Comparison of the Histological Structure of the Posterior Silk Gland in spinning Cocoons and Non-Spinning Silkworms (Bombyx mori L.)

Authors

DOI:

https://doi.org/10.24925/turjaf.v13i6.1571-1576.7702

Keywords:

Silkworm, Silk Gland, Non-Spinning Syndrome, Pesticide , Metamorphosis

Abstract

This study was conducted to compare the histological differences between the silk glands obtained from cocoon-spinning and non-cocoon-spinning silkworm larvae, and in this context, the changes that occur in the middle silk gland at the end of the larval period were examined using histological techniques. In the study, the cocoon spinning process started in the cocoon-spinning group as of the 7th day of the 5th instar and the cocoon spinning process was completed within the expected normal period. In the non-cocoon-spinning group, it was determined that the cocoon spinning process could not start within the normal period, and therefore the 5th instar period was extended until the 13th day. In the cocoon-spinning group, the tight connection of cells in the posterior silk gland, increased condensation in the nucleus, and the observation of autophagic vacuoles within the cells indicated that pupal metamorphosis continued healthily. On the other hand, in the non-cocoon-spinning group, the lack of nuclear condensation, the inability to distinguish autophagic vacuoles, and the absence of changes related to cell death indicated that the larval process continued. The regional observation of the non-spinning syndrome is thought to be due to pesticide residues in mulberry leaves. It is thought that the last instar in silkworm larvae is prolonged and the pupal metamorphosis process is prevented when mulberry leaves become contaminated with pesticides.

References

Ahsan, F., Ansari, T.M., Usmani, S., & Bagga, P. (2018). An insight on silk protein sericin: from processing to biomedical application. Drug Research, 68(6), 317–327. https://doi.org/10.1055/s-0043-121464

Akai, H. (1998). Silk glands. Microscopic anatomy of invertebrates, Insecta, 11(A), 219–253.

Azuma, M., & Ohta, Y. (1998). Changes in H+- translocating vacuolar –type ATPase in the anterior silk gland cell of Bombyx mori during matemorphosis. The Journal of Experimental Biology, 201(Pt 4), 479–486. https://doi.org/10.1242/jeb.201.4.479

Chen, Q., Sun, S., Yang, X., Yan, H., Wang, K., Ba, X., & Wang, H. (2023). Sublethal effects of neonicotinoid ınsecticides on the development, body weight and economic characteristics of silkworm. Toxics, 11, 402. https://doi.org/ 10.3390/toxics11050402

Dedos S.G., & Fugo H. (1999). Downregulation of the cAMP signal transduction cascade in the prothoracic glands is responsible forthe fenoxycarb-mediated induction of permanent 5th instar larvae in Bombyx mori. Insect Biochemistry and Molecular Biology, 29(8), 723–729. https://doi.org/10.1016/S0965-1748(99)00050-8

Dedos, S.G., Szurdoki, F., Szekacs, A., Mizoguchi, A. & Fugo, H. (2002). Induction of daurer pupae by fenoxycarb in the silkworm, Bombyx mori, Journal of Insect Physiology, 48(9), 857–865. https://doi.org/10.1016/S0022-1910(02)00155-5

Dubrovsky, E.B. (2005). Hormonal cross talk in insect development. Trends in Endocrinology and Metabolism, 16(1), 6–11. https://doi.org/10.1016/j.tem.2004.11.003

El Sherif, D.F., & Soliman, N.H. (2024). Adverse effects of chlorfenapyr and chlorantraniliprole on silkworm Bombyx mori L. parameters and reduction of their effects using ascorbic acid. Fayoum Journal of Agricultural Research and Development, 38(3), 413–423. https://doi.org/10.21608/fjard.2024.302794.1057

Fajfer, D., & Łochyńska, M. (2022). Impact of ecological plant protection products on mortality and cocoon shell ratio of mulberry silkworms (Bombyx mori L.) – pilot studies . Journal of Plant Protection Research, 62(3), 281–286. https://doi.org/10.24425/jppr.2022.142135

Göncü, N.E. (2006). İpekböceği Bombyx mori (Lepıdoptera: Bombycıdae) anterior ipek bezinde programlanmış hücre ölümüne juvenil hormon analoğu fenoxycarb’ın etkisi. Ege Üniv. Biyoloji ABD, Doktora Tezi, İzmir, Türkiye.

Gu, S., Chow, Y, & Yin, C. (1996). Involvement of juvenile hormone in regulation of prothoracicotropic hormone transduction during the early last larval instar of Bombyx mori. Molecular and Cellular Endocrinology, 127(1), 109–106. https://doi.org/10.1016/s0303-7207(96)03995-0

Habeanu, M., Anca, G., & Mihalcea, T. (2023). Silkworm Bombyx mori—sustainability and economic opportunity, particularly for Romania. Agriculture, 13(6), 1209. https://doi.org/10.3390/agriculture13061209

Kamimura, M., & Kiuchi, M. (1998). Effects of a juvenile hormone analog, fenoxycarb, on 5th stadium of the larvae of the silkworm, Bombyx mori (Lepidoptera:Bombycidae). Applied Entomology and Zoology, 33(2), 333–338. https://doi.org/10.1303/aez.33.333

Kodrik D., & Sehnal, F. (1994). Juvenile hormone counteracts the action of ecdysterone on silk glands of Galleria mellonella L. (Lepidoptera: Pyralidae). International Journal of Insect Morphology and Embryology, 23(1), 39–56. https://doi.org/10.1016/0020-7322(94)90014-0

Lu, Z., Li, M., Fang, Y., Qu, J., Ye, W., Dai, M., Bian, D., Mao, T., Li, F., Sun, H., & Li, B. (2020). The mechanism of damage to the posterior silk gland by trace amounts of acetamiprid in the silkworm, Bombyx mori. Pesticide Biochemistry and Physiology. 170, 104676. https://doi.org/10.1016/j.pestbp.2020.104676

Santorum, M., Costa, R.M., dos Reis, G.H., dos Santos, D.C. (2020). Novaluron impairs the silk gland and productive performance of silkworm Bombyx mori (Lepidoptera: Bombycidae) larvae. Chemosphere, 239 (2020), 126497. https://doi.org/10.1016/j.chemosphere.2019.124697

Shi, Y, Lin, G-L, Fu, X-L, Keller, M, Smagghe, G., Liu, T-X. (2020). Cocoon-spinning behavior and 20-hydroxyecdysone regulation of fibroin genes in Plutella xylostella. Frontiers in Physiology, 11, 574800. https://doi.org/10.3389/fphys.2020.574800

Silva, A.S., Costa, E.C., Reis, S., Spencer, C., Calhelha, R.C., Miguel, S.P., Ribeiro, M.P., Barros, L., Vaz, J.A., & Coutinho, P. (2022). Silk sericin: A promising sustainable biomaterial for biomedical and pharmaceutical applications. Polymers, 14, 4931. https://doi.org/10.3390/polym14224931

Sonavane, S., Westermark, P., Rising, A., & Holm, L. (2023). Regionalization of cell types in silk glands of Larinioides sclopetarius suggest that spider silk fibers are complex layered structures. Scientific Reports, 13: 22273. https://doi.org/10.1038/s41598-02349587-z

Şahan, Ü., Gül, Z., & Büyükuysal, L.R. (2020). Biochemical changes in hemolymph of spinning and non-spinning silkworm larvae, Bombyx mori (L., 1758) (Lepidoptera: Bombycidae), reared on fresh mulberry leaves: possible reasons for non-spinning syndrome. Turkish Journal of Entomology, 44(4), 571–579. https://doi.org/10.16970/entoted.737773

Takahashi, M., Kikuchi, K., Tomita, S., Imanishi, S., Nakahara, Y., Kiuchi, M., & Kamimura, M. (2003). Transient in vivo reporter gene assay for ecdysteroid action in the Bombyx mori silk gland. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology. 135(3), 431–437. https://doi.org/10.1016/s1096-4959(03)00094-0

Wilson, T.G. (2004). The molecular site of action of juvenile hormone and juvenile hormone ınsecticides during metamorphosis: how these compounds kill insects. Journal of Insect Physiology, 50(2-3), 111–121. https://doi.org/10.1016/j.jinsphys.2003.12.004

Downloads

Published

28.06.2025

How to Cite

Öziş Altınçekiç, Şeniz, Avcı Küpeli, Z., & Sözcü, A. (2025). Comparison of the Histological Structure of the Posterior Silk Gland in spinning Cocoons and Non-Spinning Silkworms (Bombyx mori L.). Turkish Journal of Agriculture - Food Science and Technology, 13(6), 1571–1576. https://doi.org/10.24925/turjaf.v13i6.1571-1576.7702

Issue

Section

Research Paper