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Dietary supplementation with ovine serum immunoglobulin attenuates acute effects on growth, organ weights, gut morphology and intestinal mucin production in the growing rat challenged with Salmonella enteritidis

Published online by Cambridge University Press:  27 May 2011

P. Balan
Affiliation:
Riddet Institute, Massey University, Private Bag 11 222, Palmerston North, New Zealand
K. S. Han
Affiliation:
Riddet Institute, Massey University, Private Bag 11 222, Palmerston North, New Zealand
S. M. Rutherfurd
Affiliation:
Riddet Institute, Massey University, Private Bag 11 222, Palmerston North, New Zealand
H. Singh
Affiliation:
Riddet Institute, Massey University, Private Bag 11 222, Palmerston North, New Zealand
P. J. Moughan*
Affiliation:
Riddet Institute, Massey University, Private Bag 11 222, Palmerston North, New Zealand
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Abstract

The aim was to determine the effect of orally administered ovine serum immunoglobulin (Ig) on growth performance, organ weight, gut morphology and mucin production in the Salmonella enteritidis – gavaged growing rat. Four groups consisted of non-gavaged rats fed a casein-based control basal diet (BD) and three groups of rats gavaged with 1 × 107 CFU S. enteritidis and fed a casein-based diet, a diet containing freeze-dried ovine Ig (FDOI) or a casein-based diet containing inactivated ovine Ig (IOI). The rats were randomly allocated to one of the four groups (n = 15/group) and received their respective diets for an 18-day experimental study. Gavaging took place on day 15. Average daily gain and body gain : feed ratio (post-gavage, 3 days) were significantly (P < 0.05) higher for the Salmonella-challenged rats fed the FDOI diet compared to those fed the BD and IOI diets. At the end of the study, the small intestine and colon were significantly (P < 0.05) heavier for the gavaged rats fed the FDOI diet compared to the gavaged rats fed either the BD or IOI diet. Moreover, the relative weights of the caecum, liver and spleen of the gavaged rats fed the BD or IOI diet were significantly (P < 0.05) heavier compared to the gavaged rats fed the FDOI diet. Generally, the gavaged rats fed the FDOI diet had significantly (P < 0.05) higher goblet cell counts and luminal mucin protein contents than the gavaged rats fed either the BD or IOI diet and had a more functional gut morphology. Overall, the FDOI fraction prevented the acute effects of S. enteritidis.

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Full Paper
Copyright
Copyright © The Animal Consortium 2011

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References

Animal Welfare Advisory Committee 1995. Code of recommendations for minimum standards for the care and use of animals for scientific purposes. Ministry of Agriculture, Wellington, New Zealand.Google Scholar
Association of Official Analytical Chemists (AOAC) 2003. Official methods of analysis, vol. 1, 17th edition. AOAC, Gaithersburg, MD, USA.Google Scholar
Balan, P 2010. Effects of orally administered ovine serum immunoglobulin in the normal and Salmonella enteritidis – challenged growing rat. PhD, Massey University, New Zealand.Google Scholar
Balan, P, Han, KS, Rutherfurd, SM, Singh, H, Moughan, PJ 2009. Orally administered ovine serum immunoglobulin influences growth performance, organ weights, and gut morphology in growing rats. Journal of Nutrition 139, 244249.CrossRefGoogle ScholarPubMed
Balan, P, Han, KS, Rutherfurd-Markwick, K, Singh, H, Moughan, PJ 2010. Immunomodulatory effects of ovine serum immunoglobulin in the growing rat. Animal 4, 17021708.CrossRefGoogle ScholarPubMed
Blum, PM, Phelps, DL, Ank, BJ, Krantman, HJ, Stiehm, ER 1981. Survival of oral human immune serum globulin in the gastrointestinal tract of low birth weight infants. Pediatric Research 15, 12561260.CrossRefGoogle ScholarPubMed
Bogstedt, AK, Johansen, K, Hatta, H, Kim, M, Casswall, T, Svensson, L, Hammarström, L 1996. Passive immunity against diarrhoea. Acta Paediatrica 85, 125128.CrossRefGoogle ScholarPubMed
Bosi, P, Casini, L, Finamore, A, Cremokolini, C, Merialdi, G, Trevisi, P, Nobili, F, Mengheri, E 2004. Spray-dried plasma improves growth performance and reduces inflammatory status of weaned pigs challenged with enterotoxigenic Escherichia coli K88. Journal of Animal Science 82, 17641772.CrossRefGoogle ScholarPubMed
Casswall, TH, Hammarström, L, Veress, B, Nord, CE, Bogstedt, A, Brockstedt, U, Dahlstrom, KA 1996. Oral IgA treatment of chronic non-specific diarrhoea in infants and children. Acta Paediatrica 85, 11261128.Google Scholar
Coffey, RD, Cromwell, GL 1995. The impact of the environment and antimicrobial agents on the growth response of early-weaned pigs to spray-dried porcine plasma. Journal of Animal Science 73, 25322539.CrossRefGoogle ScholarPubMed
Corl, BA, Harrell, RJ, Moon, HK, Phillips, O, Weaver, EM, Campbell, JM, Arthington, JD, Odle, J 2007. Effect of animal plasma proteins on intestinal damage and recovery of neonatal pigs infected with rotavirus. Journal of Nutritional Biochemistry 18, 778784.CrossRefGoogle ScholarPubMed
Demas, GE, Chefer, V, Talan, MI, Nelson, RJ 1997. Metabolic costs of mounting an antigen-stimulated immune response in adult and aged C57BL/6J mice. American Journal of Physiology 273, 16311637.Google ScholarPubMed
Eibl, MM, Wolf, HM, Furnkranz, H, Rosenkranz, A 1988. Prevention of necrotizing enterocolitis in low-birth-weight infants by IgA-IgG feeding. New England Journal of Medicine 319, 17.CrossRefGoogle ScholarPubMed
Gatnau, R, Cain, C, Drew, M, Zimmerman, D 1995. Mode of action of spray-dried porcine plasma in weanling pigs. Journal of Animal Science 73, 82.Google Scholar
Hammarström, V, Smith, CI, Hammarström, L 1993. Oral immunoglobulin treatment in Campylobacter jejuni enteritis. Lancet 341, 1036.CrossRefGoogle ScholarPubMed
Hansen, JA, Nelssen, JL, Goodband, RD, Weeden, TL 1993. Evaluation of animal protein supplements in diets of early-weaned pigs. Journal of Animal Science 71, 18531862.CrossRefGoogle ScholarPubMed
Johnson, RW 1997. Inhibition of growth by pro-inflammatory cytokines: an integrated view. Journal of Animal Science 75, 12441255.CrossRefGoogle ScholarPubMed
Kats, LJ, Nelssen, JL, Tokach, MD, Goodband, RD, Hansen, JA, Laurin, JL 1994. The effect of spray-dried porcine plasma on growth performance in the early-weaned pig. Journal of Animal Science 72, 20752081.CrossRefGoogle ScholarPubMed
King, MR, Morel, PCH, Pluske, JR, Hendriks, WH 2008. A comparison of the effects of dietary spray-dried bovine colostrum and animal plasma on growth and intestinal histology in weaner pigs. Livestock Science 119, 167173.CrossRefGoogle Scholar
Lambert, ME, Schofield, PF, Ironside, AG, Mandal, BK 1979. Campylobacter colitis. British Medical Journal 1, 857859.CrossRefGoogle ScholarPubMed
Lindén, SK, Florin, TH, McGuckin, MA 2008. Mucin dynamics in intestinal bacterial infection. PLoS One 3, e3952e3766.CrossRefGoogle ScholarPubMed
Lu, R, Wu, S, Liu, X, Xia, Y, Zhang, Y, Sun, J 2010. Chronic effects of a salmonella type III secretion effector protein AvrA in vivo. PLoS One 5, e10505e10518.CrossRefGoogle ScholarPubMed
Mack, DR, Michail, S, Wei, S, McDougall, L, Hollingsworth, MA 1999. Probiotics inhibit enteropathogenic E. coli adherence in vitro by inducing intestinal mucin gene expression. The American Journal of Physiology 276, G941G950.Google Scholar
National Research Council (NRC) 1995. Nutrient requirements of laboratory animals, 4th edition. National Academy Press, Washington DC, USA.Google Scholar
Owen, KQ, Nelssen, JL, Goodband, RD, Tokach, MD, Friesen, KG, Ricert, BT, Smith, JW, Russell, LE 1995. Effects of various fractions of spray-dried porcine plasma on performance of early-weaned pigs. Journal of Animal Science 73, 81.Google Scholar
Owusu-Asiedu, A, Baidoo, SK, Nyachoti, CM, Marquardt, RR 2002. Response of early-weaned pigs to spray-dried porcine or animal plasma-based diets supplemented with egg-yolk antibodies against entertoxigenic Escherichia coli. Journal of Animal Science 80, 28952903.CrossRefGoogle ScholarPubMed
Pérez-Bosque, A, Miro, L, Polo, J, Russell, L, Campbell, J, Weaver, E, Crenshaw, J, Moretó, M 2008. Dietary plasma proteins modulate the immune response of diffuse gut-associated lymphoid tissue in rats challenged with Staphylococcus aureus enterotoxin B. Journal of Nutrition 138, 533537.CrossRefGoogle ScholarPubMed
Pérez-Bosque, A, Miro, L, Polo, J, Russell, L, Campbell, J, Weaver, E, Crenshaw, J, Moretó, M 2010. Dietary plasma protein supplements prevent the release of mucosal proinflammatory mediators in intestinal inflammation in rats. Journal of Nutrition 140, 2530.Google Scholar
Pierce, JL, Cromwell, GL, Lindemann, MD, Russell, LE, Weaver, EM 2005. Effects of spray-dried animal plasma and immunoglobulins on performance of early weaned pigs. Journal of Animal Science 83, 28762885.CrossRefGoogle ScholarPubMed
Roos, N, Mahé, S, Benamouzig, R, Sick, H, Rautureau, J, Tomé, D 1995. 15N-labeled immunoglobulins from bovine colostrum are partially resistant to digestion in human intestine. Journal of Nutrition 125, 12381244.Google ScholarPubMed
Tjellstrom, B, Stenhammar, L, Eriksson, S, Magnusson, KE 1993. Oral immunoglobulin A supplement in treatment of Clostridium difficile enteritis. Lancet 341, 701702.CrossRefGoogle ScholarPubMed
Trompette, A, Blanchard, C, Zoghbi, S, Bara, J, Claustre, J, Jourdan, G, Chayvialle, JA, Plaisance, P 2004. The DHE cell line as a model for studying rat gastro-intestinal mucin expression: effects of dexamethasone. European Journal of Cell Biology 83, 347358.CrossRefGoogle Scholar
Vermeer, AW, Norde, W 2000. The thermal stability of immunoglobulin: unfolding and aggregation of a multi-domain protein. Biophysical Journal 78, 394404.CrossRefGoogle ScholarPubMed