Nutritional Plasticity, Waste Bioconversion, and Insect Detoxification in the Anthropocene
Simple Summary
Abstract
1. Introduction
2. Nutritional Needs of Insects in the Anthropocene Context: Bases for Metabolic Plasticity
2.1. Essential Nutrients and Metabolic Plasticity of Insects in Anthropogenic Environments
2.2. The Crucial Role of Gut Microbiota in Insect Adaptation in the Anthropocene
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- Improved Digestive Efficiency: The microbiota enables the insect to digest and assimilate nutrients from complex and recalcitrant substrates, such as cellulose, hemicellulose, and lignin, often abundant in agro-industrial and urban waste [14]. This capacity broadens the spectrum of resources that the insect can use as food, transforming what would be useless to others into a viable energy source
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- Synthesis of Essential Nutrients: In nutritionally unbalanced or deficient diets, the microbiota can synthesize essential vitamins (notably B-complex) and amino acids, filling nutritional gaps for the host and ensuring full development [8].
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- Detoxification Mechanisms and Xenobiotic Tolerance: The gut microbiota plays a critical role in the biotransformation and detoxification of plant secondary compounds, as well as xenobiotics and pollutants present in waste and the anthropogenic environment. This ability to neutralize potentially toxic substances is a cornerstone of insect resilience in contaminated ecosystems [22].
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- Immunity Modulation and Pathogen Resistance: A balanced microbiota contributes to the overall health of the insect, aiding in defense against pathogens and strengthening its immune response [23].
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- Hermetia illucens (Black Soldier Fly Larvae): Their gut microbiota demonstrates remarkable shifts in community structure and function when larvae are reared on diverse organic waste streams (e.g., municipal food waste, agricultural residues). These microbial adaptations enhance the breakdown of complex biopolymers and optimize nutrient cycling, allowing for efficient bioconversion and biomass accumulation [22].
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- Tenebrio molitor (Mealworm Larvae): When fed diets containing recalcitrant materials like polystyrene, the mealworm’s gut microbiome adapts, with an increased abundance of specific bacterial taxa that contribute to polymer depolymerization and utilization, showcasing its role in novel waste valorization [24].
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- Detoxification Mechanisms: The gut microbiota also plays a crucial role in detoxifying xenobiotics. For instance, in the coffee berry borer (Hypothenemus hampei), gut bacteria facilitate the detoxification of caffeine, enabling the insect to thrive on coffee beans as its primary food source [25].
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- Nutrient Compensation: In various insect species, particularly those on nutritionally imbalanced or deficient diets, changes in the gut microbial community can lead to enhanced synthesis of essential vitamins (e.g., B-complex vitamins) and amino acids, thus compensating for dietary gaps and ensuring host development [8,13].
3. Dietary Plasticity and Persistence Strategies in the Anthropocene: Evidence and Implications
Metabolic Flexibility and Exploitation of Anthropogenic Substrates
4. Detoxification Mechanisms and Biochemical Adaptation to Anthropogenic Substrate
5. Challenges and Risk Management in the Application of Insects in the Circular Bioeconomy
6. Conclusions
Author Contributions
Funding
Data Availability Statement
Conflicts of Interest
References
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Insect Composition | Protein | Crude Fiber | Carb | Fats | Vitamin A | Vitamin B2 | Vitamin C | Fe | Ca | Zn | P | Mg |
---|---|---|---|---|---|---|---|---|---|---|---|---|
(%) | (mg/100 g) | |||||||||||
Cirina forda (larvae) | 20.2 | 1.8 | ND * | ND * | 3.0 | 2.2 | 2.0 | 64.0 | 15.4 | 8.6 | 110.0 | 1.9 |
Brachytrupes membranaceus (adult) | 53.4 | 15.0 | 15.1 | 53.0 | 0.0 | 0.0 | 0.0 | 0.7 | 9.2 | ND * | 126.9 | 0.1 |
Brachytrupes spp. (adult) | 6.3 | 1.0 | ND * | ND * | 0.0 | 0.0 | 0.0 | 0.7 | 9.2 | ND * | 126.9 | 0.1 |
Rhynchophorus phoenicis (larvae) | 28.4 | 2.8 | ND * | ND * | 11.3 | 2.2 | 4.3 | 12.2 | 39.6 | ND * | 126.4 | 7.5 |
Carebara vidua (adult) | 42.5 | 9.1 | ND * | 38.2 | 12.4 | 3.2 | 10.3 | 25.2 | 15.4 | ND * | 125.5 | 5.2 |
Humans’ total requirements of nutrients | Protein | Crude Fiber | Carb | Fats | Vitamin A | Vitamin B2 | Vitamin C | Fe | Ca | Zn | P | Mg |
RDA ** (g/day) | AI *** | RDA ** (g) | RDA (μg) | RDA ** (mg) | AI *** | RDA ** (mg) | ||||||
Women (age 19–30) | 46.0 | 25.0 | 130.0 | ND * | 700.0 | 1.1 | 75.0 | 18.0 | 1000.0 | 8.0 | 700.0 | 400.0 |
Women (age 31–50) | 46.0 | 21.0 | 130.0 | ND * | 700.0 | 1.1 | 75.0 | 18.0 | 1000.0 | 8.0 | 700.0 | 420.0 |
Men (age 19–30) | 56.0 | 38.0 | 130.0 | ND * | 900.0 | 1.3 | 90.0 | 8.0 | 1000.0 | 11.0 | 700.0 | 400.0 |
Men (age 31–50) | 56.0 | 30.0 | 130.0 | ND * | 900.0 | 1.3 | 90.0 | 8.0 | 1000.0 | 11.0 | 700.0 | 420.0 |
Animals’ total requirements of nutrients | Protein | Crude Fiber | Carb | Fats | Vitamin A | Vitamin B2 | Vitamin C | Fe | Ca | Zn | P | Mg |
(%) | IU | mg | mg/ kg | (%) | mg/ kg | (%) | ||||||
Swine (7–11 kg) | ND * | ND * | ND * | ND * | 2200.0 | 3.5 | * ND | 100.0 | 0.8 | 100.0 | 0.65 | 0.04 |
Swine (75–100 kg) | ND * | ND * | ND * | ND * | 1300.0 | 2.0 | * ND | 40.0 | 0.52 | 50.0 | 0.47 | 0.04 |
Tilapia | 41.3 | ND * | ND * | ND * | 4769.0 | ND * | 600.0 | 60.0 | ND * | 79.51 | 0.65 | * ND |
Deer | ND * | ND * | ND * | ND * | ND * | ND * | ND * | 50.0 | 0.35 | 50.0 | 0.25 | 0.2 |
Chickens (6–8 weeks) | 19–21 | ND * | ND * | ND * | 1500.0 | 3.0 | ND * | 80.0 | 0.8 | 40.0 | 0.3 | ND * |
Source | Insect | Stage | Parameters | Results | Conclusion | References |
---|---|---|---|---|---|---|
Varied protein and carbohydrate content (macronutrient restriction) and caloric density (calorie restriction) | Drosophila melanogaster (fruit fly) | Larval and adult | Body weight, wing and femur size | Macronutrient restriction was more detrimental to adult size than caloric restriction. For adult body weight, a rich adult diet mitigated the negative effects of larval malnutrition for both types of diets. Poor diet of larvae caused smaller wing and femur sizes without recovery using adult diet. | The nutritional conditions of the larvae play a dominant role in determining adult body weight and wing and femur size, the adult diet may adjust body weight as flies age. | [26] |
Artificial diet based on corn, rice, or cotton leaves | Spodoptera frugiperda (fall armyworm) | Eclosion to the sixth instar | Identify differences in metabolite profiles of the larval gut | The metabolome of the midgut of insects varied according to the larval diet | Effects of diet on the metabolome, differential digestive metabolism, and identified marker metabolites. | [31] |
Mulberry leaves, artificial diet, and artificial diet + mulberry leaves | Bombyx mori (silkworm) | 1st instar to the 3rd instars, 4th instar to mature larvae (cocooning stage) | Physiological characteristics and the underlying mechanisms | Compensatory growth occurred, and genes related to metabolism and development in the midgut of the silkworm showed differences. | Compensated for developmental delay and body weight loss after changing nutritional status, as well as severe physiological changes (body weight gain, altered digestive juice activity, and altered gene expression in the midgut). | [32] |
Sugars (glucose, fructose, sucrose, trehalose, melibiose, melezitose, and sorbitol); two types of honeydew | Psyttalia concolor Szépligeti | - | Longevity and parasitism capacity | The longevity of females increased with sorbitol and melibiose and males with hexose nectars. Feeding with honeydew showed better results. | Source of carbohydrates (sugar or honeydew) is important for longevity and reproduction, especially for females. | [33] |
Diets with protein to carbohydrate ratio and nutritional content | Cricket (Gryllodes sigillatus) | Replicate populations (for >37 generations) | Hemocyte counts, the zone of inhibition, and total phenoloxidase | After three generations, in males and females, immunity was higher on protein. Although females exhibited superior immunity for all assays, the sexes showed similar immune changes across diets. | Indicated that populations evolved with dietary manipulation. | [34,35] |
Six sugarcane cultivars (total phenolic, flavonoids, and anthocyanins contents) | Pink stem stalk borer (Sesamia cretica Lederer) | Fifth instar larvae | Nutritional responses and body weight; digestive enzymatic activity | One cultivar was less suitable due to low relative consumption rates and relative growth rate, related to low nutritional level, biochemical properties, and high concentration of protein inhibitors. | Indicated remarkable differences in the nutritional properties and digestive function; significant variations in the phytochemical metabolites were detected | [34] |
Cowpea, sunflower, sorghum, and a mixture of the three plant species | Glassy-winged sharpshooter (Homalodisca vitripennis (Germar) | 9 wk oviposition period and adults emerging | Nymphal development, oogenesis, and fecundity | On nymphal diets, active females produced more eggs in plant mixtures. In choice testes, adult females opted for cowpea, but most eggs were deposited in sorghum. | Fecundity is largely determined by the quality of the adult diet, although the stimulus that initiates oogenesis does not appear to be related to nutrition. | [36] |
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Christ-Ribeiro, A.; Zacheski, J.B.A.; da Silva Lucas, A.J.; Kupski, L. Nutritional Plasticity, Waste Bioconversion, and Insect Detoxification in the Anthropocene. Insects 2025, 16, 915. https://doi.org/10.3390/insects16090915
Christ-Ribeiro A, Zacheski JBA, da Silva Lucas AJ, Kupski L. Nutritional Plasticity, Waste Bioconversion, and Insect Detoxification in the Anthropocene. Insects. 2025; 16(9):915. https://doi.org/10.3390/insects16090915
Chicago/Turabian StyleChrist-Ribeiro, Anelise, Janaína Barreto Alves Zacheski, Andressa Jantzen da Silva Lucas, and Larine Kupski. 2025. "Nutritional Plasticity, Waste Bioconversion, and Insect Detoxification in the Anthropocene" Insects 16, no. 9: 915. https://doi.org/10.3390/insects16090915
APA StyleChrist-Ribeiro, A., Zacheski, J. B. A., da Silva Lucas, A. J., & Kupski, L. (2025). Nutritional Plasticity, Waste Bioconversion, and Insect Detoxification in the Anthropocene. Insects, 16(9), 915. https://doi.org/10.3390/insects16090915