Analysis of Drosophila melanogaster reproduction and preadult mortality after the influence of microwave radiation
Abstract
A new type of anthropogenic impact – low-intensity electromagnetic radiation of extremely high frequencies (EHF EMR) demonstrates various genetic effects. The questions of the organism adaptive response formation to short-term exposure of EMR that depends on the individual’s genotype are of particular interest. The objective of this study was to analyze the reproductive ability and preadult mortality in Drosophila melanogaster with whiteapticot mutation after the influence of microwave radiation. We used D. melanogaster stocks that carry whiteapticot mutation, but differ in the genetic background on which this mutation is located: wa(C-S), wa(Or) and wa. Virgin flies were irradiated. The parameters of the external influence were power flux density W=10 μW/cm2, frequency F=65 GHz, exposure time t=5 minutes. The stages of embryo death, number of adult offspring, and mortality rate at the pupal stage were analyzed. The results of the study showed that the effect of electromagnetic radiation on virgin imagoes of Drosophila with an impaired tryptophan metabolism modifies the survival rate of the offspring at the preimaginal stages of ontogenesis. In the offspring of young flies (at the age of 3–8 days) the frequency of embryonic mortality decreases during the 0–5.5 hours period (initial stages of cleavage and blastoderm formation) and 5.5–17 hours period (stage of gastrulation and embryo segmentation, histogenesis) of embryogenesis. The total number of offspring at the adult stage does not differ from the control values; the mortality rate at the pupal stage also does not change in the offspring of young parents after exposure to EMR. An increase in the age of parental couples that were exposed to short-term EMR on the first day after eclosion from pupae (20–25 days aged) leads to a decrease in the embryonic mortality rate of offspring during the 17–22 hours of embryogenesis (organogenesis stage and larval exit from chorion). The total embryonic mortality rate is determined solely by the age of the parents. The strength of this factor for the stocks is h2wa=69.7 %, h2wa(C-S)=52.2 % and h2wa(Or)=64.9 % respectively. The impact of EMR affects the embryonic mortality rate only for the wa(Or) (h2EMR=18.3 %). External exposure does not change the number of imago offspring in individuals aged 0–5 days; the number of adult offspring increased by 1,2 times in individuals aged 20–25 days in the stock wa(C-S). A decrease in the number of dead individuals at the pupal stage in the descendants of 20–25-day-old parents after exposure to EMR EHF on average by three times was shown.
Downloads
References
Atramentova L.О., Utevska O.M. (2007). Statistical methods in biology. Kharkiv: V.N.Karazin KhNU. 288 p. [In Ukrainian]
Gorenskaya O.V., Gavrilov A.B., Shckorbatov Yu.G., Katrich V.A. (2010). Influence of genotype on viability of drosophila under small doses of microwave radiation. Bulletin of Problems in Biology and Medicine, 1, 52–56. [In Russian]
Gorenskaya O.V., Kostenko V.V., Vorobyova L.I., Taglina O.V. (2015). The influence of allelic state of locus white on some parameters of fitness in Drosophila melanogaster. Bulletin of Problems in Biology and Medicine, 1, 74–79. [In Russian]
Gorenskaya O.V., Navrotskaya V.V. (2019). Analysis of the role of tryptophan-kynurenine pathway in the life span control in Drosophila melanogaster. Factors of Experimental Evolution of Organisms, 25, 32–38. https://doi.org/10.7124/FEEO.v25.1135 [In Russian]
Gorenskaya O.V., Shckorbatov Y.G., Gavrilov A.B. (2016). Features of the adaptive response to the short-term influence of microwave radiation in Drosophіla melanogaster stocks with black mutation. The Journal of V.N.Karazin Kharkiv National University. Series "Biology", 26, 108–116. [In Russian]
Dyka L.D., Strashnyuk V.Yu., Shkorbatov Yu.G. Fitness components in Drosophila melanogaster after the exposure to microwave radiation. The Journal of V.N.Karazin Kharkiv National University. Series "Biology", 26, 65–73. [In Ukrainian]
Zhuravlev A.V., Nikitina E.A., Savvateeva-Popova E.V. (2020). Role of kynurenines in regulation of behavior and memory processes in Drosophila. Integrative Physiology, 1(1), 40–50. https://doi.org/10.33910/2687-1270-2020-1-1-40-50 [In Russian]
Kostenko V.V., Kolot N.V., Vorobyova L.I. (2015). Research of embryonic mortality stages of Drosophila melanogaster depending on age and starvation of an imago. Russ. J. Dev. Biol., 46, 381–388. https://doi.org/10.1134/S1062360415060065
Nekrasova A.V., Zolotykh I.V., Lavrik A.A. (2000). Genetic control of spontaneous mutation during aging in Drosophila melanogaster. Bulletin of the Kharkov Entomological Society, VIII(1), 175–178. [In Russian]
Adler M.I., Cassidy E.J., Fricke C., Bonduriansky R. (2013). The lifespan-reproduction trade off under dietary restriction is sex-specific and context-dependent. Exp. Gerontol., 48, 539–548. https://doi.org/10.1016/j.exger.2013.03.007
Atli E., Unlü H. (2007). The effects of microwave frequency electromagnetic fields on the fecundity of Drosophila melanogaster. Turk. J. Biol., 31, 1–5.
Averous J., Bruhat A., Mordier S., Fafournoux P. (2003). Recent advances in the understanding of amino acid regulation of gene expression. J. Nutr., 133(6), 2040S–2045S. https://doi.org/10.1093/jn/133.6.2040S
Blackman C.F., Blank M., Kundi M. et al. (2007). The bioinitiative report – a rationale for a biologically-based public exposure standard for electromagnetic fields (ELF and RF). http://www.bioinitiative.org
Drummond-Barbosa D., Spradling A.C. (2001). Stem cells and their progeny respond to nutritional changes during Drosophila oogenesis. Dev. Biol., 231, 265–278. https://doi.org/10.1006/dbio.2000.0135
Harvey C., French P.W. (2000). Effects on protein kinase C and gene expression in a human mast cell line, HMC-1, following microwave exposure. Cell. Biol. Int., 23, 739–748. https://doi.org/10.1006/cbir.1999.0436
Hill D.L. (1945). Chemical removal of the chorion from Drosophila eggs. Drosophila Information Service, 19, 62.
Johansson O. (2009). Disturbance of the immune system by electromagnetic fields – a potentially underlying cause for cellular damage and tissue repair reduction which could lead to disease and impairment. Pathophysiology, 16, 157–177. https://doi.org/10.1016/j.pathophys.2009.03.004
Margaritis L.H., Manta A.K., Kokkaliaris K.D. et al. (2014). Drosophila oogenesis as a bio-marker responding to EMF sources. Electromagn. Biol. Med., 33(3), 165–189. https://doi.org/10.3109/15368378.2013.800102
Markovа E., Hillert L., Malmgren L. et al. (2005). Microwaves from GSM mobile telephones affect 53BP1 and gamma-H2AX foci in human lymphocytes from hypersensitive and healthy persons. Environ. Health Perspect, 113(9), 1172–1177. https://doi.org/10.1289/ehp.7561
Memmi B.K., Ünlü H. (2007). The effects of short duration microwave exposure on the life span and the induction of sex-linked recessive lethal mutations in Drosophila melanogaster. Hacettepe J. Biol. & Chem., 35(3), 173–179.
Panagopoulos D.J. (2012). Gametogenesis, embryonic and post-embryonic development of Drosophila melanogaster, as a model system for the assessment of radiation and environmental genotoxicity / In: Drosophila melanogaster: Life Cycle, Genetics. Nova Science Publishers, Inc., pp. 1–38.
Panagopoulos D.J., Karabarbounis A., Margaritis L.H. (2004). Effect of GSM 900-MHz mobile phone radiation on the reproductive capacity of Drosophila melanogaster. Electromagnetic Biology and Medicine, 23(1), 29–43. https://doi.org/10.1081/JBC-120039350
Panagopoulos D.J., Margaritis L.H. (2003). Effects of electromagnetic fields on the Reproductive Capacity of Drosophila melanogaster / In: P.Stavroulakis (Ed.), “Biological Effects of Electromagnetic Fields”. Springer, pp. 545–578.
Sagioglou N.E., Manta A.K., Giannarakis I.K. et al. (2016). Apoptotic cell death during Drosophila oogenesis is differentially increased by electromagnetic radiation depending on modulation, intensity and duration of exposure. Electromagn. Biol. Med., 35(1), 40–53. https://doi.org/10.3109/15368378.2014.971959
Shakina L.A., Pasiuga V.N., Dumin O.M., Shckorbatov Y.G. (2011). Effects of microwaves on the puffing pattern of D. melanogaster. Central European Journal of Biology, 6(4), 524–530. https://doi.org/10.2478/s11535-011-0032-x
Vermeulen C.J., Loeschcke V. (2007). Longevity and the stress response in Drosophila. Exp. Gerontol., 42(3), 153–159. https://doi.org/10.1016/j.exger.2006.09.014
Weisbrot D., Lin H., Ye L. et al. (2003). Effects of mobile phone radiation on reproduction and development in Drosophila melanogaster. J. Cell. Biochem., 89(1), 48–55. https://doi.org/10.1002/jcb.10480
Authors retain copyright of their work and grant the journal the right of its first publication under the terms of the Creative Commons Attribution License 4.0 International (CC BY 4.0), that allows others to share the work with an acknowledgement of the work's authorship.