Next Article in Journal
Observation of Agonistic Behavior in Pacific White Shrimp (Litopenaeus vannamei) and Transcriptome Analysis
Previous Article in Journal
Significant Differences in Intestinal Bacterial Communities of Sympatric Bean Goose, Hooded Crane, and Domestic Goose
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effects of Defatted and Hydrolyzed Black Soldier Fly Larvae Meal as an Alternative Fish Meal in Weaning Pigs

1
Swine Science Division, National Institute of Animal Science, Rural Development Administration, Cheonan 31000, Republic of Korea
2
Chungcheongbuk-do Agricultural Research and Extension Service, Cheongju 28130, Republic of Korea
3
Department of Animal Science, Chungbuk National University, Cheongju 28644, Republic of Korea
*
Author to whom correspondence should be addressed.
Animals 2024, 14(11), 1692; https://doi.org/10.3390/ani14111692
Submission received: 30 April 2024 / Revised: 3 June 2024 / Accepted: 4 June 2024 / Published: 5 June 2024
(This article belongs to the Section Animal Nutrition)

Abstract

:

Simple Summary

Substitution with black soldier fly larvae meal (BLM, Hermetia illucens L.) has been studied as a possible means of replacing expensive protein sources such as soybean meal and fish meal. However, availability of BLM can differ depending on the substrate and its processing. We investigated the effect of supplementation with defatted and hydrolyzed BLM as an alternative to fish meal in weaning pigs. We found that supplementation with defatted BLM improved nutrient digestibility, growth performance, and economic returns when compared with fish meal (FM) in weaning pigs.

Abstract

In Experiment 1, a total of eighteen crossbred ([Landrace × Yorkshire] × Duroc) barrows with an initial body weight of 6.74 ± 0.68 kg were randomly divided into three dietary treatments (one pig per cage and six replicates per treatment) and housed in metabolic cages that were equipped with a feeder and slatted floor to collect urine and feces. In Experiment 2, a total of 96 crossbred ([Landrace × Yorkshire] × Duroc) barrows with an initial body weight of 8.25 ± 0.42 kg were used in the 6-week trial. The pigs were randomly divided into three dietary treatments (three pigs per pen and eight replicates per treatment). In Experiment 1, nutrient composition of defatted black soldier fly larvae meal (BLM) was superior to that of hydrolyzed BLM but lower than that of fish meal (FM). Also, defatted BLM and FM had better apparent total track digestibility (ATTD) of crude protein (CP) and better nitrogen retention (p < 0.05) than hydrolyzed BLM, but there was no significant difference (p > 0.05) between defatted BLM and FM. In Experiment 2, defatted BLM improved (p < 0.05) average daily gain (ADG), feed conversion ratio (FCR), and feed cost per kg gain (FCG) compared with FM. Defatted BLM could replace soybean meal and fish meal as an alternative protein source for weaning pigs.

1. Introduction

As global population and incomes increase, the consumption of meat originating from monogastric animals is growing, and among these animals, approximately one-third of global meat production is from pork [1,2,3]. Simultaneously, this globally increased consumption has caused high pressure on feed resources [4]. On average, 33% of arable land is used to produce livestock feed, and the livestock produced accounts for 25% of all human protein production [5]. It is difficult to produce feed protein for livestock due to limited arable land and unstable fish catches [6]. Protein feed ingredients are one of the most expensive types of feed (accounting for approximately 60% to 80% of the total feed cost) and limiting feed ingredients in livestock diets [7]. Thus, extensive studies have been conducted to find suitable feed protein alternatives that do not alter the growth performance in animals. Insect meal is known as having high quality protein as well as other essential nutrients for livestock, such as fat and minerals, and even active compounds such as antibiotics that can have a positive effect on livestock health [8,9]. Moreover, insects can consume animal manure and food waste, which reduces environmental pollution and converts the waste into protein [10,11]. In particular, black soldier fly larvae meal (BLM; Hermetia illucens) is easily obtained since these insects are widespread in the tropics and warm temperate regions of the world [12]. The meal contains 7–39% fat and 37–63% protein on a dry matter basis, and has an essential amino acid content similar to that of fish meals [8]. Therefore, BLM has been considered as an effective alternative to fish meals, and many researchers have conducted investigations to evaluate the effects of BLM supplementation on growth performance, nutrient digestibility, blood profiles, and even gut health in pigs in various phases [13,14,15,16].
However, the quality and/or composition of insect meals can be different depending on the substrate used for their rearing. It is also dependent on feed processing, which can be used to increase availability and reduce anti-nutritive factors [17,18]. Cho et al. [17] reported that hydrolyzed mealworm larvae meal improved in vitro digestibility and even apparent ileal digestibility (AID) of nutrients compared with defatted mealworm larvae meal. Moreover, the processing and thermal-conditioning techniques showed a tendency to improve digestibility of amino acids (AAs) in BLM [19]. However, although protein ingredients are crucial during the weaning period, which is the most important phase for early growth, there is little research comparing hydrolyzed and defatted black soldier fly larvae, which are protein sources. Therefore, we conducted an investigation to compare the effect of hydrolyzed and defatted BLM on growth performance, nutrient digestibility, economic returns, and blood profiles in pigs.

2. Materials and Methods

2.1. Ethics

The protocol for this study was approved by the Institutional Animal Care and Use Committee of Chungbuk National University, Cheongju, Republic of Korea (No. CBNUA-2184-23-02).

2.2. Black Soldier Fly Larvae Meal Sample

Defatted BLM obtained from Agricultural Research and Extension Services (Cheongju, Republic of Korea) and hydrolyzed BLM obtained from Jeju National University (Jeju, Republic of Korea) were evaluated (Table 1). The defatted BLM used black soldier flies harvested by rearing 3rd-instar larvae hatched from eggs on wet feed (food waste; 70% moisture) for 10 days. After first drying the harvested black soldier fly larvae using a microwave dryer (M-200, Entomo, Siheung, Republic of Korea), secondary drying was performed using a roaster (M-201, Entomo, Siheung, Republic of Korea) to remove moisture to within 1%. After drying, the larvae were milked using a screw-type insect oil press machine (M-202, Entomo, Siheung, Republic of Korea), and then ground to 100 mesh or less using a fine grinder (M-205, Entomo, Siheung, Republic of Korea). The hydrolyzed BLM used black soldier flies harvested by rearing 3rd instar larvae for 10 days on 1:1 wet feed mixed with citrus peel and poultry offal. After harvesting, primary and secondary drying was carried out as for the defatted BLM and then hydrolyzed using alcalase at 50 °C for 12 h. After the reaction, it went through a concentration step and was dried with hot air. Afterward, it was ground to 100 mesh or less and powdered.

2.3. Digestibility Trial (Experiment 1)

2.3.1. Experimental Animals and Design

A total of 18 crossbred ([Landrace × Yorkshire] × Duroc) barrows with initial body weight of 6.74 ± 0.68 kg at 4 weeks of age were randomly divided into three dietary treatments (1 pig per cage and 6 replicates per treatment) and housed in metabolic cages (45 × 55 × 45 cm) that were equipped with a feeder and slatted floors to collect urine and feces. This experiment was conducted in a room with a heater and fan installed to maintain a 23 ± 1.5 °C temperature with 83 ± 2.3% relative humidity and 0.25 ± 0.03 m/s wind speed.

2.3.2. Diets and Feeding

The dietary treatments were as follows: (1) basal diet based on 5% fish meal (FM), (2) 100% fish meal replacement with defatted BLM, and (3) 100% fish meal replacement with hydrolyzed BLM. All diets were formulated to meet and exceed the National Research Council nutrient requirements for pigs (Table 2) [20]. The daily feeding allowance was calculated at 4% of mean BW of pigs (approximate 3.2 times the estimated metabolize energy (ME) requirement for maintenance ([197 kcal ME per kg body weight0.60]) in each period, divided into two equal portions and fed twice daily at 0800 and 1700 h. Pigs had free access to water throughout the experiment.

2.3.3. Sampling and Analysis

Pigs were weighed at the beginning of experiment and the amount of feed consumed was recorded daily. The total experiment period was 18 days. The initial 5 days were considered the adaptation period to the diet followed by 4 days of total fecal and urine collection according to the marker to marker procedure for the first week [21]. This procedure was repeated in the second week. Briefly, feces were collected from when the first marker appeared in the feces after 6 days and collection stopped when the second marker appeared in the feces after 8 days. Urine was collected from the morning of the fourth day to the morning of the sixth day. Urine was collected into the buckets containing 50 mL of 6 mol/L H2SO4 which were located under the metabolism cages. During the collection period, feces and 20% of the urine were weighted and stored at −20 °C. Leftover feeds were collected and weighed daily to determine feed intake. All collected samples were dried at 65 °C for 72 h in a forced-air oven and ground through 1 mm screen and thoroughly mixed before further analysis. Dried samples, including feces, urine, and feeds, were analyzed in duplicate for dry matter (DM), gross energy (GE), crude protein (CP), and AAs, referring to AOAC methods [22]. The GE, nitrogen, and AAs were analyzed using a bomb calorimeter (Model 6400, Parr Instruments, Moline, IL, USA), a Kjeltec TM 8400 (FOSS Inc., Eden Prairie, MN, USA) with subsequent calculation of CP by a conversion factor of 6.25 for FM and a conversion factor of 4.67 for BLMs [23], and chromatography (Shimadzu model LC-10AT, Shimadzu, Kyoto, Japan), respectively. Using the analyzed values of nutrient concentration in feeds, the nutrient digestibility was calculated using the following equation: apparent total track digestibility (ATTD, %) = [(Ni − Nf) / Ni] × 100 where Ni is the total intake of energy of nutrient and Nf is the fecal output of energy or nutrient originating from the feeds. Nitrogen retention was calculated using following equation: nitrogen retention (%) = {Ni − ((Nf + Nu)/Ni)} × 100 where Ni is nitrogen (N) intake, and Nf and Nu are N output in feces and urine. For blood profiles, at the end of the week, blood was collected from the jugular vein of all pigs using 5 mL syringes and stored in a K3EDTA vacuum tube and a serum separator tube. Piglets had their feed and water withdrawn 12 h before blood collection. Samples were centrifuged at 12,500× g for 15 min at 4 °C. White blood cells (WBCs), red blood cells (RBCs), lymphocytes, and neutrophils; and blood urea nitrogen (BUN) and total protein concentrations were measured using an automatic blood analyzer (ADVIA 120, Bayer, Leverkusen, Germany) and automatic biochemistry blood analyzer (HITACHI 747; Hitachi, Tokyo, Japan), respectively.

2.4. Performance Trial (Experiment 2)

2.4.1. Experimental Animals and Design

A total of 96 crossbred ([Landrace × Yorkshire] × Duroc) barrows at 4 weeks of age (average body weight of 8.25 ± 0.42 kg) were used in the 6-week trial. Pigs were randomly divided into three dietary treatments in a completely randomized block design based on initial BW. There were 3 pigs in a pen with 8 replicate pens for each treatment. The dietary treatments were same as those for Experiment 1: (1) basal diets based on 5% fish meal (FM), (2) 100% fish meal replacement with defatted BLM, and (3) 100% fish meal replacement with hydrolyzed BLM. All diets were formulated to meet and exceed the National Research Council nutrient requirements for pigs (Table 2) [20]. Each pen was equipped with a self-feeder and nipple drinker to allow ad libitum access to feed and water. This experiment was conducted in a room with a heater and fan installed to maintain at 23 ± 1.5 °C temperature with 83 ± 2.3% relative humidity and 0.25 ± 0.03 m/s wind speed.

2.4.2. Sampling and Analysis

To measure growth performance, all piglets were weighed at the start of the experiment, after 2 weeks, after 4 weeks, and at the end of experiment (6 weeks), and feed consumption was recorded to calculate average daily gain (ADG), average daily feed intake (ADFI), and feed conversion ratio (FCR). Economic evaluation was based on the data obtained from each treatment. It was categorized as total weight gain and total feed intake. Total weight gain (TWG) and total feed intake (TFI) were calculated by multiplying the average daily gain and average daily feed intake by the total experimental period, respectively. Feed cost per weight gain (FCG) was calculated by multiplying the TFI by feed cost (USD 0.76/kg, Korea Institute for Animal Products Quality Evaluation, Sejong, Republic of Korea) and then dividing by TWG. When FCG was estimated, only feed cost was considered without taking into account other things such as electricity and porterage, because other expenses were charged, in common, to each treatment.

2.5. Statistical Analysis

All data were statistically analyzed by one-way analysis of variance (ANOVA) using JMP 16.0 (SAS Institute Inc., Cary, NC, USA) with post hoc analysis using Tukey’s honest significant difference (HSD) test. p < 0.05 was considered a statistically significant difference.

3. Results

3.1. Experimant 1

3.1.1. Nutrient Digestibility

Effects of defatted and hydrolyzed BLM on ATTD of DM, CP, and GE as a fish-meal substitute in weaning pigs are presented in Table 3. There was no significant effect (p > 0.05) on ATTD of nutrients in week 1 among treatments. In week 2, there was no significant difference in ATTD (p > 0.05) of CP between FM and defatted BLM, while hydrolyzed BLM had lower ATTD of CP (p < 0.05) than other treatments. Although there was no significant difference (p > 0.05) in ATTD of DM and GE between treatments, FM and defatted BLM numerically increased ATTD of DM and GE compared with hydrolyzed BLM. The effects of defatted and hydrolyzed BLM as a fish-meal substitute on ATTD of amino acids in weaning pigs are presented in Table 4 and Table 5. There was no significant difference (p > 0.05) on ATTD of essential and non-essential amino acids between treatments in weeks 1 and 2. FM and defatted BLM numerically increased the ATTD of essential and non-essential amino acids in weeks 1 and 2 compared with hydrolyzed BLM.

3.1.2. Nitrogen Retention

The effects of defatted and hydrolyzed BLM as a fish-meal substitute on N retention in weaning pigs are presented in Table 6. There was no significant difference (p > 0.05) on nitrogen retention in week 1 between treatments. Defatted BLM did not change (p > 0.05) nitrogen retention in week 2 compared to FM, while hydrolyzed BLM had lower nitrogen retention (p < 0.05) than FM.

3.1.3. Blood Profiles

The effects of defatted and hydrolyzed BLM as a fish-meal substitute on blood profiles in weaning pigs are presented in Table 7. There was no significant difference (p > 0.05) on WBCs, RBCs, lymphocytes, neutrophils, or total protein concentration between treatments. Defatted BLM did not change (p > 0.05) BUN concentration compared to FM, while hydrolyzed BLM had higher BUN concentration (p < 0.05) than FM.

3.2. Experimant 2

Production Performance

The effects of defatted and hydrolyzed BLM as a fish-meal substitute on production performance in weaning pigs are presented in Table 8. There was no significant difference (p > 0.05) in BW between treatments for the entire experiment except for week 6. After 6 weeks, pigs fed defatted BLM had a higher BW (p < 0.05) than those fed FM. Neither type of BLM affected (p > 0.05) ADG, ADFI, or FCR during weeks 0 to 2 weeks and weeks 4 to 6 compared to FM. Defatted BLM significantly increased (p < 0.05) ADG during weeks 2 to 4 compared with FM. During the entire experiment, the defatted BLM group had a higher ADG and FCR (p < 0.05) than the FM group. However, there was no significant difference (p > 0.05) in ADG during weeks 2 to 4, or in ADG and FCR during weeks 0 to 6 weeks between pigs fed defatted or hydrolyzed BLM.
There was no significant difference (p > 0.05) in FCG during weeks 0 to 2 weeks and weeks 4 to 6 weeks between treatments. During weeks 2 to 4 and 0 to 6, defatted BLM significantly increased (p < 0.05) FCG compared with FM although there was no significant difference (p > 0.05) between the two types of BLM.

4. Discussion

According to previous studies, CP concentration of BLM ranged from 30 to 51% although their substrates were different [14,24]. Furthermore, recent studies have reported that full fat and defatted BLM had 41% and 71.2% CP concentration, respectively [25,26]. In our study, CP concentration of defatted and hydrolyzed BLM represented 56.02% and 59.97%, respectively, although their CP concentrations were lower than those of conventional FM. Likewise, defatted BLM had better amino acid profiles of both essential and non-essential amino acids than hydrolyzed BLM despite the fact that their components did not reach those of FM. Lys, classified as belonging to the epsilon amino group, is most susceptible to heat damage and thus Lys concentration of heat-damaged feed ingredients could be decreased while heat damage usually does not affect CP concentration [27]. The Lys:CP ratio has been considered as an indicator of heat damage [28,29]. In this study, the Lys:CP ratio in FM was 0.083, whereas the ratios in defatted and hydrolyzed BLM were 0.062 and 0.057, respectively. High pressure is required for the defatting process, which probably results in heat damage to BLM, leading to a slight reduction in the Lys:CP ratio compared with that of FM. Moreover, the hydrolyzing process is more necessary than the defatting process, and hydrolyzed BLM, therefore, had the lowest Lys concentration compared with other ingredients. According to Dabbou et al. [30], BLM contains a greater amount of lipids, which could represent a higher energy concentration. We found that hydrolyzed BLM had a slightly higher GE concentration than FM and defatted BLM. This finding may be due to the high EE concentration of hydrolyzed BLM. The EE concentration of BLM ranges from 3.4% to 38.6% [31]. Previous studies have reported that nutrient components including CP and EE concentration of insect meals could be altered depending on species, growth phase, harvest point, and processing technique [8,32,33].
In the digestibility trial, no significant difference was observed between treatments for ATTD of DM, CP, or GE in week 1, and ATTD of DM and GE in week 2. Likewise, there was no significant difference in ATTD of indispensable and dispensable amino acids between treatments. Nevertheless, defatted BLM and FM increased ATTD of CP in week 2 compared with hydrolyzed BLM, while there was no significant difference between FM and defatted BLM. Our results were in agreement with those of previous studies which found that dietary BLM supplementation and even partial replacement of soybean meal with defatted BLM did not change nutrient digestibility compared to a basal diet in piglets [16,34]. The main factor of BLM, which could affect nutrient digestibility of livestock, is chitin concentration. BLM is known to contain chitin and this even has a negative effect on nutrient digestion, especially protein and lipid in the animals [35]. Some in vivo studies have reported that chitin supplementation can decrease CP and OM digestibility compared with control diets [36,37]. Likewise, an in vitro study showed that chitin concentration in BLM was negatively correlated with DM, OM, and CP digestibility [38]. Although we did not estimate chitin concentration of both BLMs in this study, it is considered that the lowest ATTD of CP in hydrolyzed BLM may be due to the chitin concentration which is included in the BLM. Our results for N retention and BUN could indirectly prove the above-mentioned mechanism. Chitin, one of the major component of the insect cuticle, increases the actual protein content due to chitinous nitrogen [39,40]. Compared with defatted BLM and FM, N excretion in feces in hydrolyzed BLM was increased at each time point and thus, hydrolyzed BLM had a lower N retention percentage than the other treatments, especially during week 2. Moreover, hydrolyzed BLM had higher BUN concentration, which is inversely correlated to protein utilization in blood, than FM and defatted BLM. As a consequence, increased N excretion of hydrolyzed BLM in feces may mainly be due to the chitin concentration, causing poor N digestibility of hydrolyzed BLM. On the other hand, ATTD of CP and BUN concentrations in blood in pigs fed defatted BLM was similar to that of FM. Rumpold and Schlüter [41] suggested the partial removal of chitin through high pressure processing as a method to solve the reduction in digestion of BLM. Therefore, the positive effects of defatted BLM on nutrient digestibility may have been mainly due to reduction in chitin through the use of high pressure in the defatting process and the preservation of Lys concentration compared with hydrolyzed BLM. However, some studies have shown that DM and CP digestibility was increased by gradually increasing dried mealworm in diets for piglets [42]. Also, according to our previous study, defatted BLM had similar GE and CP digestibility to that of FM, while hydrolyzed BLM had higher CP digestibility than defatted BLM in broilers [43]. These inconsistent results may be mainly due to differences in animals, components of BLM, and the environment.
In the performance trial, defatted BLM supplementation during the entire experimental period improved BW, ADG, and FCR compared with FM. This result was in agreement with a previous study which reported that mealworm supplementation improved growth performance, although the type of insect used and the affected phase were different [42,44]. Unlike our results, other studies have reported that heterogeneous insect meals including full fat and defat types did not influence growth performance and 3.5% FM replacement with defatted BLM also did not affect growth performance of pigs [14,16,34,45,46]. Also, 75% soybean meal replacement with BLM slightly reduced growth performance including growth, feed intake, and protein efficiency in piglets [15]. These inconsistent results may be due to the nutrition difference depending on species and substrate for rearing the insects. As mentioned above, the CP concentration ranged from about 36% to 48%, and EE concentration ranged from about 37% to 48%, although the same dried full-fat BLM was used [16,47,48]. Furthermore, the contrasting results in studies related to the effect of partial BLM supplementation on growth performance could be attributed to the chitin concentration in insect meal. The existence of chitin brings positives and negatives. For example, as mentioned above, chitin could inhibit the nutrient digestibility of pigs. However, many studies have reported that increasing chitin through increased BLM supplementation could activate or boost the innate immune responses in animals and improve intestinal immunoglobulin A (IgA) [6,49,50]. Therefore, the improvement in growth in this study could be attributed to the positive effects on immunity of the chitin contained in both BLMs. In the economic evaluation in this study, defatted BLM and hydrolyzed BLM as FM replacement slightly decreased FCG compared with FM. This result may be attributed to increased ADG and BW in both BLM groups with no alteration in FI. Moreover, the price of defatted and hydrolyzed BLM was USD 2.88/kg and USD 2.95/kg, respectively, and they were cheaper than FM (USD 3.18/kg). Additionally, this price advantage may be attributed to improved economic evaluations of both BLMs.

5. Conclusions

This study suggests that full replacement of fish meal with defatted black soldier fly larvae meal (BLM) did not have a negative effect in terms of nutrient digestibility, but rather, had a positive effect in terms of growth performance and economic evaluation in piglets in Experiments 1 and 2. Therefore, defatted BLM can replace fish meal as an alternative protein source for weaning pigs. However, since the nutrient composition could be different depending on growth phase, substrate, and processing technique, further studies should be performed while maintaining stable nutrient components from BLM.

Author Contributions

Conceptualization, J.L., Y.P., and J.C.; methodology, J.L., Y.P., D.S., and S.C.; investigation, J.L., Y.P., D.S., and S.C.; writing—original draft preparation, J.L.; writing—review and editing, J.L., Y.P., D.S., S.C., and J.C. All authors have read and agreed to the published version of the manuscript.

Funding

This work was carried out with the support of the “Cooperative Research Program for Agriculture Science and Technology Development (Project No. RS-2022-RD009981)” from the Rural Development Administration, Republic of Korea.

Institutional Review Board Statement

The protocol for this study was approved by the Institutional Animal Care and Use Committee of Chungbuk National University, Cheongju, Republic of Korea (No. CBNUA-2184-23-02).

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in this paper.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Bruinsma, J. Agriculture: Towards 2015/2030; A FAO Perspective; Earthscan: London, UK, 2003; p. 432. [Google Scholar]
  2. Komarek, A.M.; Dunston, S.; Enahoro, D.; Godfray, H.C.J.; Herrero, M.; Mason-D’Croz, D.; Rich, F.M.; Scarborough, P.; Springmann, M.; Sulser, T.B.; et al. Income, consumer preferences, and the future of livestock-derived food demand. Glob. Environ. Chang. 2021, 70, 102343. [Google Scholar] [CrossRef]
  3. Miller, V.; Reedy, J.; Cudhea, F.; Zhang, J.; Shi, P.; Erndt-Marino, J.; Coates, F.; Micha, R.; Webb, P.; Mozaffarian, D.; et al. Global, regional, and national consumption of animal-source foods between 1990 and 2018: Findings from the Global Dietary Database. Lancet Planet. Health 2022, 6, 243–256. [Google Scholar] [CrossRef]
  4. Zhao, J.; Ban, T.; Miyawaki, H.; Hirayasu, H.; Izumo, A.; Iwase, S.I.; Kasai, K.; Kawasaki, K. Long-term dietary fish meal substitution with the black soldier fly larval meal modifies the caecal microbiota and microbial pathway in laying hens. Animals 2023, 13, 2629. [Google Scholar] [CrossRef]
  5. van Huis, A.; Gasco, L. Insects as feed for livestock production. Science 2023, 379, 138–139. [Google Scholar] [CrossRef]
  6. Yu, M.; Li, Z.; Chen, W.; Wang, G.; Rong, T.; Liu, Z.; Wang, F.; Ma, X. Hermetia illucens larvae as a fishmeal replacement alters intestinal specific bacterial populations and immune homeostasis in weanling piglets. J. Anim. Sci. 2020, 98, skz395. [Google Scholar] [CrossRef]
  7. Parisi, G.; Tulli, F.; Fortina, R.; Marino, R.; Bani, P.; Dalle Zotte, A.; De Angelis, A.; Piccolo, G.; Pinotti, L.; Schiavone, A.; et al. Protein hunger of the feed sector: The alternatives offered by the plant world. Ital. J. Anim. Sci. 2020, 19, 1204–1225. [Google Scholar] [CrossRef]
  8. 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. [Google Scholar] [CrossRef]
  9. Gasco, L.; Józefiak, A.; Henry, M. Beyond the protein concept: Health aspects of using edible insects on animals. J. Insects. Food. Feed. 2021, 7, 715–741. [Google Scholar] [CrossRef]
  10. Slade, E.M.; Riutta, T.; Roslin, T.; Tuomisto, H.L. The role of dung beetles in reducing greenhouse gas emissions from cattle farming. Sci. Rep. 2016, 6, 18140. [Google Scholar] [CrossRef]
  11. Chavez, M.; Uchanski, M. Insect left-over substrate as plant fertilizer. J. Insects. Food. Feed. 2021, 7, 683–694. [Google Scholar] [CrossRef]
  12. Sheppard, D.C.; Newton, G.L.; Thompson, S.A.; Savage, S. A value added manure management system using the black soldier fly. Bioresour. Technol. 1994, 50, 275–279. [Google Scholar] [CrossRef]
  13. Bondari, K.; Sheppard, D.C. Soldier fly, Hermetia illucens L., larvae as feed for channel catfish, Ictalurus punctatus (Rafinesque), and blue tilapia, Oreochromis aureus (Steindachner). Aquac. Res. 1987, 18, 209–220. [Google Scholar] [CrossRef]
  14. Driemeyer, H. Evaluation of Black Soldier Fly (Hermetia illucens) Larvae as an Alternative Protein Source in Pig Creep Diets in Relation to Production, Blood and Manure Microbiology Parameters. Ph.D. Dissertation, Stellenbosch University, Stellenbosch, South Africa, 2016. [Google Scholar]
  15. Velten, S.; Neumann, C.; Dorper, A.; Liebert, F. Response of piglets due to amino acid optimization of mixed diets with 75% replacement of soybean-meal by partly defatted insect meal (H. illucens). In Proceedings of the INSECTA, Berlin, Germany, 7–8 September 2017; p. 63. [Google Scholar]
  16. Spranghers, T.; Michiels, J.; Vrancx, J.; Ovyn, A.; Eeckhout, M.; De Clercq, P.; De Smet, S. Gut antimicrobial effects and nutritional value of black soldier fly (Hermetia illucens L.) prepupae for weaned piglets. Anim. Feed. Sci. Technol. 2018, 235, 33–42. [Google Scholar] [CrossRef]
  17. Cho, K.H.; Kang, S.W.; Yoo, J.S.; Song, D.K.; Chung, Y.H.; Kwon, G.T.; Kim, Y.Y. Effects of mealworm (Tenebrio molitor) larvae hydrolysate on nutrient ileal digestibility in growing pigs compared to those of defatted mealworm larvae meal, fermented poultry by-product, and hydrolyzed fish soluble. Asian-Australas. J. Anim. Sci. 2020, 33, 490. [Google Scholar] [CrossRef] [PubMed]
  18. Luparelli, A.V.; Saadoun, J.H.; Lolli, V.; Lazzi, C.; Sforza, S.; Caligiani, A. Dynamic changes in molecular composition of black soldier fly prepupae and derived biomasses with microbial fermentation. Food. Chem. X 2022, 14, 100327. [Google Scholar] [CrossRef] [PubMed]
  19. Hosseindoust, A.; Ha, S.; Mun, J.; Kim, J. Effects of meal processing of black soldier fly on standardized amino acids digestibility in pigs. J. Anim. Sci. Technol. 2023, 65, 1014. [Google Scholar] [CrossRef] [PubMed]
  20. NRC (National Research Council). Nutrient Requirements of Swine, 11th ed.; The National Academy Press: Washington, DC, USA, 2012.
  21. Adeola, O. Digestion and balance techniques in pigs. In Swine Nutrition; CRC Press: Boca Raton, FL, USA, 2000; pp. 923–936. [Google Scholar]
  22. AOAC. Official Methods of Analysis, 18th ed.; AOAC International: Washington, DC, USA, 2005. [Google Scholar]
  23. Smets, R.; Claes, J.; Van Der Borght, M. On the nitrogen content and a robust nitrogen-to-protein conversion factor of black soldier fly larvae (Hermetia illucens). Anal. Bioanal. Chem. 2021, 413, 6365–6377. [Google Scholar] [CrossRef] [PubMed]
  24. 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 Aquacult. Soc. 2007, 38, 59–67. [Google Scholar] [CrossRef]
  25. Murawska, D.; Daszkiewicz, T.; Sobotka, W.; Gesek, M.; Witkowska, D.; Matusevičius, P.; Bakuła, T. Partial and total replacement of soybean meal with full-fat black soldier fly (Hermetia illucens L.) larvae meal in broiler chicken diets: Impact on growth performance, carcass quality and meat quality. Animals 2021, 11, 2715. [Google Scholar] [CrossRef]
  26. Van der Heide, M.E.; Nørgaard, J.V.; Engberg, R.M. Performance, nutrient digestibility and selected gut health parameters of broilers fed with black soldier fly, lesser mealworm and yellow mealworm. J. Insects. Food. Feed. 2021, 7, 1011–1022. [Google Scholar] [CrossRef]
  27. Almeida, F.N.; Htoo, J.K.; Thomson, J.; Stein, H.H. Effects of heat treatment on the apparent and standardized ileal digestibility of amino acids in canola meal fed to growing pigs. Anim. Feed. Sci. Technol. 2014, 187, 44–52. [Google Scholar] [CrossRef]
  28. Stein, H.H.; Shurson, G.C. Board-invited review: The use and application of distillers dried grains with solubles in swine diets. J. Anim. Sci. 2009, 87, 1292–1303. [Google Scholar] [CrossRef] [PubMed]
  29. Rodriguez, D.A.; Lee, S.A.; Stein, H.H. Digestibility of amino acids, but not fiber, fat, or energy, is greater in cold-fermented, low-oil distillers dried grains with solubles (DDGS) compared with conventional DDGS fed to growing pigs. J. Anim. Sci. 2020, 98, skaa297. [Google Scholar] [CrossRef] [PubMed]
  30. 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. [Google Scholar] [CrossRef] [PubMed]
  31. Tschirner, M.; Simon, A. Influence of different growing substrates and processing on the nutrient composition of black soldier fly larvae destined for animal feed. J. Insects. Food. Feed. 2015, 1, 249–259. [Google Scholar] [CrossRef]
  32. Khan, S.; Khan, R.U.; Alam, W.; Sultan, A. Evaluating the nutritive profile of three insect meals and their effects to replace soya bean in broiler diet. J. Anim. Physiol. Anim. Nutr. 2018, 102, 662–668. [Google Scholar] [CrossRef] [PubMed]
  33. Zozo, B.; Wicht, M.M.; Mshayisa, V.V.; Van Wyk, J. The nutritional quality and structural analysis of black soldier fly larvae flour before and after defatting. Insects 2022, 13, 168. [Google Scholar] [CrossRef] [PubMed]
  34. 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. [Google Scholar] [CrossRef] [PubMed]
  35. Kroeckel, S.; Harjes, A.G.; Roth, I.; Katz, H.; Wuertz, S.; Susenbeth, A.; Schulz, C. 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 2012, 364, 345–352. [Google Scholar] [CrossRef]
  36. 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. [Google Scholar] [CrossRef]
  37. Bovera, F.; Piccolo, G.; Gasco, L.; Marono, S.; Loponte, R.; Vassalotti, G.; Mastellone, V.; Lombardi, P.; Attia, Y.A.; Nizza, A. Yellow mealworms larvae (Tenebrio molitor L.) as protein source for broilers: Effects on growth performance and blood profiles. Br. Poult. Sci. 2015, 56, 569–575. [Google Scholar] [PubMed]
  38. Kim, J.; Park, K.; Ji, S.Y.; Kim, B.G. Nutrient digestibility in black soldier fly larva was greater than in adults for pigs and could be estimated using fiber. J. Anim. Sci. Technol. 2023, 65, 1002. [Google Scholar] [CrossRef]
  39. Caligiani, A.; Marseglia, A.; Leni, G.; Baldassarre, S.; Maistrello, L.; Dossena, A.; Sforza, S. Composition of black soldier fly prepupae and systematic approaches for extraction and fractionation of proteins, lipids and chitin. Food. Res. Int. 2018, 105, 812–820. [Google Scholar] [CrossRef] [PubMed]
  40. Do, S.; Koutsos, L.; Utterback, P.L.; Parsons, C.M.; De Godoy, M.R.; 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, skz363. [Google Scholar] [CrossRef]
  41. Rumpold, B.A.; Schlüter, O.K. Potential and challenges of insects as an innovative source for food and feed production. Innov. Food. Sci. Emerg. Technol. 2013, 17, 1–11. [Google Scholar] [CrossRef]
  42. Jin, X.H.; Heo, P.S.; Hong, J.S.; Kim, N.J.; Kim, Y.Y. Supplementation of dried mealworm (Tenebrio molitor larva) on growth performance, nutrient digestibility and blood profiles in weaning pigs. Asian-Australas. J. Anim. Sci. 2016, 29, 979. [Google Scholar] [CrossRef] [PubMed]
  43. Chang, S.; Song, M.; Lee, J.; Oh, H.; Song, D.; An, J.; Cho, H.; Park, S.; Jeon, K.; Lee, B.; et al. Effect of black soldier fly larvae as substitutes for fishmeal in broiler diet. J. Anim. Sci. Technol. 2023, 65, 1290–1307. [Google Scholar] [CrossRef]
  44. Crosbie, M.; Zhu, C.; Karrow, N.A.; Huber, L.A. The effects of partially replacing animal protein sources with full fat black soldier fly larvae meal (Hermetia illucens) in nursery diets on growth performance, gut morphology, and immune response of pigs. Transl. Anim. Sci. 2021, 5, txab057. [Google Scholar] [CrossRef] [PubMed]
  45. Nekrasov, R.; Zelenchenkova, A.; Chabaev, M.; Ivanov, G.; Antonov, A.; Pastukhova, N. PSIII-37 Dried Black Soldier Fly larvae as a dietary supplement to the diet of growing pigs. J. Anim. Sci. 2018, 96, 314. [Google Scholar] [CrossRef]
  46. Chia, S.Y.; Tanga, C.M.; Osuga, I.M.; Alaru, A.O.; Mwangi, D.M.; Githinji, M.; Subramanian, S.; Fiaboe, K.K.M.; Ekesi, S.; van Loon, J.J.A.; 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. [Google Scholar] [CrossRef]
  47. Yu, M.; Li, Z.; Chen, W.; Rong, T.; Wang, G.; Ma, X. Hermetia illucens larvae as a potential dietary protein source altered the microbiota and modulated mucosal immune status in the colon of finishing pigs. J. Anim. Sci. Biotechnol. 2019, 10, 50. [Google Scholar] [CrossRef] [PubMed]
  48. 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. Translnal. Anim. Sci. 2020, 4, txaa104. [Google Scholar] [CrossRef] [PubMed]
  49. Jozefiak, A.; Engberg, R.M. Insect proteins as a potential source of antimicrobial peptides in livestock production. A review. J. Anim. Feed. Sci. 2017, 26, 87–99. [Google Scholar] [CrossRef]
  50. Cho, K.H.; Sampath, V.; Kim, A.J.; Yoo, J.S.; Kim, I.H. Evaluation of full-fatted and hydrolysate mealworm (Tenebrio molitor) larvae as a substitute for spray-dried plasma protein diet in weaning pigs. J. Anim. Physiol. Anim. Nutr. 2023, 107, 589–597. [Google Scholar] [CrossRef]
Table 1. Chemical composition of fish meal, defatted black soldier fly larvae (BLM), and hydrolyzed black soldier fly larvae meal (BLM) 1.
Table 1. Chemical composition of fish meal, defatted black soldier fly larvae (BLM), and hydrolyzed black soldier fly larvae meal (BLM) 1.
ItemsFMDefatted
BLM
Hydrolyzed
BLM
General Components      
  GE, kcal/kg4542.204578.124638.92
  DM, %93.0093.2593.41
  CP, %67.0056.0259.97
  EE, %9.006.2611.44
  CF, %0.3010.288.62
  Ash, %10.0216.9310.02
Essential Amino Acids, %      
  Lys5.603.513.40
  Thr3.102.202.00
  Trp1.050.610.54
  Met2.561.030.83
  Phe2.222.272.42
  Ile2.712.292.41
  Leu4.423.803.87
  His2.211.701.48
  Arg4.372.772.68
  Val3.483.853.55
Non-Essential Amino Acids, %      
  Ala4.733.554.24
  Asp6.505.035.11
  Glu7.856.116.14
  Gly4.703.083.03
  Ser2.772.382.07
  Tyr1.833.283.66
  Cys0.910.550.37
  Pro2.833.273.55
1 Abbreviations: BLM, black soldier fly larvae; CP, crude protein; EE, ether extract; CF, crude fiber; Lys, lysine; Thr, threonine; Met, methionine; Phe, phenylalanine; Ile, isoleucine; Leu, leucine; His, histidine; Arg, arginine; Val, valine; Ala, alanine; Asp, aspartic acid; Gly, glycine; Ser; serine; Tyr, tyrosine; Cys, cysteine; Pro, proline.
Table 2. Chemical composition of fish meal (FM), defatted black soldier fly larvae (BLM), and hydrolyzed black soldier fly larvae meal (BLM) (Exp. 1 and 2) 1.
Table 2. Chemical composition of fish meal (FM), defatted black soldier fly larvae (BLM), and hydrolyzed black soldier fly larvae meal (BLM) (Exp. 1 and 2) 1.
ItemsFMDefatted
BLM
Hydrolyzed
BLM
Ingredients, %      
  Corn36.4336.1236.07
  Extruded corn15.0015.0015.00
  Lactose10.0010.0010.00
  Soybean meal, 44% CP14.5014.8114.86
  Soy protein concentrate, 65% CP8.008.008.00
  Fishmeal5.00--
  Defatted BLM-5.00-
  Hydrolyzed BLM--5.00
  Whey5.005.005.00
  Soy oil2.202.202.20
  Monocalcium phosphate1.261.261.26
  Limestone1.401.401.40
  L-Lysine-HCl, 78%0.060.060.06
  DL-Methionine, 50%0.150.150.15
  Choline chloride, 25%0.100.100.10
  Vitamin premix 20.250.250.25
  Trace mineral premix 30.250.250.25
  Salt0.400.400.40
Total100.00100.00100.00
Calculated Value      
  ME, kcal/kg349334933493
  CP, %20.5520.5520.55
  Lysine, %1.551.551.55
  Methionine, %0.410.410.41
Analyzed Value      
  ME, kcal/kg3442.023426.983427.33
  CP, %19.6119.5619.60
  Lysine, %1.481.441.43
  Methionine, %0.490.430.39
1 Abbreviation: FM, basal diet with fishmeal; defatted BLM, basal diet with 100% replacement of fishmeal with defatted BLM; hydrolyzed BLM, basal diet with 100% replacement of fishmeal with hydrolyzed BLM; CP, crude protein; ME, metabolize energy. 2 Provided per kg of complete diet: vitamin A, 11,025 IU; vitamin D3, 1103 IU; vitamin E, 44 IU; vitamin K3, 4.4 mg; riboflavin, 8.3 mg; niacin, 50 mg; thiamine, 4 mg; d-pantothenic, 29 mg; choline, 166 mg; and vitamin B12, 33 mg. 3 Provided per kg of complete diet without zinc: Cu (as CuSO4·5H2O), 12 mg; Mn (as MnO2), 8 mg; I (as KI), 0.28 mg; and Se (as Na2SeO3·5H2O), 0.15 mg.
Table 3. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on apparent total tract digestibility (ATTD) of DM, CP, and GE in weaned pigs (Exp. 1) 1.
Table 3. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on apparent total tract digestibility (ATTD) of DM, CP, and GE in weaned pigs (Exp. 1) 1.
Items, %FMDefatted
BLM
Hydrolyzed
BLM
SEp-Value
Week 1          
  DM84.5585.4084.031.8060.865
  CP74.9876.0475.072.8420.958
  GE83.8084.9582.291.9130.624
Week 2          
  DM84.5085.4282.091.3680.240
  CP80.27 a80.36 a73.19 b1.9030.026
  GE84.3884.9680.661.4890.120
1 Abbreviation: DM, dry matter; CP, crude protein; GE, gross energy; FM, basal diet with fishmeal; defatted BLM, basal diet with 100% replacement of fishmeal with defatted BLM; hydrolyzed BLM, basal diet with 100% replacement of fishmeal with hydrolyzed BLM; SE, standard error; a,b means within a row with different letters are significantly different at p < 0.05.
Table 4. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on apparent total tract digestibility (ATTD) of amino acids in week 1 in weaned pigs (Exp. 1) 1.
Table 4. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on apparent total tract digestibility (ATTD) of amino acids in week 1 in weaned pigs (Exp. 1) 1.
Items, %FMDefatted
BLM
Hydrolyzed
BLM
SEp-Value
Essential Amino Acids          
  Lys76.4877.7474.882.6790.756
  Thr72.4473.2969.193.4000.673
  Trp66.2266.9164.584.0090.916
  Met79.7375.1872.763.1620.314
  Phe76.8275.6974.942.8730.898
  Ile62.2463.5860.994.3470.915
  Leu70.7369.8368.573.2410.895
  His70.8268.5569.513.0580.871
  Arg73.3575.3170.532.9420.528
  Val66.0566.5863.693.1640.792
  Total71.7171.6369.273.1430.826
Non-Essential Amino Acids          
  Ala65.7364.0864.414.1080.956
  Asp80.5779.4978.302.4710.813
  Glu77.6580.1775.962.7300.561
  Gly66.6064.4762.993.7890.798
  Ser79.0379.3777.972.5470.922
  Tyr70.3868.9868.612.9580.905
  Cys69.9869.7763.032.7710.165
  Pro74.1975.3773.293.0880.893
  Total74.7074.6972.522.9230.833
1 Abbreviation: FM, basal diet with fishmeal; defatted BLM, basal diet with 100% replacement of fishmeal with defatted BLM; hydrolyzed BLM, basal diet with 100% replacement of fishmeal with hydrolyzed BLM; SE, standard error.
Table 5. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on apparent total tract digestibility (ATTD) of amino acids in week 2 in weaned pigs (Exp. 1) 1.
Table 5. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on apparent total tract digestibility (ATTD) of amino acids in week 2 in weaned pigs (Exp. 1) 1.
Items, %FMDefatted
BLM
Hydrolyzed
BLM
SEp-Value
Essential Amino Acids          
  Lys79.3179.5574.671.8770.152
  Thr74.8476.0469.462.4500.163
  Trp70.5071.5068.972.8690.823
  Met83.7679.6078.271.6710.084
  Phe77.0776.6775.442.1420.856
  Ile63.3464.9761.242.8610.661
  Leu74.5972.8570.042.1060.332
  His74.6373.6171.762.2920.676
  Arg75.0378.2271.592.0620.109
  Val67.7468.1563.772.8660.507
  Total74.1874.0170.222.1700.369
Non-Essential Amino Acids          
  Ala66.8268.3665.012.6410.675
  Asp82.5882.1579.291.5590.298
  Glu79.6482.1480.061.9850.643
  Gly69.7667.4465.982.8500.648
  Ser82.6083.1780.441.5100.425
  Tyr74.0273.0870.712.3070.591
  Cys74.7775.6571.102.0710.287
  Pro76.7478.3874.132.0280.354
  Total77.1977.8175.041.9740.591
1 Abbreviation: FM, basal diet with fishmeal; defatted BLM, basal diet with 100% replacement of fishmeal with defatted BLM; hydrolyzed BLM, basal diet with 100% replacement of fishmeal with hydrolyzed BLM; SE, standard error.
Table 6. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on nitrogen (N) retention in weaned pigs (Exp. 1) 1.
Table 6. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on nitrogen (N) retention in weaned pigs (Exp. 1) 1.
ItemsFMDefatted
BLM
Hydrolyzed
BLM
SEp-Value
Week 1          
  N intake, g/d18.0716.9318.241.6250.827
  N excretion in urine, g/d2.152.202.290.2500.921
  N excretion in feces, g/d4.443.994.760.6820.731
  Total N excretion, g/d6.596.197.050.7400.720
  N retention, g/d11.4810.7411.191.1490.901
  N retention, % of N intake63.0663.0061.722.3910.906
Week 2          
  N intake, g/d17.9916.7817.651.1880.765
  N excretion in urine, g/d2.402.232.000.2560.543
  N excretion in feces, g/d3.593.424.800.5120.149
  Total N excretion, g/d5.995.656.800.4040.155
  N retention, g/d11.9911.1310.850.8810.644
  N retention, % of N intake66.73 a65.80 ab61.30 b1.3680.030
1 Abbreviation: N, nitrogen; FM, basal diet with fishmeal; defatted BLM, basal diet with 100% replacement of fishmeal with defatted BLM; hydrolyzed BLM, basal diet with 100% replacement of fishmeal with hydrolyzed BLM; SE, standard error; a,b means within a row with different letters are significantly different at p < 0.05.
Table 7. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on blood profiles in weaned pigs (Exp. 1) 1.
Table 7. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on blood profiles in weaned pigs (Exp. 1) 1.
ItemsFMDefatted
BLM
Hydrolyzed
BLM
SEp-Value
WBCs, 103/μL21.5521.1221.840.7680.800
RBCs, 106/μL6.546.646.890.2480.601
Lymphocytes, %59.9061.6560.172.5960.877
Neutrophils, %36.1734.1734.782.3820.833
Total protein, g/dL4.734.725.000.1950.529
BUN, mg/dL8.00 b9.33 ab10.67 a0.6890.048
1 Abbreviation: WBCs, white blood cells; RBCs, red blood cells; BUN, blood urea nitrogen; FM, basal diet with fishmeal; defatted BLM, basal diet with 100% replacement of fishmeal with defatted BLM; hydrolyzed BLM, basal diet with 100% replacement of fishmeal with hydrolyzed BLM; SE, standard error; a,b means within a row with different letters are significantly different at p < 0.05.
Table 8. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on production performance in weaned pigs (Exp. 2) 1.
Table 8. Effects of defatted and hydrolyzed black soldier fly larvae meal (BLM) as a fish-meal substitute on production performance in weaned pigs (Exp. 2) 1.
ItemsFMDefatted
BLM
Hydrolyzed
BLM
SEp-Value
BW, kg          
  Initial8.198.178.380.3770.908
  Week 2 11.3311.3211.490.3530.926
  Week 415.8816.8716.410.4220.276
  Week 621.80 b23.68 a22.81 ab0.4220.017
Weeks 0–2           
  ADG, g224.20225.00222.3210.5610.983
  ADFI, g408.33393.30395.4914.3650.730
  FCR1.821.751.780.1120.721
  FCG, USD/kg gain1.261.141.180.0740.566
Weeks 2–4           
  ADG, g325.27 b396.61 a351.34 ab14.9750.010
  ADFI, g631.47662.87646.5417.8510.474
  FCR1.941.671.840.0800.077
  FCG, USD/kg gain1.31 a1.10 b1.22 ab0.0530.039
Weeks 4–6           
  ADG, g422.68486.61457.1424.8890.216
  ADFI, g962.26991.44976.8819.0480.565
  FCR2.282.042.140.1280.401
  FCG, USD/kg gain1.561.361.430.0850.270
Weeks 0–6           
  ADG, g324.05 b369.40 a343.60 ab7.2810.001
  ADFI, g667.35682.53672.979.7940.550
  FCR2.06 a1.85 b1.96 ab0.0520.031
  FCG, USD/kg gain1.38 a1.21 b1.29 ab0.0340.009
1 Abbreviation: BW, body weight, ADG, average daily gain; ADFI, average daily feed intake; FCR, feed conversion ratio; FCG, feed cost per kg gain; FM, basal diet with fishmeal; defatted BLM, basal diet with 100% replacement of fishmeal with defatted BLM; hydrolyzed BLM, basal diet with 100% replacement of fishmeal with hydrolyzed BLM; SE, standard error; a,b means within a row with different letters are significantly different at p < 0.05.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Lee, J.; Park, Y.; Song, D.; Chang, S.; Cho, J. Effects of Defatted and Hydrolyzed Black Soldier Fly Larvae Meal as an Alternative Fish Meal in Weaning Pigs. Animals 2024, 14, 1692. https://doi.org/10.3390/ani14111692

AMA Style

Lee J, Park Y, Song D, Chang S, Cho J. Effects of Defatted and Hydrolyzed Black Soldier Fly Larvae Meal as an Alternative Fish Meal in Weaning Pigs. Animals. 2024; 14(11):1692. https://doi.org/10.3390/ani14111692

Chicago/Turabian Style

Lee, Jihwan, Younguk Park, Dongcheol Song, Seyeon Chang, and Jinho Cho. 2024. "Effects of Defatted and Hydrolyzed Black Soldier Fly Larvae Meal as an Alternative Fish Meal in Weaning Pigs" Animals 14, no. 11: 1692. https://doi.org/10.3390/ani14111692

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop