Effect of the dietary inclusion of soybean components on the innate immune system in zebrafish

Zebrafish

Volumn 11, Issue 1, 2014, Pages 41-49

  Fuentes Appelgren, Pamela ^a,b   Opazo, Rafael ^a   Barros, Luis ^a   Feijoó, Carmen G ^c   Urzúa, Victoria ^a   Romero, Jaime ^a  

^a UNIVERSITY OF CHILE   (Chile)

^b UNIVERSIDAD DE SANTIAGO DE CHILE   (Chile)

^c UNIVERSIDAD ANDRÉS BELLO   (Chile)

Author keywords

[No Author keywords available]

Indexed keywords

SAPONIN;

ANIMAL; ARTICLE; CYTOLOGY; DRUG EFFECT; GASTROINTESTINAL TRACT; GENE EXPRESSION; GENETICS; GRANULOCYTE; IMMUNOLOGY; INNATE IMMUNITY; NEUTROPHIL; SOYBEAN; ZEBRA FISH;

ANIMALS; GASTROINTESTINAL TRACT; GENE EXPRESSION; GRANULOCYTES; IMMUNITY, INNATE; NEUTROPHILS; SAPONINS; SOY FOODS; SOYBEANS; ZEBRAFISH;

EID: 84892909189     PISSN: 15458547     EISSN: None     Source Type: Journal    
DOI: 10.1089/zeb.2013.0934     Document Type: Article

References (50)

1. Rawls JF, Samuel BS, Gordon JI. Gnotobiotic zebrafish reveal evolutionarily conserved responses to the gut microbiota. Proc Natl Acad Sci USA 2004;101:4596-4601
2. Kiron V. Fish immune system and its nutritional modulation for preventive health care. Anim Feed Sci Technol 2012;173: 111-133
3. Levraud J-P, Colucci-Guyon E, Redd MJ, Lutfalla G, Herbomel P. In vivo analysis of zebrafish innate immunity. Methods Mol Biol 2008;415:337-363
4. Stevens CE, Hume ID. Contributions of microbes in vertebrate gastrointestinal tract to production and conservation of nutrients. Physiol Rev 1998;78:393-427
5. Clements KD, Raubenheimer D. Feeding and nutrition. In: The Physiology of Fishes. Evans DH, Claiborne JB (eds), Boca Raton, FL: Taylor and Francis Group, 2006
6. Oliva-Teles A. Nutrition and health of aquaculture fish. J Fish Dis 2012;35:83-108
7. Swiatczak B, Rescigno M. How the interplay between antigen presenting cells and microbiota tunes host immune responses in the gut. Semin Immunol 2012;24:43-49
8. Wacyk J, Powell M, Rodnick K, Overturf K, Hill R, Hardy R. Dietary protein source significantly alters growth performance, plasma variables and hepatic gene expression in rainbow trout (Oncorhynchus mykiss) fed amino acid balanced diets. Aquaculture 2012;356-357:223-234
9. Sales J. The effect of fish meal replacement by soyabean products on fish growth: A meta-Analysis. Br J Nutr 2009;102:1709-1722
10. Hart SD, Bharadwaj AS, Brown PB. Soybean lectins and trypsin inhibitors, but not oligosaccharides or the interactions of factors, impact weight gain of rainbow trout (Oncorhynchus mykiss). Aquaculture 2010;306:310-314
11. Santigosa E, García-Meilán I, Valentin JM, Pérez-Sánchez J, Médale F, Kaushik S, et al. Modifications of intestinal nutrient absorption in response to dietary fish meal replacement by plant protein sources in sea bream (Sparus aurata) and rainbow trout (Onchorynchus mykiss). Aquaculture 2011;317:146-154
12. Gatlin DM, Barrows FT, Brown P, Dabrowski K, Gaylord TG, Hardy RW, et al. Expanding the utilization of sustainable plant products in aquafeeds: A review. Aquacult Res 2007;38:551-579
13. Bakke-McKellep AM, Press CM, Baeverfjord G, Krogdahl A, Landsverk T. Changes in immune and enzyme histochemical phenotypes of cells in the intestinal mucosa of Atlantic salmon, Salmo salar L., with soybean meal-induced enteritis. J Fish Dis 2000;23:115-127
14. Krogdahl A, Bakke-McKellep AM, Baeverfjord G. Effects of graded levels of standard soybean meal on intestinal structure, mucosal enzyme activities, and pancreatic response in Atlantic salmon (Salmo salar L.). Aquacult Nutr 2003;9:361-371
15. Goncalves AA, Urán PA, Taverne-Thiele JJ, Schrama JW, Verreth JA, Rombout JH. Soybean meal induces intestinal inflammation in common carp (Cyprinus carpio L.). Fish Shellfish Immunol 2008;25:751-760
16. Urán PA, Schrama JW, Rombout JH, Taverne-Thiele JJ, Obach A, Koppe W, et al. Time-related changes of the intestinal morphology of Atlantic salmon, Salmo salar L., at two different soybean meal inclusion levels. J Fish Dis 2009;32:733-744
17. Knudsen D, Urán P, Arnous A, Koppe W, Frøkiaer H. Saponin-containing subfractions of soybean molasses induce enteritis in the distal intestine of Atlantic salmon. J Agric Food Chem 2007;55:2261-2267
18. Knudsen D, Jutfelt F, Sundh H, Sundell K, Koppe W, Frøkiaer H. Dietary soya saponins increase gut permeability and play a key role in the onset of soyabean-induced enteritis in Atlantic salmon (Salmo salar L.). Br J Nutr 2008;100:120-129
19. Sørensen M, Penn M, El-Mowafi A, Storebakken T, Chunfang C, Øverland M, et al. Effect of stachyose, raffinose and soya-saponins supplementation on nutrient digestibility, digestive enzymes, gut morphology and growth performance in Atlantic salmon (Salmo salar, L). Aquaculture 2011;314:145-152
20. Krogdahl A°, Penn M, Thorsen J, Refstie S, Bakke AM. Important antinutrients in plant feedstuffs for aquaculture: An update on recent findings regarding responses in salmonids. Aquacult Res 2010;41:333-344
21. Chen W, Ai Q, Mai K, Xu W, Liufu Z, Zhang W, et al. Effects of dietary soybean saponins on feed intake, growth performance, digestibility and intestinal structure in juvenile Japanese flounder (Paralichthys olivaceus). Aquaculture 2011;318: 95-100
22. Kortner T, Skugor S, Penn MH, Mydland LT, Djordjevic B, Hillestad M, Krasnov A and Krogdahl A° . Dietary soyasaponin supplementation to pea protein concentrate reveals nutrigenomic interactions underlying enteropathy in Atlantic salmon (Salmo salar). BMC Vet Res 2012;8:101
23. Chikwati EM, Venold FF, Penn MH, Rohloff J, Refstie S, Guttvik A, et al. Interaction of soyasaponins with plant ingredients in diets for Atlantic salmon, Salmo salar L. Br J Nutr 2012;107:1570-1590
24. Guo P, Piao X, Ou D, Li D, Hao Y. Characterization of the antigenic specificity of soybean protein beta-conglycinin and its effects on growth and immune function in rats. Arch Anim Nutr 2007;61:189-200
25. Sun P, Li D, Dong B, Qiao S, Ma X. Effects of soybean glycinin on performance and immune function in early weaned pigs. Arch Anim Nutr 2008;62:313-321
26. Xu J, Zhou A, Wang Z, Ai D. Effects of glycinin and bconglycinin on integrity and immune responses of mouse intestinal epithelial cells. J Ani Plant Sci 2010;20:170-174
27. Collins S, Desai A, Mansfield G, Hill J, Van Kessel A, Drew M. The effect of increasing inclusion rates of soybean, pea and canola meals and their protein concentrates on the growth of rainbow trout: Concepts in diet formulation and experimental design for ingredient evaluation. Aquaculture 2012;344-349:90-99
28. Brandon DL, Friedman M. Immunoassays of soy proteins. J Agric Food Chem 2002;50:6635-6642
29. Ulloa PE, Iturra P, Neira R, Araneda C. Zebrafish as a model organism for nutrition and growth: Towards comparative studies of nutritional genomics applied to aquacultured fishes. Rev Fish Biol Fish 2011;21:649-666
30. Brugman S, Liu K, Lindenbergh-Kortleve D, Samsom J, Furuta GT, Renshaw SA, et al. Oxazolone-induced enterocolitis in zebrafish depends on the composition of the intestinal microbiota. Gastroenterology 2009;137:1757-1767
31. Sissener NH, Johannessen LE, Hevrøy EM, Wiik-Nielsen CR, Berdal KG, Nordgreen A, et al. Zebrafish (Danio rerio) as a model for investigating the safety of gm feed ingredients (soya and maize); performance, stress response and uptake of dietary DNA sequences. Br J Nutr 2010;103:3-15
32. Westerfield M. The Zebrafish Book: A Guide for the Laboratory Use Of the Zebrafish (Danio rerio). Oregon: University of Oregon Press, 1994
33. Kimmel CB, Ballard WW, Kimmel SR, Ullmann B, Schilling TF. Stages of embryonic development of the zebrafish. Dev Dyn 1995;203:253-310
34. Haffter P, Granato M, Brand M, Mullins MC, Hammerschmidt M, Kane DA, et al. The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio. Development 1996;123:1-36
35. Rønnestad I, Kamisaka Y, Conceiçäo LE, Morais S, Tonheim SK. Digestive physiology of marine fish larvae: Hormonal control and processing capacity for proteins, peptides and amino acids. Aquaculture 2007;268:82-97
36. Renshaw S, Loynes C, Trushell D, Elworthy S, Ingham P and Whyte M. A transgenic zebrafish model of neutrophilic inflammation. Blood 2006;108:3976-3978
37. Pfaffl MW, Horgan GW, Dempfle L. Relative Expression Software Tool (REST) for group-wise comparison and statistical analysis of relative expression results in real-Time PCR. Nucleic Acids Res 2002;30:e36
38. Fleming A, Jankowski J, Goldsmith P. In vivo analysis of gut function and disease changes in a zebrafish larvae model of inflammatory bowel disease: A feasibility study. Inflamm Bowel Dis 2010;16:1162-1172
39. Oehlers SH, Flores MV, Okuda KS, Hall CJ, Crosier KE, Crosier PS. A chemical enterocolitis model in zebrafish larvae that is dependent on microbiota and responsive to pharmacological agents. Dev Dyn 2011;240:288-298
40. Kaushik S, Georga I, Koumoundouros G. Growth and body composition of zebrafish (Danio rerio) larvae fed a compound feed from first feeding onward: Toward implications on nutrient requirements. Zebrafish 2011;8:87-95
41. Rombout JH, Abelli L, Picchietti S, Scapigliati G, Kiron V. Teleost intestinal immunology. Fish Shellfish Immunol 2010;31:616-626
42. Wang Z, Du J, Lam SH, Mathavan S, Matsudaira P. Morphological and molecular evidence for functional organization along the rostrocaudal axis of the adult zebrafish intestine. BMC Genom 2010;11:392
43. Palic D, Andreasen CB, Ostojic J, Tell RM, Roth JA. Zebrafish (Danio rerio) whole kidney assays to measure neutrophil extracellular trap release and degranulation of primary granules. J Immunol Methods 2007;319:87-97
44. Walters KB, Green JM, Surfus JC, Yoo SK, Huttenlocher A. Live Imaging of neutrophil motility in a zebrafish model of WHIM syndrome. Blood 2010;116:2803-2811
45. Herbomel P, Thisse B, Thisse C. Ontogeny and behaviour of early macrophages in the zebrafish embryo. Development 1999;126:3735-3745
46. Bureau DP, Harris AM, Cho CY. The effects of purified alcohol extracts from soy products on feed intake and growth of chinook salmon (Oncorhynchus tshawytscha) and rainbow trout (Oncorhynchus mykiss). Aquaculture 1998;161:27-43
47. Boshra H, Li J, Sunyer JO. Recent advances on the complement system of teleost fish. Fish Shellfish Immunol 2006;20:239-262
48. Heppell LM, Sissons JW, Pedersen HE. A comparison of the antigenicity of soya-bean-based infant formulas. Br J Nutr 1987;58:393-403
49. Bayne CJ, Gerwick L. The acute phase response and innate immunity of fish. Dev Comp Immunol 2001;25:205-217
50. Sahlmann C, Sutherland B, Kortner TM, Koop B, Krogdahl A°, Bakke AM. Early response of gene expression in the distal intestine of Atlantic salmon (Salmo salar L.) during the development of soybean meal induced enteritis. Fish Shellfish Immunol 2013;34:599-609