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JFST 2018, 7(1): 9-16 |
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Kazemi M, Abediankenari A, Rabiei R. Effect of Marine Macroalgae on Growth Performance and Immune Response in Rainbow Trout Fingerlings
. JFST 2018; 7 (1) :9-16
URL: http://jfst.modares.ac.ir/article-6-12442-en.html
URL: http://jfst.modares.ac.ir/article-6-12442-en.html
1- Department of Aquaculture, Faculty of Natural Resources and Marine Sciences, Tarbiat Modares University, Mazandaran, Noor, Iran
2- ,aabedian@modares.ac.ir
3- Hormozgan Agricultural and Natural Resources Research Center, Agricultural Research, Education and Promotion Organization, Ministry of Jihad-e-Agriculture, Bandar Abbas, Iran
2- ,
3- Hormozgan Agricultural and Natural Resources Research Center, Agricultural Research, Education and Promotion Organization, Ministry of Jihad-e-Agriculture, Bandar Abbas, Iran
Abstract: (14175 Views)
Aims: Sargassum bovianum, Polycladia myrica, and Gracilariopsis persica can be used in aquatic diets due to their significant biomass and mass production capacity for artificial rearing. The aim of this study was to investigate the effect of marine macroalgae on growth performance and immune response in rainbow trout (Oncorhynchus mykiss) fingerlings.
Materials & Methods: The present experimental study was carried out on 210 rainbow trout fingerlings, which were randomly selected and cultured in Aquatic Laboratory, Faculty of Marine Sciences, Tarbiat Modares University, Noor, in 2016. These fingerlings were placed in 7 experimental treatments, including a diet without marine macroalgae (control) and by replacing different marine macroalgae powder levels of 5% and 10% with wheat flour. Lindo 5.3 software was used to analyze food items and SPSS 20 software was used to analyze the data.
Findings: The lowest weight gain, the lowest growth factor, the lowest protein efficiency ratio, and the highest feed conversion ratio were in the treatment containing 10% Sargassum bovianum powder and it had a significant difference with other treatments. Condition factor (CF) was at the highest level in control treatment and no significant difference was observed between treatments. There was no significant difference in survival of different treatments. The highest level of serum lysozyme was in the treatment containing 5% Gracilariopsis persica powder and the highest serum hemolytic complement activity was in the treatment containing 5% Sargassum bovianum.
Conclusion: Gracilariopsis persica, Sargassum bovianum, and Polycladia myrica have no effect on the improvement of growth performance in rainbow trout fingerlings, Gracilariopsis persica and Sargassum bovianum have an impact on their immune response.
Materials & Methods: The present experimental study was carried out on 210 rainbow trout fingerlings, which were randomly selected and cultured in Aquatic Laboratory, Faculty of Marine Sciences, Tarbiat Modares University, Noor, in 2016. These fingerlings were placed in 7 experimental treatments, including a diet without marine macroalgae (control) and by replacing different marine macroalgae powder levels of 5% and 10% with wheat flour. Lindo 5.3 software was used to analyze food items and SPSS 20 software was used to analyze the data.
Findings: The lowest weight gain, the lowest growth factor, the lowest protein efficiency ratio, and the highest feed conversion ratio were in the treatment containing 10% Sargassum bovianum powder and it had a significant difference with other treatments. Condition factor (CF) was at the highest level in control treatment and no significant difference was observed between treatments. There was no significant difference in survival of different treatments. The highest level of serum lysozyme was in the treatment containing 5% Gracilariopsis persica powder and the highest serum hemolytic complement activity was in the treatment containing 5% Sargassum bovianum.
Conclusion: Gracilariopsis persica, Sargassum bovianum, and Polycladia myrica have no effect on the improvement of growth performance in rainbow trout fingerlings, Gracilariopsis persica and Sargassum bovianum have an impact on their immune response.
Article Type: Research Article |
Subject:
fish and shellfish physiology
Received: 2016/10/9 | Published: 2018/03/20
Received: 2016/10/9 | Published: 2018/03/20
References
1. Reverter M, Bontemps N, Lecchini D, Banaigs B, Sasal P. Use of plant extracts in fish aquaculture as an alternative to chemotherapy: Current status and future perspectives. Aquaculture. 2014;433:50-61. [Link] [DOI:10.1016/j.aquaculture.2014.05.048]
2. Hebb CD, Castell JD, Anderson DM, Batt J. Growth and feed conversion of juvenile winter flounder (Pleuronectes americanus) in relation to different protein-to-lipid levels in isocaloric diets. Aquaculture. 2003;221(1-4):439-49. [Link] [DOI:10.1016/S0044-8486(03)00064-4]
3. Barrows FT, Gaylord TG, Stone DAJ, Smith CE. Effect of protein source and nutrient density on growth efficiency, histology and plasma amino acid concentration of rainbow trout (Oncorhynchus mykiss Walbaum). Aquac Res. 2007;38(16):1747-58. [Link] [DOI:10.1111/j.1365-2109.2007.01854.x]
4. Nakagawa H, Sato M, Gatlin DM. Dietary supplements for the health and quality of cultured fish. Wallingford: Cabi; 2007. [Link] [DOI:10.1079/9781845931995.0000]
5. Hashim R, Mat Saat MA. The utilization of seaweed meals as binding agents in pelleted feeds for snakehead (Channa striatus) fry and their effects on growth. Aquaculture. 1992;108(3-4):299-308. [Link] [DOI:10.1016/0044-8486(92)90114-Z]
6. Pereira L. A review of the nutrient composition of selected edible seaweeds. In: Pomin VH. Seaweed: Ecology, nutrient composition and medicinal uses. Pomin VH, editor. New York: Nova Science; 2012. pp. 15-47. [Link]
7. Burtin P. Nutritional value of seaweeds. Electron J Environ Agric Food Chem. 2003;2(4):498-503. [Link]
8. Rabiei R, Asadi M, Sohrabipour J, Nejadsattari T, Majd A. Algae species diversity of Gracilaria salicornia on the Persian Gulf Coast-Qeshm Island. J Res Constr. 2007;20(2):47-53. [Persian] [Link]
9. Nakagawa H, Sato M, Gatlin DM. Dietary supplements for the health and quality of cultured fish. Abedian Kenari A, Sotoudeh E, translators. Tehran: Tarbiat Modares University Press; 2012. p. 391. [Persian] [Link]
10. Sohrabipour J, Rabiei R. Algal vegetation in southern coastline of Iran. Iran Nat. 2017;2(1):62-8. [Persian] [Link]
11. Stirk WA, Reinecke DL, van Staden RJ. Seasonal variation in antifungal, antibacterial and acetylcholinesterase activity in seven South African seaweeds. J Appl Phycol. 2007;19(3):271-6. [Link] [DOI:10.1007/s10811-006-9134-7]
12. Volk RB, Furkert FH. Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth. Microbiol Res. 2006;161;(2):180-6. [Link] [DOI:10.1016/j.micres.2005.08.005]
13. Jiao L, Li X, Li T, Jiang P, Zhang L, Wu M, et al. Characterization and anti-tumor activity of alkali-extracted polysaccharide from Enteromorpha intestinalis. Int Immunopharmacol. 2009;9(3):324-9. [Link] [DOI:10.1016/j.intimp.2008.12.010]
14. Kumar M, Kumari P, Trivedi N, Shukla MK, Gupta V, Reddy CRK, et al. Minerals, PUFAs and antioxidant properties of some tropical seaweeds from Saurashtra coast of India. J Appl Phycol. 2011;23(5):797-810. [Link] [DOI:10.1007/s10811-010-9578-7]
15. Bellorin AM, Buriyo A, Sohrabipour J, Oliveira MC, Oliveira EC. Gracilariopsis mclachlanii sp. nov. and Gracilariopsis persica sp. nov. of the Gracilariaceae (Gracilariales, Rhodophyceae) from the Indian Ocean. J Phycol. 2008;44(4):1022-32. [Link] [DOI:10.1111/j.1529-8817.2008.00552.x]
16. Agardh JG. Species, genera and orders Algae or a succinct descriptions of species, genera and orders of Algae kingdom. 2nd Volume. Lund: CWK Gleerup; 1851. [Latin] [Link]
17. Draisma SGA, Ballesteros E, Rousseau F, Thibaut T. DNA sequence data demonstrate; the polyphyly of the genus Cystoseira and other Sargassaceae genera (Phaeophyceae). J Phycol. 2010;46(6):1329-45. [Link] [DOI:10.1111/j.1529-8817.2010.00891.x]
18. Clerck OD, Coppejans E. Marine algae of the Jubail Marine Wildlife Sanctuary, Saudi Arabia. In: Krupp F, Abuzinada AH, Nader IA, editors. A marine wildlife sanctuary for the Arabian Gulf environmental research and conservation following the 1991 gulf war oil spill. Frankfurt: Senckenberg Research Institute; 1996. [Link]
19. Subcommittee on Fish Nutrition, National Research Council. Nutrient requirements of fish. Washington, DC: National Academy Press; 1993. [Link]
20. Abedian Kenari A, Sotoudeh E, Rezaei MH. Dietary soybean phosphatidylcholine affects growth performance and lipolytic enzyme activity in Caspian Brown Trout (Salmo Trutta Caspius) alevin. Aquac Res. 2011;42(5):655-63. [Link] [DOI:10.1111/j.1365-2109.2010.02587.x]
21. Fynn-Aikins K, Hung SS, Liu W, Li H. Growth, lipogenesis and liver composition of juvenile white sturgeon fed different levels of D-glucose. Aquaculture. 1992;105(1):61-72. [Link] [DOI:10.1016/0044-8486(92)90162-E]
22. Clerton P, Troutaud D, Verlhac V, Gabaudan J, Deschaux P. Dietary vitamin E and rainbow trout (Oncorhynchus mykiss) phagocyte functions: Effect on gut and on head kidney leucocytes. Fish Shellfish Immunol. 2001;11(1):1-13. [Link] [DOI:10.1006/fsim.2000.0287]
23. Amar EC, Kiron V, Satoh S, Watanabe T. Effects of dietary beta-carotene on the immune response of rainbow trout Oncorhynchus mykiss. Fish Sci. 2000;66:1068-75.
https://doi.org/10.2331/suisan.66.1068 [Link] [DOI:10.1046/j.1444-2906.2000.00170.x]
24. Zar JH. Biostatistical analysis. 4th Edition. Upper Saddle River, New Jersey: Prentice Hall; 1999. [Link]
25. Yangthong M, Oncharoen S, Sripanomyom J. Effect of Sargassum meal supplementation on growth performance of sex-reversed tilapia (Oreochromis niloticus Linn.). In: Proceedings Kasetsart University Annual Conference. Chatuchak, Bangkok: Kasetsart University; 2014. pp. 234-41. [Link]
26. Güroy BK, Cirik Ş, Güroy D, Sanver F, Tekinay AA. Effects of Ulva rigida and Cystoseira barbata meals as a feed additive on growth performance, feed utilization, and body composition of Nile Tilapia, Oreochromis niloticus. Turk J Vet Animal Sci. 2007;31(2):91-7. [Link]
27. Kim KW, Kim SS, Khosravi S, Rahimnejad S, Lee KJ. Evaluation of sargassum fusiforme and ecklonia cava as dietary additives for olive flounder (Paralichthys olivaceus). Turk J Fish Aquat Sci. 2014;14:321-30. [Link] [DOI:10.4194/1303-2712-v14_2_03]
28. Pham MA, Lee K, Lee B, Lim S, Kim S, Lee Y, et al. Effects of dietary Hizikia fusiformis on growth and immune responses in juvenile olive flounder (Paralichthys olivaceus). Asian Aust J Anim Sci. 2006;19(12):1769-75. [Link] [DOI:10.5713/ajas.2006.1769]
29. Wassef EA, El-Sayed AFM, Sakr EM. Sakr EM. Pterocladia (Rhodophyta) and Ulva (Chlorophyta) as feed supplements for European seabass, Dicentrarchus labrax L., fry. J Appl Phycol. 2013;255:1369-76. [Link] [DOI:10.1007/s10811-013-9995-5]
30. Mustafa G, Wakamatsu S, Takeda TA, Umino T, Nakagawa H. Effects of Algae meal as feed additive on growth, feed efficiency, and body composition in Red Sea bream. Fish Sci. 1995;61(1):25-8. [Link] [DOI:10.2331/fishsci.61.25]
31. Soler-Vila A, Coughlan S, Guiry MD, Kraan S. The red alga Porphyra dioica as a fish-feed ingredient for rainbow trout (Oncorhynchus mykiss): Effects on growth, feed efficiency, and carcass composition. J Appl Phycol. 2009;215:617-24. [Link] [DOI:10.1007/s10811-009-9423-z]
32. Fujiki K, Yano T. Effects of sodium alginate on the non-specific defence system of the common carp (Cyprinus carpioL.). Fish Shellfish Immunol. 1997;7(6):417-27. [Link] [DOI:10.1006/fsim.1997.0095]
33. Skjermo J, Defoort T, Dehasque M, Espevik T, Olsen Y, Skjak-brfek, et al. Immunostimulation of juvenile turbot (Scophthalmusmaximus L.) using an alginate with high mannuronic acid content administered via the live food organism Artemia. Fish Shellfish Immunol. 1995;5(7):531-4. [Link] [DOI:10.1016/S1050-4648(95)80053-0]
34. Dalmo RA, Seljelid R. The immunomodulatory effect of LPS, laminaran and sulphated laminaran [β(l,3)-D-glucan] on Atlantic salmon, Salmo salar L., macrophages in vitro. J Fish Dis. 1955;18(2):175-85. [Link] [DOI:10.1111/j.1365-2761.1995.tb00275.x]
35. Yeh SP, Chang CA, Chang CY, Liu CH, Cheng W. Dietary sodium alginate administration affects fingerling growth and resistance to Streptococcus sp. and iridovirus, and juvenile non-specific immune responses of the orange-spotted grouper, Epinephelus coioides. Fish Shellfish Immunol. 2008;25(1-2):19-27. [Link] [DOI:10.1016/j.fsi.2007.11.011]
36. Cheng AC, Tu CW, Chen YY, Nan FH, Chen JC. The immunostimulatory effects of sodium alginate and iota-carrageenan on orange-spotted grouper Epinephelus coicoides and its resistance against Vibrio alginolyticus. Fish Shellfish Immunol. 2007;22(3):197-205. [Link] [DOI:10.1016/j.fsi.2006.04.009]
37. Chiu ShT, Tsai RT, Hsu JP, Liu ChH, Cheng W. Dietary sodium alginate administration to enhance the non-specific immune responses, and disease resistance of the juvenile grouper Epinephelus fuscoguttatus. Aquaculture. 2008;277(1-2):66-72. [Link] [DOI:10.1016/j.aquaculture.2008.01.032]
38. Fujiki K, Matsuyama H, Yano T. Protective effect of sodium alginates against bacterial infection in common carp, Cyprinus carpio L. J Fish Dis. 1994;17(4):349-55. [Link] [DOI:10.1111/j.1365-2761.1994.tb00230.x]
39. Liang L, Sun X. A genetic linkage map of common carp (Cyprinus carpio L.) and mapping of a locus associated with cold tolerance. Aquaculture. 2004;238(1-4):165-72. [Link] [DOI:10.1016/S0044-8486(03)00445-9]
40. Valente LMP, Araújo M, Batista S, Peixoto MJ, Sousa-Pinto I, Brotas V, et al. Carotenoid deposition, flesh quality and immunological response of Nile tilapia fed increasing levels of IMTA-cultivated Ulva spp. J Appl Phycol. 2016;28(1):691-701. [Link] [DOI:10.1007/s10811-015-0590-9]
41. Araújo M, Rema P, Sousa-Pinto I, Cunha LM, Peixoto MJ, Pires MA, et al. Dietary inclusion of IMTA-cultivated Gracilaria vermiculophylla in rainbow trout (Oncorhynchus mykiss) diets: Effects on growth, intestinal morphology, tissue pigmentation, and immunological response. J Appl Phycol. 2016;28:679-89. [Link] [DOI:10.1007/s10811-015-0591-8]
42. Zamannejad N, Emadi H, Hosseinzade Sahafi O. Effects of Sargassum illicifolium algae feeding on IgM level and lysozyme activity in Rainbow trout (Onchorhynchus mykiss). J Marine Sci Technol. 2016;10(4):57-70. [Persian] [Link]
43. Yano T. Assays of hemolytic complement activity. In: Stolen JS, Fletcher TC, Anderson DP, Kaattari SL, Rowley AF, editors. Techniques in fish immunology. 2nd Volume. Cambridge: SOS Publications; 1992. pp. 131-41. [Link]
44. Mauri I, Romero A, Acerete L, MacKenzie S, Roher N, Callol A, et al. Changes in complement responses in Gilthead seabream (Sparus aurata) and European seabass (Dicentrarchus labrax) under crowding stress, plus viral and bacterial challenges. Fish Shellfish Immunol. 2011;30(1):182-8. [Link] [DOI:10.1016/j.fsi.2010.10.006]
45. Timmis J, Knight T, de Castro LN, Hart E. An overview of artificial immune systems. In: Paton R, Bolouri H, Holcombe WML, Parish JH, Tateson R, editors. Computation in cells and tissues. Berlin: Springer Berlin Heidelberg; 2004. pp. 51-91. [Link] [DOI:10.1007/978-3-662-06369-9_4]
46. Wyban JA, Lee CS, Sato VT, Sweeney JN, Richards Jr WK. Effect of stocking density on shrimp growth rates in manure-fertilized ponds. Aquaculture. 1987;61(1):23-32. [Link] [DOI:10.1016/0044-8486(87)90334-6]
47. Gabrielsen BO, Austreng E. Growth, product quality and immune status of Atlantic salmon, Salmo salar L., fed wet feed with alginate. Aquac Res. 1988;29(6):397-401. [Link] [DOI:10.1111/j.1365-2109.1998.tb01146.x]
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