Enhancing chicken manure with bread waste and black soldier fly associated bacteria to increase larval biomass

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Enhancing chicken manure with bread waste and black soldier fly associated bacteria to increase larval biomass

References

  1. Makkar, H. P., Tran, G., Heuzé, V. & Ankers, P. State-of-the-art on use of insects as animal feed. Anim. Feed Sci. Technol. 197, 1–33. https://doi.org/10.1016/j.anifeedsci.2014.07.008 (2014).

    Google Scholar 

  2. Abd El-Hack, M. E. et al. Black soldier fly (Hermetia illucens) meal as a promising feed ingredient for poultry: A comprehensive review. Agriculture 10, 339. https://doi.org/10.3390/agriculture10080339 (2020).

    Google Scholar 

  3. Awasthi, M. K., Duan, Y., Liu, T., Awasthi, S. K. & Zhang, Z. Relevance of Biochar to influence the bacterial succession during pig manure composting. Bioresour. Technol. 304, 122962. https://doi.org/10.1016/j.biortech.2020.122962 (2020).

    Google Scholar 

  4. Lakshmi, N. M., Binod, P., Sindhu, R., Awasthi, M. K. & Pandey, A. Microbial engineering for the production of isobutanol: current status and future directions. Bioengineered 12, 12308–12321 https://doi.org/10.1080/21655979.2021.1978189 (2021).

    Google Scholar 

  5. Mahmoud, I., Hassan, H., Eldlebshany, A. A. & Abdel-Wareth, A. Application of black soldier fly larvae as alternative source of protein in poultry nutrition. A review. SVU-International J. Agricultural Sci. 4, 67–78. https://doi.org/10.21608/svuijas.2022.180821.1253 (2022).

    Google Scholar 

  6. Chia, S. et al. Black soldier fly larval meal in feed enhances growth performance, carcass yield and meat quality of finishing pigs. J. Insects as Food Feed. 7, 433–447. https://doi.org/10.3920/JIFF2020.0072 (2021).

    Google Scholar 

  7. Wang, Q. et al. Improvement of the composition and humification of different animal manures by black soldier fly bioconversion. J. Clean. Prod. 278, 123397. https://doi.org/10.1016/j.jclepro.2020.123397 (2021).

    Google Scholar 

  8. Kumar, V. et al. Active pharmaceutical ingredient (API) chemicals: a critical review of current biotechnological approaches. Bioengineered 13, 4309–4327. https://doi.org/10.1080/21655979.2022.2031412 (2022).

    Google Scholar 

  9. Das, S., Goswami, L. & Bhattacharya, S. S. in Current Developments in Biotechnology and Bioengineering 79–102 (Elsevier, 2020).

  10. Ddiba, D., Andersson, K., Rosemarin, A., Schulte-Herbrüggen, H. & Dickin, S. The circular economy potential of urban organic waste streams in low-and middle-income countries. Environ. Dev. Sustain. 24, 1116–1144. https://doi.org/10.1007/s10668-021-01487-w (2022).

    Google Scholar 

  11. Al Sagan, A. A., Al-Abdulkader, A. M., Al-Dakhil, A. I., Khalil, S. & Al-Khuraish, M. M. Technical and economic potentials of the unconventional extruded dried Arabic bread wastes in broilers diets. Saudi J. Biol. Sciences. 28, 262–271. https://doi.org/10.1016/j.sjbs.2020.09.058 (2021).

    Google Scholar 

  12. State Information Service. Helping the poultry industry. Al-Ahram Weekly. (2022). Available at: https://english.ahram.org.eg/News/479370.aspx

  13. ResearchGate. Bread and Bakery Products Waste in Selected Mediterranean Arab Countries. Bread_and_Bakery_Products_Waste_in_Selected_Mediterranean_Arab_Countries. https://www.researchgate.net/publication/301696018 (2016).

  14. Engel, P. & Moran, N. A. The gut microbiota of insects–diversity in structure and function. FEMS Microbiol. Rev. 37, 699–735. https://doi.org/10.1111/1574-6976.12025 (2013).

    Google Scholar 

  15. Chen, B. et al. Biodiversity and activity of the gut microbiota across the life history of the insect herbivore spodoptera littoralis. Sci. Rep. 6, 29505. https://doi.org/10.1038/srep29505 (2016).

    Google Scholar 

  16. Jiang, C. L. et al. Black soldier fly larvae (Hermetia illucens) strengthen the metabolic function of food waste biodegradation by gut Microbiome. Microb. Biotechnol. 12, 528–543. https://doi.org/10.1111/1751-7915.13393 (2019).

    Google Scholar 

  17. Crotti, E. et al. Microbial symbionts: a resource for the management of insect-related problems. Microb. Biotechnol. 5, 307–317. https://doi.org/10.1111/j.1751-7915.2011.00312.x (2012).

    Google Scholar 

  18. Yu, G. et al. Inoculating poultry manure with companion bacteria influences growth and development of black soldier fly (Diptera: Stratiomyidae) larvae. Environ. Entomol. 40, 30–35. https://doi.org/10.1603/EN10126 (2011).

    Google Scholar 

  19. Prosdocimi, E. M., Mapelli, F., Gonella, E., Borin, S. & Crotti, E. Microbial ecology-based methods to characterize the bacterial communities of non-model insects. J. Microbiol. Methods. 119, 110–125. https://doi.org/10.1016/j.mimet.2015.10.010 (2015).

    Google Scholar 

  20. Varotto Boccazzi, I. et al. A survey of the mycobiota associated with larvae of the black soldier fly (Hermetia illucens) reared for feed production. PloS One. 12, e0182533. https://doi.org/10.1371/journal.pone.0182533 (2017).

    Google Scholar 

  21. Broderick, N. A., Buchon, N. & Lemaitre, B. Microbiota-induced changes in Drosophila melanogaster host gene expression and gut morphology. MBio 5, 01117–01114 https://doi.org/10.1128/mBio.01117-14 (2014).

    Google Scholar 

  22. Peterson, B. F. & Scharf, M. E. Lower termite associations with microbes: synergy, protection, and interplay. Front. Microbiol. 7, 422. https://doi.org/10.3389/fmicb.2016.00422 (2016).

    Google Scholar 

  23. Sabree, Z. L., Kambhampati, S. & Moran, N. A. Nitrogen recycling and nutritional provisioning by Blattabacterium, the cockroach endosymbiont. Proceedings of the National Academy of Sciences. 106, 19521–19526 https://doi.org/10.1073/pnas.0907504106 (2009).

  24. Mazza, L. et al. Management of chicken manure using black soldier fly (Diptera: Stratiomyidae) larvae assisted by companion bacteria. Waste Manage. 102, 312–318. https://doi.org/10.1016/j.wasman.2019.10.055 (2020).

    Google Scholar 

  25. Sukmawati, D. et al. Isolation and screening microorganisms from black soldier fly larvae (Hermetia illucens) that producing Amylase, protease and cellulase. Jurnal Penelitian Pendidikan IPA. 9, 9784–9793. https://doi.org/10.29303/jppipa.v9i11.4516 (2023).

    Google Scholar 

  26. Association of Official Analytical Chemists. Official Methods of Analysis of the Association of Official Analytical Chemists 18th edn, Vol. 2 (The Association, 2007).

  27. Broeckx, L. et al. Growth of black soldier fly larvae reared on organic side-streams. Sustainability 13, 12953. https://doi.org/10.3390/su132312953 (2021).

    Google Scholar 

  28. Benson, H. J. Microbiological Applications: a Laboratory Manual in General Microbiology ([McGraw-Hill], 2002).

  29. Leboffe, M. J. & Pierce, B. E. Microbiology: Laboratory Theory and Application (Morton Publishing Company, 2015).

  30. Garrity, G., Bell, J. A. & Lilburn, T. The proteobacteria, part B the Gammaproteobacteria. Bergey’s Man. Syst. Bacteriol. 2, 323–337 (2005).

    Google Scholar 

  31. Niall, A. L. & Paul, D. V. Genus Bacillus. In: Paul, D.V., M.G. George, J. Dorothy, R.K. Noel, L. Wolfgang, A.R. Fred, S. Karl-Heinz and B.W. William (Eds), Bergey’s manual of systematic bacteriology. Vol. 3 (2nd edition). pp. 21–128 (Springer, New York, 2009).

  32. Parte, A. et al. Bergey’s manual of systematic bacteriology: volume 5: the Actinobacteria (Springer Science & Business Media, 2012).

  33. White, T. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. PCR Protocols: A guide to methods and applications/Academic Press, Inc (1990).

  34. Pellet, P. L. & Young, V. R. In Nutritional evaluation of protein foods. Food and Nutrition Bulletin, Supplement No. 4. Published the United Nations University. Tokyo, Japan pp: 546 (1980).

  35. Bryman, A. & Cramer, D. Quantitative Data Analysis with IBM SPSS 17, 18 & 19: A Guide for Social Scientists (Routledge, 2012). https://doi.org/10.4324/9780203180990

  36. Singh, G., Shamsuddin, M. R. & Lim, S. W. December. Characterization of chicken manure from manjung region. IOP conference series: materials science and engineering. 458(1), 012084 (2018).

  37. Maj, I. Significance and challenges of poultry litter and cattle manure as sustainable fuels: a review. Energies 15, 8981 (2022).

    Google Scholar 

  38. Al-Dalain, S. Y. & Morsy, M. K. Effect of Pullulan and hydrocolloids on rheological properties and quality parameters of wheat-soy Baladi bread. Food Nutr. Sci. 9, 32–45 (2018).

    Google Scholar 

  39. Siddiqui, S. A. et al. Black soldier fly larvae (BSFL) and their affinity for organic waste processing. Waste Management. 140, 1–13. https://doi.org/10.1016/j.wasman.2021.12.044 (2022).

    Google Scholar 

  40. Barragan-Fonseca, K. B., Gort, G., Dicke, M. & van Loon, J. J. A. Effects of dietary protein and carbohydrate on life-history traits and body protein and fat contents of the black soldier fly Hermetia illucens. Physiol. Entomol. 44, 148–159. https://doi.org/10.1111/phen.12285 (2019).

    Google Scholar 

  41. Eggink, K. M., Donoso, I. G. & Dalsgaard, J. Optimal dietary protein to carbohydrate ratio for black soldier fly (Hermetia illucens) larvae. J. Insects as Food Feed. 9, 789–798. https://doi.org/10.3920/JIFF2022.0102 (2023).

    Google Scholar 

  42. ur Rehman, K. et al. Enhanced bioconversion of dairy and chicken manure by the interaction of exogenous bacteria and black soldier fly larvae. J. Environ. Manage. 237, 75–83. https://doi.org/10.1016/j.jenvman.2019.02.048 (2019).

    Google Scholar 

  43. Danieli, P. P., Lussiana, C., Gasco, L., Amici, A. & Ronchi, B. The effects of diet formulation on the yield, proximate composition, and fatty acid profile of the black soldier fly (Hermetia illucens L.) Prepupae intended for animal feed. Animals 9, 178. https://doi.org/10.3390/ani9040178 (2019).

    Google Scholar 

  44. Belperio, S. et al. Assessing substrate utilization and bioconversion efficiency of black soldier fly (Hermetia illucens) larvae: effect of diet composition on growth and development temperature. Animals 14, 1340 https://doi.org/10.3390/ani14091340 (2024).

    Google Scholar 

  45. Cattaneo, A. et al. First step towards black soldier fly larvae (Diptera: Stratiomyidae) welfare by considering dietary regimes (Part I). Insects 15, 817. https://doi.org/10.3390/insects15100817 (2024).

    Google Scholar 

  46. Generalovic, T. N. et al. Variation in strain performance and estimates of heritability of body size indicate considerable potential for genetic improvement of the black soldier fly (Hermetia illucens). Entomol. Exp. Appl. 173 (6), 558–574. https://doi.org/10.17863/CAM.116993 (2025).

    Google Scholar 

  47. Nguyen, T. T., Tomberlin, J. K. & Vanlaerhoven, S. Ability of black soldier fly (Diptera: Stratiomyidae) larvae to recycle food waste. Environ. Entomol. 44, 406–410. https://doi.org/10.1093/ee/nvv002 (2015).

    Google Scholar 

  48. Jucker, C., Erba, D., Leonardi, M. G., Lupi, D. & Savoldelli, S. Assessment of vegetable and fruit substrates as potential rearing media for Hermetia illucens (Diptera: Stratiomyidae) larvae. Environ. Entomol. 46, 1415–1423. https://doi.org/10.1093/ee/nvx154 (2017).

    Google Scholar 

  49. Zhou, Z. et al. The effect of dietary Chitin on the autochthonous gut bacteria of A Tlantic Cod (G adus Morhua L). Aquac. Res. 44, 1889–1900. https://doi.org/10.1111/j.1365-2109.2012.03194.x (2013).

    Google Scholar 

  50. Msangi, J., Mweresa, C. & Ndong’a, M. Using organic wastes as feed substrate for black soldier fly larvae. J. Insects as Food Feed. 8, 357–366. https://doi.org/10.3920/JIFF2021.0047 (2022).

    Google Scholar 

  51. Jalil, N., Abdullah, S., Ahmad, I., Basri, N. & Mohamed, Z. Decomposition of food waste from protein and carbohydrate sources by black soldier fly larvae, hermetia illucens L. J. Environ. Biol. 42, 756–761. https://doi.org/10.22438/jeb/42/3(SI)/JEB-04 (2021).

    Google Scholar 

  52. Farooq, M. A. et al. Biosynthesis and industrial applications of α-amylase: a review. Arch. Microbiol. 203, 1281–1292. https://doi.org/10.1007/s00203-020-02128-y (2021).

    Google Scholar 

  53. Pamaya, D. et al. Isolasi Bakteri Penghasil Enzim protease Bacillus amyloliquefacienns IROD2 Pada Oncom Merah Pasca fermentasi 48 jam. National Seminar Educ. Technology pp. 31–39, (2018).

  54. Masi, C., Fazil, A. M. & Parthasarathi, N. A comparative study on the protease producing bacteria isolated from dairy effluents of Chennai region, identification, characterization and application of enzyme in detergent formulation. Asian J. Microbiol. Biotechnol. Environ. Sci. 16, 41–46 (2014).

    Google Scholar 

  55. Putri, A. L. O. & Kusdiyantini, E. Isolation and identification of lactic acid bacteria from fish-based fermented food (Inasua) traded in Maluku-Indonesia. J. Trop. Biology. 1, 6–12 (2018).

    Google Scholar 

  56. Mekonnen, E. et al. Isolation and characterization of Urease-Producing soil bacteria. Int. J. Microbiol. 1 https://doi.org/10.1155/2021/8888641 (2021).

  57. Phang, I. R. K., Chan, Y. S., Wong, K. S. & Lau, S. Y. Isolation and characterization of urease-producing bacteria from tropical peat. Biocatal. Agric. Biotechnol. 13 (2-s2), 168–175. https://doi.org/10.1016/j.bcab.2017.12.006 (2018).

    Google Scholar 

  58. Cuzman, O. A., Rescic, S., Richter, K., Wittig, L. & Tiano, P. Sporosarcina pasteurii use in extreme alkaline conditions for recycling solid industrial wastes. J. Biotechnol. 214 (2-s2), 49–56. https://doi.org/10.1016/j.jbiotec.2015.09.011 (2015).

    Google Scholar 

  59. Kim, C. H. et al. Use of black soldier fly larvae for food waste treatment and energy production in Asian countries: A review. Processes 9, 161. https://doi.org/10.3390/pr9010161 (2021).

    Google Scholar 

  60. Callegari, M. et al. Hydrolytic profile of the culturable gut bacterial community associated with Hermetia illucens. Front. Microbiol. 11, 1965 https://doi.org/10.3389/fmicb.2020.01965 (2020).

  61. Zhang, Y. et al. Hermetia illucens L. larvae–associated intestinal microbes reduce the transmission risk of zoonotic pathogens in pig manure. Microb. Biotechnol. 15, 2631–2644. https://doi.org/10.1111/1751-7915.14113 (2022).

    Google Scholar 

  62. Mannaa, M., Mansour, A., Park, I., Lee, D. W. & Seo, Y. S. Insect-based agri-food waste valorization: agricultural applications and roles of insect gut microbiota. Environ. Sci. Ecotechnology. 17, 100287. https://doi.org/10.1016/j.ese.2023.100287( (2024).

    Google Scholar 

  63. Klammsteiner, T. et al. The core gut Microbiome of black soldier fly (Hermetia illucens) larvae Raised on low-bioburden diets. Frontires Microbiol. 11, 993. https://doi.org/10.3389/fmicb.2020.00993 (2020).

    Google Scholar 

  64. Memon, F. U. et al. Gut microbial communities and transcriptional profiles of black soldier fly (Hermetia illucens) larvae fed on fermented sericulture waste. Waste Manage. 194, 158–168, https://doi.org/10.1016/j.wasman.2025.01.011(2025).

  65. Gorrens, E., Van Moll, L., Frooninckx, L., De Smet, J. & Van Campenhout, L. Isolation and identification of dominant bacteria from black soldier fly larvae (Hermetia illucens) envisaging practical applications. Front. Microbiol. 13, 900729. https://doi.org/10.3389/fmicb.2022.900729 (2022).

    Google Scholar 

  66. Vandeweyer, D. et al. Bacterial biota composition in gut regions of black soldier fly larvae reared on industrial residual streams: revealing community dynamics along its intestinal tract. Front. Microbiol. 14, 1276187. https://doi.org/10.3389/fmicb.2023.1276187 (2023).

    Google Scholar 

  67. Spranghers, T. et al. Nutritional composition of black soldier fly (Hermetia illucens) Prepupae reared on different organic waste substrates. J. Sci. Food. Agric. 97, 2594–2600. https://doi.org/10.1002/jsfa.8081 (2017).

    Google Scholar 

  68. Nguyen, T. T., Tomberlin, J. K. & Vanlaerhoven, S. Ability of black soldier fly (Diptera: Stratiomyidae) 870 larvae to recycle food waste. Environ. Entomol. 44, 406–410. https://doi.org/10.1093/ee/nvv002 (2015).

    Google Scholar 

  69. Sealey, W. M. et al. Sensory analysis of rainbow trout, Oncorhynchus mykiss, fed enriched black soldier fly prepupae, hermetia illucens. J. World Aquaculture Soc. 42, 34–45. https://doi.org/10.1111/j.1749-7345.2010.00441.x (2011).

    Google Scholar 

  70. Schmidt, K. & Engel, P. Mechanisms underlying gut microbiota–host interactions in insects. J. Exp. Biol. 224 (jeb207696), 202. https://doi.org/10.1242/jeb.207696 (2021).

    Google Scholar 

  71. Jing, T. Z., Qi, F. H. & Wang, Z. Y. Most dominant roles of insect gut bacteria: digestion, detoxification, or essential nutrient provision? Microbiome 8, 1–20. https://doi.org/10.1186/s40168-020-00823-y (2020).

    Google Scholar 

  72. Smetana, S., Palanisamy, M., Mathys, A. & Heinz, V. Sustainability of insect use for feed and food: life cycle assessment perspective. J. Clean. Prod. 137, 741–751. https://doi.org/10.1016/j.jclepro.2016.07.148 (2016).

    Google Scholar 

  73. Salomone, R. et al. Environmental impact of food waste bioconversion by insects: application of life cycle assessment to process using Hermetia illucens. J. Clean. Prod. 140, 890e905. https://doi.org/10.1016/j.jclepro.2016.06.154 (2017).

    Google Scholar 

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