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Effects of a dietary crude fibre concentrate on growth in weaned piglets

Published online by Cambridge University Press:  20 March 2017

P. Superchi*
Affiliation:
Department of Veterinary Science, University of Parma, Via del Taglio 10, 43126 Parma, Italy
R. Saleri
Affiliation:
Department of Veterinary Science, University of Parma, Via del Taglio 10, 43126 Parma, Italy
P. Borghetti
Affiliation:
Department of Veterinary Science, University of Parma, Via del Taglio 10, 43126 Parma, Italy
G. Ferrarini
Affiliation:
Department of Veterinary Science, University of Parma, Via del Taglio 10, 43126 Parma, Italy
V. Cavalli
Affiliation:
Department of Veterinary Science, University of Parma, Via del Taglio 10, 43126 Parma, Italy
M. Sereni
Affiliation:
Department of Veterinary Science, University of Parma, Via del Taglio 10, 43126 Parma, Italy
S. Zavattini
Affiliation:
Department of Veterinary Science, University of Parma, Via del Taglio 10, 43126 Parma, Italy
A. Sabbioni
Affiliation:
Department of Veterinary Science, University of Parma, Via del Taglio 10, 43126 Parma, Italy
*
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Abstract

Many fibre sources can help the adaptation of piglets at weaning, improving the growth. In this study, the effects of a dietary crude fibre concentrate (CFC) on piglet’s growth was investigated. From 31 to 51 days of age, 108 weaned piglets (D×(Lw×L)), had access to two isofibrous, isoenergetic and isonitrogenous diets, supplemented with 1% of CFC (CFC group) or not (control (CON) group). From days 52 to 64 all piglets received the same starter diet. During the dietary treatment period the CFC group showed higher average daily gain, average daily feed intake and feed efficiency (P<0.001) than CON group. At 64 days of age, BW was higher in CFC group compared with CON group (P<0.001). Blood samples were collected at days 31, 38, 45 and 52 of age. From days 31 to 52 significant differences in the somatotropic axis between groups were observed. In particular, growth hormone levels were higher only at the end of the 1st week of dietary treatment (P<0.05) in CFC group animals compared with CON group animals. The IGF-I trend was similar between groups even if the IGF-I levels were higher in the CFC group than CON group 1 week after starting treatment (P<0.01). The IGF-binding protein 3 (IGFBP-3) levels were higher in the first 2 weeks of dietary treatment and lower in the 3rd week in CON group compared with CFC group (P<0.01). Specifically, the IGFBP-3 profile was consistent with that of IGF-I in CFC group but not in CON group. At the same time, an increase of leptin in CFC compared with CON group was observed (P<0.05). Piglets fed the CFC diet showed a lower diarrhoea incidence (P<0.05) and a lower number of antibiotic interventions (P<0.05) than CON diet from 31 to 51 days of age. Pig-major acute-phase protein plasma level (P<0.01) and interleukin-6 gene expression (P<0.05) were higher in CON group than CFC group at the end of 1st week of dietary treatment. In conclusion, this study showed that CFC diet influences the hormones related to energy balance enhancing the welfare and growth of piglets. Furthermore, the increase in feed intake during 3 weeks of dietary treatment improved the feed efficiency over the entire post-weaning period.

Type
Research Article
Copyright
© The Animal Consortium 2017 

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References

Bach Knudsen, KE, Hedemann, MS and Lærke, HN 2012. The role of carbohydrates in intestinal health of pigs. Animal Feed Science and Technology 173, 4153.CrossRefGoogle Scholar
Baratta, M, Saleri, R, Mainardi, GL, Valle, D, Giustina, A and Tamanini, C 2002. Leptin regulates growth hormone gene expression and secretion and nitric oxide production in pig pituitary cells. Endocrinology 143, 551557.Google Scholar
Borghetti, P, Morganti, M, Saleri, R, Ferrari, L, De Angelis, E, Cavalli, V, Cacchioli, A, Corradi, A and Martelli, P 2013. Innate pro-inflammatory and adaptive immune cytokines in PBMC of vaccinated and unvaccinated pigs naturally exposed to porcine circovirus type 2 (PCV2) infection vary with the occurrence of the disease and the viral burden. Veterinary Microbiology 163, 4253.Google Scholar
Borghetti, P, Saleri, R, Mocchegiani, E, Corradi, A and Martelli, P 2009. Infection, immunity and the neuroendocrine response. Veterinary Immunology and Immunopathology 130, 141162.Google Scholar
Campbell, JM, Crenshaw, JD and Polo, J 2013. The biological stress of early weaned piglets. Journal of Animal Science and Biotechnology 4, 1922.Google Scholar
Ferrari, L, Borghetti, P, Gozio, S, De Angelis, E, Ballotta, L, Smeets, J, Blanchaert, A and Martelli, P 2011. Evaluation of the immune response induced by intradermal vaccination by using a needle-less system in comparison with the intramuscular route in conventional pigs. Research in Veterinary Science 90, 6471.Google Scholar
Fisher, T, Buttner, M and Rziha, HJ 2006. T helper 1-type cytokine transcription in peripheral blood mononuclear cells of pseudorabies virus (Suid herpesvirus 1)-primed swine indicates efficient immunization. Immunology 101, 378387.CrossRefGoogle Scholar
Gautron, L and Elmquist, JK 2011. Sixteen years and counting: an update on leptin in energy balance. Journal of Clinical Investigation 121, 20872093.Google Scholar
Gerritsen, R, van der Aar, P and Molist, F 2012. Insoluble nonstarch polysaccharides in diets for weaned piglets. Journal of Animal Science 90, 318320.CrossRefGoogle ScholarPubMed
Grau-Roma, L, Heegaard, PM, Hjulsager, CK, Sibila, M, Kristensen, CS, Allepuz, A, Piñeiro, M, Larsen, LE, Segalés, J and Fraile, L 2009. Pig-major acute phase protein and haptoglobin serum concentrations correlate with PCV2 viremia and the clinical course of postweaning multisystemic wasting syndrome. Veterinary Microbiology 138, 5361.Google Scholar
Hedemann, MS, Eskildsen, M, Laerke, HN, Pedersen, C, Lindberg, JE, Laurinen, P and Bach Knudsen, KE 2006. Intestinal morphology and enzymatic activity in newly weaned pigs fed contrasting fiber concentrations and fiber properties. Journal of Animal Science 84, 13751386.Google Scholar
Hevener, W, Almond, GW, Armstrong, JD and Richards, RG 1997. Effects of acute endotoxemia on serum somatotropin and insulin-like growth factor I concentrations in prepubertal gilts. American Journal of Veterinary Research 58, 10101013.Google Scholar
Jha, R and Berrocoso, JD 2015. Review: dietary fiber utilization and its effects on physiological functions and gut health of swine. Animal 9, 14411452.Google Scholar
Lahtinen, P, Liukkonen, S, Pere, J, Sneck, A and Kangas, H 2014. A comparative study of fibrillated fibers from different mechanical and chemical pulps. BioResources 9, 21152127.Google Scholar
Lim, VP Jr, Juan, JJ, Celestino, OF, San Andres, JV and Martin, EA 2013. Beneficial effects of insoluble raw fiber concentrate addition to layer diet. Philippines Journal of Veterinary and Animal Sciences 39, 4352.Google Scholar
Lindberg, JE 2014. Fiber effects in nutrition and gut health in pigs. Journal of Animal Science and Biotechnology 5, 1521.Google Scholar
Livak, KJ and Schmittgen, TD 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) method. Methods 25, 402408.Google Scholar
Meissonnier, GM, Pinton, P, Laffitte, J, Cossalter, AM, Gong, YY, Wild, CP, Bertin, G, Galtier, P and Oswald, IP 2008. Immunotoxicity of aflatoxin B1: impairment of the cell-mediated response to vaccine antigen and modulation of cytokine expression. Toxicology and Applied Pharmacology 231, 142149.Google Scholar
Molist, F, Gómez de Segura, A, Gasa, J, Hermes, RG, Manzanilla, EG, Anguita, M and Pérez, JF 2009. Effects of dietary fibre on physicochemical characteristics of digesta, microbial activity and gut maturation in early weaned piglets. Animal Feed Science and Technology 149, 346353.CrossRefGoogle Scholar
Montagne, L, Pluske, JR and Hampson, DJ 2003. A review of interactions between dietary fiber and the intestinal mucosa, and their consequences on digestive health in young non-ruminants animals. Animal Feed Science and Technology 108, 95117.Google Scholar
Noblet, J and Perez, JM 1993. Prediction of digestibility of nutrients and energy values of pig diets from chemical analysis. Journal of Animal Science 71, 33893398.Google Scholar
Odle, AK, Haney, A, Allensworth-James, M, Akhter, N and Childs, GV 2014. Adipocyte versus pituitary leptin in the regulation of pituitary hormones: somatotropes develop normally in the absence of circulating leptin. Endocrinology 155, 43164328.Google Scholar
Piñeiro, C, Piñeiro, M, Morales, J, Carpintero, R, Campbell, FM, Eckersall, PD, Toussaint, MJM, Alava, MA and Lampreave, F 2007. Pig acute-phase protein levels after stress induced by changes in the pattern of food administration. Animal 1, 133139.Google Scholar
SAS Institute Inc. 2012. Statistical Analysis System (SAS), user’s guide: statistics (version 9.4). SAS Institute Inc., Cary, NC, USA.Google Scholar
Slifierz, MJ, Friendship, R, de Lange, CFM, Slavic, D, Grgic, H and Farzan, A 2014. Immunomodulatory factors and infectious agents associated with the hepatic gene expression of the IGF system in nursery pigs. Animal 8, 844851.CrossRefGoogle ScholarPubMed
Summer, A, Saleri, R, Malacarne, M, Bussolati, S, Beretti, V, Sabbioni, A and Superchi, P 2009. Leptin in sow: influence on the resumption of cycle activity after weaning and on the piglet gain. Livestock Science 124, 107111.Google Scholar
Ulbrich, M and Flöter, E 2014. Impact of high pressure homogenization modification of a cellulose based fiber product on water binding properties. Food Hydrocolloids 41, 281289.CrossRefGoogle Scholar
Van Soest, PJ and Wine, RH 1967. Use of detergents in the analysis of fibrous feeds. IV. Determination of plant cell-wall constituents. Journal of the Association of Official Analytical Chemists 50, 5055.Google Scholar
von der Hardt, K, Kandler, MA, Fink, L, Schoof, E, Dotsch, J, Brandenstein, O, Bohle, RM and Rascher, W 2004. High frequency oscillatory ventilation suppresses inflammatory response in lung tissue and microdissected alveolar macrophages in surfactant depleted piglets. Pediatric Research 55, 339346.Google Scholar