Growth, body composition and digestive enzyme activities of rainbow trout fed with dietary Beta-glucan containing mannan oligosaccharide

Keywords: Prebiotic, Oncorhynchus mykiss, growth rate, feed conversion, protein efficiency

Abstract

This study investigated the impact of a yeast containing the prebiotic β-glucans, on the growth parameters and enzyme activities of rainbow trout (Oncorhynchus mykiss) at various dosage levels. The fish were randomly placed in plastic tanks (120 x 50 x 32 cm) in three trial groups and replicates, with an average weight of 73.37 ± 0.21 g (n = 90). Three different diets were prepared; 0 g.kg-¹ in group G-1 (control), 0.5 g.kg-¹ of the prebiotic (mannan oligosaccharides + β-glucan) in group G-2 and 1 g.kg-¹ ratio prebiotic (mannan oligosaccharides + β-glucan) were added to group G-3. The fish were fed these experimental feeds for 60 days. By the end of the experiment, the G-2 group had achieved the highest average live weight and weight gain, with values of 155.38 ± 0.19 g and 81.76 ± 0.16 g respectively. Feed conversion ratio, specific growth rate, protein efficacy ratio and survival rate showed the best values (1.13 ± 0.03, 1.24 ± 0.003, 1.91 ± 0.001, and 93.33 ± 3.33, respectively) were observed in the G-2 group (P < 0.05). Pepsin activity was also significantly higher in the G-2 group (163.94 ± 2.23 U/mg protein; P < 0.05). Similarly, the highest trypsin, amylase, and lipase activities were recorded in the G-2 group, with values of 1.09 ± 0.05, 5.31 ± 0.22, and 4.38 ± 0.11 U/mg protein, respectively (P < 0.05). No significant differences were detected among the groups with respect to muscle proximate composition (P > 0.05). Both β-glucan–supplemented yeast groups positively influenced the growth performance and digestive enzyme activities of trout. However, the group receiving 0.5 g.kg-¹ β-glucan supplementation exhibited significantly superior results compared to the other groups (P < 0.05).

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References

Serra V, Pastorelli G, Tedesco DEA, Turin L, Guerrini A. Alternative protein sources in aquafeed: Current scenario and future perspectives. [Internet]. Vet. Anim. Sci. 2024; 25:100381. doi: https://doi.org/hbgbxh DOI: https://doi.org/10.1016/j.vas.2024.100381

Boyd CE, McNevin AA. Aquaculture, resource use, and the environment. Oxford: Wiley-Blackwell. [Internet]. 2015; doi: https://doi.org/q62q DOI: https://doi.org/10.1002/9781118857915

Ringø E, Van Doan H, Lee SH, Soltani M, Hoseinifar SH, Harikrishnan R, Song SK. Probiotics, lactic acid bacteria and bacilli: interesting supplementation for aquaculture. J. Appl. Microbiol. [Internet]. 2020; 129:(1):116-136. doi: https://doi.org/ggpwtr DOI: https://doi.org/10.1111/jam.14628

Wee W, Abdul-Hamid NK, Mat K, Raja-Khalif RIA, Rusli ND, Rahman MM, Kabir MA. Wei LS. The effects of mixed prebiotics in aquaculture: A review. Aquac. Fish. [Internet]. 2024; 9(1):28-34. doi: https://doi.org/q62x DOI: https://doi.org/10.1016/j.aaf.2022.02.005

Saad N, Delattre C, Urdaci M, Schmitter JM, Bressollier P. An overview of the last advances in probiotic and prebiotic field. LWT. Food Sci. Technol. [Internet]. 2013; 50(1):1-16. doi: https://doi.org/gfwkkr DOI: https://doi.org/10.1016/j.lwt.2012.05.014

Dawood MAO, Koshio S. Recent advances in the role of probiotics and prebiotics in carp aquaculture: A review. Aquaculture. [Internet]. 2016; 454:243-251. doi: https://doi.org/q623 DOI: https://doi.org/10.1016/j.aquaculture.2015.12.033

Özkan-Yılmaz F, Özlüer-Hunt A, Berköz M. Investigation on paraoxonase enzyme activity and malondialdehyde level in liver of Oreochromis niloticus fed with MOS supplemented diet. [Internet]. Turk. J. Agric. Food Sci. Technol. 2015; 3(8):639-643. doi: https://doi.org/q624

Özlüer-Hunt A, Berköz M, Özkan F, Yalin S, Erçen Z, Erdoğan E, Gündüz SG. Effect of mannan oligosaccharide on growth, body composition, and antioxidant enzyme activity of tilapia (Oreochromis niloticus). Isr. J. Aquac. Bamidgeh. [Internet]. 2011 [cited 20 Jan 2026]; 63(2):619-627. Available in: https://goo.su/GHxYUvU

Ebrahimi G, Ouraji H, Khalesi MK, Sudagar M, Barari A, Zarei-Dangesaraki M, Jani-Khalili KH. Effects of a prebiotic, Immunogen®, on feed utilization, body composition, immunity and resistance to Aeromonas hydrophila infection in the common carp Cyprinus carpio (Linnaeus) fingerlings. J. Anim. Physiol. Anim. Nutr. [Internet]. 2012; 96(4):591-599. doi: https://doi.org/cnr69p DOI: https://doi.org/10.1111/j.1439-0396.2011.01182.x

Martins de Brito J, Urbich AV, Pereira da Cruz T, Panczevicz PAP, Galioto-Miranda JA, Wernick B, Furuya VRB, Furuya WM. Xylanase and β-glucanase improve growth performance, gut barrier, and microbiota of pre-growout Nile tilapia, Oreochromis niloticus fed a vegetable-based diet. Aquaculture. [Internet]. 2022; 561:738653. doi: https://doi.org/q625

Samrongpan C, Areechon N, Yoonpundh R, Srisapoome P. Effects of mannan-oligosaccaharide on growth, survival and disease resistance of Nile Tilapia (Oreochromis niloticus, Linneaeus) Fry. 8th Interntional Symposium on Tilapia in Aquaculture. [Internet]. 2008; 345-353 Available in: https://goo.su/jztuZC

Torrecillas S, Makol A, Cabellero D, Montero R, Gines J, Sweetmen M, Izquierdo M. Improved feed utilization, intestinal mucus production and immune parameters in sea bass (Dicentrarchus labrax) fed mannan oligosaccharides (MOS). Aquac. Nutr. [Internet]. 2011; 17:223-233. doi: https://doi.org/c3gv3h DOI: https://doi.org/10.1111/j.1365-2095.2009.00730.x

Magouz FI, Salem MFI, Emara AEI, Hassan MM, Dawood MAO. A mixture of β-glucan and mannanoligosaccharide ameliorated the growth rate, digestive enzyme activity, intestinal morphometry, and immunity of common carp (Cyprinus carpio). Annals Anim. Sci. [Internet]. 2021; 21(3):1027-1041. doi: https://doi.org/q626 DOI: https://doi.org/10.2478/aoas-2021-0002

Schmidt J, Bischoff AA, Weiß M, Kim SK, Frickenhaus S, Slater MJ, Buck BH. Effect of beta-1-3-glucan and mannans on growth and fitness of starry flounder (Platichthys stellatus): A potential new candidate for aquaculture in temperate regions. J. Fish. Sci. [Internet]. 2017; 11(3):17-25. doi: https://doi.org/q628 DOI: https://doi.org/10.21767/1307-234X.1000125

Spencer JFT, de Spencer AR, Laluce C. Non-conventional yeasts. Appl. Microbiol. Biotechnol. [Internet]. 2002; 58:147-156. doi: https://doi.org/fvp9kc DOI: https://doi.org/10.1007/s00253-001-0834-2

ADM Animal Nutrition. CitriStim®. [Internet]. Quincy, Ilinois, USA: ADM Animal Nutrition. 2026 [cited 20 Jan 2026]; 0917. Avalabile from: https://goo.su/3tGUUF

Smith RR. Nutritional energetics. In: Halver JE, Editor. Fish Nutrition. (2nd ed.) New York, USA: Academic Press. 1989; p. 2-31.

Ricker WE. Growth rates and models. In: Hoar WS, Randall DJ, Brett JR, Editors. Fish Physiology, VIII, Bioenergetics and Growth. New York, USA: Academic Press, 1979; 677-743 pp. DOI: https://doi.org/10.1016/S1546-5098(08)60034-5

Tarak RR, Yadav MK, Saxena S, Kher D. Effect of leaf powder of giloy (Tinospora cordifolia) in fish feed on survival and growth of post larvae of Cyprinus carpio fingerlings. Int. J. Adv. Biochem. Res. [Internet]. 2025; 9(8):532-536. doi: https://doi.org/q63f DOI: https://doi.org/10.33545/26174693.2025.v9.i8g.5247

Martínez-Llorens S, Moñino AV, Tomás A, Pla M, Jover M. Soybean meal as a protein source in gilthead sea bream (Sparus aurata L.) diets: effects on growth and nutrient utilization. Aquac. Res. [Internet]. 2007; 38:82-90. doi: https://doi.org/c86w7r DOI: https://doi.org/10.1111/j.1365-2109.2006.01637.x

Official Methods of Analysis of Association of Official Analytical Chemists (AOAC). Arlington, Virginia, USA: AOAC. [Internet]. 15th edition. 1990. [cited 20 Jan 2026]. 771 p. Available in: https://goo.su/aTWze

Worthington CC, Worthington V, Worthington K, Decher L, Hackler D, Worthinton A. Worthington Enzyme Manual. Enzymes and Related Biochemicals Worthington Chemical. New Jersey, USA: Worthington Biochemical Corporation. [Internet]. 2016. [cited 20 Jan 2026]. 782 p. Available in: https://goo.su/ICc9U

Erlanger B, Kokowsky N, Cohen W. The preparation and properties of two new cromogenic substrates of trypsin. Arch. Biochem. Biophys. [Internet]. 1961; 95(2):271-278. doi: https://doi.org/d8jjvr DOI: https://doi.org/10.1016/0003-9861(61)90145-X

Benjakul S, Visessanguan W, Thummaratwasik P. Isolation and characterization of trypsin inhibitors from some Thai legume seeds. J. Food Biochem. [Internet]. 2007; 24(2):107-127. doi: https://doi.org/d8qf4f DOI: https://doi.org/10.1111/j.1745-4514.2000.tb00689.x

Bernfeld P. Amylases, α and β. Methods in enzymol. [Internet]. 1995; 1:149-158. doi: https://doi.org/dc9pbx DOI: https://doi.org/10.1016/0076-6879(55)01021-5

Winkler UK, Stuckman M. Glycogen, hyaluronate, and some other polysaccharides greatly enhance the formation of exo-lipase by Serratia marescens. J. Bacteriol. [Internet]. 1979; 138(3):663-670. doi: https://doi.org/q63k DOI: https://doi.org/10.1128/jb.138.3.663-670.1979

Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the folin phenol reagent. J. Biol. Chem. [Internet]. 1951; 193(1):265-275. doi: https://doi.org/ghv6nr DOI: https://doi.org/10.1016/S0021-9258(19)52451-6

Ringø E, Olsen RE. Gifstad TØ, Dalmo RA, Amlund H, Hemre GI, Bakke AM. Prebiotic in aquaculture, review. Aquac. Nutr. [Internet]. 2010; 16:117-136. doi: https://doi.org/dhb32j DOI: https://doi.org/10.1111/j.1365-2095.2009.00731.x

Grisdale-Helland B, Helland SJ, Gatlin-III DM. The effects of dietary supplementation with mannanoligosaccharide, fructooligosaccharide or galactooligosaccharide on the growth and feed utilization of Atlantic salmon (Salmo salar). Aquaculture. [Internet]. 2008; 283(1-4):163-167. doi: https://doi.org/b3dmz8 DOI: https://doi.org/10.1016/j.aquaculture.2008.07.012

Salze G, McLean E, Schwarz MH, Craig SR. Dietary mannan oligosaccharide enhances salinity tolerance and gut development of larval cobia. Aquaculture. [Internet]. 2008; 274(1):148-152. doi: https://doi.org/b3dmz8, 111, 112] DOI: https://doi.org/10.1016/j.aquaculture.2007.11.008

Torrecillas S, Makol A, Caballero MJ, Montero D, Robaina L, Real F, Sweetman J, Tort L, Izquierdo MS. Immune stimulation and improved infection resistance in European sea bass (Dicentrarchus labrax) fed mannan oligosaccharides. Fish Shellfish Immunol. [Internet]. 2007; 23(5):969-981. doi: https://doi.org/fw379x DOI: https://doi.org/10.1016/j.fsi.2007.03.007

Staykov Y, Spring P, Denev S, Sweetman J. Effect of a mannan oligosaccharide on the growth performance and immune status of rainbow trout (Oncorhynchus mykiss). Aquac. Int. [Internet]. 2007; 15:153-161. doi: https://doi.org/bm5vh5 DOI: https://doi.org/10.1007/s10499-007-9096-z

Aramli MS, Kamangar B, Nazari RM. Effects of dietary β-glucan on the growth and innate immune response of juvenile Persian sturgeon, Acipenser persicus. Fish Shellfish Immunol. [Internet]. 2015; 47(1):606-610. doi: https://doi.org/f7zwbm DOI: https://doi.org/10.1016/j.fsi.2015.10.004

Ai Q, Mai K, Zhang L, Tan B, Zhang W, Xu W, Li H. Effects of dietary β-1,3 glucan on innate immune response of large yellow croaker, Pseudosciaena crocea. Fish Shellfish Immunol. [Internet]. 2007; 22(4):394-402. doi: https://doi.org/d47mt2 DOI: https://doi.org/10.1016/j.fsi.2006.06.011

Misra CK, Das BK, Mukherjee SC, Pattnaik P. Effect of long term administration of dietary β-glucan on immunity, growth and survival of Labeo rohita fingerlings. Aquaculture. [Internet]. 2006; 255(1-4):82-94. doi: https://doi.org/bwv2j8 DOI: https://doi.org/10.1016/j.aquaculture.2005.12.009

Bai N, Zhang WB, Mai KS, Wang XJ, Xu W, Ma, HM. Effects of discontinuous administration of β-glucan and glycyrhizin on the growth and immunity of white shrimp Litopenaeus vannamei. Aquaculture. [Internet]. 2010; 306(1-4):218-224. doi: https://doi.org/fsc3wb DOI: https://doi.org/10.1016/j.aquaculture.2010.06.017

Khodadadi M, Abbasi N, Adorian TJ, Farsani HG, Hedayati A, Hoseini SM. Growth performance, survival, body composition, hematological parameters, intestinal histomorphology, and digestive enzymes' activity in juvenile rainbow trout (Oncorhynchus mykiss) fed dietary Immunogen®. J. Appl. Aquac. [Internet]. 2018; 30(2):174-186. doi: https://doi.org/q64s DOI: https://doi.org/10.1080/10454438.2017.1420515

Brito JM, Urbich AV, Cruz TP, Panczevicz PAP, Miranda JAG, Wernick B, Furuya VRB, Furuya WM. Xylanase and β-glucanase improve growth performance, gut barrier, and microbiota of pre-growout Nile tilapia, Oreochromis niloticus fed a vegetable-based diet. Aquaculture. [Internet]. 2022; 561:738653. doi: https://doi.org/q625 DOI: https://doi.org/10.1016/j.aquaculture.2022.738653

Welker TL, Lim C, Yıldırım-Aksoy M, Shelby R, Klesius PH. Immune response and resistance to stress and Edwardsiella ictaluri challenge in channel catfish, Ictalurus punctatus, fed diets containing commercial whole-cell yeast or yeast subcomponents. J. World Aquac. Soc. [Internet] 2007; 38(1):24-35. doi: https://doi.org/d62qqr DOI: https://doi.org/10.1111/j.1749-7345.2006.00070.x

Castro C, Pérez-Jiménez A, Coutinho F, Pousão-Ferreira P, Brandão T.M, Oliva-Teles A, Peres H. Digestive enzymes of meagre (Argyrosomus regius) and white seabream (Diplodus sargus). Effects of dietary brewer's spent yeast supplementation. Aquaculture. [Internet]. 2013; 416-417:322-327. doi: https://doi.org/q64t DOI: https://doi.org/10.1016/j.aquaculture.2013.09.042

Dehaghani PG, Baboli MJ, Moghadam AT, Ziaei-Nejad S, Pourfarhadi M. Effect of synbiotic dietary supplementation on survival, growth performance, and digestive enzyme activities of common carp (Cyprinus carpio) fingerlings. Czech J. Anim. Sci. [Internet]. 2015; 60(5):224-232. doi: https://doi.org/q64v DOI: https://doi.org/10.17221/8172-CJAS

Özlüer-Hunt A, Özkan-Yılmaz F, Engin K, Berköz M, Gündüz SG, Yalın S, Şahin NÖ. The effects of fish meal replacement by yeast based nucleotides on growth, body composition and digestive enzyme activity in rainbow trout juveniles (Onchorchyncus mykiss). Isr. J. Aquac - Bamidgeh. [Internet]. 2014 [cited 20 Jan 2026]; 66:964-973. Available in: https://goo.su/If9B DOI: https://doi.org/10.46989/001c.20745

Xu B, Wang Y, Li J, Lin Q. Effect of prebiotic xylooligosaccharides on growth performances and digestive enzyme activities of allogynogenetic crucian carp (Carassius auratus gibelio). Fish Physiol. Biochem. [Internet]. 2009; 35(3):351-357. doi: https://doi.org/bw9kzp DOI: https://doi.org/10.1007/s10695-008-9248-8

Ringø E, Strøm E, Tabachek JA. Intestinal microflora of salmonids: a review. Aquac. Res. [Internet]. 1995; 26:773-789. doi: https://doi.org/fd83m6 DOI: https://doi.org/10.1111/j.1365-2109.1995.tb00870.x

Özlüer-Hunt A, Çetinkaya M, Özkan-Yılmaz F, Yıldırım M, Berköz M, Yalın S. Effect of dietary supplementation of Inulin on growth performance, digestion enzyme activities and antioxidant status of rainbow trout (Oncorhynchus mykiss). Turk J. Agric. Food Sci. Technol. [Internet]. 2019; 7(9):1344-1353. doi: https://doi.org/m4cq DOI: https://doi.org/10.24925/turjaf.v7i9.1344-1353.2581

Ringø E, Gatesoupe FJ. Lactic acid bacteria in fish: a review. Aquaculture. [Internet]. 1998; 160(3-4):177-203. doi: https://doi.org/fqcgjm DOI: https://doi.org/10.1016/S0044-8486(97)00299-8

Lemieux H, Blier P, Dutil JD. Do digestive enzymes set a physiological limit on growth rate and food conversion efficiency in the Atlantic cod (Gadus morhua)? Fish Physiol. Biochem. [Internet]. 1999; 20:293-303. doi: https://doi.org/bbvf64 DOI: https://doi.org/10.1023/A:1007791019523

Bongers A, Van den Huevel EGHM. Prebiotics and the bioavailability of mineral and trace elements. Food Rev. Int. [Internet]. 2003; 19(4):397-422. doi: https://doi.org/djrnpr DOI: https://doi.org/10.1081/FRI-120025482

Ganguly S, Paul I, Mukhopadhayay SK. Application and effectiveness of immunostimulants, probiotics, and prebiotics in aquaculture: A review. Isr. J. Aquacult. Bamidgeh. [Internet]. 2010 [cited 20 Jan 2026]; 62(3):130-138. Available in: https://goo.su/n6KDB DOI: https://doi.org/10.46989/001c.38880

Published
2026-05-22
How to Cite
1.
Özlüer-Hunt A, Özkan-Yılmaz F. Growth, body composition and digestive enzyme activities of rainbow trout fed with dietary Beta-glucan containing mannan oligosaccharide. Rev. Cient. FCV-LUZ [Internet]. 2026May22 [cited 2026May25];36(2):9. Available from: http://www.produccioncientifica.luz.edu.ve/index.php/cientifica/article/view/45622
Section
Animal Production