Comparative Effects of Lactose-Free and Regular Kefir on Lifespan of Drosophila Melanogaster
DOI:
https://doi.org/10.24925/turjaf.v13i9.2632-2639.7714Keywords:
Kefir, Lactose-free kefir, Drosophila melanogaster, Lifespan, Gompertz modelAbstract
This study investigated the effects of lactose-free and regular kefir on Drosophila melanogaster lifespan, by applying four doses (5%, 10%, 15%, 20%) to assess their impact on aging through mathematical modeling. We hypothesized that kefir's probiotic content could extend lifespan through its bioactive compounds, with the observed differences potentially attributable to lactose content and dosage. Wild-type flies were divided into groups: a control group fed with a standard diet (SDB), and groups fed regular or lactose-free kefir at varying concentrations. Each group comprised 100 male and 100 female flies, with three replicates, maintained at 25°C and 60% humidity. Daily survival data were collected and analyzed using the Gompertz model to evaluate lifespan and aging rates. Results showed that regular 15% kefir increased average lifespan from 61.2 to 68.2 days for females, and 63.5 to 70.0 days for males, while lactose-free kefir at the same dose extended it to 72.4 and 73.9 days, respectively. Aging rates decreased most significantly at 15% lactose-free kefir, indicating slower aging. However, at 20%, lifespan gains diminished, indicating a complex dose-response relationship that warrants further investigation. These findings suggest kefir's anti-aging potential, with lactose-free kefir showing greater efficacy (18.3% increase in females and 16.4% increase in males), and highlight the importance of dose optimization in aging research.
References
Ahn, J. S., Mahbub, N. U., Kim, S., Kim, H. B., Choi, J. S., Chung, H. J., & Hong, S. T. (2023). Nectandrin B significantly increases the lifespan of Drosophila-Nectandrin B for longevity. Aging (Albany NY), 15(22), 12749. https://doi.org/10.18632/aging.205234.
Ashburner, M., Hawley, R. S., & Golic, K. G. (2005). Drosophila. A Laboratory Handbook. Cold Spring Harbor Lab.
Belyi, A. A., Alekseev, A. A., Fedintsev, A. Y., Balybin, S. N., Proshkina, E. N., Shaposhnikov, M. V., & Moskalev, A. A. (2020). The resistance of Drosophila melanogaster to oxidative, genotoxic, proteotoxic, osmotic stress, infection, and starvation depends on age according to the stress factor. Antioxidants, 9(12), 1239. https://doi.org/10.3390/antiox9121239.
Broderick, N. A., & Lemaitre, B. (2012). Gut-associated microbes of Drosophila melanogaster. Gut microbes, 3(4), 307-321. https://doi.org/10.4161/gmic.19896
Chiang, M. H., Ho, S. M., Wu, H. Y., Lin, Y. C., Tsai, W. H., Wu, T., ... & Wu, C. L. (2022). Drosophila model for studying gut microbiota in behaviors and neurodegenerative diseases. Biomedicines, 10(3), 596. https://doi.org/10.3390/biomedicines10030596
Cloutier, C., Guay, J. F., & Champagne-Cauchon, W. (2022). Postdiapause reproduction of spotted-wing drosophila (Diptera: Drosophilidae) in realistically simulated cold climatic springtime conditions of Québec, Canada. The Canadian Entomologist, 154(1), e22. https://doi.org/10.4039/tce.2022.3.
Deepashree, S., Niveditha, S., Shivanandappa, T., & Ramesh, S. R. (2019). Oxidative stress resistance as a factor in aging: evidence from an extended longevity phenotype of Drosophila melanogaster. Biogerontology, 20, 497-513. https://doi.org/10.1007/s10522-019-09812-7
Deepashree, S., Shivanandappa, T., & Ramesh, S. R. (2022). Genetic repression of the antioxidant enzymes reduces the lifespan in Drosophila melanogaster. Journal of Comparative Physiology B, 192(1), 1-13. https://doi.org/10.1007/s00360-021-01412-7
Donati Zeppa, S., Agostini, D., Ferrini, F., Gervasi, M., Barbieri, E., Bartolacci, A., ... & Stocchi, V. (2022). Interventions on gut microbiota for healthy aging. Cells, 12(1), 34. https://doi.org/10.3390/cells12010034.
Fidan, M., & Ayar, A. (2023). Investigation of effect of probiotic use on organism behaviours in Drosophila melanogaster. Sabuncuoglu Serefeddin Health Sciences, 4(3), 1-13. https://doi.org/10.55895/sshs.1201900.
Gavrilova, E., Kostenko, V., Zadorina, I., Khusnutdinova, D., Yarullina, D., Ezhkova, A., ... & Nikitina, E. (2023). Repression of Staphylococcus aureus and Escherichia coli by Lactiplantibacillus plantarum strain ag10 in Drosophila melanogaster in vivo model. Microorganisms, 11(5), 1297. https://doi.org/10.3390/microorganisms11051297
Gompertz, B. (1825). On the nature of the function expressive of the law of human mortality. Philosophical Transactions of the Royal Society of London, 115, 513-585.
Güneş, E., & Bayram, Ş. B. (2021). The Effect of Feeding With Pumpkin Seed Membrane on Survival, Development and Longevity in Model Organism. Kahramanmaraş Sütçü İmam Üniversitesi Tarım ve Doğa Dergisi, 24(6), 1327-1332. https://doi.org/10.18016/ksutarimdoga.vi.839884.
Han, Q., Li, H., Jia, M., Wang, L., Zhao, Y., Zhang, M., Liu, X., Chen, X., & Zhu, L. (2021). Age-related changes in metabolites in young donor livers and old recipient sera after liver transplantation from young to old rats. Aging Cell, 20(7), Article e13425. https://doi.org/10.1111/acel.13425.
Karatas, A., & Ozgumus Demir, E. (2018). Dairy products added in media affect the development of Drosophila melanogaster (Diptera: Drosophilidae). Journal of Insect Science, 18(3), Article 19. https://doi.org/10.1093/jisesa/iey058.
Kong, Y., Wang, L., & Jiang, B. (2021). The role of gut microbiota in aging and aging related neurodegenerative disorders: Insights from Drosophila model. Life, 11(8), 855. https://doi.org/10.3390/life11080855
Lee, K. P., Simpson, S. J., & Wilson, K. (2020). Dietary protein and lifespan in Drosophila: Effects of milk-derived nutrients. Journal of Experimental Biology, 223(5), Article jeb215277. https://doi.org/10.1242/jeb.215277.
Lewis, E. B. (1960). A new standard food medium. Drosophila information service, 34(117), 1-55.
Malacrida, S., De Lazzari, F., Mrakic-Sposta, S., Vezzoli, A., Zordan, M. A., Bisaglia, M., ... & Megighian, A. (2022). Lifespan and ROS levels in different Drosophila melanogaster strains after 24 h hypoxia exposure. Biology Open, 11(6), bio059386. https://doi.org/10.1242/bio.059386.
Malta, S. M., Batista, L. L., Silva, H. C. G., Franco, R. R., Silva, M. H., Rodrigues, T. S., Correia, L. I. V., Martins, M. M., Venturini, G., Espindola, F. S., da Silva, M. V., & Ueira-Vieira, C. (2022). Identification of bioactive peptides from a Brazilian kefir sample, and their anti-Alzheimer potential in Drosophila melanogaster. Scientific Reports, 12, 11065. https://doi.org/10.1038/s41598-022-15297-1.
Malta, S. M., Rodrigues, T. S., Silva, M. H., Marquez, A. S., Ferreira, R. B., do Prado Mascarenhas, F. N. A., ... & Ueira-Vieira, C. (2024). Brazilian kefir fraction attenuates Alzheimer-like phenotype in Drosophila melanogaster with β-amyloid overexpression model. Scientific Reports, 14(1), 25474. https://doi.org/10.1038/s41598-024-76601-9.
Marco, M. L., Heeney, D., Binda, S., Cifelli, C. J., Cotter, P. D., Foligné, B., Gänzle, M., Kort, R., Pasin, G., Pihlanto, A., Smid, E. J., & Hutkins, R. (2021). The role of Lactobacilli in health and disease. Nature Reviews Microbiology, 19(3), 186-197. https://doi.org/10.1038/s41579-020-00459-5.
Mulla, S., Ludlam, A. R., Elragig, A., Slack, C., Balklava, Z., Stich, M., & Cheong, A. (2023). A biphasic model of lifespan in nematode Caenorhabditis elegans worm. Royal Society Open Science, 10(2), 220991. https://doi.org/10.1098/rsos.220991.
Oak, S. J., & Jha, R. (2019). The effects of probiotics in lactose intolerance: A systematic review. Critical reviews in food science and nutrition, 59(11), 1675-1683. https://doi.org/10.1080/10408398.2018.1425977.
Piper, M. D. W., & Partridge, L. (2018). Drosophila as a model for ageing. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1864(9), 2707-2717. https://doi.org/10.1016/j.bbadis.2017.09.016.
Pletcher. (1999). Model fitting and hypothesis testing for age‐specific mortality data. Journal of Evolutionary Biology, 12(3), 430-439. https://doi.org/10.1046/j.1420-9101.1999.00058.x
Rosa, D. D., Dias, M. M. S., Grześkowiak, Ł. M., Reis, S. A., Conceição, L. L., & Peluzio, M. D. C. G. (2017). Milk kefir: Nutritional, microbiological and health benefits. Nutrition Research Reviews, 30(1), 82-96. https://doi.org/10.1017/S0954422416000275.
Rosa, D. D., Dias, M. M., Grześkowiak, Ł. M., Reis, S. A., Conceição, L. L., & Maria do Carmo, G. P. (2017). Milk kefir: nutritional, microbiological and health benefits. Nutrition research reviews, 30(1), 82-96. https://doi.org/10.1017/S0954422416000275.
Scialò, F., Sriram, A., Stefanatos, R., Spriggs, R. V., Loh, S. H., Martins, L. M., & Sanz, A. (2020). Mitochondrial complex I derived ROS regulate stress adaptation in Drosophila melanogaster. Redox biology, 32, 101450. https://doi.org/10.1016/j.redox.2020.101450
Sharma, R., & Padwad, Y. (2020). Probiotic bacteria as modulators of cellular senescence: emerging concepts and opportunities. Gut microbes, 11(3), 335-349. https://doi.org/10.1080/19490976.2019. 1697148.
Shilovsky, G. A. (2024). Calculating aging: Analysis of survival curves in the norm and pathology, fluctuations in mortality dynamics, characteristics of lifespan distribution, and indicators of lifespan variation. Biochemistry (Moscow), 89(2), 371-376. https://doi.org/10.1134/S0006297924020159.
Sonestedt, E., Borné, Y., Wirfält, E., & Ericson, U. (2021). Dairy consumption, lactase persistence, and mortality risk in a cohort from southern Sweden. Frontiers in Nutrition, 8, 779034. https://doi.org/10.3389/fnut.2021.779034.
Sun, Y., Yolitz, J., Wang, C., Spangler, E., Zhan, M., & Zou, S. (2013). Aging studies in Drosophila melanogaster. In S. M. Jazwinski, A. I. Yashin, & G. M. Martin (Eds.), Biological aging: Methods and protocols (pp. 77-93). Humana Press. https://doi.org/10.1007/978-1-62703-556-9_7.
Tan, F. H. P., Shamsuddin, S., & Zainuddin, A. (2023). Ageing and the gut-brain axis: lessons from the Drosophila model. Beneficial Microbes, 14(6), 591-607. https://doi.org/10.1163/18762891-20230056.
Tyson, J. J., Monshizadeh, A., Shvartsman, S. Y., & Shingleton, A. W. (2023). A dynamical model of growth and maturation in Drosophila. Proceedings of the National Academy of Sciences, 120(49), e2313224120. https://doi.org/10.1073/pnas.2313224120.
Westfall, S., Lomis, N., & Prakash, S. (2018). A novel polyphenolic prebiotic and probiotic formulation have synergistic effects on the gut microbiota influencing Drosophila melanogaster physiology. Artificial cells, nanomedicine, and biotechnology, 46(sup2), 441-455. https://doi.org/10.1080/21691401.2018.1458731.
Westfall, S., Lomis, N., & Prakash, S. (2018). Longevity extension in Drosophila through gut-brain communication. Scientific Reports, 8(1), Article 8362. https://doi.org/10.1038/s41598-018-25382-z.
Wilmanski, T., Diener, C., Rappaport, N., Patwardhan, S., Wiedrick, J., Lapidus, J., ... & Price, N. D. (2021). Gut microbiome pattern reflects healthy ageing and predicts survival in humans. Nature metabolism, 3(2), 274-286. https://doi.org/10.1038/s42255-021-00348-0.
Yi, Y., Xu, W., Fan, Y., & Wang, H. X. (2021). Drosophila as an emerging model organism for studies of food-derived antioxidants. Food Research International, 143, 110307. https://doi.org/10.1016/j.foodres.2021.110307.
Yusuf, A. O., Danborno, B., Bauchi, Z. M., Sani, D., & Ndams, I. S. (2024). Aging impaired locomotor and biochemical activities in Drosophila melanogaster Oregon R (fruit fly) model. Experimental Gerontology, 197, 112593.
Zanco, B., Mirth, C. K., Sgrò, C. M., & Piper, M. D. (2021). A dietary sterol trade-off determines lifespan responses to dietary restriction in Drosophila melanogaster females. Elife, 10, e62335. https://doi.org/10.7554/eLife.62335.
Downloads
Published
Issue
Section
License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.






