Skip to main content

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



Dietary supplementation of full-fat black soldier fly larvae (BSFL full-fat meal; alone or in combination with multi-probiotics) was tested as an alternative to dietary antibiotics in weaning piglets. We also tested the effects of these diets on growth performance, nutrient digestibility coefficients, immune status, oxidative stress, intestinal histomorphology, and rectal microbial modulations in weaned pigs. A total of 80 piglets [(Landrace × Large White) × Duroc] of both sexes (a ratio of gilts and barrows; 1:1), were randomly allotted to four diet groups: positive control (PC) diet supplemented with 0.02% amoxicillin; negative control (NC) diet without supplement addition; BSFL12 diet (NC + 12% BSFL full-fat meal); and BSFL + Pro diet (BSFL full-fat meal + 0.1% multi-probiotics, including Bacillus subtilis, B. licheniformis, and Saccharomyces cerevisiae). All groups had five replicates, with four piglets per replicate.


Dietary BSFL + Pro improved the overall average daily gain (P = 0.013), and gain-to-feed ratio (P = 0.032). The BSFL12 and BSFL + Pro diets improved nutrient digestibility and increased the serum levels of immunoglobulin A and glutathione peroxidase, while reducing the levels of pro-inflammatory cytokines. The spleen weight was higher and caecal pH was lower in pigs fed the BSFL + Pro diet than in those fed the NC diet (P = 0.011 and P = 0.021, respectively). Pigs fed the BSFL diets had longer duodenal villi, a higher villus height-to-crypt depth ratio (P = 0.004), and shorter crypt depth (P = 0.017) than those fed NC. The BSFL + Pro diet also increased faecal Lactobacillus spp. count (P = 0.008) and reduced Escherichia coli (P = 0.021) counts compared with that seen with PC and NC diets, respectively.


Dietary supplementation with BSFL or BSFL + multi-probiotics can improve the growth performance and intestinal health of pigs and may be an effective strategy to replace antibiotics for weaned pigs.

Peer Review reports


For several years, amoxicillin has been widely used to control post-weaning diarrhoea in piglets. However, the excessive use of antimicrobials in food animal production has led to concerns regarding the spread of multidrug-resistant pathogens. Since 28 January 2022, the use of amoxicillin in the food animal production industry has been regulated by the European Medicines Agency [1]. To curb the escalating problem of antibiotic resistance, the bioactive properties of black soldier fly larva full-fat meal (BSFL) and multi-strain probiotics (i.e., Bacillus subtilis, B. licheniformis, and Saccharomyces cerevisiae) have been suggested as effective alternatives to in-feed antibiotics. The BSFL is an attractive protein source for monogastric animals, especially because of its high crude protein content (40.11 ± 7.1%), ether extract (32.54 ± 11.2%), essential amino acid content (0.7 ± 0.4% methionine, 2.3 ± 0.9% lysine, and 1.8 ± 1.2% arginine), and lauric acid content (64 ± 7.8%) [2,3,4,5]. BSFL-derived antimicrobial peptides (AMPs) and chitin also inhibit the proliferation of harmful bacteria and activate immunity [6, 7]. Previous studies have demonstrated that the BSFL full-fat meal can be used in dietary formulations at a concentration of 8% in weanling pigs [8] and 18.5% in growing pigs [9], without any detrimental effects on growth performance. In addition, multi-strain probiotics are well-established to have better antibacterial, anti-inflammatory, and antioxidant properties than single-strain probiotics [10, 11]. Recently, a multi-strain Bacillus subtilis-based probiotic has been shown to improve the growth performance of pigs and the nutrient digestibility of essential amino acids [12]. Moreover, the inclusion of up to 0.3% probiotic mixture improves the growth performance of weaning pigs, inhibits the growth of harmful microbes, and reduces faecal NH3 emissions [13].

To our knowledge, few studies have examined how BSFL and multi-strain probiotics (alone or in combination), when used as substitutes for amoxicillin, affect growth performance, nutrient digestibility coefficients, immune status, oxidative stress, intestinal histomorphology, and rectal microbial modulation in weaned pigs. We hypothesised that when used in combination, BSFL full-fat meal and multi-strain probiotics were more likely to enhance the growth performance and gut health of weaned pigs than in-feed antibiotics. This would help mitigate the problem of antimicrobial resistance due to the escalating use of amoxicillin.


This study was reported in accordance with ARRIVE guidelines and was conducted in strict accordance with the guidelines of the National Research Council of Thailand. Protocols were approved by the Institutional Animal Care and Use committee of Khon Kaen University (Khon Kaen, Thailand; approval number 125/64 on 18 November, 2021).

BSFL and probiotics

The BSFL (Hermetia illucens) were obtained locally (Ban Dangnoi, Khon Kaen, Thailand), reared under constant conditions (27 ± 1 °C, 65% relative humidity, and L12:D12 photoperiod) and fed broiler feed substrate without any feed additive, coccidiostats, or antibiotic growth promoters (expect for 29 mg of CuSO4 and 108 mg of ZnSO4). Larvae were harvested on day 13 of larval development and killed by freezing at − 20 °C for 6 h. Next, the samples were dried at 65 °C for 72 h, and their nutrient composition was analysed before they were added to the dietary formulation. The nitrogen-to-protein conversion factor (kp) for BSFL full-fat meal is 5.33 [14]. This was subsequently used to calculate crude protein percentage as 5.33 x the nitrogen (N) content. The main components of BSFL are crude protein (CP, 35.88%), ether extract (EE, 30.58), lysine (2.31%), total essential amino acids (15.81%), non-essential amino acids (18.59%), lauric acid (9.17%), total saturated fatty acids (21.09%), unsaturated fatty acids (11.62%), and chitin (4.26%) (Table 1). The multi-probiotics included Bacillus subtilis (1 × 1011 cfu/kg), Bacillus licheniformis (1 × 109 cfu/kg), and Saccharomyces cerevisiae (1 × 109 cfu/kg).

Table 1 Analysed values of BSF larvae (Hermetia illucens, dry matter basis)

Animals, treatments, and management

A total of 80 piglets [(Landrace × Large White) × Duroc] weaned at 28 ± 3 days of age (7.34 ± 0.21 kg body weight, BW) were divided into four experimental groups and fed the following diets: PC, basal diet supplemented with 0.02% amoxicillin; NC, basal diet without supplementation; BSFL12, basal diet supplemented with 12% full-fat BSFL; and BSFL + Pro, basal diet supplemented with BSFL + 0.1% multi-probiotics. Each treatment had five replicates. Each animal pen had an equal number of gilts and barrows (1:1 ratio) in a randomised complete block design with initial body weight as the blocking factor. Pigs were housed in pens with slatted concrete flooring (20 pens, 1.6 × 2.1 m; stocking density, 0.8 m2/pig) furnished with a low-pressure nipple drinker, stainless steel trough, and heating lamp. Rice straw and gunny bags were supplied as bedding materials during the 14-day post-weaning period and were changed twice daily (0600 and 1900), following the guidelines of the EU Directive 2010/63/EC for animal experiments. All pigs were vaccinated against Aujeszky’s disease, salmonellosis, and transmissible gastroenteritis. Mash diets were formulated to meet or exceed the nutrient requirements for pigs weighing 11–25 kg. The diets were formulated in two phases (Phase I, 1–2 weeks post-weaning; Phase II, 3–4 weeks post-weaning) as suggested by the National Research Council (NRC) [15] (Table 2). All pigs had free access to feed and water throughout the experimental period.

Table 2 Ingredients and nutrient values of the experimental diet (% as fed basis)

Measurement of growth performance and incidence of diarrhoea

On days 1, 15, and 29 post-weaning, each pig was weighed individually at 0600. Following this, pen-based feed disappearance was recorded to determine the average daily gain (ADG), average daily feed intake (ADFI), and gain-to-feed ratio (G:F, calculated as ADG/ADFI). The severity of diarrhoea was measured visually using a faecal consistency score: 0, firm and shape faeces; 1, soft and shaped faeces; 2, loose faeces; and 3, watery faeces. Scores of 0 and 1 represented normal faeces, whereas scores of 2 and 3 represented diarrhoea. Diarrhoeal rate (%) was calculated using the following formula:

$$\textrm{Diarrhoeal}\ \textrm{rate}=\textrm{number}\ \textrm{of}\ \textrm{pigs}\ \textrm{with}\ \textrm{diarrhoea}/\left(\textrm{total}\ \textrm{number}\ \textrm{of}\ \textrm{pigs}\ \textrm{by}\ \textrm{treatment}\times \textrm{days}\ \textrm{with}\ \textrm{diarrhoea}\right)\times 100$$

Apparent total tract digestibility (ATTD)

A total of 20 barrows (initial average BW = 10.26 ± 2.36 kg) were chosen separately from the feeding trial and assigned to each dietary treatment in five replicates in a completely randomised design. The pigs were housed individually in cages (0.58 m × 0.83 m) equipped with a grid and slurry pit for a 7-d adaption and 5-d faecal collection period. The experimental diets were offered at 12-h intervals in an amount equalling 3× the maintenance energy requirement (106 kcal of metabolisable energy per kg of BW0.75) [15]. During the faecal collection period, two indigestible indicators, chromic oxide and ferric oxide were homogenously mixed with all the experimental diets (5 g/kg feed of each marker) at the first and last meal, respectively, according to the marker-to-marker method [19]. The collection of faecal output started and ended when the initial and final marker appeared in the faeces, respectively. The faecal collection was performed daily at 1900 hrs. Pooled faeces were weighed and dried in a forced air-drying oven (60 °C for 72 h) and subsequently ground in a hammer mill using a 0.88 mm screen. Representative samples of pooled faeces and diets were used to measure the levels of dry matter (DM, method #930.15), CP (method #984.13), crude ash (method #942.15), and EE method (#920.39) using standard Association of Official Analytical Chemists protocols [20]. These values were used to calculate ATTD using following formula [19]:

$$\textrm{X}\ \textrm{apparent}\ \textrm{digestibility}=\frac{\textrm{X}\ \textrm{ingested}-\textrm{X}\ \textrm{excreted}}{\textrm{X}\ \textrm{ingested}}\times 100$$

where X represents DM, CP, crude ash, or EE in feed and faeces, respectively.

Blood collection and analyses

On day 29, one healthy pig per pen (n = 20), weighing the BW average of the pen, was selected for blood sampling (10 mL) from the anterior vena cava. Blood samples were collected in serum-coated tubes with silica (Grener Bio-one, Chonburi, Thailand), allowed to clot at room temperature for 60 min, centrifuged for 10 min at 4 °C at 13,000×g, and then frozen at − 20 °C. Serum concentrations of immunoglobulin A (IgA), immunoglobulin G (IgG), immunoglobulin M (IgM), interleukin-1β (IL1β), interleukin-6 (IL6), and tumour necrosis factor alpha (TNFα) were quantified using porcine enzyme-linked immunosorbent kits (Abcam, Cambridge, UK). The concentrations of total antioxidant capacity (TAC), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and malondialdehyde (MDA) were determined using commercial kits (Sigma-Aldrich, St. Louis, MO). All assays were performed as outlined by the manufacturer and conducted in triplicate to control for variation.

Organ weight

After blood collection, all selected pigs were slaughtered after 12 h of fasting. The digestive tract was eviscerated to harvest the heart, liver, kidney, stomach, and spleen. Each organ was separately flushed with 0.9% phosphate-buffer saline solution, blot-dried, and weighed using a digital scale. Segments of the colon, cecum, and small intestine were also collected for later examination.

Digesta pH

The cecum and colon (proximal, middle, and distal portions) tissues collected were immediately used to measure the hindgut pH with a pH metre (AP 110, Fisher Scientific, Pittsburgh, PA, USA).

Intestinal histomorphology

Segments of the small intestine were collected immediately after euthanasia. Longitudinal dissections of the duodenum (50 cm caudal to pyloric sphincter), jejunum (5 cm from the pyloric sphincter), and ileum (20 cm from the ileocecal orifice) were performed carefully. Each sample was rinsed with saline solution and fixed with a neutral buffer (pH 7.0) and formaldehyde solution (10% vol/vol) for 72 hours. The tissue samples were embedded with ethanol and xylene and then transversely cut into 5-μm-thick sections using a rotary microtome (Leica RM2235, Wetzlar, Germany). The tissue sections were placed on glass slides and stained with haematoxylin-eosin (H&E staining, Sigma-Aldrich, St Louis, MO, USA). In total, 20 well-oriented villi (per stained section) and crypt columns were used to determine villus height (VH, from the tip of the villus to the basolateral membrane) and crypt depth (CD, from the villus–crypt junction and the submucosa) using an optical light microscope at 10× magnification. Average VH and CD values were recorded, and the villus height-to-crypt depth ratio (VH/CD) was calculated.

Microbial count

Faecal samples were collected by rectal massage of the pigs (5 samples per treatment) and suspended in 0.9% (w/v) sodium chloride solution at 1:10 dilution. A 0.1 mL aliquot of each dilution was spread-plated in triplicate onto deMan, Rogosa, and Sharpe (Difco™ Lactobacillus MRS agar, Becton, Dickinson and Company, USA), MacConkey (Himedi™, HiMedia Laboratories, India), and SalmonellaShigella agar (Oxoid™ SS Agar, Oxoid Limited, Thermo Fisher Scientific Inc., UK) for the determination of Lactobacillus spp., Escherichia coli, and Salmonella spp., respectively, following the manufacturer’s guidelines. The average growth of each microbe was log-transformed and represented as log10 colony-forming unit (CFU)/g of faeces.

Statistical analysis

Data were analysed using general linear models in SAS (version 9.4, SAS Inst. Inc., Cary, NC, USA) using a randomised complete block design with “pen” as the experimental unit for growth performance and diarrhoea rate, and “each pig” as the experimental unit for digestibility, blood analyses, organ weight, hindgut pH, intestinal morphology, and microbial counts. The statistical model was:

$$Yij=\mu +{\alpha}_i+{\beta}_j+{\varepsilon}_{ij}$$

where Yij is the jth observation of the ith treatment; μ is the overall mean; αi is the effect of the ith block (i = 1–5); βj is the effect of the jth treatment (j = 1–4); and εij is the error term.

Normal probability was assessed using the Shapiro-Wilk test and homogeneity of error variance among treatments was verified using the Hartley’s test. If the data was not characterised by the normal distribution, the nonparametric analysis was verified using the Friedman’s test. Duncan’s new multiple range test was used to test for significant differences among dietary treatments using the SAS package. All data were represented as the mean ± standard error of the mean (SEM), and P < 0.05 was considered statistically significant.


Growth performance and diarrhoeal rate

During the experimental period, the values of ADG (P = 0.013) and G:F (P = 0.032) were increased by 18.16 and 18.21%, respectively, compared to those obtained using the NC diet (Table 3). Outcomes of the BSFL + Pro diet were comparable to those of the positive control diet (PC, basal diet supplemented with 0.02% amoxicillin) in all experimental periods. However, the BW, ADFI and the incidence of diarrhoea was unaffected by dietary treatment during Phases I and II (P > 0.05).

Table 3 Effect of dietary BSFL full-fat meal and probiotic mixture to replace antibiotics on growth performance and diarrhoeal rate in weaning pigs1,2

Nutrient digestibility coefficients

Diets supplemented with BSFL12 (basal diet supplemented with 12% BSFL full-fat meal) and BSFL + Pro groups increased the ATTD of DM (P = 0.047), CP (P = 0.022), and EE (P = 0.019) compared to that seen in the NC-fed group (Table 4); however, ATTD was comparable to that in the PC-fed group. However, there were no differences in the ATTD of crude ash among dietary treatments (P > 0.05).

Table 4 Effect of dietary BSFL full-fat meal and probiotic mixture to replace antibiotics on the apparent total tract digestibility (ATTD) in weaning pigs on day 281,2

Blood-related gut health and antioxidative stress

The concentration of IgA (P = 0.044) was higher in the BSFL-supplemented diets, whereas reduced IL1β (P = 0.031) and MDA (P = 0.006) concentrations occurred in comparison to NC (Table 5). In addition, the pigs fed BSFL+ Pro diet had higher IgG (P = 0.008), SOD (P = 0.033), and GSH-Px (P = 0.026), with a lower secretion of TNFα than those fed the NC diet (P = 0.044). However, the dietary treatments did not affect serum concentrations of IgM, IL6, and TAC (P > 0.05).

Table 5 Effect of dietary BSFL full-fat meal and probiotic mixture to replace antibiotic on the blood-related gut health and antioxidative stress in weaning pigs1,2

Organ weight

Pigs that were fed the BSFL + Pro diet had the highest spleen weight compared to pigs who were fed other treatments (P = 0.011; Table 6). However, the organ weights of heart, liver, kidney, and stomach were unaffected by dietary treatment (P > 0.05).

Table 6 Effect of dietary BSFL full-fat meal and probiotic mixture to replace antibiotics on organ weight in weaning pigs1,2

Digesta pH

The digesta pH in the caecal, proximal, middle, and distal small intestinal segments was not affected by any of the dietary treatments (P > 0.05; Table 7). However, a tendency for a lower pH value in the caecum was observed in the BSFL + Pro (P = 0.069) treatment.

Table 7 Effect of dietary BSFL full-fat meal and probiotic mixture to replace antibiotic on digesta pH in weaning pigsa,b

Intestinal histomorphology

The VH and VH/CD in the duodenum were higher in the BSFL-supplemented treatments (P = 0.033, and 0.004, respectively; Table 8). However, the duodenum CD and all intestinal histomorphology measurements in the jejunum and ileum were similar among all treatments (P > 0.05).

Table 8 Effect of dietary BSFL full-fat meal and probiotic mixture to replace antibiotics on the intestinal histomorphology in weaning pigs1,2

Microbial count

The BSFL + Pro treatment increased faecal Lactobacillus spp. Count by 29.26 and 64.90% compared with that seen with the PC and NC treatments, respectively (P = 0.008; Table 9). Simultaneously, faecal E. coli count decreased in the BSFL + Pro treatment group in comparison to that in the NC group (P = 0.021). No differences were detected in the faecal Salmonella spp. counts among the dietary treatments (P > 0.05).

Table 9 Effect of dietary BSFL full-fat meal and probiotic mixture to replace antibiotics on the microbial count (log colony-forming unit [CFU]/g faeces) in weaning pigs1,2


Growth performance and diarrhoeal rate

The extensive in-feed administration of antibiotics in swine production and lack of awareness regarding its effects are driving the accelerated and widespread emergence of antibiotic-resistant bacteria [11]. Dietary supplements, BSFL full-fat meal, and multi-probiotics have been proposed as substitutes for antibiotics for future generations of weanling pigs. However, the combined effects of these supplements on overall growth performance and the incidence of diarrhoea in piglets have not well-established. In this study, these two combinations demonstrated improvements in growth performance and feed efficiency. Although the underlying mechanism remains unknown, it may have exerted an effect because of the unique properties of the diet in not only providing an excellent source of protein, essential amino acids, and energy but also providing several active compounds [2, 6, 7]. Supplementation positively enhanced the overall growth performance and health benefits for the weaned pigs. According to Jin et al. [21], dietary supplementation with 8% BSFL full-fat meal improves overall growth performance in a dose-dependent manner. However, BSFL-supplemented diets did not affect the growth performance of piglets when fed at a concentration below 4% [22]. The BSFL full-fat meal is normally relatively high in lauric acid (12.83% DM) [5], which accounted for ~ 1.52% of our calculated value in the BSFL-supplemented diet. The chitin content will trigger the secretion of growth hormone and insulin-like growth factor 1, leading to a heavier body weight in weaning pigs [23]. Other factors might be associated with the action of AMPs in promoting ADG when supplied at of 2 mg/kg AMPs [24]. However, there is no available data of insect-derived AMPs in improving growth performance and feed efficiency in monogastrics; therefore, further research is needed to elucidate the in vivo effects. Taken together with probiotic mixtures, strong antimicrobial and growth-promoting effects may be expected at inclusions of > 0.1% [13].

In the present study, we found that, compared with the NC diet, supplementation with BSFL alone did not exert considerable effect on the growth performance of pigs in any period. However, the combination of BSFL full-fat meal can be used to decrease the quantity of soybean meal (28.88% vs. 17.31%) in diets for weaned piglets. This will have the added value of essential amino acid recovery over soybean meal (44.06% vs. 41.30%) [15], leading to better protein utilisation with less undigestible protein loss. Furthermore, the higher EE in Phase I (3.83% vs. 7.53%) and II (3.72% vs. 7.02%) in the BSFL-supplemented diets may positively increase nutrient uptake.

Addition of the Bacillus spp. probiotic mixture has been proposed to produce several active enzymes in the digestion of soluble or insoluble fractions of feed that will rapidly increase the absorbability of nutrients by enterocytes and their ability to maintain health status of pigs during the post-weaning period [25]. These unique characteristics facilitate faster gut recovery and better nutrient uptake to support growth performance of the weaning pigs. This was evidenced by the increase in BW and ADG in the BSFL+ Pro-supplemented diet.


The inclusion of insect protein (BSFL) and multi-probiotics has been shown to increase the nutrient digestibility of DM, CP, and EE in weaned pigs [26]. Previous studies have also reported that B. licheniformis and B. subtilis produce several extracellular enzymes that are beneficial to hosts, including α-amylase, proteinase, lipase, xylanase, cellulase, and pectinase [27]. Indeed, B. subtilis exceeds B. licheniformis in producing glycosyl hydrolase, which assists in the degradation of glycosidic linkages in complex sugars [28]. BSFL full-fat meal has a high protein content and is a good source of amino acids, which can further improve CP digestibility [29]. Inclusion of BSFL at 12% had no effect on protein digestibility, indicating the possibility of replacing soybean meal with BSFL full-fat meal as a protein source. This increases the digestion and absorption of nutrients in the dietary treatment supplemented with BSFL full-fat meal.

The high fat content and degree of saturation of fatty acids may be a major reason for the improved digestibility of EE in BSFL-supplemented diets over in NC diets (7.02–7.53% vs. 3.72–3.83%). In this study, C12:0—which is rapidly utilised and passively absorbed by the animals—was the main component of saturated fatty acids in the BSFL12 diet. Combined with microbial lipase secretion from Bacillus-based probiotics, C12:0 may have broad effects in the hydrolysed 1- and 3- positions of dietary triglycerides. Although the experimental dietary combinations showed improved nutrient digestibility compared to the NC diet, their effects were comparable to those of the PC diet, suggesting the greater availability of nutrients beyond the antibiotic treatment.

Blood-related gut health and antioxidative stress

Serum immunoglobulins can be used to determine cellular responses and the ability of an animal’s body to recognise pathogenic invasion [30]. Our study showed that serum IgA concentrations increased in pigs fed the BSFL12 and BSFL + Pro diets. Serum IgA can subsequently interact with lactoferrin and/or transferrin for bacteriostatic action by increasing the adhesion to epithelial cells (to improve their adhesion to the mucus) and neutralising bacterial toxins. Therefore, increased levels of serum IgA prompt the initial defence against infection by pathogens [31]. Serum IgG inhibits various stressors, including diseases and intestinal disorders, during the first week post-weaning [32]. Therefore, higher levels of serum IgG can suppress invading pathogens and activate long-lasting immunity. The feedback regulation of IgG also induces the secretion of novel IgG antibodies via the activation of B lymphocytes [31]. This is consistent with previous reports that dietary inclusion of B. subtilis will increase serum IgA and IgG levels in rabbits and neonatal piglets [33, 34]. The higher C12:0 content of BSFL-supplemented diets may also activate interleukin production, which in turn promotes the production of immunoglobulins [35]. However, the mechanism by which BSFL (alone or in combination with Bacillus-based probiotics) promotes immunoglobulin secretion is still unclear. It is possible that the binding site of Bacillus-based probiotics can bind with IgG Fc-receptors as additional ligands, which can subsequently influence immunoglobulin secretion [36].

Pro-inflammatory cytokines (such as IL1β, IL6, and TNFα) are known to be secreted as part of the innate immune response [37]. These factors have detrimental effects on intestinal mucosal injury and dysfunction, impair nutrient digestion and absorption, and subsequently lead to a poor growth rate [37]. However, dietary BSFL can activate intestinal development, immunity, and anti-inflammation [37, 38] via the direct utilisation of C12:0 by enterocytes for energy production, thereby maintaining the integrity of the intestinal mucosa in young piglets [39]. Peptidoglycans in the insect skeleton can also attach to the binding sites of pathogens, thus triggering IgA release into the intestinal lumen and inhibiting the secretion of pro-inflammatory factors. Chitin and its derivatives have also been reported to polarise faecal calprotectin, which is a sensitive and non-invasive marker of active inflammation in the gastrointestinal tract. They also regulate a main receptor for commensal recognition in gut innate immunity [40], thus reducing inflammation in the lower intestine. It is unclear how BSFL supplementation lowers the serum TNFα concentration. Although possible factors may be attributed to the molecular weight, degree of saturation, particle size, source, and the purification level of the BSFL [41], further research is warranted. Our study observed a positive response on lowering TNFα when applied with the Bacillus-based probiotic combination. It is well-established that Bacillus genera can synthesise bacteriocins, which have a widely antimicrobial action, to suppress the growth of several gram-positive bacteria via the permeability of their cytoplasmic membrane [42], thereby decreasing the penetration of the inflammatory cells. Furthermore, B. subtilis has a stronger ability to enhance innate immunity via β-defensin, which can have a direct effect on pathogenic colonisation and more predominantly involve the initiation and regulation of the adaptive immune response [34]. We thus propose that the decreased pro-inflammatory and increased anti-inflammatory cytokines caused by the Bacillus-based probiotic mixture may be linked to the capacity of these bacteria to decrease the increased inflammatory status associated with the transition at weaning.

An increase in the antioxidant enzyme activity of SOD and GSH-Px is also associated with antioxidant defence mechanisms. The SOD is an effective antioxidant enzyme for radical detoxification at the beginning of the free radical formation, whereas the enzymatic GSH-Px effectively inhibits the harmful accumulation of intracellular hydrogen peroxide, thus preventing damage to DNA, proteins, and membrane lipids in the animal body. The BSFL has appropriate amount of total phenolic compounds (32–35 mg/gallic acid equivalents g DM), whereas action of the Bacillus probiotic mixture (caused by the utilisation of antioxidant enzymes), modulates the host’s antioxidant system and probiotic-mediated antioxidant signalling mechanism [43]. This contributes to the scavenging of reactive oxygen species [44]. This is consistent with the increase in antioxidant enzymes and decrease in MDA concentrations, as shown in the current study. Therefore, it is suggested that the active substances derived from BSFL and probiotic mixtures may have been absorbed sufficiently for activating antioxidant enzymes in experimental pigs.

Organ weight

The spleen is an important immune organ that can be used to evaluate immune responses in weaned pigs. Changes in the immune organ index indicate immune function and resistance to pathogenic invasion in animals. In the present study, the relative weight of the spleen increased after 4 weeks of feeding with BSFL + Pro. Previous studies have reported an increase in the spleen weight following the dietary inclusion of B. subtilis (1 × 106 cfu/g) or chitin and its derivatives [34, 45]. This increase in spleen weight may enhance the immune function of weaned pigs, help them overcome weaning stress, and therefore improve their overall growth performance.

Digesta pH

The digesta pH was substantially lower in the BSFL + Pro treatment group, indicating that these pigs were capable of generating acidic conditions to facilitate microbial growth and colonisation. The underlying mechanism of this process may be related to the large amount of chitin and its derivatives (rather than fibre content) passing through the large intestine [46], which causes a shift in hindgut fermentation and leads to the generation of short-chain fatty acids that supply energy for the growth of lactic acid-producing bacteria, thus lowering the number of pathogens [47]. This is consistent with our observation of faecal microbial counts in this study. However, the content of short-chain fatty acids should be assessed to explore this positive effect in more detail.

Intestinal histomorphology

Changes in intestinal histomorphology—including VH, CD, and VH:CD—are indicative of gut health in pigs. A longer VH increases the mucosal surface area, facilitating improved digestion and absorption of available nutrients. Moreover, a shorter CD suppresses the rapid turnover of the intestinal epithelium, thus facilitating the renewal of villi in response to normal sloughing or inflammation from pathogenic invasion. The VH:CD ratio is typically associated with increased epithelial turnover [48]. Our results indicate that dietary BSFL12 and BSFL + Pro increased duodenal VH in weaned pigs. This may be because BSFL-supplemented diets promoted the activity of digestive enzymes (including membrane-bound peptidases) and facilitated more efficient utilisation of CP, amino acids, and EE [49]. This likely increased the availability of nutrients for the maturation of undifferentiated cells. Han et al. [38] also reported that chitin derivatives enhanced enterocyte proliferation and diminished villous atrophy. This suggests that the presence of 0.52% chitin in the BSFL full-fat meal diets can be efficiently utilised by chitin-degrading enzymes in the piglets’ stomach [50] and via hindgut microbial fermentation (47). Furthermore, the increased VH in the duodenum of pigs fed the BSFL full-fat meal diet suggests an increased surface area for greater digestion and absorption of the available nutrients. In addition, the combination with Bacillus-based probiotics has been reported to enhance various exogenous enzyme secretions including protease, lipase, phytase, and cellulase [51]. This action possibly increases the digestion and nutrient absorption of fat and CP from the BSFL full-fat meal, thus enhancing nutrient availability for greater differentiation of epithelial cells.

Microbial count

The presence of calculated C12:0 in the BSFL-supplemented diet (~ 1.10%) is beneficial for the intestinal microbiota of weaning pigs, facilitates the semi-permeable membrane of pathogenic microbes, and improves the intestinal structure of piglets [52]. Therefore, in combination with chitin and its derivatives, C12:0 may have desirable effects on the gut microbiota of pigs. Chitin is a major fibrous compound in arthropod exoskeletons. It is strongly attached with β-glucan in the chitin–glucan complex, which is selectively used as a fibrous substrate by host microorganisms for their own growth [53]. This promotes the adherence of beneficial microbiota (such as Lactobacillus spp.) while reducing the faecal E. coli count in the hindgut [49, 54]. This is consistent with previous findings in which the inclusion of lower amounts of chitin had a greater influence on colonic microbiota than chitin supplementation in high amounts [55]. In addition, Yu et al. [56], demonstrated that pigs fed 4% BSFL showed a substantially higher abundance of Lactobacillus spp. than those fed 8% BSFL (0.19% vs. 0.37% chitin, respectively). This may indicate that feeding low levels of BSFL full-fat meal has desirable effects on the faecal microbiota of weaning pigs, compared to those on the PC diet. Interestingly, the combination of BSFL+ Pro produced a greater colonisation of Lactobacillus spp. and lower E. coli than both the control and NC diets, respectively. A previous study demonstrated that the addition of 0.1% multi-probiotics (consisting of B. subtilis, B. licheniformis, and S. cerevisiae) had a beneficial effect on maintaining faecal microbiota count by promoting growth of Lactobacillus spp. in growing pigs [57]. One possible explanation for this outcome is that Bacillus-based probiotics are considered facultative anaerobes with high resistance to acidic conditions (such as the gastrointestinal tract of animals) [58]. This unique characteristic may allow these microbes to attach with the gut surface and produce various bacteriolytic proteins [27]. This explanation is supported by our finding of the digesta pH being appropriate for the increased activity and proliferation of lactic acid-producing bacteria in this study. Another explanation is that it might be because of the interaction between the insect AMPs and microbial bacteriocins, and gut microbiota community. With the production of bacteriocins, Bacillus spp. probiotics have an inhibitory effect on pathogenic growth via the activation of their virulent genes and production of elastase and endopeptidase [59]. This mechanism can destroy the early cells of Gram-negative bacteria [59]. This is a potential inhibitor of E. coli, acting directly on the cell wall by inhibiting peptidoglycan or lipopolysaccharide O-antigen synthesis by permeabilising the membrane, resulting in ion leakage of the cellular content and cell death [60]. Taken together with insect AMPs, which include both hydrophobic and hydrophilic structures with a highly positive charge (ranging from + 2 to + 9) [61], they can interact with the negative charge of bacterial cell membrane. There is a concomitant increase in the permeability of the bacterial membrane, including interference with bacterial metabolism, disruption of bacterial cell integrity, and targeting of cytoplasmic components [61, 62], which ultimately retards gram-negative bacterial growth. It has been reported that H. illucens is an enriching source of AMPs, owing to the larval instar that feeds on decaying organic substrates and protects itself from the pathogens and restores substrate health via the reduction of E. coil [63]. It is suggested that the combinations of both substrates effectively enhanced the microbial populations in weaned pigs.


The BSFL + Pro has the potential to activate IgG, GSH-Px, and Lactobacillus spp. growth more than the in-feed antibiotic treatment. Growth performance, nutrient digestibility coefficients, and intestinal histomorphology were comparable among the two treatments. Therefore, it is a viable alternative to antibiotics in nursery diets, without any impairment of growth performance and gut health in weaning pigs.

Availability of data and materials

All datasets are available from the corresponding author on reasonable request.



Average daily feed intake


Average daily gain


Apparent total tract digestibility


Full-fat black soldier fly larvae


Negative control plus 12% BSFL full-fat meal

BSFL + Pro:

BSFL full-fat meal plus 0.1% multi-probiotics


Crypt depth


Crude protein


Dry matter


Ether extract


Gross energy


Gain-to-feed ratio


Glutathione peroxidase


Immunoglobulin A


Immunoglobulin G


Immunoglobulin M






Nitrogen-to-protein conversion factor




Metabolisable energy


Negative control


Not detected


Positive control


Saturated fatty acids


Superoxide dismutase


Total antioxidant capacity


Tumour necrosis factor alpha


Unsaturated fatty acids


Villus height


Villus height-to-crypt depth ratio


  1. European Medicines Agency. Final programming document 2022–2024. Accessed 12 May 2022.

  2. Kierończyk B, Rawski M, Mikołajczak Z, Homska N, Jankowski J, Ognik K, et al. Available for millions of years but discovered through the last decade: Insects as a source of nutrients and energy in animal diets. Anim Nutr. 2022;11:60–79.

    Article  Google Scholar 

  3. Barragan-Fonseca KB, Dicke M, van Loon JJA. Nutritional value of the black soldier fly (Hermetia illucens L.) and its suitability as animal feed. J Insects Food Feed. 2017;3:105–20.

    Article  Google Scholar 

  4. Spranghers T, Ottoboni M, Klootwijk C, Ovyn A, Deboosere S, De Meulenaer B, et al. Nutritional composition of black soldier fly (Hermetia illucens) prepupae reared on different organic waste substrates. J Sci Food Agric. 2017;97:2594–600.

    Article  CAS  Google Scholar 

  5. de Souza VJ, Andronicos NM, Kolakshyapati M, Hilliar M, Sibanda TZ, Andrew NR, et al. Black soldier fly larvae in broiler diets improve broiler performance and modulate the immune system. Anim Nutr. 2021;7:695–706.

    Article  Google Scholar 

  6. Elieh AKD, Sharma L, Cruz CSD. Chitin and its effects on inflammatory and immune responses. Clin Rev Allergy Immunol. 2018;54:213–23.

    Article  Google Scholar 

  7. Xia J, Ge C, Yao H. Antimicrobial peptides from black soldier fly (Hermetia illucens) as potential antimicrobial factors representing an alternative to antibiotics in livestock farming. Animals. 2021;11:1937.

    Article  Google Scholar 

  8. Yu M, Li Z, Chen W, Wang G, Rong T, Liu Z, et al. Hermetia illucens larvae as a fishmeal replacement alters intestinal specific bacterial populations and immune homeostasis in weanling piglets. J Anim Sci. 2020;98:skz395.

    Article  Google Scholar 

  9. Chia SY, Tanga CM, Osuga IM, Alaru AO, Mwangi M, Githinji M, 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.

    Article  Google Scholar 

  10. Yan L, Kim IH. The apparent total tract digestibility, apparent ileal digestibility and fecal noxious gas content of growing pigs fed probiotics in diets. Wayamba J Anim Sci. 2021;3:121–3.

    Google Scholar 

  11. Kwoji ID, Aiyegoro OA, Okpeku M, Adeleke MA. Multi-strain probiotics: synergy among isolates enhances biological activities. Biology. 2021;10:322.

    Article  CAS  Google Scholar 

  12. Lewton JR, Woodward AD, Moser RL, Thelen KM, Moeser AJ, Trottier NL, et al. Effects of a multi-strain Bacillus subtilis-based direct-fed microbial on weanling pig growth performance and nutrient digestibility. Trans. Anim Sci. 2021;5:txab058.

    Google Scholar 

  13. Nguyen DH, Nyachoti CM, Kim IH. Evaluation of effect of probiotics mixture supplementation on growth performance, nutrient digestibility, faecal bacterial enumeration, and noxious gas emission in weaning pigs. Ital J Anim Sci. 2019;18:466–73.

    Article  CAS  Google Scholar 

  14. Boulos S, Tännler A, Nyström L. Nitrogen-to-protein conversion factors for edible insects on the Swiss market: T. molitor, A. domesticus, and L. migratoria. Front Nutr. 2020;7:89.

    Article  Google Scholar 

  15. National Research Council (NRC). Nutrient requirements of swine. Washington, DC: National Academies Press; 2012.

    Google Scholar 

  16. Crosbie M, Zhu C, Shoveller AK, Huber LA. 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. Trans Anim Sci. 2020;4:1–10.

    Article  CAS  Google Scholar 

  17. Osunbami OT, Adeola O. Regression method-derived digestible and metabolizable energy concentrations of partially defatted black soldier fly larvae meal for broiler chickens and pigs. Livest Sci. 2022;264:105042.

    Article  Google Scholar 

  18. Kierończyk B, Rawski M, Stuper-Szablewska K, Józefiak D. First report of the apparent metabolisable energy value of black soldier fly larvae fat used in broiler chicken diets. Animal. 2022;16:100656.

    Article  Google Scholar 

  19. Adeola O. Digestion and balance techniques in pigs. In: Lewis AJ, Southern LL, editors. Swine nutrition. Washington, DC: CRC Press; 2001. p. 923–36.

    Google Scholar 

  20. Association of Official Analytical Chemists (AOAC). Official methods of analysis. Gaithersburg: AOAC; 2000.

    Google Scholar 

  21. Jin X, Yuan B, Liu M, Zhu M, Zhang X, Xie G, et al. Dietary Hermetia illucens larvae replacement alleviates diarrhoea and improves intestinal barrier function in weaned piglets challenged with enterotoxigenic Escherichia coli K88. Front Vet Sci. 2021;8:746224.

    Article  Google Scholar 

  22. Yu M, Li Z, Chen W, Rong T, Wang G, Wang F, et al. Evaluation of full-fat Hermetia illucens larvae meal as a fishmeal replacement for weanling piglets: effects on the growth performance, apparent nutrient digestibility, blood parameters and gut morphology. Anim Feed Sci Technol. 2020;264:114431.

    Article  CAS  Google Scholar 

  23. Xu Y, Shi B, Yan S, Li T, Guo T, Li J. Effects of chitosan on body weight gain, growth hormone and intestinal morphology in weaning pigs. Asian-Australas J Anim Sci. 2013;6:1484–9.

    Google Scholar 

  24. Zhang L, Guo T, Zhan N, Sun T, Shan A. Effects of the antimicrobial peptide WK3 on diarrhea, growth performance and intestinal health of weaned piglets challenged with enterotoxigenic Escherichia coli K88. Food Nutr Res. 2021;65:1–9.

    Article  Google Scholar 

  25. Hu S, Cao X, Wu Y, Mei X, Xu H, Wang Y, et al. Effects of probiotic Bacillus as an alternative of antibiotics on digestive enzymes activity and intestinal integrity of piglets. Front Microbiol. 2018;9:2427.

    Article  Google Scholar 

  26. Cheng L, Kim IH. Effects of dietary supplementation with Baciallu licheniformis derived-proteinase on growth performance, nutrient digestibility and fecal microbial shedding in post-weaned growing pigs. J Appl Anim Res. 2019;47:322–5.

    Article  CAS  Google Scholar 

  27. Su Y, Liu C, Fang H, Zhang D. Bacillus subtilis: a universal cell factory for industry, agriculture, biomaterials and medicine. Microb Cell Factories. 2020;19:173.

    Article  Google Scholar 

  28. Larsen N, Thorsen L, Kpikpi EN, Stuer-Lauridsen B, Cantor MD, Nielsen B, et al. Characterization of Bacillus spp. strains for use as probiotic additives in pig feed. Appl Microbiol Biotechnol. 2014;98:1105–18.

    Article  CAS  Google Scholar 

  29. Do S, Koutsos L, Utterback PL, Parsons CM, de Godoy MRC, Swanson KS. 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.

    Article  Google Scholar 

  30. Elgert KD. Immunology: understanding the immune system. New York: Wiley & Liss, Inc.; 2009.

    Google Scholar 

  31. Reyneveld GI, Savelkoul HFJ, Parmentier HK. Current understanding of natural antibodies and exploring the possibilities of modulation using veterinary models. A review. Front Immunol. 2020;11:2139.

    Article  Google Scholar 

  32. Yoon JH, Ingale SL, Kim JS, Kim KH, Lee SH, Park YK, et al. Effects of dietary supplementation of antimicrobial peptide-A3 on growth performance, nutrient digestibility, intestinal and fecal microflora and intestinal morphology in weanling pigs. Anim Feed Sci Technol. 2012;177:98–7.

    Article  CAS  Google Scholar 

  33. Yeruva L, Spencer NE, Saraf MK, Hennings L, Bowlin AK, Cleves MA, et al. Formula diet alters small intestine morphology, microbial abundance and reduces VE-cadherin and Il-10 expression in neonatal porcine model. BMC Gastroenterol. 2016;16:40.

    Article  Google Scholar 

  34. Guo M, Wu F, Hao G, Qi Q, Li R, Li N, et al. Bacillus subtilis improves immunity and disease resistance in rabbits. Front Immunol. 2017;8:354.

    Article  Google Scholar 

  35. Kawano Y, Noma T. Role of interleukin-2 and interferon-gamma in inducing production of IgG subclasses in lymphocytes of human newborns. Immunology. 1996;88:40–8.

    Article  CAS  Google Scholar 

  36. Flesch BK, Neppert J. Functions of the Fc receptors for immunoglobulin G. J Clin Lab Anal. 2000;14:141–56.

    Article  CAS  Google Scholar 

  37. Liu Y. Fatty acids, inflammation and intestinal health in pigs. J Anim Sci Biotechnol. 2015;6:41.

    Article  Google Scholar 

  38. Jackman JA, Boyd RD, Elrod CC. Medium-chain fatty acids and monoglycerides as additives for pig production: towards gut health improvement and feed pathogen mitigation. J Anim Sci Biotechnol. 2020;11:44.

    Article  Google Scholar 

  39. Lauridsen C. Effects of dietary fatty acids on gut health and function of pigs pre- and post-weaning. J Anim Sci. 2020;98:skaa086.

    Article  Google Scholar 

  40. Xiao D, Wang Y, Liu G, He J, Qiu W, Hu X, et al. Effects of chitosan on intestinal inflammation in weaned pigs challenged by enterotoxigenic Escherichia coli. PLoS One. 2014;9:e104192.

    Article  Google Scholar 

  41. Alvarez FJ. The effect of chitin size, shape, source and purification method on immune recognition. Molecules. 2014;19:4433–51.

    Article  Google Scholar 

  42. Abriouel H, Franz CMAP, Omar NB, Gálvez A. Diversity and applications of Bacillus bacteriocins. FEMS Microbiol Rev. 2011;35:201–32.

    Article  CAS  Google Scholar 

  43. Wang Y, Wu Y, Wang Y, Xu H, Mei X, Yu D, et al. Antioxidant properties of probiotic bacteria. Nutrients. 2017;9:521.

    Article  Google Scholar 

  44. Ravi HK, Guidou C, Costil J, Trespeuch C, Chemat F, Vian MA. Novel insights on the sustainable wet mode fractionation of black soldier fly larvae (Hermetia illucens) into lipids, proteins and chitin. Processes. 2021;9:1888.

    Article  CAS  Google Scholar 

  45. Deng X, Li X, Liu P, Yuan S, Zang J, Li S, et al. Effect of chito-oligosaccharide supplementation on immunity in broiler chickens. Asian-Australas J Anim Sci. 2008;21:1651–8.

    Article  CAS  Google Scholar 

  46. Beier S, Bertilsson S. Bacterial chitin degradation—mechanisms and ecophysiological strategies. Front Microbiol. 2013;4:149.

    Article  CAS  Google Scholar 

  47. Nakatani M, Inoue R, Tomonaga S, Fukuta K, Tsukahara T. Production, absorption, and blood flow dynamics of short-chain fatty acids produced by fermentation in piglet hindgut during the suckling-weaning period. Nutrients. 2018;10:1220.

    Article  Google Scholar 

  48. Parker A, Maclaren OJ, Fletcher AG, Muraro D, Kreuzaler PA, Byrne HM, et al. Cell proliferation within small intestinal crypts is the principal driving force for cell migration on villi. FASEB J. 2017;31:636–49.

    Article  CAS  Google Scholar 

  49. Wan J, Jiang F, Xu Q, Chen D, Yu B, Huang Z, et al. New insights into the role of chitosan oligosaccharide in enhancing growth performance, antioxidant capacity, immunity and intestinal development of weaned pigs. RSC Adv. 2017;7:9669–79.

    Article  CAS  Google Scholar 

  50. Kawasaki K, Osafune T, Tamehira S, Yano K. Piglets can secrete acidic mammalian chitinase from the pre weaning stage. Sci Rep. 2021;11:1297.

    Article  CAS  Google Scholar 

  51. Latorre JD, Hernandez-Velasco X, Wolfenden RE, Vicente JL, Wolfenden AD, Menconi A, et al. Evaluation and selection of Bacillus species based on enzyme production, antimicrobial activity, and biofilm synthesis as direct-fed microbial candidates for poultry. Front Vet Sci. 2016;3:95.

    Article  Google Scholar 

  52. Hanczakowska E. The use of medium-chain fatty acids in piglet feeding—a review. Ann Anim Sci. 2017;17:967–77.

    Article  CAS  Google Scholar 

  53. Lopez-Santamarina A, Mondragon ADC, Lamas A, Miranda JM, Franco CM, Cepeda A. Animal-origin prebiotics based on chitin: a n alternative for the future? A critical review. Foods. 2020;9:782.

    Article  CAS  Google Scholar 

  54. Selenius O, Korpela J, Salminen S, Gallego CG. Effect of chitin and chitooligosaccharide on in vitro growth of Lactobacillus rhamnosus GC and Escherichia coli TG. Appl Food Biotechnol. 2018;5:163–2.

    CAS  Google Scholar 

  55. Tran HT, Barnich N, Mizoguchi E. Potential role of chitinases and chitin-binding proteins in host-microbial interactions during the development of intestinal inflammation. Histol Histopathol. 2011;26:1453–64.

    CAS  Google Scholar 

  56. 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.

    Article  CAS  Google Scholar 

  57. Wang H, Ha BD, Kim IH. Effects of probiotics complex supplementation in low nutrient density diet on growth performance, nutrient digestibility, faecal microbial, and faecal noxious gas emission in growing pigs. Ital J Anim Sci. 2021;20:163–70.

    Article  CAS  Google Scholar 

  58. Hong HA, Duc LH, Cutting SM. The use of bacterial spore formers as probiotics. FEMS Microbiol Rev. 2005;29:813–35.

    Article  CAS  Google Scholar 

  59. Miller MB, Bassler BL. Quorum Sensing in Bacteria. Annu Rev Microbiol. 2001;55:165–99.

    Article  CAS  Google Scholar 

  60. Darbandi A, Asadi A, Mahdizade AM, Ohadi E, Talebi M, Halaj ZM, et al. Bacteriocins: Properties and potential use as antimicrobials. J Clin Lab Anal. 2022;36:e24093.

    Article  CAS  Google Scholar 

  61. Manniello MD, Moretta A, Salvia R, Scieuzo C, Lucchetti D, Vogel H, et al. Insect antimicrobial peptides: potential weapons to counteract the antibiotic resistance. Cell Mol Life Sci. 2021;78:4259–82.

    Article  CAS  Google Scholar 

  62. Erickson MC, Islam M, Sheppard C, Liao J, Doyle MP. Reduction of Escherichia coli O157:H7 and Salmonella enterica serovar Enteritidis in chicken manure by larvae of the black soldier fly. J Food Prot. 2004;67:685–90.

    Article  Google Scholar 

  63. Liu Q, Tomberlin JK, Brady JA, Sanford MR, Yu Z. Black soldier fy (Diptera: Stratiomyidae) larvae reduce Escherichia coli in dairy manure. Environ Entomol. 2008;37:1525–30.

    Article  Google Scholar 

Download references


Not applicable.


The authors sincerely thank the Fundamental Fund of Khon Kaen University, which received funding from the National Science, Research, and Innovation Fund.

Author information

Authors and Affiliations



Conceptualization, WB and PP; methodology, WB and JH; data curation, PP and WB; formal analysis, PP, WB, YYK, and JH; investigation, PP and WB; project administration, PP and WB; funding acquisition, PP, JH and WB; writing—original draft preparation, WB, JH, AW; writing - review and editing, WB, JH, AW, and YYK. All authors have read and agreed to the published version of the manuscript.

Corresponding author

Correspondence to Waewaree Boontiam.

Ethics declarations

Ethics approval and consent to participate

Animal trials were conducted in strict accordance with the guidelines of the National Research Council of Thailand, and the protocols were approved by the Institutional Animal Care and Use committee of Khon Kaen University (Khon Kaen, Thailand; approval number 125/64 on 18 November, 2021).

Consent for publication

Not applicable.

Competing interests

All authors have no conflicts of interest to declare.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Phaengphairee, P., Boontiam, W., Wealleans, A. et al. 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 19, 7 (2023).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: