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Performance of weanling piglets offered low-, medium- or high-lactose diets supplemented with a seaweed extract from Laminaria spp.

Published online by Cambridge University Press:  01 January 2009

D. A. Gahan ,
M. B. Lynch ,
J. J. Callan ,
J. T. O’Sullivan  and
J. V. O’Doherty
D. A. Gahan
Affiliation:
UCD School of Agriculture, Food Science and Veterinary Medicine, Lyons Research Farm, Newcastle, Co. Dublin, Ireland
M. B. Lynch
Affiliation:
UCD School of Agriculture, Food Science and Veterinary Medicine, Lyons Research Farm, Newcastle, Co. Dublin, Ireland
J. J. Callan
Affiliation:
UCD School of Agriculture, Food Science and Veterinary Medicine, Lyons Research Farm, Newcastle, Co. Dublin, Ireland
J. T. O’Sullivan
Affiliation:
Bioatlantis Ltd, Tom Crean Business Centre, Kerry Technology Park, Tralee, County Kerry, Ireland
J. V. O’Doherty*
Affiliation:
UCD School of Agriculture, Food Science and Veterinary Medicine, Lyons Research Farm, Newcastle, Co. Dublin, Ireland
*
E-mail: john.vodoherty@ucd.ie
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Abstract

An experiment (3 × 4 factorial arrangement) was conducted to investigate the interaction between different levels of lactose (60 v. 150 v. 250 g/kg) and seaweed extract (0 v. 1 v. 2 v. 4 g/kg) containing both laminarin and fucoidan derived from Laminaria spp. on growth performance and nutrient digestibility of weanling pigs. In all, 384 piglets (24 days of age, 7.5 kg (s.d. 1 kg) live weight) were blocked on the basis of live weight and were assigned to one of 12 dietary treatments (eight replicates per treatment). Piglets were offered diets containing either low (60 g/kg), medium (150 g/kg) or high (250 g/kg) lactose levels with one of the following levels of seaweed extract additive: (1) 0 g/kg, (2) 1 g/kg, (3) 2 g/kg or (4) 4 g/kg seaweed extract. The pigs were offered the diets ad libitum for 21 days post weaning. There was a significant lactose × seaweed extract interaction (P < 0.05) in average daily gain (ADG) during the experimental period (days 0 to 21). At the low and medium levels of lactose, there was an increase in ADG as the level of seaweed extract increased to 2 g/kg (P < 0.05). However, at the high level of lactose there was no further response in ADG as the level of seaweed extract increased above 1 g/kg. There was a significant lactose × seaweed extract interaction during the experimental period (days 0 to 21) (P < 0.05) on the food conversion ratio (FCR). At the low level of lactose, there was a significant improvement in FCR as the levels of seaweed extract increased to 4 g/kg (P < 0.01). At the medium level of lactose, there was a significant improvement in FCR as seaweed extract increased to 2 g/kg. However, there was no significant effect of seaweed extract on FCR at the high levels of lactose (P > 0.05). There was a linear increase in average daily feed intake (ADFI) during the experimental period (days 0 to 21) (P < 0.05) as levels of seaweed extract increased. There was a linear increase in ash digestibility (P < 0.01) during the experimental period (days 0 to 21) as the level of lactose increased. There was a quadratic decrease (P < 0.01) in nitrogen (N) and neutral detergent fibre digestibility as the levels of lactose increased. In conclusion, pigs responded differently to the inclusion levels of seaweed extract at each level of lactose supplementation. The inclusion of a laminarin–fucoidan extract in piglet diets may alleviate the use for high-lactose diets (>60 g/kg) and would also alleviate some of the common problems that occur post weaning.

Keywords

lactose, laminarinfucoidanpig
Type
Full Paper
Information
animal , Volume 3 , Issue 1 , January 2009 , pp. 24 - 31
Copyright
Copyright © The Animal Consortium 2008

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References

Alexopoulos, C, Georgoulakis, IE, Tzivara, A, Kyriakis, CS, Govaris, A, Kyriakis, SC 2004. Field evaluation of the effect of a probiotic-containing Bacillus licheniformis and Bacillus subtilis spores on the health status, performance, and carcass quality of grower and finisher pigs. Journal of Veterinary Medicine 51, 306–312.CrossRefGoogle ScholarPubMed
Allen, VG, Pond, KR, Saker, KE, Fontenot, JP, Bagley, CP, Ivy, RL, Evans, RR, Schmidt, RE, Fike, JH, Zhang, X, Ayad, JY, Brown, CP, Miller, MF, Montgomery, JL, Mahan, J, Wester, DB, Melton, C 2001. Tasco: influence of a brown seaweed on antioxidants in forages and livestock – a review. Journal of Animal Science 79, E21–E31.CrossRefGoogle Scholar
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. 123–140. Nottingham University Press, London, UK.Google Scholar
Cummings, JH, Macfarlane, GT 1991. The control and consequences of bacterial fermentation in the human colon. Journal of Applied Bacteriology 70, 443–459.CrossRefGoogle ScholarPubMed
Devillé, C, Damas, J, Forget, P, Dandrifosse, G, Peulen, O 2004. Laminarin in the dietary fibre concept. Journal of the Science of Food and Agriculture 84, 1030–1038.CrossRefGoogle Scholar
Dritz, SS, Shi, J, Kielian, TL, Goodband, RD, Nelssen, JL, Tokach, MD, Chengappa, MM, Smith, JE, Blecha, F 1995. Influence of dietary beta-glucan on growth performance, nonspecific immunity, and resistance to Streptococcus suis infection in weanling pigs. Journal of Animal Science 73, 3341–3350.CrossRefGoogle ScholarPubMed
Ekstrom, KE, Benevenga, NJ, Grummer, H 1975. Changes in the intestinal lactase in the small intestine of two breeds of swine from birth to 6 weeks of age. Journal of Nutrition 105, 1032–1038.CrossRefGoogle ScholarPubMed
Estrada, A, Drew, MD, Van Kessel, A 2001. 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, 141–148.CrossRefGoogle Scholar
Gardiner, GE, Campbell, AJ, O’Doherty, JV, Pierse, E, Lynch, PB, Leonard, FC, Stanton, C, Ross, RP, Lawlor, PG 2008. Effects 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, 259–273.CrossRefGoogle Scholar
Kim, KI, Jewell, DE, Benevenga, NJ, Grummer, RH 1978. The fraction of dietary lactose available for fermentation in the caecum and colon of pigs. Journal of Animal Science 46, 1658–1665.CrossRefGoogle ScholarPubMed
Kogan, G, Masler, L, Šandula, J, Navarová, J, Trnovec, T 1989. Recent results on the structure and immunomodulating activities of yeast glucan. In Biomedical and biotechnological advances in industrial polysaccharides (ed. V Crescenzi, ICM Dea, S Paoletti, SS Stivala and IW Sutherland), pp. 251–258. Gordon and Breach Science Publishers, New York.Google Scholar
Kyriakis, SC, Tsiloyiannis, VK, Vlemmas, J, Sarris, K, Tsinas, AC, Alexopoulos, C, Jansegers, L 1999. The effect of probiotic LSP 122 on the control of post-weaning diarrhoea syndrome of piglets. Research in Veterinary Science 67, 223–228.CrossRefGoogle ScholarPubMed
Lassen, SF, Breinholt, J, Ostergaard, PR, Brugger, R, Bischoff, A, Wyss, M, Fuglsang, CC 2001. Expression, gene cloning, and characterization of five novel phytases from four b asidiomycete fungi: Peniophora lycii, Agrocybe pediades, a Ceriporia sp., and Trametes pubescens. Applied and Environmental Microbiology 67, 4701–4707.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, 1091–1094.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, 349–364.CrossRefGoogle Scholar
Macfarlane, S, Macfarlane, GT 2003. Regulation of short-chain fatty acid production. The Proceedings of the Nutrition Society 62, 67–72.CrossRefGoogle ScholarPubMed
Majtán, J, Kogan, G, Kováčová, E, Bíliková, K, Šimúth, J 2005. Stimulation of TNF-α release by fungal cell wall polysaccharides. Zeitschrift fur Naturforschung. Section C. Biosciences 60c, 921–926.CrossRefGoogle 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, 19–26.CrossRefGoogle ScholarPubMed
Ministry of Agriculture, Fisheries and Food 1991. The Feeding Stuffs Regulations 1991. Statutory Instrument No 2840, 9. Her Majesty Stationery Office, London, p. 76.Google Scholar
O’Connell, JM, Callan, JJ, O’Doherty, JV 2005a. The interaction between cereal type and lactose level on piglet performance post weaning. Animal Science 81, 265–269.CrossRefGoogle Scholar
O’Connell, JM, Sweeney, T, Callan, JJ, O’Doherty, JV 2005b. 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, 357–364.CrossRefGoogle Scholar
O’Doherty, JV, Nolan, CS, Callan, JJ, McCarthy, P 2004. The interaction between lactofeed level and soya bean meal on growth performance of weanling pigs. Journal of Animal Science 78, 419–427.CrossRefGoogle Scholar
O’Doherty, JV, Nolan, CS, McCarthy, PC 2005. Interaction between lactose levels and antimicrobial growth promoters on growth performance of weanling pigs. Journal of the Science of Food and Agriculture 85, 371–380.CrossRefGoogle Scholar
Percival E and Mc Dowell RH 1967. Chemistry and enzymology of marine algae polysaccharides, pp. 53–71. Mag Westerlo, London.Google 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, 313–318.CrossRefGoogle Scholar
Pierce, KM, Sweeney, T, Brophy, PO, Callan, JJ, Fitzpatrick, E, McCarthy, P, O’Doherty, JV 2006. The effect of lactose and inulin on intestinal morphology, selected microbial populations and volatile fatty acid concentration in the gastrointestinal tract of the weanling pig. Animal Science 82, 311–318.CrossRefGoogle Scholar
Pluske, JR, Thompson, MJ, Atwood, CS, Bird, PH, Williams, IH, Hartmann, PE 1996. Maintenance of villus height and crypt depth, and enhancement of disaccharide digestion and monosaccharide absorption, in piglets fed on cows’ whole milk after weaning. British Journal of Animal Nutrition 76, 409–422.CrossRefGoogle ScholarPubMed
Reale, A, Konietzny, U, Coppola, R, Sorrentino, E, Greiner, R 2007. The importance of lactic acid bacteria for phytate degradation during cereal dough fermentation. Journal of Agriculture and Food Chemistry 55, 2993–2997.CrossRefGoogle ScholarPubMed
Reilly P, Sweeney T, Pierce KM, Callan JJ, Julka A and O’Doherty JV 2008. The effect of seaweed extract inclusion on gut health and immune status of the weaned pig. Animal (In press).Google Scholar
Schoenherr, WD, Pollmann, DS, Coalson, JA 1994. Titration of MacroGuard™-S on growth performance of nursery pigs. Journal of Animal Science 72 (suppl. 2), 57.Google Scholar
Shibata, H, Limuro, M, Uchiya, N, Kawamori, T, Nagaoka, M, Ueyama, S, Hashimoto, S, Yokokura, T, Sugimura, T, Wakabayashi, K 2003. Preventive effects of Cladosiphon fucoidan against Helicobacter pylori in Mongolian gerbils. Helicobacter 8, 59–65.CrossRefGoogle ScholarPubMed
Statistical Analysis Systems Institute 1985. Statistical analysis systems, version 6.12. SAS Institute Inc., Cary, NC.Google Scholar
Tokach, MD, Nelssen, JL, Allee, GL 1989. Effect of protein and (or) carbohydrate fractions of dried whey on performance and nutrient digestibility of early weaned pigs. Journal of Animal Science 67, 1307–1312.CrossRefGoogle ScholarPubMed
Turner, JL, Dritz, SS, Higgins, JJ, Minton, JE 2002. Effects of Ascophyllum nodosum extract on growth performance and immune function of young pigs challenged with Salmonella typhimurium. Journal of Animal Science 80, 1947–1953.CrossRefGoogle ScholarPubMed
Usov, AI, Smirnova, GP, Klochkova, NG 2001. Algae polysaccharides. 55. Polysaccharide composition of some brown Kamchatka algae. Bioorganicheskaia Khimiia 27, 444–448.Google ScholarPubMed
Whittemore, CT 1993. The science and practice of pig production. Longman, Harlow, UK.Google Scholar
Williams, CH, David, DJ, Iismaa, O 1962. The determination of chromic oxide in faeces samples by atomic absorption spectrophotometry. Journal of Animal Science 63, 381–385.Google Scholar
Williams, BA, Verstegen, MWA, Tamminga, S 2001. Fermentation in the large intestine of single stomached animals and its relationship to human health. Nutrition Research Reviews 14, 207–227.CrossRefGoogle Scholar
Zhuang, C, Itoh, H, Mizuno, T, Ito, H 1995. Antitumor active fucoidan from the brown seaweed, umitoranoo (Sargassum thunbergii). Bioscience, Biotechnology, and Biochemistry 59, 563–567.CrossRefGoogle ScholarPubMed
Zvyagintseva, TN, Shevchenko, NM, Popivnich, IB, Isakov, VV, Scobun, AS, Sundukova, EV, Elyakova, LA 1999. A new procedure for the separation of water-soluble polysaccharides from brown seaweeds. Carbohydrate Research 322, 32–39.CrossRefGoogle Scholar
Zvyagintseva, TN, Shevchenko, NM, Chizhov, AO, Krupnova, TN, Sundukova, EV, Isakov, VV 2003. Water-soluble polysaccharides of some far-eastern brown seaweeds. Distribution, structure, and their dependence on the developmental conditions. Journal of Experimental Marine Biology and Ecology 294, 1–13.CrossRefGoogle Scholar