Introduction
The white-spotted flower chafer, Protaetia brevitarsis (Coleop- tera; Scarabaeidae), is used as a traditional medicine for treating diseases such as hepatic cancer, breast cancer, in- flammatory disease, liver cirrhosis, and hepatitis [20]. In 2016, the Ministry of Food and Drug Safety of Korea regis- tered P. brevitarsis larvae as a general food ingredient. Owing to increased interest, producers have launched businesses for mass production of these larvae for food and feed; how- ever, this has led to the emergence of several bacterial, viral, and fungal diseases among these insects. Insect diseases can be lethal and cause serious economic damage to farms rear- ing the insects [8,33]. Thus, these insect diseases must be prevented and controlled.
Serratia marcescens is an opportunistic gram-negative bac- terium in the Enterobacteriaceae family. S. marcescens was originally thought to be a non-pathogenic saprophytic water organism that formed red colonies [13]. Animal and insect infections caused by S. marcescens have been increasingly re- ported since 1960 [7,11]. Importantly, S. marcescens was shown to be lethal to insects [15, 23, 32]; thus, production of consistently safe and high-quality insects is necessary. Sprouted grain has been suggested as a method of pro- ducing fresh forage grains with little water.
Sprouted barley ([SB], Hordeum vulgare L.) is a young barley leaf grown to approximately 20 cm and harvested at 10-15 days after sowing. Barley is one of the most important crops world- wide and is the second most consumed grain after rice in Korea [17]. Several reports have shown that SB is a valuable source of nutrients, such as amino acids, minerals, vitamins, dietary fiber, and other bioactive substances such as super- oxide dismutase, catalase, carotenoids, and chlorophyll [5,25]. Several researchers have investigated feeding sprouted grain to cattle, pigs, and poultry with a sustainable product quality [1, 12, 16, 22, 31]. These studies revealed an increased performance in both lambs and cattle fed barley grain. Additionally, the barley fodder helped reduce operating costs and improve product quality. However, SB is rarely used as a feed supplement in insect farming. Therefore, the present study was designed to evaluate the effects of SB as an insect feed supplement using 5% and 10% w/w of feed.
Materials and Methods
Insects
P. brevitarsis eggs were purchased from a private seller (Wanju-gun, Jeollabuk-do, Korea). After hatching, the larvae were reared in a laboratory regulated at 26±1℃ and 40%~ 60% relative humidity. The larvae were individually reared and checked once weekly to measure their body weight and larval period. Twenty larvae were tested per group, and each treatment was repeated three times.
Feed with different SB contents
To test the effects of SB on P. brevitarsis larval growth, different amounts of SB were mixed with oak sawdust and fermented for at least 1 month (Table 1). The Korea Feed Ingredients Association recommended that the content of feed additives be added to less than 15% of the total feed. In this study, SB was added at the levels of 5% and 10% as an additive for insect feeds. SB was kindly provided by the National Institute of Crop Science.
Table 1. Formulation of experimental feed concentrate composi-tion (%)
S. marcescens and colony counting
The bacterial strain S. marcescens (Korean Agricultural Culture Collection [KACC] No. 10502) was obtained from the KACC (Wanju-gun, Jeollabuk-do, Korea). The strains were incubated on nutrient agar medium (Becton, Dickinson and Co., Inc., Franklin Lakes, NJ, USA). For the antibacterial assays, S. marcescens cultures treated with 1%, 5%, and 10% SB were incubated on an orbital shaker at 200 rpm and seri- ally diluted to 10-fold. Ten microliters of the 3-fold dilution was spread on nutrient agar. The plates were incubated overnight at 30℃ in the dark. The colony-forming numbers were determined, and the bacterial concentration in each original sample was calculated. The tests were performed in triplicate. Each data point was composed of the average of three independent samples.
S. marcescens infection of Protaetia brevitarsis
Bioassays were performed by injecting healthy third-in- star P. brevitarsis larvae with 10 μl of bacterial suspension containing 105 bacteria per larva, directly into the hemocoel. The negative- and positive-control larvae were injected with 10 μl of nutrient broth and bacterial suspension, respectively, and fed control feed. Survival rates and larval weights were checked weekly. Each treatment included ten larvae and was repeated four times.
Proximate analysis
Proximate analysis was performed according to the stand- ard methods of the Association of Official Analytical Chemists [2] for determining moisture, crude fiber, protein, and fat content in the samples. The proximate values were reported as percentages. Moisture contents of the samples were determined by oven-drying at 105℃ to a constant weight. The Kjeldahl method was used to determine the pro- tein content with a conversion factor of 6.25. Crude fat was extracted with hexane via the Soxhlet method. Crude fiber content was determined via the digestion method, and the ash content was estimated by ashing at 550℃ for 3 hr.
Mineral, amino acid, and heavy metal compositions
The mineral elements in the P. brevitarsis larvae, i.e., cop-per, zinc, potassium, magnesium, and phosphorus were de-termined using an atomic absorption spectrophotometer as per the AOAC methods. The mineral values were reported in milligrams per kilogram (mg/kg). Amino acids were de- termined using an automated Amino Acid Analyzer (Beck- man 6300, Brea, CA, USA). The amino acid compositions were expressed as percentage. Heavy metals were deter- mined using an atomic absorption spectrophotometer as per the AOAC methods. The results were expressed as mg/kg dry weight.
Statistical analysis
Values from each experiment are expressed as the mean ± standard deviation (SD) and compared with the controls. Comparisons between means were performed using one- way analysis of variance, followed by Tukey’s multiple com-parisons test. The significance level was set at p<0.05.
Results and Discussion
Growth performance of larvae fed SB-added feed
Table 2 shows the effect of SB as a feed additive on P. brevitarsis larval growth. Maximum larval weights of the 5% and 10% SB-fed groups were 3.45 g and 3.56 g, respectively. The 5% and 10% SB-fed groups reached their maximum weights markedly earlier than did the control group. Maxim- um larval weights (p<0.001) and the days at which the max- imum larval weight (p<0.001) differed significantly. For com- mercial use in animal feed and human food, each third-in- star larva should weigh >2.0 g. Thus, insects fed SB were more efficient and cost-effective to produce. Feeds contain- ing 5% and 10% SB yielded larvae that could be used in feed and food at 6 and 5 weeks of feeding, respectively. SB improved the larval growth and weight gain compared with those of the control larvae. Thus, using SB could reduce rear- ing costs and labor supplies for insect farms.
Table 2. Growth parameters of P. brevitarsis after feeding feeds treated with different concentrations of sprouted barley
Columns with different letters differed significantly. Means followed by the same letters within a column do not significantly differ (p>0.05); based on Tukey’s multiple comparisons test.
At the end of the trial, the average survival rate for all three groups was >90% (Table 2). The pupation rates of lar- vae fed both 5% and 10% SB were higher than that of the control (Table 2); all larvae fed SB pupated 9 or 10 weeks after hatching. In the control group, pupation was delayed by 17 weeks. Survival and pupation rates did not sig- nificantly differ among the groups.
The improvements in P. brevitarsis growth performance after SB treatment were attributed to the nutrients in the SB. Researchers have reported that SB can be used to en- hance growth performance in lambs [1,12]. Additionally, feeding SB to growing goats increased nutrient digestibility, body weight gain and feed conversion efficiency [16]. The improved performance of SB-supplemented livestock could be due to the ability of the supplements to supply necessary nutrients. The higher performance of P. brevitarsis in the present study was consistent with these studies, although differences existed among the species. SB is a rich source of nutrients and contains enzymes that promote growth per- formance [25,34].
Table 3 showed the larval periods for each P. brevitarsis larval instar. Larvae fed 5% and 10% SB had shorter larval periods than did the control larvae at each stage. Interestingly, the average larval periods of the third instar larvae fed 5% and 10% SB were 75.1% and 76.7% shorter, respectively, than those of the control. Therefore, larvae fed SB grew faster, and nutrients in the SB contributed to this growth. Thus, SB could be used as a nutritive additive for P. brevitarsis to promote larval growth and reduce the labor and costs to rear the larvae.
Table 3. Larval periods for each P. brevitarsis instar treated with three formulations
Growth-inhibitory effect of SB against entomoph- agous S. marcescens
To evaluate the in vitro antibacterial activity of SB, bio- assays were performed by counting colonies on nutrient agar plates. Significantly fewer S. marcescens colonies grew in 5% and 10% SB agar than in the control agar (p<0.01; Fig. 1), possibly because of the antibacterial effect of polico- sanol in the SB. Policosanol is a natural mixture of higher aliphatic primary alcohols (C24-C36). Many studies have re-ported that policosanols substantially inhibit bacterial growth [28-30].
Fig. 1. Effect of sprouted barley on the antibacterial activity against S. marcescens. Columns with different letters dif-fered significantly (p<0.01). Error bars represent the standard deviation of the mean (n=3).
S. marcescens inhabits soil and exhibits entomopathogenic characteristics [15, 23, 32]. In Korea, S. marcescens is the most common bacterium to cause bacterial diseases in P. brevi- tarsis on domestic insect farms. To confirm the in vivo anti- bacterial activity of SB, S. marcescens was injected into the hemocoels of third-instar P. brevitarsis larvae fed feeds sup- plemented with or without SB (Table 4). Approximately 50% of the positive-control larvae, which were infected with S. marcescens and fed control feed, died 4 weeks postin- oculation, revealing that inoculation of entomopathogenic S. marcescens could kill P. brevitarsis larvae. S. marcescens may secrete toxins and damage the larvae during the inoculation period. Despite the bacterial infection, larvae fed SB ex- hibited a survival rate of >70%. Components in the SB seemed to confer the nutrition and immunity required for the infected larvae to survive. Weight gained by the larvae fed control feed was 54%-57%. The final body weights of the infected larvae fed 5% and 10% SB increased by 68% and 75%, respectively. Arabinoxylan polysaccharides and γ -aminobutyric acid (GABA) in the SB causes the im- munomodulatory activity [17,18]. Immunomodulatory com- pounds can interact with the immune system and enhance specific host response mechanisms [9, 18, 34]. Thus, the im- mune enhancement associated with these functional in- gredients might occur in infected larvae fed SB. Further studies on the mechanisms of immunomodulatory mole- cules would help determine their functional roles or involve- ment in insect immune responses.
Table 4. Survival rates and body weights of S. marcescens-infected P. brevitarsis larvae fed different feeds
Nutrient composition of P. brevitarsis with different feeds
The Korean Ministry of Food and Drug Safety registered P. brevitarsis larvae as a general food ingredient in 2016. To guarantee the safety of their use in foods and feeds, we ana- lyzed larval nutrient compositions in different feeds. Table 5 presented the proximate larvla compositions. Crude pro- tein contents in the 5% and 10% SB (59.29% and 55.03%) were significantly higher than those in the control feed (43.68%; 5% SB, p<0.01; 10% SB, p<0.05). Crude protein in meat is ~22% and varies according to source (e.g., beef and pork) [26]. Edible insects are considered a good protein source [4,6]. Larvae fed SB-added feeds had much higher protein concentrations than did other meats. Crude fat was high in the larvae fed 5% SB (3.49%) and 10% SB (3.03%). Crude fiber percentages differed significantly at 5.13% in the control larvae and 6.83% in the larvae fed 10% SB (p<0.001). Therefore, SB might be a nutritional feed source for P. brevitarsis.
Table 5 showed the mineral compositions. Larvae fed SB had higher copper levels than did the controls. Zinc and potassium levels varied significantly (p<0.001) in larvae fed 5% and 10% SB compared with those of the controls. Animals need copper for growth and nerve fiber health [14,27]. Zinc is essential for animal nutrition and physiology [14,24]. Potassium is a major mineral in intracellular fluid and is important for body health and cellular functions in hu-mans and animals [21]. The high levels of copper, zinc, and potassium in the 5% and 10% SB may enhance P. brevitarsis larval growth.
Table 6 showed the larval amino acid profiles. The highest essential amino acid concentrations were for tyrosine at 1.48% (5% SB) and 1.66% (10% SB). The lowest were for me- thionine (0.27% for 5% SB; 0.28% for 10% SB); however, the larvae fed SB-added feeds showed higher methionine con- tents than those of the controls. Methionine is important for animal growth [10]. For non-essential amino acids, the high- est concentrations were for glutamic acid at 1.71% (5% SB) and 1.79% (10% SB). Cysteine had the lowest concentrations (0.22% for both 5% and 10% SB), but the rate of increase in its contents in both groups was the highest of all amino acids compared with those of the controls. Cysteine can be synthesized from methionine, and increased cysteine con- tents were likely due to the increased methionine contents. Adding SB would improve the nutritional value of the larvae as food and feed sources, because these amino acids can sup- port larval growth performance.
However, as the use of insects as food sources has in- creased, concerns have been raised regarding food in- securities such as chemical hazards. Heavy metals can pose serious health hazards to humans and contribute to mortal- ity. No heavy metals, such as arsenic, cadmium, or lead, were detected in any tested samples (Table 5), thus indicating that larvae fed SB are safe and immediately available as food and feed sources.
Acknowledgment
This study was supported by a grant from the National Institute of Agricultural Sciences, Rural Development Administration, Korea (Project No.: PJ014215012021).
The Conflict of Interest Statement
The authors declare that they have no conflicts of interest with the contents of this article.
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