Alterations in the lipid composition of pectoral muscles in honey bees (Apis mellifera) in relation to brood-rearing activity

  • I. V. Kovalskyi Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • М. A. Druzhbiak Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • L. M. Kovalska Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • A. J. Druzhbiak Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • A. M. Tybinka Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • O. Y. Klym Institute of Agriculture in the Carpathian Region NAAS
  • A. O. Boyko Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • V. V. Zhmur Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • R. V. Havdan Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • D. P. Perig Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • I. M. Lunyk Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • L. M. Fiialovych Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • O. P. Petryshak Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • G. A. Paskevych Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • B. S. Barylo Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • I. S. Leshchyshyn Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • M. D. Perig Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
  • V. A. Grynyk Stepan Gzhytsky Lviv National University of Veterinary Medicine and Biotechnology
Keywords: honey bees, muscles, total lipids, lipid classes, brood quantity, hypobiosis, productivity level.

Abstract

Colony preparation for hypobiosis is associated with the emergence of highly viable individuals. Autumn bees possess significantly greater longevity due to a physiological state defined by reduced metabolic activity. This preparatory process is evidenced by diminished brood rearing and decreased flight activity in response to natural factors. Consequently, young bees cease brood care and begin to accumulate increased quantities of proteins, lipids, and glycogen in the fat body. In this context, intensive brood rearing may be regarded as a stressor that significantly affects both energy metabolism and plastic processes within the insect organism. Research findings indicate that this factor determines both the total lipid content and the distribution of lipid classes in various tissues prior to the onset of hypobiosis, with particular reference to the thoracic flight muscles of bees. Given their principal role in thermogenesis, the structural organization of muscle tissue and its functional state substantially influence the metabolic activity and physiological condition of the insects, thereby affecting the overall success of colony overwintering. The pectoral musculature of honey bees constitutes a highly specialized, energy-demanding system whose activity is supported by the mobilization of reserves from the fat body. Accordingly, lipid accumulation within these muscles for winter survival does not take place. The lipids present are largely associated with mitochondria and serve as substrates for prompt oxidative metabolism, rather than as strategic reserves. Their proportion in muscle tissue is considerably lower than that of proteins and glycogen. Analysis revealed that the total lipid content in the pectoral muscles of worker bees ranged from 62.4 to 80.1 mg/g of tissue mass. The cessation of brood rearing in the experimental colonies led to significant quantitative and qualitative changes in muscle total lipid composition, affecting both total lipid levels and the relative distribution of lipid fractions. Specifically, total lipid content increased by 17.6% in the experimental group (P < 0.001). Additionally, the complete cessation of brood rearing resulted in a 2.75% increase in phospholipid content within the pectoral muscles (P < 0.001), a change that influences the functional stability of cellular membranes. The experimental group also exhibited a 4.6% reduction in free cholesterol levels, a key determinant of membrane fluidity. Furthermore, the 2.89% increase in triacylglycerol content observed in the experimental group suggests an adaptive response to low-temperature conditions. In general, the changes associated with the brood-rearing factor exert a detr i mental effect on the physiological status of autumn bees. As a consequence, these individuals acquire features typical of aged summer bees and demonstrate a shortened lifespan, thereby reducing their capacity to successfully endure the winter period. This ultimately compromises colony overwintering success, spring development, and productivity in the subsequent season.

References

Amdam, G., & Omholt, S. (2012). The regulatory anatomy of honeybee lifespan. Journal of Theoretical Biology, 16(2), 209–228.

Amdam, G., Rueppell, O., Fondrk, K, Page, R., & Nelson, C. (2009). The nurse’s load: Early-life exposure to brood-rearing affects behavior and lifespan in honey bees (Apis mellifera). Experimental Gerontology, 44(6–7), 467–471.

Arien, Y., Dag, A, Yona, S, Tietel, Z, Cohen, T., & Shafir, S. (2020). Effect of diet lipids and omega-6:3 ratio on honey bee brood development, adult survival and body composition. Journal of Insect Physiology, 124, 104074.

Azeez, O. I., Meintjes, R., & Chamunorwa, J. P. (2014). Fat body, fat pad and adipose tissues in invertebrates and vertebrates: The nexus. Lipid in Health and Disease, 13, 71.

Basualdo, M., Barragán, S., Vanagas, L., García, C., Solana, H., Rodríguez, E., & Bedascarrasbure, E. (2013). Conversion of high and low pollen protein diets into protein in worker honey bees (Hymenoptera: Apidae). Journal of Economic Entomology, 106(4), 1553–1558.

Begum, H., Idrees, A., & Afzal, A. (2023). Impact of different pollen protein diets on the physiology of Apis mellifera L. (Hymenoptera: Apidae) workers from essential plant sources. Journal of King Saud University, 35(2), 102511.

Brejcha, M., Prušáková, D., Sábová, M., Peska, V., Černý, J., Kodrík, D., Konopová, B., & Frydrychová, R. (2023). Seasonal changes in ultrastructure and gene expression in the fat body of worker honey bees. Journal of Insect Physiology, 146, 104504.

Brodschneider, R., & Crailsheim K. (2010). Nutrition and health in honey bees. Apidologie, 41(3), 278–294.

Bryś, M. S., Olszewski, K., Bartoń, M., & Strachecka, A. (2025). Changes in the activities of antioxidant enzymes in the fat body and hemolymph of Apis mellifera L. due to pollen monodiets. Antioxidants, 14(1), 69.

Bryś, M. S.; Staniec, B., & Strachecka, A. (2024). The effect of pollen monodiets on fat body morphology parameters and energy substrate levels in the fat body and hemolymph of Apis mellifera L. Scientific Reports, 14(1), 15177.

Castaños, C. E., Boyce, M. C., Bates, T., Millar, A. H., Flematti, G., Lawler, N. G., & Grassl, J. (2023). Lipidomic features of honey bee and colony health during limited supplementary feeding. Insect Molecular Biology, 32(6), 658–675.

Chan, Q. W. T., Mutti, N. S., Foster, L. J., Kocher, S. D., Amdam, G. V., & Wolschin, F. (2011). The worker honeybee fat body proteome is extensively remodeled preceding a major life-history transition. PLoS One, 6(9), e24794.

Corby-Harris, V., Snyder, L., & Meador, C. (2019). Fat body lipolysis connects poor nutrition to hypopharyngeal gland degradation in Apis mellifera. Journal of Insect Physiology, 116, 1–9.

Dai, Y., Tang, H., & Pang, S. (2021). The crucial roles of phospholipids in aging and lifespan regulation. Frontiers in Physiology, 12, 775648.

Debnam, S. E., McCormick, M. B., Callaway, R. M., & Woods, H. A. (2024). Energetic costs of raising brood in honey bee colonies are high, but heater bees are cheap. Journal of Insect Physiology, 153, 104613.

Deeter, M., Snyder, L., Meador, C., & Harris, V. (2023). Accelerated abdominal lipid depletion from pesticide treatment alters honey bee pollen foraging strategy, but not onset, in worker honey bees. Journal of Experimental Biology, 226(7), 245404.

Folch, J. (1957). A simple method for the isolation and purification of total lipids from animal tissues. Journal of Biological Chemistry, 226, 497–500.

Guler, A., Ekinci, D., Biyik, S., & Garipoğlu, A. (2018). Effects of feeding honey bees (Hymenoptera: Apidae) with industrial sugars produced by plants using different photosynthetic cycles (carbon C3 and C4) on the colony wintering ability, lifespan, and forage behavior. Journal of Economic Entomology, 111(5), 2003–2010.

Güneşdoğdu, M., Sarıoğlu-Bozkurt, A., Şekeroğlu, A., & Abacı, S. (2024). Changes in vitellogenin, abdominal lipid content, and hypopharyngeal gland development in honey bees fed diets with different protein sources. Insects, 15(4), 215.

Heinrich, B. (1987). Thermoregulation by individual honeybees. In: Menzel, R., & Mercer, A. (Eds.). Neurobiology and behavior of honeybees. Springer, Berlin, Heidelberg. Pp. 102–111.

Hopkins, B., Chakrabarti, P., Lucas, H., Sagili, R., & Sheppard, W. (2021). Impacts of different winter storage conditions on the physiology of diutinus honey bees (Hymenoptera: Apidae). Journal of Economic Entomology, 114(1), 409–414.

Jang, H., Ghosh, S., Sun, S., Cheon, K. J., & Jung, M. (2022). Chlorella-supplemented diet improves the health of honey bee (Apis mellifera). Frontiers in Ecology and Evolution, 10, 922741.

Kovalskyi, Y., Gutyj, B., Fedak, V., Kovalska, L., & Druzhbiak, А. (2021). The influence of feed quality on the development and productivity of bee queens. Scientific Messenger of LNU of Veterinary Medicine and Biotechnologies, Series: Agricultural Sciences, 23(95), 71–75.

Kutby, R., Baer-Imhoof, B., Robinson, S., Porter, L., & Baer, B. (2024). The effect of hive type on colony homeostasis and performance in the honey bee (Apis mellifera). Insects, 15(10), 800.

Sheng, L., Xiaoqiang, Y., & Qili, F. (2019). Fat body biology in the last decade. Annual Review of Entomology, 64, 315–333.

Tawfik, A., Ahmed, Z., Abdel-Rahman, M., & Moustafa, A. (2020). Influence of winter feeding on colony development and the antioxidant system of the honey bee, Apis mellifera. Journal of Apicultural Research, 59(5), 752–763.

Tkachuk, V., & Stapay, P. (2011). Doslidzhennya vosku zhyropotu i lipidiv vovny ovetsʹ [Research on wool grease wax and lipids in sheep wool]. Instytut Biolohiyi Tvaryn Natsionalʹnoyi Akademiyi Ahrarnykh Nauk, L’viv (in Ukrainian).

Wegener, J., Jakop, U., Schiller, J., & Müller, K. (2018). The membrane phospholipid composition of honeybee (Apis mellifera) workers reflects their nutrition, fertility, and vitellogenin stores. Insectes Sociaux, 65(3), 381–391.

Wegener, J., Krause, S., Parafianczuk, V., Chaniotakis, I., Schiller, J., Dannenberger, D., & Engel, K. (2022). Lipidomic specializations of honeybee (Apis mellifera) castes and ethotypes. Journal of Insect Physiology, 142, 104439.

Westerterp, K. R. (2017). Control of energy expenditure in humans. European Journal of Clinical Nutrition, 71(3), 340–344.

Wright, G. A., Nicolson, S. W., & Shafir, S. (2018). Nutritional physiology and ecology of honey bees. Annual Review of Entomology, 63, 327–344.

Published
2026-05-10
How to Cite
Kovalskyi, I. V., DruzhbiakМ. A., Kovalska, L. M., Druzhbiak, A. J., Tybinka, A. M., Klym, O. Y., Boyko, A. O., Zhmur, V. V., Havdan, R. V., Perig, D. P., Lunyk, I. M., Fiialovych, L. M., Petryshak, O. P., Paskevych, G. A., Barylo, B. S., Leshchyshyn, I. S., Perig, M. D., & Grynyk, V. A. (2026). Alterations in the lipid composition of pectoral muscles in honey bees (Apis mellifera) in relation to brood-rearing activity. Regulatory Mechanisms in Biosystems, 17(3), e26064. https://doi.org/10.15421/0226064