Efficacy of insect larval meal to replace fish meal in juvenile barramundi, Lates calcarifer reared in freshwater
The present experiment was conducted to evaluate the efficacy of dietary protein from black soldier fly, Hermetia illucens, larval meal (BSFL) to replace fish meal (FM) protein in juvenile barramundi, Lates calcarifer. Larvae of black soldier fly were fed with the underutilised crop, sesbania, Sesbania grandiflora. Five isonitrogenous (44% crude protein) and isocaloric (16.0 kJ available energy/g) experimental diets were formulated to replace FM using processed BSFL meal at 0 (control), 25% (BSFL25), 50% (BSFL50), 75% (BSFL75) and 100% (BSFL100). Data for proximate and amino acid analysis suggested BSFL meal as an inferior protein ingredient than FM, but parallel to soybean meal. At the end of 8 weeks of fish feeding trial, there were no significant differences in the average weight gain (WG) and specific growth rate among the group of fish-fed control, BSFL25 and BSFL50 diets (P < 0.05). Although numerical differences were recorded in the fish whole-body proximate composition, crude protein and moisture content were not much affected by the different dietary treatments. Essential amino acids including arginine, histidine, lysine and methionine were found to be higher in the whole body of fish-fed BSFL100 diet. Broken line regression analysis of average WG showed an optimum FM replacement level of 28.4% with BSFL meal. Therefore, the present experiment clearly demonstrates that the maximal dietary inclusion level of BSFL meal as FM protein replacer for the optimum growth of juvenile barramundi reared in freshwater could be greater than 28.4% but less than 50%, without any adverse effects on the fish whole-body proximate and amino acid composition.
KeywordsBlack soldier fly Fish meal Growth Amino acids Barramundi
Aquaculture has become the fastest growing food-producing industry around the world; however, the production efficiency of aquaculture could be further increased through the development of nutritious and cost-effective alternatives to traditional and finite marine protein feedstuffs such as fish meal (FM) (Suarez et al. 2013; Katya et al. 2014). Numerous studies have been carried out to replace or reduce the inclusion level of FM and to identify promising alternative protein sources in aquafeeds. Some of the thoroughly investigated ingredients to partially replace FM in fish feed include plant protein sources such as soybean meal, corn gluten meal and soy protein concentrate, by-products of mushroom (Carter and Hauler 2000; Refstie et al. 2001; Choi et al. 2004; Lim et al. 2004; Kim et al. 2008; Katya et al. 2014) and animal protein sources such as meat and bone meal, blood meal, feather meal, poultry by-product meal and lysine by-product (Bai et al. 1997, 1998; Lee and Bai 1997a, b). However, least attention has been given to access the use of unconventional but promising feedstuffs such as insect meal in commercial fish feed formulation.
In last few years, a considerable number of researches have shed the light on the efficacy of dietary insect meal in several aquaculture species including tilapia, Oreochromis niloticus, salmon, Salmo salar, African catfish, Clarias gariepinus, turbot, Psetta maxima, and rainbow trout, Oncorhynchus mykiss (Kroeckel et al. 2012; Fasakin et al. 2003; Lock et al. 2015; St-Hilaire et al. 2007a, b; Ogunji et al. 2007, 2008; Rana et al. 2015) feeds. Among a number of promising insect species, farming of black soldier fly, Hermetia illucens larvae/pre-pupae has received top priority for the commercial exploitation (Lock et al. 2015). The overall nutrient content viz. crude protein, lipid and essential amino acid content of insect meal closely resemble with FM, and the pre-pupae meal have been demonstrated to be suitably alternative for FM (Kroeckel et al. 2012; Lock et al. 2015; Rana et al. 2015) in several aquaculture species.
Barramundi or Asian sea bass, Lates calcarifer is one of the commercially important fish species widely cultured in several Asian countries. Nutrient requirements for this species has been well defined, considerable efforts have also been made in the three decades to develop nutritionally balanced and cost-effective diets (Glencross 2003). The commercial feed formulation for this species heavily depends upon the FM as the primary protein source. Although, a number of FM alternative ingredients of plant and animal origin have been investigated (Boonyaratpalin et al. 1998; Glencross 2003), use of locally available but nutritionally efficient feedstuff in barramundi feeds is warranted. Therefore, the present experiment was conducted to evaluate the replacement efficacy of protein from BSFL meal with FM protein in juvenile barramundi, reared in freshwater.
Materials and methods
Insects rearing and larval meal production
The insectarium and larval rearing units were set up at the field research center of Crops for The Future (CFF), Kuala Lumpur, Malaysia. Based upon the experience on behaviors of adult insects as well as using the knowledge on the life cycle of black soldier fly, a calm place was selected and natural environment were simulated to attract and induce the mating of adult insects. Six small plastic buckets filled with banana leaves and hay were hanged around the corners and center of the insectarium to collect insect eggs every morning. A series of round bottom 500 L capacity plastic tanks were filled one-third with the blend of underutilized crop sesbania, Sesbania grandiflora. Self-harvesting larvae collection chambers were prepared using flat wooden sheet fixed at 45° angle opening outside the plastic tanks. The BSFL production method were similar that is used by Ajani et al. (2004) and Adesulu and Mustapha (2000) for housefly maggot meal.
Experimental design and diets
Formulation and proximate composition of the experimental control diet (% dry matter base)
Squid liver powder
Procedures for diet preparation and storage were as previously described by Bai and Kim (1997). After thoroughly mixing the dry ingredients and fish oil with 30%-filtered tap water, experimental diets were pelleted with a laboratory pelleting machine without heating, using a 2-mm diameter module (MK-NG 1500 WSL food grinder). All the feeds were air-dried for 24 h and after processing, all diets were kept at −4 °C in the cold storage until use.
Experimental fish and feeding trial
Juvenile size barramundi, Lates calcarifer fish acclimated to freshwater were obtained from the hatchery Biodesaru, Gelang Patah Johor, Malaysia. Fish were transported to the experimental station (FishPLUS laboratory, FRC, Crops for The Future) and acclimated to the experimental conditions for 2 weeks before the feeding trial began. During the acclimation period, fish were fed control diet twice daily (10:00 and 1800 h) at approximately 3% of wet body weight/day. Twenty barramundi fish averaging 6.7 ± 0.1 g (mean ± standard deviation) were randomly distributed in fifteen individual fish groups to each of fifteen aquaria. Each aquarium was then randomly assigned to one of three replicates of five experimental diets. Triplicate groups of fish were fed one of the experimental diet twice daily (10:00 and 17:00 h) at approximately 2% of wet body weight/day at the beginning and 3% of wet body weight/day at the end of the feeding trial for 8 weeks. Total fish weight in each aquarium was determined every 2 weeks, and the amount of feeds fed to the fish was adjusted accordingly.
The feeding trial was conducted in an indoor semi-recirculation system with fifteen 300 L of aquaria receiving filtered freshwater from the center tank. Supplemental aeration was provided to maintain dissolved oxygen levels near 6.5 ± 0.5 (mean ± SD) ppm. Water temperature was 24 ± 1 °C (mean ± SD); pH was 7.5 ± 0.3 (mean ± SD) and the photoperiod of 12:12 (light: dark) was maintained throughout the experimental period.
Sample collection and analysis
At the end of the feeding trial, all of the fish were weighed and counted for the calculation of weight gain (WG), specific growth rate (SGR), feed conversion ratio (FCR) and survival rate. Growth performance parameters including WG, SGR and FCR were calculated using formulas.
Protocol for the feeding trial, fish anesthesia, sample collection and analysis were followed as prescribed and approved by the Animal ethics committee, University of Nottingham. After the final weighing, five fish were randomly collected from each aquaria and frozen at −20 °C for analysis. The proximate composition and amino acid analysis of the experimental diets, ingredients and fish whole body was performed by the standard methods of AOAC (1995). Samples were dried to a constant weight at 105 °C to determine moisture content. Ash was determined by incineration at 550 °C, crude lipid by soxhlet extraction using a Soxtec system 1046 (Tecator AB, Hoganas, Sweden), and crude protein by Kjeldahl method (N × 6.25) after acid digestion. Amino acid analysis was carried out using Ninhydrin method (Sykam Amino Acid Analyzer S433; Sykam, Eresing, Germany).
All data were analyzed by one-way ANOVA (Statistix 3.1, Analytical Software, St. Paul, MN, USA) to test the effects of the dietary treatments. When a significant treatment effect was observed, a least significant difference (LSD) test was used to compare means. Treatment effects were considered at P < 0.05 level of significance. Broken line model (Robbins et al. 1979) was used to evaluate the optimum dietary level of black soldier fly larval meal as fish meal replacer in barramundi.
Nutrient profile of protein ingredients
Analyzed nutrient composition (% DM base) of fish meal, soybean meal and black soldier fly, Hermetia illucens larval (BSFL) meal used as the major protein ingredients in the experimental diets formulation
Growth performance of barramundi, Lates calcarifer-fed black soldier fly, Hermetia illucens larval (BSFL) meal as a fish meal replacer for 8 weeks
136.3 ± 6a
119 ± 8ab
110.3 ± 7ab
92.3 ± 11b
24.3 ± 6c
2 ± 0.06a
1.8 ± 0.08ab
1.7 ± 0.08ab
1.5 ± 0.13b
0.5 ± 0.12c
2 ± 0.1b
2.3 ± 0.1b
2.4 ± 0.1b
3.2 ± 0.1b
11.3 ± 3.6a
94.4 ± 3.9ab
94.4 ± 3.9ab
80.5 ± 14.1b
86.1 ± 10.3ab
Fish whole-body proximate composition
Whole body proximate composition (% dry weight basis) of barramundi, Lates calcarifer-fed black soldier fly Hermetia illucens larval (BSFL) meal as a fish meal replacer for 8 weeks
Fish whole-body essential amino acid composition
Whole body amino acids (ppm) composition of barramundi, Lates calcarifer fed black soldier fly, Hermetia illucens larval (BSFL) meal as a fish meal replacer for 8 weeks
Essential amino acids
Identifying promising alternative ingredients to minimize the inclusion level of dietary fish meal has been a much debated and extensively researched topic in aquaculture. Unfortunately, despite three decades of numerous replacement research, fish meal remains the prime protein ingredient in the majority of commercial fish feeds. Among plant protein, soybean meal is the extensively used ingredient in aquaculture diets due to its wide availability, comparatively low market price and promising nutrient profile (Akiyama et al. 1989; Gatlin et al. 2007; Trosvik et al. 2012; Cummins et al. 2013; Cummins et al. 2017). However, the price of soybean meal and other plant feedstuff has also increased dramatically due to their growing demand for the direct human consumption (FAO 2009). Therefore, attention could be directed towards the locally available and cheaper protein source, which may create flexibility in diet formulations and insect meal has been identified as one such ingredient (Rumpold and Schlüter 2013; Van der Spiegel et al. 2013; Van Huis 2013; Lock et al. 2015).
Black soldier fly was early been recognized as the potential candidate ingredient due to its rich nutritional profile comprised of 40% protein and 35% lipid (Bondari and Sheppard 1987). However, limited and scattered information on nutrient profile and culture techniques has restricted the use of insect larval meal in commercial fish feed formulation. Our observations for the protein content of BSFL meal closely resembled with those of previous reports, indicating 40–45% crude protein content in the larvae of black soldier fly (Yu and Chen 2009; Van Huis 2013). On the other hand, crude lipid content was found to be comparatively lower (16.7 vs. 30%) than those of values reported in these aforementioned studies. It is worthy to note that published reports on insect body composition show large differences between (Sanchez-Muros et al. 2015) and within species. It appears, the substrates used to feed the insect larvae might have profound effects on the final nutrient profile of processed larval meal. Whereas, data for amino acid comparison between fish meal and black soldier fly larval meal showed inferior but not limiting to be used in fish feed formulation, similar to the observation of Sanchez-Muros et al. (2015) with the insect, Tenebrio molitor meal. Overall performances for the the nutrient content (Table 2; Fig. 1) suggested, black soldier fly larvae meal as an inferior protein source than fish meal but closely similar with soybean meal.
The growth performance of barramundi, Lates calcarifer clearly demonstrated that larval meal of black soldier fly could be a promising alternative of fish meal in the feed of carnivorous fish species. Although WG and SGR decreased with fish meal replacement, no significant differences were recorded in these parameters among those of fish fed the BSFL-free diet and those fed-fish meal replaced with 25 and 50% of BSFL meal (P < 0.05). Whereas, published reports on BSFL meal as an alternative of fish meal are extremely few, but has been increasing recently (Cummins et al. 2017). Our results are in consistence with those of previous studies, suggesting an optimum fish meal replacement level of 20–50% using insect meal (Wing-Keong et al. 2001; St-Hilaire et al. 2007b; Alegbeleye et al. 2002; Cummins et al. 2017) in different aquaculture species. Similar to our observation, these aforementioned studies also reported the limitations in replacing fish meal beyond 50% of diet using insect meal. The possible reason for the reduction in fish growth performance with a corresponding increase in the dietary insect meal inclusion could be due to the substantial increase in chitin content (Sanchez-Muros et al. 2015) in addition to the deficiency in essential amino acid content (Cummins et al. 2017). Insect exoskeletons contain chitin and the b1, 4 bond in chitin has been reported to be indigestible for several fish species (Rust 2002). The ability of fish to degrade and digest chitin by the chitinase depends upon the fish species (Smith et al. 1989) and available gut bacteria. For instance, in red tilapia, O. niloticus × O. hornorum and nile tilapia, dietary fishmeal could be significantly replaced with shrimp meal, which is a rich source of chitin, without any adverse effects on the fish performance (El-Sayed 1998; Mansour 1998). Conversely, in the other species of tilapia, O. niloticus x O. aureus, the inclusion of chitin depressed growth (Shiau and Yu 1999). Our observations from the present study suggest, barramundi, Lates calcarifer might have limited efficiency to digest chitin thereby insect meal. Further investigation in this regard are recommended to study the chitin content in the larvae of black soldier fly and the ability of carnivorous fish species to digest chitin.
Further in the current experiment, whole-body proximate composition of fish was not much affected by the black soldier fly larvae inclusion as the fish meal replacer in the diets. Essential amino acids viz. arginine and histidine tend to be higher in the whole body of fish-fed fish meal-free diet, overall performance suggested no adverse effects of black soldier fly inclusion on the amino acid profile. Rainbow trout, Onchrynchus mykiss whole body showed a decreasing trend with a corresponding increase in the dietary black soldier fly inclusion (St-Hilaire et al. 2007a). Whereas, these authors found no difference in whole-body crude protein content in trout-fed different experimental diets. Likewise, in a recent study, the nutrient profile of shrimp whole body has been reported not much affected by fish meal replacement with dietary black soldier fly larval meal (Cummins et al. 2017). Our findings closely resembled with these two previous studies, suggesting negligible effects of dietary black soldier fly larval meal inclusion on the whole-body nutrient profile of aquaculture species. Overall observations from the present experiment are in agreement with those of previous reports, suggesting the potential benefit of using insect larval meal as fish meal alternative in fish feeds. Further studies are recommended to investigate the chitin content and efficiency of carnivorous fish species to digest it, with the view to further enhance the digestibility, and thereby use of insect meal in commercial fish feeds.
In conclusion, the current experiment opens a new avenue for the culture of insect larvae, using underutlised crop, Sesbania, Sesbania grandiflora as the substrate. Observations from the fish feeding trial, augment well for the use of black soldier fly larval meal as the dietary protein source in fish feeds. The maximal dietary inclusion level of protein from black soldier fly larval meal as fish meal protein replacer could be greater than 28.4 but less than 50%, characterized by the optimum growth performance, fish whole-body proximate and amino acid compositions in barramundi, Lates calcarifer reared in freshwater.
This study was conducted under NEWTON Ungku Omar fund—Insect and Underutilised Crops Aquafeed Project (IUCAP), funded by British council and MIGHT, Malaysia. Authors also wish to thank, all the researchers, technical and field staffs of Crops for The Future, (CFF) for all their support during this project.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
- Adesulu EA, Mustapha AK (2000) Use of housefly maggots as a fishmeal replacer in tilapia culture: a recent vogue in Nigeria. In: Ftzimmons K, Filho JC (eds) Proceedings of the fifth international symposium on tilapia aquaculture, pp 138–143Google Scholar
- Ajani EK, Nwanna LC, Musa BO (2004) Replacement of fishmeal with maggot meal in the diets of Nile tilapia, Oreochromis niloticus. J World Aquac Soc 35(52–277):54Google Scholar
- AOAC (1995) Official methods of analysis, 16th edn. Association of Official Analytical Chemists, ArlingtonGoogle Scholar
- Bai SC, Kim KW (1997) Effects of dietary animal protein sources on growth and body composition in Korean rockfish, Sebastes schlegelii. J Aquac 10:77–85 (in Korean with English Abstract) Google Scholar
- Bai SC, Jang HK, Kim KH (1997) Evaluation of feather meal and meat and bone meal as the fish meal replacer in Israeli carp diets. J Aquac 10:153–161Google Scholar
- Bai SC, Jang HK, Cho ES (1998) Possible use of the animal by-product mixture as a dietary fish meal replacer in growing common carp (Cyprinus carpio). J Korean Fish Soc 31:380–385Google Scholar
- Cummins VC, Webster CD, Thompson KR, Velasquez A (2013) Replacement of fish meal with soybean meal, alone or in combination with distiller’s dried grains with solubles, in practical diets for Pacific white shrimp, Litopenaeus vannamei, grown in a clear-water culture system. J World Aquac Soc 44:775–785CrossRefGoogle Scholar
- Cummins VC Jr, Rawles SD, Thompson KR, Velasquez A, Kobayashi Y, Hager J, Webster CD (2017) Evaluation of black soldier fly (Hermetia illucens) larvae meal as partial or total replacement of marine fish meal in practical diets for Pacific white shrimp (Litopenaeus vannamei). Aquaculture 473:337–344CrossRefGoogle Scholar
- FAO (Food and Agricultural Organization of the United Nations) (2009) State of world fisheries and aquaculture 2008 (SOFIA). FAO Fisheries and Aquaculture Department, RomeGoogle Scholar
- Gatlin DM, Barrows FT, Brown P, Dabrowski K, Gaylord TG, Hardy RW, Herman E, Hu G, Krogdahl A, Nelson R, Overturf K, Rust M, Sealy W, Skonberg D, Souza EJ, Stone D, Wilson R, Wurtele E (2007) Expanding the utilization of sustainable plant products in aquafeeds: a review. Aquac Res 38:551–579CrossRefGoogle Scholar
- Glencross BD (2003) Can modelling assist with the determination of nutrient requirements in fish diet? In: van Barneveld RJ (ed) FRDC aquaculture nutrition subprogram annual workshop, Fremantle, WA, Australia. 29 May. pp 65–68Google Scholar
- Katya K, Yun YH, Park G, Lee JY, Yoo G, Bai SC (2014) Evaluation of the efficacy of fermented by-product of mushroom, Pleurotus ostreatus, as a fish meal replacer in juvenile Amur catfish, Silurus asotus: effects on growth, serological characteristics and immune responses. Asian Australas J Anim Sci 27(10):1478–1486CrossRefGoogle Scholar
- Kroeckel S, Harjes A-GE, Roth I, Katz H, Wuertz S, Susenbeth A, Schulz C (2012) When a turbot catches a fly: evaluation of a pre-pupae meal of the black soldier fly (Hermetia illucens) as fish meal substitute—growth performance and chitin degradation in juvenile turbot (Psetta maxima). Aquaculture 364:345–352CrossRefGoogle Scholar
- Lock ER, ArisIwala T, Wagbo R (2015) Insect larval meal as an alternative source of nutrients in the diet of Atlantic salmon (Salmo salar) postmolt. Aquac Nutr 22(6):1–4Google Scholar
- Mansour CR (1998) Nutrient requirements of red tilapia fingerlings. MSc. Thesis, Faculty of Science. University of Alexandria, Alexandria, Egypt, p 121Google Scholar
- Ogunji JO, Nimptsch J, Wiegand C, Schultz C (2007) Evaluation of the influence of housefly maggot meal (magmeal) diets on catalase, glutathione S-transferase and glycogen concentration in the liver of Oreochromis niloticus fingerling. Comp Biochem Physiol Part A: Mol Integr Physiol 147:942–947CrossRefGoogle Scholar
- Rana KS, Salam MA, Hashem S, Islam MA (2015) Development of black soldier fly larvae production technique as an alternate fish feed. Int J Res Fish Aquac 5(1):41–47Google Scholar
- Robbins KR, Norton HW, Baker DH (1979) Estimation of nutrient requirements from growth data. J Nutr. 109(10):1710–1714Google Scholar
- Rust MB (2002) Nutritional physiology. In: Halver JE, Hardy RW (eds) Fish nutrition. Academic Press, New York, pp 368–446Google Scholar
- Suarez JA, Tudela C, Davis D, Daugherty Z, Taynor M, Glass L, Hoenig R, Buentello A, Beenetti DD (2013) Replacement of fish meal by a novel non-GM variety of soybean meal in cobia, Rachycentron canadum: ingredient nutrient digestibility and growth performance. Aquaculture 416–417:328–333CrossRefGoogle Scholar
- Trosvik KA, Rawles SD, Thompson KR, Metts LA, Gannam A, Twibell R, Webster CD (2012) Growth and body composition of Nile tilapia, Oreochromis niloticus, fry fed organic diets containing yeast extract and soybean meal as replacement for fish meal, with and without supplemental lysine and methionine. J World Aquac Soc 43:635–647CrossRefGoogle Scholar
- Yu GH, Chen YH (2009) Research progression on the larvae and prepupae of black soldier fly Hermetia illucens used as animal feedstuff. Chin Bull Entomol 46(1):41–45Google Scholar
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.