antiviral fucoidan from sporophyll of Undaria pinnatifida (Mekabu). Chemical and Pharmaceutical Bulletin 52, 10911094.CrossRefGoogle ScholarPubMed
Lynch, MB, Callan, JJ, O’Doherty, JV 2007. The interaction between lactose level and enzyme supplementation and form of barley processing on performance, digestibility and faecal volatile fatty acid concentration of weanling pigs fed barley based diets. Animal Feed Science and Technology 140, 349364.CrossRefGoogle Scholar
Lynch, MB, Sweeney, T, Callan, JJ, O’Sullivan, JT, O’Doherty, JV 2009. The effect of laminaria hyperborea derived laminarin and fucoidan on nutrient digestibility, nitrogen utilisation, intestinal microflora and volatile fatty acid concentrations in pigs. 11th International Symposium on Digestive Physiology of Pigs, Hotel Termes de Montbrió, Montbrió del Camp, Costa Daurada, Spain, 20–22 May, 2009, abstract 2.24, p. 68.Google Scholar
McClure, MO, Moore, JP, Blanc, DF, Scotting, P, Cook, GM, Keynes, RJ, Weber, JN, Davies, D, Weiss, RA 1992. Investigations into the mechanism by which sulfated polysaccharides inhibit HIV infection in vitro. AIDS Research and Human Retroviruses 8, 1926.CrossRefGoogle ScholarPubMed
Macfarlane, S, Macfarlane, GT 2003. Regulation of short-chain fatty acid production. The proceedings of the nutrition society 62, 6772.CrossRefGoogle ScholarPubMed
Michel, C, Lahaye, M, Bonnet, C, Mabeau, S, Barry, J-L 1996. In vitro fermentation by human faecal bacteria of total and purified dietary fibres from brown seaweeds. British Journal of Nutrition 75, 263280.CrossRefGoogle ScholarPubMed
Miller, BG, Newby, TJ, Stokes, CR, Bourne, FJ 1984. Influence of diet on postweaning malabsorption and diarrhoea in the pig. Research in Veterinary Science 36, 187193.CrossRefGoogle ScholarPubMed
O’Connell, JM, Sweeney, T, Callan, JJ, O’Doherty, JV 2005. The effect of cereal type and exogenous enzyme supplementation in pig diets on nutrient digestibility, intestinal microflora, volatile fatty acid concentration and manure ammonia emissions from finisher pigs. Animal Science 81, 357364.CrossRefGoogle Scholar
O’Connell, M, Callan, JJ, O’Doherty, JV 2006. The effect of dietary crude protein level, cereal type and exogenous enzyme supplementation on nutrient digestibility, nitrogen excretion, faecal volatile fatty acid concentration and ammonia emissions from pigs. Animal Feed Science and Technology 127, 7388.CrossRefGoogle Scholar
O’Doherty, JV, Nolan, CS, McCarthy, P 2004. Interaction between lactofeed level and soybean meal on growth performance of weanling pigs. Animal Science 78, 419427.CrossRefGoogle Scholar
Pierce, KM, Callan, JJ, McCarthy, P, O’ Doherty, JV 2005. Performance of weanling pigs offered low or high lactose diets supplemented with avilamycin or inulin. Animal Science 80, 313318.CrossRefGoogle Scholar
Pierce, KM, Callan, JJ, Brophy, PO, McCarthy, P, Sweeney, T, Fitzpatrick, E, Byrne, C, NiCheallaigh, S, O’Doherty, JV 2006. The effect of lactose and inulin on intestinal morphology, microbiology and volatile fatty acids of the weanling pig. Animal Science 82, 311318.CrossRefGoogle Scholar
Pierce, KM, Callan, JJ, McCarthy, P, O’Doherty, JV 2007. The interaction between lactose level and crude protein concentrations on piglet post-weaning performance, nitrogen metabolism, selected faecal microbial populations and faecal volatile fatty acid concentrations. Animal Feed Science and Technology 132, 267382.CrossRefGoogle Scholar
Pluske, JR, Hampson, DJ, Williams, IH 1997. Factors influencing the structure and function of the small intestine in the weaned pig: a review. Livestock Production Science 51, 215236.CrossRefGoogle Scholar
Prohaszka, L, Baron, F 1980. The predisposing role of high dietary protein supplies in enteropathogenic Escherichia coli infections in weaned pigs. Zentralbl. Veterinarmed. [C] 27B, 222232.Google Scholar
Reilly, P, Sweeney, T, Pierce, KM, Callan, JJ, Julka, A, O’Doherty, JV 2008. The effect of seaweed extract inclusion on gut health and immune status of the weaned pig. Animal 2, 14651473.CrossRefGoogle Scholar
Rice, PJ, Adams, EL, Ozment-Skelton, T, Gonzalez, AJ, Goldman, MP, Lockhart, BE 2006. Oral delivery and gastrointestinal absorption of soluble glucans stimulate increased resistance to infectious challenge. Journal of Pharmacology and Experimental Therapeutics 314, 10791086.CrossRefGoogle Scholar
Rupérez, P, Ahrazem, O, Leal, JA 2002. Potential antioxidant capacity of sulfated polysaccharides from the edible marine brown seaweed: fucus vesiculosus. Journal of Agricultural and Food Chemistry 50, 840845.CrossRefGoogle ScholarPubMed
Salyers, AA 1979. Energy sources of major intestinal fermentative anaerobes. The American Journal of Clinical Nutrition 32, 158163.CrossRefGoogle ScholarPubMed
Salyers, AA, West, SEH, Vercellotti, JR, Wilkins, TD 1977. Fermentation of mucins and plant polysaccharides by anaerobic bacteria from the human colon. Applied and Environmental Microbiology 34, 529533.CrossRefGoogle ScholarPubMed
Sauvant, D, Perez, J-M, Tran, G 2004. Tables of Composition and Nutritional Value of Feed Materials. Pigs, Poultry, Cattle, Sheep, Goats, Rabbits, Horses, Fish. Wageningen Academic Publishers, The Netherlands.CrossRefGoogle Scholar
Smith, HW, Jones, JET 1963. Observations on the alimentary tract and its bacteria flora in healthy and diseased pigs. The Journal of Pathology and Bacteriology 86, 387412.CrossRefGoogle ScholarPubMed
Statistical Analysis Systems Institute (SAS) 1985. Statistical analysis systems, version 6.12. SAS Institute Inc., Cary, NC.Google Scholar
Usov, AI, Smirnova, GP, Klochkova, NG 2001. Algae polysaccharides. 55. Polysaccharide composition of some brown kamchatka algae. Bioorganicheskaia Khimiia 27, 444448.Google ScholarPubMed
Van Soest, PJ, Robertson, JB, Lewis, BA 1991. Methods for dietary fiber, neutral detergent fiber and non starch polysaccharides in relation to animal nutrition. Journal of Dairy Science 74, 35833597.CrossRefGoogle ScholarPubMed
Zhuang, C, Itoh, H, Mizuno, T, Ito, H 1995. Antitumor active fucoidan from the brown seaweed, umitoranoo (Sargassum thunbergii). Bioscience, Biotechnology, and Biochemistry 59, 563567.CrossRefGoogle ScholarPubMed