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Stream/Area:
-
Subject:
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Paper ID:
IJSREM66678
Volume:
10 |
8 |
Aug 2026
Pages:
1-12
Publication Frequency:
Monthly (12 issues per year)
License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.

Assistant Professor and Head, Department of Zoology
Hutatma Jayvantrao Patil Mahavidyalaya, Himayatnagar, Nanded–431802, Maharashtra, India.
The gut microbiota of the mulberry silkworm, Bombyx mori, has emerged as a critical determinant of larval growth, nutrient utilization, immune competence, disease resistance, and silk production. Advances in high-throughput sequencing, metagenomics, metabolomics, and microbial ecology have substantially improved our understanding of the complex interactions between the silkworm host and its intestinal microbial community. The gut microbiome contributes to the digestion of mulberry leaves, biosynthesis of essential nutrients, detoxification of plant secondary metabolites, regulation of immune responses, and maintenance of intestinal homeostasis. Recent studies have demonstrated that dietary supplementation with probiotics, including Bacillus, Lactobacillus, Pediococcus, Enterococcus, and yeast species, enhances larval growth, cocoon quality, feed conversion efficiency, antioxidant capacity, and resistance against bacterial, fungal, viral, and microsporidian pathogens. Furthermore, emerging microbiome-engineering approaches, artificial diets enriched with beneficial microorganisms, and multi-omics technologies have opened new opportunities for developing sustainable and antibiotic-free sericulture. Despite significant progress, several challenges remain, including the lack of standardized probiotic formulations, geographical variation in microbial communities, incomplete understanding of host–microbe interactions, and limited commercial application. This review comprehensively summarizes recent advances in the diversity, functional roles, and manipulation of the gut microbiota of Bombyx mori, with particular emphasis on nutrition, probiotics, immunity, disease resistance, and sustainable silk production. Finally, current research gaps and future perspectives for microbiome-guided precision sericulture are discussed.
KEYWORDS
The gut microbiota of Bombyx mori has emerged as a fundamental determinant of silkworm nutrition, immunity, metabolism, disease resistance, and silk production. Advances in next-generation sequencing, metagenomics, transcriptomics, metabolomics, and other multi-omics technologies have significantly expanded our understanding of the composition, diversity, and functional significance of the silkworm intestinal microbiome. Beneficial microorganisms, particularly members of the genera Lactobacillus, Enterococcus, Bacillus, Pediococcus, and Pantoea, contribute to the degradation of complex dietary components, synthesis of essential nutrients, modulation of immune responses, detoxification of plant secondary metabolites, maintenance of gut homeostasis, and enhancement of antioxidant defense systems. These microbial activities collectively improve larval growth, feed conversion efficiency, cocoon quality, and silk yield while reducing susceptibility to bacterial, viral, fungal, and microsporidian infections. Recent research has demonstrated that manipulation of the gut microbiota through probiotics, prebiotics, synbiotics, phytogenic feed additives, and optimized artificial diets represents a promising and environmentally sustainable strategy for improving silkworm health and productivity. Furthermore, microbiome-based interventions offer an effective alternative to antibiotics and chemical growth promoters, thereby supporting eco-friendly and sustainable sericulture. Nevertheless, substantial challenges remain, including limited knowledge of fungal, archaeal, and viral communities, incomplete understanding of host–microbe interactions, lack of standardized probiotic formulations, and insufficient field validation under commercial rearing conditions. These knowledge gaps emphasize the need for integrated multidisciplinary investigations combining microbiology, molecular biology, nutrition, immunology, bioinformatics, and systems biology. Future research should focus on functional microbiome engineering, precision nutrition, synthetic microbial communities, artificial intelligence-assisted microbiome prediction, and multi-omics integration to elucidate the complex mechanisms governing host–microbiota interactions. The development of standardized probiotic formulations and microbiome-guided feeding strategies will facilitate improved disease management, enhanced silk productivity, and reduced environmental impacts. Additionally, integrating genomic selection with microbiome profiling may enable the identification of silkworm strains exhibiting superior microbial associations and enhanced resistance to environmental stress and infectious diseases.Overall, the gut microbiota represents a valuable biological resource for advancing modern sericulture. Continued exploration of microbial diversity, functional mechanisms, and microbiome-based technologies will not only deepen our understanding of silkworm biology but also accelerate the development of innovative, sustainable, and precision-based sericultural practices. Such approaches have the potential to improve the economic viability of silk production while contributing to global efforts toward sustainable agriculture, environmental conservation, and the circular bioeconomy.
1. Goldsmith, M. R., Shimada, T., & Abe, H. (2005). The genetics and genomics of the silkworm, Bombyx mori. Annual Review of Entomology, 50, 71–100. https://doi.org/10.1146/annurev.ento.50.071803.130456 2. Xia, Q., Zhou, Z., Lu, C., Cheng, D., Dai, F., Li, B., Zhao, P., Zha, X., Cheng, T., Chai, C., Pan, G., Xu, J., Liu, C., Lin, Y., Qian, J., Hou, Y., et al. (2004). A draft sequence for the genome of the domesticated silkworm (Bombyx mori). Science, 306(5703), 1937–1940. https://doi.org/10.1126/science.1102210 3. International Silkworm Genome Consortium. (2008). The genome of a lepidopteran model insect, the silkworm Bombyx mori. Insect Biochemistry and Molecular Biology, 38(12), 1036–1045. https://doi.org/10.1016/j.ibmb.2008.11.004 4. Engel, P., & Moran, N. A. (2013). The gut microbiota of insects—Diversity in structure and function. FEMS Microbiology Reviews, 37(5), 699–735. https://doi.org/10.1111/1574-6976.12025 5. Douglas, A. E. (2009). The microbial dimension in insect nutritional ecology. Functional Ecology, 23(1), 38–47. https://doi.org/10.1111/j.1365-2435.2008.01442.x 6. Chen, B., Du, K., Sun, C., Vimalanathan, A., Liang, X., Li, Y., Wang, B., Lu, X., Li, L., & Shao, Y. (2018). Gut bacterial and fungal communities of the domesticated silkworm (Bombyx mori) and wild mulberry-feeding relatives. The ISME Journal, 12(9), 2252–2262. https://doi.org/10.1038/s41396-018-0174-1 7. Hou, C., Shi, Y., Wang, H., Li, R., Nartey, M. A., & Guo, X. (2018). Composition and diversity analysis of intestinal microbiota in the fifth instar silkworm, Bombyx mori L. Invertebrate Survival Journal, 15(1), 223–233. https://doi.org/10.25431/1824-307X/isj.v15i1.223-233 8. Qin, L., Qi, J., Shen, G., Qin, D., Wu, J., Song, Y., Cao, Y., Zhao, P., & Xia, Q. (2022). Effects of microbial transfer during food-gut-feces circulation on the health of Bombyx mori. Microbiology Spectrum, 10(6), e02357-22. https://doi.org/10.1128/spectrum.02357-22 9. Shu, Q., Wang, Y., Gu, H., Zhu, Q., Liu, W., Dai, Y., Li, F., & Li, B. (2023). Effects of artificial diet breeding on intestinal microbial populations at the young stage of silkworm (Bombyx mori). Archives of Insect Biochemistry and Physiology, 113(3), e22019. https://doi.org/10.1002/arch.22019 10. Xin, L., Chen, Y., Rong, W., Qin, Y., Li, X., & Guan, D. (2024). Gut microbiota analysis in silkworms (Bombyx mori) provides insights into identifying key bacteria for inclusion in artificial diet formulations. Animals, 14(9), 1261. https://doi.org/10.3390/ani14091261
Publication Date
8/11/2026
Peer Review Type
Double-Blind Peer Review
Review Rounds: 2
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