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Salahuddin, M.; Abdel-Wareth, A.A.A.; Hiramatsu, K.; Tomberlin, J.K.; Luza, D.; Lohakare, J. Black Soldier Fly Larvae Nutrients Digestibility and Bioavailability. Encyclopedia. Available online: https://encyclopedia.pub/entry/54888 (accessed on 05 July 2024).
Salahuddin M, Abdel-Wareth AAA, Hiramatsu K, Tomberlin JK, Luza D, Lohakare J. Black Soldier Fly Larvae Nutrients Digestibility and Bioavailability. Encyclopedia. Available at: https://encyclopedia.pub/entry/54888. Accessed July 05, 2024.
Salahuddin, Md, Ahmed A. A. Abdel-Wareth, Kohzy Hiramatsu, Jeffery K. Tomberlin, Daylan Luza, Jayant Lohakare. "Black Soldier Fly Larvae Nutrients Digestibility and Bioavailability" Encyclopedia, https://encyclopedia.pub/entry/54888 (accessed July 05, 2024).
Salahuddin, M., Abdel-Wareth, A.A.A., Hiramatsu, K., Tomberlin, J.K., Luza, D., & Lohakare, J. (2024, February 08). Black Soldier Fly Larvae Nutrients Digestibility and Bioavailability. In Encyclopedia. https://encyclopedia.pub/entry/54888
Salahuddin, Md, et al. "Black Soldier Fly Larvae Nutrients Digestibility and Bioavailability." Encyclopedia. Web. 08 February, 2024.
Black Soldier Fly Larvae Nutrients Digestibility and Bioavailability
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This entry is adapted from the peer-reviewed paper 10.3390/ani14030510

The black soldier fly (BSF) is a distinct member of the Stratiomyidae family within the Diptera order. BSF, primarily thriving in South America, has adapted to a wide range of climates including temperate, subtropical, and tropical regions, with its ideal living conditions being temperatures between 25 °C and 30 °C. Outside of industrial production, they cannot live in northwestern Europe and locations with temperatures below 5 °C due to their inability to withstand the cold. Today, the BSF is estimated to inhabit over 80% of the world, particularly between latitudes 46 N and 42 S. Incredibly prolific in humid tropical areas, the BSF is drawn to regions abundant in decomposing organic materials.

black soldier fly larvae (BSFL) nutrients protein digestibility fat bioavailability mineral chitin

1. Introduction

By 2050, the world’s population is anticipated to reach 10 billion, leading to a rise in global food requirements by about 35% to 56% from 2010 levels, as reported by Van Dijk et al. [1]. Animal products currently account for nearly 70% of worldwide food consumption, a figure projected to grow, primarily due to changing dietary preferences and rising economic status, particularly in regions with lower incomes [2]. To accommodate this surge in demand for animal-based products, the global poultry industry needs to enhance its productivity and adopt more eco-friendly practices. Sustainable feeding practices are essential for the poultry sector to achieve environmental and economic sustainability. The choice and management of animal feed play a pivotal role in this process, influencing the overall impact of livestock production on the environment and its economic viability. The high cost of poultry feeds is primarily influenced by the scarcity of critical ingredients like soybean and fishmeal [3]. These components are favored in poultry diets due to their palatability and high protein content. However, their reliance on imports and the associated high costs have prompted researchers to explore alternative protein sources that could substitute soybean and fishmeal in poultry feeds.
In recent years, the quest for sustainable and environmentally friendly alternatives within the animal feed industry has led to a growing interest in black soldier fly larvae (BSFL), scientifically known as Hermetia illucens (L.) (Diptera: Stratiomyidae) [4][5][6][7]. This species, originating from South America, and its larvae have demonstrated remarkable adaptability across various climates, including temperate, subtropical, and tropical regions. Thriving best in temperatures of 25 °C to 30 °C, BSFL can also grow in a range of environmental conditions, showcasing their resilience. Their natural inclination toward habitats rich in decomposing organic material, coupled with this adaptability, highlights their pivotal role in sustainable agriculture and waste management, suitable for diverse geographical locations [8][9][10]. These larvae, which can grow up to 27 mm in length and weigh approximately 220 mg, are nutritionally dense, with a composition rich in proteins and fats [11][12][13][14][15][16][17]. This makes them an invaluable source of nutrients compared with conventional feed ingredients, suitable for a range of animals including poultry [18][19][20][21][22][23], aquaculture species such as fish [24][25][26][27], and swine [28][29][30]. Furthermore, BSFL significantly reduces waste volume by rapidly eating organic waste, providing a practical substitute for conventional landfill disposal techniques. This contributes to reducing methane emissions, a potent greenhouse gas frequently emitted by decomposing organic matter in landfills, and waste accumulation [31][32][33].
In the field of animal nutrition, BSFL have emerged as a highly viable and sustainable source of protein. They present an environmentally friendly alternative to conventional feed ingredients such as soybean meal and fishmeal, which are often linked to environmental challenges like deforestation and overfishing. Additionally, traditional feed components like soybean meal and fishmeal with other feed ingredients can account for up to 70% of total poultry production costs [34]. The nutrient-dense nature of BSFL, which is rich in proteins and lipids, makes them an excellent solution to the growing need for quality feed in chicken raising. The fact that BSFL can feed on various organic wastes not only demonstrates their sustainability but also contributes to significant waste reduction. The dual role of BSFL in delivering vital feed while reducing waste has piqued the interest of the animal feed industry. Their efficient waste conversion into usable biomass adheres to circular economy concepts, establishing BSFL as a trailblazer in advancing sustainable poultry farming operations. The nutritional benefits of BSFL have been shown to be the most appealing to the feed business, with a balanced amino acid composition and a high concentration of protein, energy, and mono- and poly-unsaturated fatty acids [35].
BSFL have been used as a potential alternative source of animal feed, especially for poultry, due to their high digestibility and bioavailability of nutrients.

2. Protein Digestibility

The utilization of nutrients from BSFL is typically efficient. Larval composition allows for the effective utilization of nutrients by broilers, leading to improved growth performance. The protein digestibility of BSFL in poultry is a topic of interest for many researchers and producers, as BSFL have a high protein content and a low environmental impact. The protein digestibility of BSFL in animals and poultry may vary depending on the larvae meal’s age, processing method, and inclusion level. Some studies have reported that BSFL can be used as a partial or complete replacement for conventional protein sources in animal feeds, such as soybean meal, fish meal, or insect meal [36][37][38][39][40]. Recent studies on the protein digestibility of BSFL reveal that the dried larvae protein exhibits a digestibility of 48%, highlighting the need for efficient processing methods to enhance its nutritional value [41]. When the larvae biomass is defatted, the protein digestibility significantly improves to 75%, indicating the impact of fat content on protein availability [41]. The high protein content in BSFL, constituting up to 50% of their dry weight, positions them as a potential sustainable alternative to traditional protein sources in animal feeds [42]. BSFL full-fat meal has a high protein content and is a good source of amino acids, which can further improve CP digestibility [43]. Another interesting recent study has investigated the relationship between inclusion level and nutrient digestibility by using the full-fatted BSFL in diets and found that a moderate inclusion (3%) of full-fatted BSFL in the diet significantly enhanced the digestibility of crude protein [37]. This indicated that these nutrients are better absorbed and used even at lower inclusion levels. The requirement for a balanced approach in feed formulation is shown by the adverse effects of more extensive BSFL inclusions (9%) on nutritional digestibility [37].

3. Fat Bioavailability

BSFL also contain significant amounts of lipids (fats), providing a source of energy for broilers. The fat bioavailability of BSFL in poultry refers to how effectively poultry can digest and utilize the fats present in BSFL as a food source. BSFL are increasingly recognized as a sustainable and efficient protein source for animal feed, including poultry diets. The concept of fat bioavailability is crucial in animal nutrition, as it influences the energy value of the feed and the health of the animals. The lipid profile of BSFL is a significant factor in determining their bioavailability as a feed ingredient, particularly in poultry diets. This profile is characterized by a high content of saturated fatty acids (SFAs), with lauric acid (C12:0) being the most abundant [44][45]. A study demonstrated that larvae with higher weight generally contain a higher percentage of saturated fatty acids and a lower percentage of unsaturated fatty acids such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) [46]. Furthermore, research on the fatty acid composition of BSFL revealed a high content of saturated fatty acids, including a significant 58.9% concentration of lauric acid [47]. Incorporating BSFL fat into poultry diets has emerged as an innovative approach with multiple benefits, as evidenced by various studies. The dietary supplementation of BSFL oil has been shown to positively influence broiler health, suggesting its efficacy as an alternative fat source [48]. This is further supported by research on the inclusion of BSFL fat in finisher broiler chicken diets, which maintains growth performance while offering a sustainable alternative to conventional fat sources [49]. Additionally, evaluating low inclusion rates of full-fatted BSFL meal in chicken diets indicates improvements in growth performance, nutrient digestibility, and gut health [37]. This underscores the potential of BSFL as a comprehensive feed ingredient, as reviewed in studies highlighting BSFL meal’s promise for poultry nutrition. The fatty acid composition of BSFL, notably influenced by the feed substrate, presents significant applications in the feed industry, offering a balanced and nutritious feed component [50]. Research also points to the possibility of BSFL meal and fat completely replacing soybean cake and oil in diets for laying hens, indicating a substantial shift in traditional poultry feeding practices [51]. The impact of BSFL larva fat on broiler diets extends to the quality of the chicken meat itself, particularly affecting breast meat quality [52]. Furthermore, modified BSF larva fat in broiler diets has been examined for its effects on performance, carcass traits, blood parameters, histomorphological features, and gut microbiota, demonstrating its comprehensive impact on poultry health and product quality [53]. Overall, the bioavailability of fat from BSFL in poultry diets presents a multifaceted opportunity. It not only aligns with sustainable feed production but also enhances the nutritional profile of poultry diets, thereby contributing to healthier poultry and potentially higher-quality poultry products.

4. Mineral Uptake

BSFL are known to be a good source of minerals and vitamins, contributing to the overall nutritional value of broiler diets. One of the main advantages of BSFL is their high calcium content, which can reach up to 9% of dry matter (DM) [36]. Calcium is essential for bone formation and eggshell quality in poultry, and its deficiency can cause rickets, osteomalacia, and poor production performance [54][55][56]. BSFL can provide sufficient calcium to meet the requirements of broilers and layers, and may even reduce the need for supplemental limestone or oyster shell in the diet [57]. Moreover, BSFL can enhance calcium absorption and retention in poultry, as they contain a natural form of calcium carbonate that is more soluble and bioavailable than the synthetic forms [58]. Another vital mineral in BSFL is phosphorus, which can range from 0.7% to 1.5% of DM [36]. Phosphorus is involved in many metabolic processes, such as energy production, nucleic acid synthesis, and acid–base balance. Phosphorus deficiency can impair growth, bone development, and egg production in poultry [59][60]. However, most of the phosphorus in plant-based feed ingredients is in the form of phytate, which is poorly digested and utilized by poultry and can also reduce the availability of other minerals, such as calcium, zinc, and iron. Therefore, poultry diets usually require supplemental inorganic phosphorus sources, such as monocalcium phosphate or dicalcium phosphate, which are costly and can have negative environmental impacts. BSFL can offer a more sustainable and efficient source of phosphorus for poultry, as they contain mainly non-phytate phosphorus that is highly digestible and bioavailable [58]. Furthermore, BSFL can improve phytate degradation and phosphorus utilization in poultry, as they contain phytase enzymes that can hydrolyze phytate and release its bound phosphorus [61]. Besides calcium and phosphorus, BSFL also contains other essential minerals, such as magnesium, potassium, sodium, iron, zinc, copper, manganese, and selenium, in varying amounts depending on the substrate and processing method [36]. These minerals play important roles in various physiological functions, such as enzyme activity, antioxidant defense, immune response, and blood formation. However, the optimal levels and ratios of these minerals in poultry diets are not well established, and their interactions with other dietary components may affect their absorption and metabolism. Therefore, more research is needed to determine the effects of BSFL on the mineral balance and status of poultry and to optimize the inclusion levels and combinations of BSFL with other feed ingredients.

5. Chitin as a Fiber Source

The digestibility of BSFL may be affected by the fibrous material called chitin. Although some research suggests that the chitin concentration may have an impact on how nutrients are utilized, overall effects appear to be beneficial. Recent studies have underscored the potential of chitin, a polysaccharide found in the exoskeleton of insects such as BSFL, as a sustainable and beneficial fiber source in poultry diets [62]. BSFL efficiently converts organic waste into valuable nutrients like proteins, lipids, and chitin, offering an environmentally friendly solution to waste management while providing nutrient-rich feed for poultry [63][64][65]. The chitin content in BSFL, which varies based on factors like rearing substrate and life stage, has been reported to range between 5.6% to 6.7% on a DM basis, as indicated in the study findings [66][67][68][69]. This variability is crucial for determining the nutritional impact on poultry. Several studies have explored chitin’s role in enhancing nutrient digestibility in poultry. They suggest that a moderate inclusion level of this insoluble fiber stimulates the development of the gizzard and the production of digestive enzymes, thereby improving the digestion of starch, lipids, and other dietary components [70][71][72]. Additionally, chitin’s impact on poultry gut health is notable. Chitin can modulate the intestinal microbiota, enhance immune responses, and strengthen the mucosal barrier, potentially increasing the population and diversity of beneficial gut bacteria [72][73][74]. This can lead to the production of short-chain fatty acids and a lower intestinal pH, thus inhibiting pathogenic bacteria growth. Moreover, the conversion of chitin into chitosan, its deacetylated form, has been shown to positively affect poultry plasma lipid profiles. Different studies have demonstrated that chitosan can reduce total plasma cholesterol and low-density lipoprotein (LDL) cholesterol concentrations, enhancing the high-density lipoprotein (HDL) to total cholesterol ratio in broilers [70][75][76][77][78]. These findings collectively suggest that chitin from BSFL could be a valuable component in poultry diets, potentially improving nutrient utilization, feed efficiency, gut health, antioxidant function, and lipid metabolism [78][79][80]. However, further systematic research is needed to fully understand the optimal conditions and mechanisms of chitin from BSFL action in poultry nutrition.

6. Factors Influencing Nutrient Utilization

Utilizing BSFL in poultry diets has garnered increasing interest due to their rich nutritional profile and sustainable production potential. The effectiveness of BSFL as a feed ingredient largely depends on their nutritional composition, which includes high levels of protein, essential amino acids, and lipids. These nutritional characteristics are influenced by the larvae’s age and developmental stage, as well as their diet, which can vary significantly based on the substrates they are fed [14][81]. The processing methods applied to BSFL, such as drying or pelleting, also play a crucial role in determining their digestibility and nutrient availability [82]. Furthermore, the inclusion rate of BSFL in poultry diets needs careful consideration, as it can impact feed intake, nutrient absorption, and overall poultry performance. Studies have shown that while moderate inclusion rates can be beneficial, higher rates might lead to reduced palatability and intake [83]. Palatability itself is a significant factor, influencing poultry’s acceptance of BSFL-based feeds. The texture and taste of the larvae can affect feed consumption patterns, which in turn impacts nutrient utilization [84]. Anti-nutritional factors present in BSFL, such as chitin, also warrant attention, as they can impede nutrient absorption and digestion [85]. The specific poultry species and age group being fed BSFL-based diets can exhibit varied responses due to differences in nutrient requirements and digestive capabilities. For instance, the dietary requirements of laying hens differ from those of broilers, which could affect how nutrients from BSFL are utilized [86]. The health status and gut health of the birds are also crucial, as they significantly influence nutrient absorption and overall feed efficiency [87]. Finally, environmental conditions like temperature and housing can affect feed intake, metabolic rates, and growth performance, thereby impacting the utilization of nutrients derived from BSFL [88][89][90][91]. Understanding these complex interactions is essential for optimizing the use of BSFL in poultry diets and ensuring the health and productivity of the birds. Ongoing research in this area is crucial to provide insights into maximizing the benefits of BSFL in sustainable poultry nutrition.

References

  1. Van Dijk, M.; Morley, T.; Rau, M.L.; Saghai, Y. A meta-analysis of projected global food demand and population at risk of hunger for the period 2010–2050. Nat. Food 2021, 2, 494–501.
  2. OECD; Food and Agriculture Organization of the United Nations. OECD-FAO Agricultural Outlook (Edition 2022). 2022. Available online: https://www.oecd-ilibrary.org/content/data/13d66b76-en (accessed on 29 June 2022).
  3. Adeniji, A.A. Effect of replacing groundnut cake with maggot meal in the diet of broilers. Int. J. Poult. Sci. 2007, 6, 822–825.
  4. Digiacomo, K. Black soldier fly larvae protein production in Australia. Anim. Front. 2023, 13, 8–15.
  5. Sankara, F.; Sankara, F.; Pousga, S.; Coulibaly, K.; Nacoulma, J.P.; Ilboudo, Z.; Ouédraogo, I.; Somda, I.; Kenis, M. Optimization of Production Methods for Black Soldier Fly Larvae (Hermetia illucens L.) in Burkina Faso. Insects 2023, 14, 776.
  6. Dzepe, D.; Kuietche, H.M.; Magatsing, O.; Meutchieye, F.; Nana, P.; Tchuinkam, T.; Djouaka, R. From agricultural waste to chicken feed using insect-based technology. J. Basic Appl. Zool. 2023, 84, 18.
  7. Ee, K.Y.; Lam, M.Q.; Mah, J.K.; Merican, A. Black soldier fly (Hermetia illucens L.) larvae in degrading agricultural waste as a sustainable protein production: Feedstock modification and challenges. Int. J. Trop. Insect Sci. 2022, 42, 3847–3854.
  8. Lu, S.; Taethaisong, N.; Meethip, W.; Surakhunthod, J.; Sinpru, B.; Sroichak, T.; Archa, P.; Thongpea, S.; Paengkoum, S.; Purba, R.A.P.; et al. Nutritional composition of black soldier fly larvae (Hermetia illucens L.) and its potential uses as alternative protein sources in animal diets: A review. Insects 2022, 13, 831.
  9. Pazmiño-Palomino, A.; Reyes-Puig, C.; Del Hierro, A.G. How could climate change influence the distribution of the black soldier fly, Hermetiaillucens (Linnaeus)(Diptera, Stratiomyidae)? Biodivers. Data J. 2022, 10, e90146.
  10. Kaya, C.; Generalovic, T.N.; Ståhls, G.; Hauser, M.; Samayoa, A.C.; Nunes-Silva, C.G.; Roxburgh, H.; Wohlfahrt, J.; Ewusie, E.A.; Kenis, M.; et al. Global population genetic structure and demographic trajectories of the black soldier fly, Hermetia illucens. BMC Biol. 2021, 19, 94.
  11. Makkar, H.P.; Tran, G.; Heuzé, V.; Ankers, P. State-of-the-art on use of insects as animal feed. Anim. Feed Sci. Technol. 2014, 197, 1–33.
  12. Newton, G.L.; Sheppard, D.C.; Watson, D.W.; Burtle, G.J.; Dove, C.R.; Tomberlin, J.K.; Thelen, E.E. The black soldier fly, Hermetia illucens, as a manure management/resource recovery tool. In Proceedings of the Symposium on the State of the Science of Animal Manure and Waste Management, San Antonio, TX, USA, 5–7 January 2005; Volume 1, p. 57.
  13. St-Hilaire, S.; Sheppard, C.; Tomberlin, J.K.; Irving, S.; Newton, L.; McGuire, M.A.; Mosley, E.E.; Hardy, R.W.; Sealey, W. Fly prepupae as a feedstuff for rainbow trout, Oncorhynchus mykiss. J. World Aquac. Soc. 2007, 38, 59–67.
  14. Barragan-Fonseca, K.B.; Dicke, M.; van Loon, J.J. Nutritional value of the black soldier fly (Hermetia illucens L.) and its suitability as animal feed—A review. J. Insects Food Feed 2017, 3, 105–120.
  15. Ishak, S.; Kamari, A. Biodiesel from black soldier fly larvae grown on restaurant kitchen waste. Environ. Chem. Lett. 2019, 17, 1143–1150.
  16. Fajar, A. Penggunaan Eceng Gondok dan Limbah Buah Terfermentasi Sebagai Media Tumbuh BSF (Blak Soldier Fly) Terhadap Kualitas Tepung Maggot BSF; Skripsi Fakultas Peternakan Universitas Islam Lamongan: Jawa Timur, Indonesia, 2020.
  17. Scala, A.; Cammack, J.A.; Salvia, R.; Scieuzo, C.; Franco, A.; Bufo, S.A.; Tomberlin, J.K.; Falabella, P. Rearing substrate impacts growth and macronutrient composition of Hermetia illucens (L.) (Diptera: Stratiomyidae) larvae produced at an industrial scale. Sci. Rep. 2020, 10, 19448.
  18. Kawasaki, K.; Hashimoto, Y.; Hori, A.; Kawasaki, T.; Hirayasu, H.; Iwase, S.I.; Hashizume, A.; Ido, A.; Miura, C.; Miura, T.; et al. Evaluation of black soldier fly (Hermetia illucens) larvae and pre-pupae raised on household organic waste, as potential ingredients for poultry feed. Animals 2019, 9, 98.
  19. Brede, A.; Wecke, C.; Liebert, F. Does the optimal dietary methionine to cysteine ratio in diets for growing chickens respond to high inclusion rates of insect meal from Hermetia illucens? Animals 2018, 8, 187.
  20. Cullere, M.; Schiavone, A.; Dabbou, S.; Gasco, L.; Dalle Zotte, A. Meat quality and sensory traits of finisher broiler chickens fed with black soldier fly (Hermetia illucens L.) larvae fat as alternative fat source. Animals 2019, 9, 140.
  21. Dabbou, S.; Gai, F.; Biasato, I.; Capucchio, M.T.; Biasibetti, E.; Dezzutto, D.; Meneguz, M.; Plachà, I.; Gasco, L.; Schiavone, A. Black soldier fly defatted meal as a dietary protein source for broiler chickens: Effects on growth performance, blood traits, gut morphology and histological features. J. Anim. Sci. Biotechnol. 2018, 9, 49.
  22. Lee, J.; Kim, Y.M.; Park, Y.K.; Yang, Y.C.; Jung, B.G.; Lee, B.J. Black soldier fly (Hermetia illucens) larvae enhances immune activities and increases survivability of broiler chicks against experimental infection of Salmonella Gallinarum. J. Vet. Med. Sci. 2018, 80, 736–740.
  23. Mbhele, F.G.; Mnisi, C.M.; Mlambo, V. A nutritional evaluation of insect meal as a sustainable protein source for jumbo quails: Physiological and meat quality responses. Sustainability 2019, 11, 6592.
  24. Xiao, X.; Jin, P.; Zheng, L.; Cai, M.; Yu, Z.; Yu, J.; Zhang, J. Effects of black soldier fly (Hermetia illucens) larvae meal protein as a fishmeal replacement on the growth and immune index of yellow catfish (Pelteobagrus fulvidraco). Aquac. Res. 2018, 49, 1569–1577.
  25. Fawole, F.J.; Adeoye, A.A.; Tiamiyu, L.O.; Ajala, K.I.; Obadara, S.O.; Ganiyu, I.O. Substituting fishmeal with Hermetia illucens in the diets of African catfish (Clarias gariepinus): Effects on growth, nutrient utilization, haemato-physiological response, and oxidative stress biomarker. Aquaculture 2020, 518, 734849.
  26. Bruni, L.; Belghit, I.; Lock, E.J.; Secci, G.; Taiti, C.; Parisi, G. Total replacement of dietary fish meal with black soldier fly (Hermetia illucens) larvae does not impair physical, chemical or volatile composition of farmed Atlantic salmon (Salmo salar L.). J. Sci. Food Agric. 2020, 100, 1038–1047.
  27. Terova, G.; Rimoldi, S.; Ascione, C.; Gini, E.; Ceccotti, C.; Gasco, L. Rainbow trout (Oncorhynchus mykiss) gut microbiota is modulated by insect meal from Hermetia illucens prepupae in the diet. Rev. Fish Biol. Fish. 2019, 29, 465–486.
  28. Altmann, B.A.; Neumann, C.; Rothstein, S.; Liebert, F.; Mörlein, D. Do dietary soy alternatives lead to pork quality improvements or drawbacks? A look into micro-alga and insect protein in swine diets. Meat Sci. 2019, 153, 26–34.
  29. Biasato, I.; Renna, M.; Gai, F.; Dabbou, S.; Meneguz, M.; Perona, G.; Martinez, S.; Lajusticia, A.C.B.; Bergagna, S.; Sardi, L.; et al. Partially defatted black soldier fly larva meal inclusion in piglet diets: Effects on the growth performance, nutrient digestibility, blood profile, gut morphology and histological features. J. Anim. Sci. Biotechnol. 2019, 10, 12.
  30. Chia, S.Y.; Tanga, C.M.; Osuga, I.M.; Alaru, A.O.; Mwangi, D.M.; Githinji, M.; Subramanian, S.; Fiaboe, K.K.; Ekesi, S.; van Loon, J.J.; et al. Effect of dietary replacement of fishmeal by insect meal on growth performance, blood profiles and economics of growing pigs in Kenya. Animals 2019, 9, 705.
  31. Ahmad, I.K.; Peng, N.T.; Amrul, N.F.; Basri, N.E.A.; Jalil, N.A.A.; Azman, N.A. Potential Application of Black Soldier Fly Larva Bins in Treating Food Waste. Insects 2023, 14, 434.
  32. Rehman, K.U.; Hollah, C.; Wiesotzki, K.; Rehman, R.U.; Rehman, A.U.; Zhang, J.; Zheng, L.; Nienaber, T.; Heinz, V.; Aganovic, K. Black soldier fly, Hermetia illucens as a potential innovative and environmentally friendly tool for organic waste management: A mini-review. Waste Manag. Res. 2023, 41, 81–97.
  33. Boakye-Yiadom, K.A.; Ilari, A.; Duca, D. Greenhouse Gas Emissions and Life Cycle Assessment on the Black Soldier Fly (Hermetia illucens L.). Sustainability 2022, 14, 10456.
  34. Mupeta, B.; Coker, R.; Zaranyika, E. The Added Value of Sunflower Performance of Indigenous Chickens Fed a Reduce-Fibre Sunflower Cake Diet in Pens and on Free Range. 2003. Available online: www.dfid.gov.uk/r4d/pdf/outputs/R7524e.pdf (accessed on 1 January 2023).
  35. Mahmoud, I.; Hassan, H.A.; Eldlebshany, A.A.; Abdel-Wareth, A.A.A. Application of black solider fly larvae as alternative source of protein in poultry nutrition. A Review. SVU-Int. J. Agric. Sci. 2022, 4, 67–78.
  36. Seyedalmoosavi, M.M.; Mielenz, M.; Veldkamp, T.; Daş, G.; Metges, C.C. Growth efficiency, intestinal biology, and nutrient utilization and requirements of black soldier fly (Hermetia illucens) larvae compared to monogastric livestock species: A review. J. Anim. Sci. Biotechnol. 2022, 13, 31.
  37. Chu, X.; Li, M.; Wang, G.; Wang, K.; Shang, R.; Wang, Z.; Li, L. Evaluation of the low inclusion of full-fatted Hermetia illucens larvae meal for layer chickens: Growth performance, nutrient digestibility, and gut health. Front. Vet. Sci. 2020, 7, 585843.
  38. Crosbie, M.; Zhu, C.; Shoveller, A.K.; Huber, L.A. Standardized ileal digestible amino acids and net energy contents in full fat and defatted black soldier fly larvae meals (Hermetia illucens) fed to growing pigs. Transl. Anim. Sci. 2020, 4, 104.
  39. Shelomi, M. Nutrient composition of black soldier fly (Hermetia illucens). In African Edible Insects as Alternative Source of Food, Oil, Protein and Bioactive Components; Springer: Cham, Switzerland, 2020; pp. 195–212.
  40. Jian, S.; Zhang, L.; Ding, N.; Yang, K.; Xin, Z.; Hu, M.; Zhou, Z.; Zhao, Z.; Deng, B.; Deng, J. Effects of black soldier fly larvae as protein or fat sources on apparent nutrient digestibility, fecal microbiota, and metabolic profiles in beagle dogs. Front. Microbiol. 2022, 13, 1044986.
  41. Traksele, L.; Speiciene, V.; Smicius, R.; Alencikiene, G.; Salaseviciene, A.; Garmiene, G.; Zigmantaite, V.; Grigaleviciute, R.; Kucinskas, A. Investigation of in vitro and in vivo digestibility of black soldier fly (Hermetia illucens L.) larvae protein. J. Funct. Foods 2021, 79, 104402.
  42. Shumo, M.; Osuga, I.M.; Khamis, F.M.; Tanga, C.M.; Fiaboe, K.K.; Subramanian, S.; Ekesi, S.; van Huis, A.; Borgemeister, C. The nutritive value of black soldier fly larvae reared on common organic waste streams in Kenya. Sci. Rep. 2019, 9, 10110.
  43. Do, S.; Koutsos, L.; Utterback, P.L.; Parsons, C.M.; de Godoy, M.R.C.; Swanson, K.S. Nutrient and AA digestibility of black soldier fly larvae differing in age using the precision-fed cecectomized rooster assay. J. Anim. Sci. 2020, 98, 363.
  44. Spranghers, T.; Ottoboni, M.; Klootwijk, C.; Ovyn, A.; Deboosere, S.; De Meulenaer, B.; Michiels, J.; Eeckhout, M.; De Clercq, P.; De Smet, S. Nutritional composition of black soldier fly (Hermetia illucens) prepupae reared on different organic waste substrates. J. Sci. Food Agric. 2017, 97, 2594–2600.
  45. Barroso, F.G.; de Haro, C.; Sánchez-Muros, M.J.; Venegas, E.; Martínez-Sánchez, A.; Pérez-Bañón, C. The potential of various insect species for use as food for fish. Aquaculture 2014, 422, 193–201.
  46. Ewald, N.; Vidakovic, A.; Langeland, M.; Kiessling, A.; Sampels, S.; Lalander, C. Fatty acid composition of black soldier fly larvae (Hermetia illucens)—Possibilities and limitations for modification through diet. Waste Manag. 2020, 102, 40–47.
  47. Nekrasov, R.V.; Ivanov, G.A.; Chabaev, M.G.; Zelenchenkova, A.A.; Bogolyubova, N.V.; Nikanova, D.A.; Sermyagin, A.A.; Bibikov, S.O.; Shapovalov, S.O. Effect of Black Soldier Fly (Hermetia illucens L.) Fat on Health and Productivity Performance of Dairy Cows. Animals 2022, 12, 2118.
  48. Kim, B.; Bang, H.T.; Jeong, J.Y.; Kim, M.; Kim, K.H.; Chun, J.L.; Ji, S.Y. Effects of dietary supplementation of black soldier fly (Hermetia illucens) larvae oil on broiler health. J. Poult. Sci. 2021, 58, 222–229.
  49. Schiavone, A.; Dabbou, S.; De Marco, M.; Cullere, M.; Biasato, I.; Biasibetti, E.; Capucchio, M.T.; Bergagna, S.; Dezzutto, D.; Meneguz, M.; et al. Black soldier fly larva fat inclusion in finisher broiler chicken diet as an alternative fat source. Animal 2018, 12, 2032–2039.
  50. Cattaneo, A.; Meneguz, M.; Dabbou, S. The fatty acid composition of black soldier fly larvae: The influence of feed substrate and applications in the feed industry. J. Insects Food Feed 2023, 1, 1–26.
  51. Heuel, M.; Sandrock, C.; Leiber, F.; Mathys, A.; Gold, M.; Zurbrügg, C.; Gangnat, I.D.M.; Kreuzer, M.; Terranova, M. Black soldier fly larvae meal and fat can completely replace soybean cake and oil in diets for laying hens. Poult. Sci. 2021, 100, 101034.
  52. Kierończyk, B.; Rawski, M.; Mikołajczak, Z.; Szymkowiak, P.; Stuper-Szablewska, K.; Józefiak, D. Black Soldier Fly Larva Fat in Broiler Chicken Diets Affects Breast Meat Quality. Animals 2023, 13, 1137.
  53. Dabbou, S.; Lauwaerts, A.; Ferrocino, I.; Biasato, I.; Sirri, F.; Zampiga, M.; Bergagna, S.; Pagliasso, G.; Gariglio, M.; Colombino, E.; et al. Modified black soldier fly larva fat in broiler diet: Effects on performance, carcass traits, blood parameters, histomorphological features and gut microbiota. Animals 2021, 11, 1837.
  54. Bai, S.; Yang, Y.; Ma, X.; Liao, X.; Wang, R.; Zhang, L.; Li, S.; Luo, X.; Lu, L. Dietary calcium requirements of broilers fed a conventional corn-soybean meal diet from 1 to 21 days of age. J. Anim. Sci. Biotechnol. 2022, 13, 11.
  55. Carrillo, L.; Bernad, M.J.; Monroy-Barreto, M.; Coello, C.L.; Sumano, H.; Gutiérrez, L. Higher bioavailability of calcium in chickens with a novel in-feed pharmaceutical formulation. Front. Vet. Sci. 2020, 7, 343.
  56. Wilkinson, S.J.; Selle, P.H.; Bedford, M.R.; Cowieson, A.J. Exploiting calcium-specific appetite in poultry nutrition. Worlds Poult. Sci. J. 2011, 67, 587–598.
  57. Schiavone, A.; Dabbou, S.; Petracci, M.; Zampiga, M.; Sirri, F.; Biasato, I.; Gai, F.; Gasco, L. Black soldier fly defatted meal as a dietary protein source for broiler chickens: Effects on carcass traits, breast meat quality and safety. Animal 2019, 13, 2397–2405.
  58. Schiavone, A.; De Marco, M.; Martínez, S.; Dabbou, S.; Renna, M.; Madrid, J.; Hernandez, F.; Rotolo, L.; Costa, P.; Gai, F.; et al. Nutritional value of a partially defatted and a highly defatted black soldier fly larvae (Hermetia illucens L.) meal for broiler chickens: Apparent nutrient digestibility, apparent metabolizable energy and apparent ileal amino acid digestibility. J. Anim. Sci. Biotechnol. 2017, 8, 51.
  59. Valable, A.S.; Narcy, A.; Duclos, M.J.; Pomar, C.; Page, G.; Nasir, Z.; Magnin, M.; Létourneau-Montminy, M.P. Effects of dietary calcium and phosphorus deficiency and subsequent recovery on broiler chicken growth performance and bone characteristics. Animal 2018, 12, 1555–1563.
  60. Nie, W.; Wang, B.; Gao, J.; Guo, Y.; Wang, Z. Effects of dietary phosphorous supplementation on laying performance, egg quality, bone health and immune responses of laying hens challenged with Escherichia coli lipopolysaccharide. J. Anim. Sci. Biotechnol. 2018, 9, 53.
  61. Zulkifli, N.F.N.M.; Seok-Kian, A.Y.; Seng, L.L.; Mustafa, S.; Kim, Y.S.; Shapawi, R. Nutritional value of black soldier fly (Hermetia illucens) larvae processed by different methods. PLoS ONE 2022, 17, e0263924.
  62. Merzendorfer, H.; Zimoch, L. Chitin metabolism in insects: Structure, function and regulation of chitin synthases and chitinases. J. Exp. Biol. 2003, 206, 4393–4412.
  63. Naser El Deen, S.; van Rozen, K.; Elissen, H.; van Wikselaar, P.; Fodor, I.; van der Weide, R.; Hoek-van den Hil, E.F.; Rezaei Far, A.; Veldkamp, T. Bioconversion of Different Waste Streams of Animal and Vegetal Origin and Manure by Black Soldier Fly Larvae Hermetia illucens L. (Diptera: Stratiomyidae). Insects 2023, 14, 204.
  64. Yu, Y.; Zhang, J.; Zhu, F.; Fan, M.; Zheng, J.; Cai, M.; Zheng, L.; Huang, F.; Yu, Z.; Zhang, J. Enhanced protein degradation by black soldier fly larvae (Hermetia illucens L.) and its gut microbes. Front. Microbiol. 2023, 13, 1095025.
  65. Amrul, N.F.; Kabir Ahmad, I.; Ahmad Basri, N.E.; Suja, F.; Abdul Jalil, N.A.; Azman, N.A. A review of organic waste treatment using black soldier fly (Hermetia illucens). Sustainability 2022, 14, 4565.
  66. Koutsos, E.; Modica, B.; Freel, T. Immunomodulatory potential of black soldier fly larvae: Applications beyond nutrition in animal feeding programs. Transl. Anim. Sci. 2022, 6, 084.
  67. Phaengphairee, P.; Boontiam, W.; Wealleans, A.; Hong, J.; Kim, Y.Y. Dietary supplementation with full-fat Hermetia illucens larvae and multi-probiotics, as a substitute for antibiotics, improves the growth performance, gut health, and antioxidative capacity of weaned pigs. BMC Vet. Res. 2023, 19, 7.
  68. de Souza Vilela, J.; Kheravii, S.K.; Bajagai, Y.S.; Kolakshyapati, M.; Sibanda, T.Z.; Wu, S.B.; Andrew, N.R.; Ruhnke, I. Inclusion of up to 20% Black Soldier Fly larvae meal in broiler chicken diet has a minor effect on caecal microbiota. PeerJ 2023, 11, e15857.
  69. Rampure, S.M.; Velayudhannair, K.; Marimuthu, N. Characteristics of chitin extracted from different growth phases of black soldier fly, Hermetia illucens, fed with different organic wastes. Int. J. Trop. Insect Sci. 2023, 43, 979–987.
  70. Razdan, A.; Pettersson, D. Effect of chitin and chitosan on nutrient digestibility and plasma lipid concentrations in broiler chickens. Br. J. Nutr. 1994, 72, 277–288.
  71. Lokman, I.H.; Ibitoye, E.B.; Hezmee, M.N.M.; Goh, Y.M.; Zuki, A.B.Z.; Jimoh, A.A. Effects of chitin and chitosan from cricket and shrimp on growth and carcass performance of broiler chickens. Trop. Anim. Health Prod. 2019, 51, 2219–2225.
  72. Jha, R.; Mishra, P. Dietary fiber in poultry nutrition and their effects on nutrient utilization, performance, gut health, and on the environment: A review. J. Anim. Sci. Biotechnol. 2021, 12, 51.
  73. Malematja, E.; Manyelo, T.G.; Sebola, N.A.; Mabelebele, M. The role of insects in promoting the health and gut status of poultry. Comp. Clin. Pathol. 2023, 32, 501–513.
  74. Kipkoech, C. Beyond Proteins-Edible Insects as a Source of Dietary Fiber. Polysaccharides 2023, 4, 116–128.
  75. Swiatkiewicz, S.; Swiatkiewicz, M.; Arczewska-Wlosek, A.; Jozefiak, D. Chitosan and its oligosaccharide derivatives (chito-oligosaccharides) as feed supplements in poultry and swine nutrition. J. Anim. Physiol. Anim. Nutr. 2015, 99, 1–12.
  76. Harkin, C.; Mehlmer, N.; Woortman, D.V.; Brück, T.B.; Brück, W.M. Nutritional and additive uses of chitin and chitosan in the food industry. In Sustainable Agriculture Reviews 36: Chitin and Chitosan: Applications in Food, Agriculture, Pharmacy, Medicine and Wastewater Treatment; Springer: Cham, Switzerland, 2019; pp. 1–43.
  77. Tufan, T.; Arslan, C. Dietary supplementation with chitosan oligosaccharide affects serum lipids and nutrient digestibility in broilers. S. Afr. J. Anim. Sci. 2020, 50, 663–671.
  78. Ayman, U.; Akter, L.; Islam, R.; Bhakta, S.; Rahman, M.A.; Islam, M.R.; Sultana, N.; Sharif, A.; Jahan, M.R.; Rahman, M.S.; et al. Dietary chitosan oligosaccharides improves health status in broilers for safe poultry meat production. Ann. Agric. Sci. 2022, 67, 90–98.
  79. Kobayashi, S.; Terashima, Y.; Itoh, H. The effects of dietary chitosan on liver lipid concentrations in broiler chickens treated with propylthiouracil. J. Poult. Sci. 2006, 43, 162–166.
  80. Li, Y.; Zhang, Q.; Feng, Y.; Yan, S.; Shi, B.; Guo, X.; Zhao, Y.; Guo, Y. Dietary Chitosan Supplementation Improved Egg Production and Antioxidative Function in Laying Breeders. Animals 2022, 12, 1225.
  81. Rumpold, B.A.; Schlüter, O.K. Nutritional composition and safety aspects of edible insects. Mol. Nutr. Food Res. 2013, 57, 802–823.
  82. Oonincx, D.G.; Van Broekhoven, S.; Van Huis, A.; van Loon, J.J. Feed conversion, survival and development, and composition of four insect species on diets composed of food by-products. PLoS ONE 2015, 10, 0144601.
  83. Biasato, I.; De Marco, M.; Rotolo, L.; Renna, M.; Lussiana, C.; Dabbou, S.; Capucchio, M.T.; Biasibetti, E.; Costa, P.; Gai, F.; et al. Effects of dietary Tenebrio molitor meal inclusion in free-range chickens. J. Anim. Physiol. Anim. Nutr. 2016, 100, 1104–1112.
  84. Hwangbo, J.; Hong, E.C.; Jang, A.; Kang, H.K.; Oh, J.S.; Kim, B.W.; Park, B.S. Utilization of house fly-maggots, a feed supplement in the production of broiler chickens. J. Environ. Biol. 2009, 30, 609–614.
  85. De Marco, M.; Martínez, S.; Hernandez, F.; Madrid, J.; Gai, F.; Rotolo, L.; Belforti, M.; Bergero, D.; Katz, H.; Dabbou, S.; et al. Nutritional value of two insect larval meals (Tenebrio molitor and Hermetia illucens) for broiler chickens: Apparent nutrient digestibility, apparent ileal amino acid digestibility and apparent metabolizable energy. Anim. Feed Sci. Technol. 2015, 209, 211–218.
  86. Cutrignelli, M.I.; Messina, M.; Tulli, F.; Randazzo, B.; Olivotto, I.; Gasco, L.; Loponte, R.; Bovera, F. Evaluation of an insect meal of the Black Soldier Fly (Hermetia illucens) as soybean substitute: Intestinal morphometry, enzymatic and microbial activity in laying hens. Res. Vet. Sci. 2018, 117, 209–215.
  87. Stanley, D.; Hughes, R.J.; Moore, R.J. Microbiota of the chicken gastrointestinal tract: Influence on health, productivity and disease. Appl. Microbiol. Biotechnol. 2014, 98, 4301–4310.
  88. Pornsuwan, R.; Pootthachaya, P.; Bunchalee, P.; Hanboonsong, Y.; Cherdthong, A.; Tengjaroenkul, B.; Boonkum, W.; Wongtangtintharn, S. Evaluation of the Physical Characteristics and Chemical Properties of Black Soldier Fly (Hermetia illucens) Larvae as a Potential Protein Source for Poultry Feed. Animals 2023, 13, 2244.
  89. Bosch, G.; Van Zanten, H.H.E.; Zamprogna, A.; Veenenbos, M.; Meijer, N.P.; Van der Fels-Klerx, H.J.; Van Loon, J.J.A. Conversion of organic resources by black soldier fly larvae: Legislation, efficiency and environmental impact. J. Clean. Prod. 2019, 222, 355–363.
  90. Rummel, P.S.; Beule, L.; Hemkemeyer, M.; Schwalb, S.A.; Wichern, F. Black soldier fly diet impacts soil greenhouse gas emissions from frass applied as fertilizer. Front. Sustain. Food Syst. 2021, 5, 709993.
  91. da Silva, G.D.P.; Hesselberg, T. A review of the use of black soldier fly larvae, Hermetia illucens (Diptera: Stratiomyidae), to compost organic waste in tropical regions. Neotrop. Entomol. 2020, 49, 151–162.
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Subjects: Agriculture, Dairy & Animal Science
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Md Salahuddin
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Ahmed A. A. Abdel-Wareth
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Kohzy Hiramatsu
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Jeffery K. Tomberlin
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Daylan Luza
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Jayant Lohakare
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Update Date: 08 Feb 2024
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