Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Rotenone Induced Alterations in Lifecycle Parameters and Compound Eye Morphology of Drosophila Melanogaster


Affiliations
1 Toxicology Research Unit, Cytogenetics Laboratory, Department of Zoology, The University of Burdwan, Burdwan, West Bengal, India
     

   Subscribe/Renew Journal


Rotenone is a widely used natural pesticide and piscicide and a potent inhibitor of mitochondrial complex I (NADHquinone reductase) that elicits the degeneration of dopaminergic neurons. Present study explored the adverse effect of rotenone at concentrations far below the reported LC50 on several life cycle parameters and on the compound eye structure of a non-target insect, Drosophila melanogaster. Newly hatched first instar larvae were introduced in Drosophila food medium containing different concentrations (50, 100, 150, 200, 250 μg/L) of rotenone. Different life cycle parameters were recorded. Emerged adult flies were collected and studied under Scanning electron microscope. Student's t-test was performed to explore significant difference and changes in both life cycle parameter and eye architecture. Treated groups showed significant delay (p<0.05 level) in larval duration, pupal duration, and in emergence of flies when compared with the control groups. Delay in life cycle parameters significantly increased with increase of rotenone exposure. Interestingly, the compound eye structure of the treated flies was seen to be affected by rotenone. Thus these results clearly demonstrate that chronic exposure to rotenone can alter the structure and lifecycle of a non-target organism like Drosophila at sub-lethal concentrations. Thus rotenone in Drosophila at sub-lethal concentrations might be the reason for developmental toxicity.

Keywords

Rotenone, Drosophila, Ommatidia, SEM.
User
Subscription Login to verify subscription
Notifications
Font Size

  • Ott, K.C., 2006. A brief review of its chemistry, environmental fate, and the toxicity of rotenone formulations, www.newmexicotu.org/Rotenone%20summary. pdf2015 (Accessed on 1-8-15).
  • Ochi, R., Dhagia, V., Lakhkar, A., Patel, D., Wolin, M.S., Gupte, S.A.,2016. Rotenone-stimulated superoxide release from mitochondrial complex I acutely augments L-type Ca2+ current in A7r5 aortic smooth muscle cells. Am. J. Physiol. Heart. Circ. Physiol. 310(9), H1118-1128.
  • Betarbet, R., Sherer, T.B.,Testa, C.M., Seo. B.B., Richardson, J.R., Kim, H.J., Miller, G.W.,Yagi. T.,Yagi, A.M.,and Greenamyre, J.T., 2003.Mechanism of Toxicity in Rotenone Models of Parkinson’s Disease. J. Neurosci. 23(34), 10756 –10764.
  • Coulom, H., Birman, S., 2004. Chronic Exposure to Rotenone Models Sporadic Parkinson’s Disease in Drosophila melanogaster. J. Neurosci. 24(48), 10993–10998.
  • US EPA (United States Enviornmental Protection Agency) 2007. https://archive.epa.gov/pesticides/reregistration/ web/pdf/rotenone_red.pdf. (Accessed July 7, 2016)
  • Meyer, S., Schulz, J., Jeibmann, A., Taleshi, M.S., Ebert, F., Francesconi, K.A., Schwerdtle, T., 2014. Arsenic-containing hydrocarbons are toxic in the in vivo model Drosophila melanogaster. Metallomics. 6, 2010-2014.
  • Kang, H.L., Benzer, S., Min, K.T., 2001 Life extension in Drosophila by feeding a drug. PNAS. 99, 838-843.
  • Zivanovcurils, J., Tomin, J., Bojanic, V., Bojanic, J., Najman, S., Katic, K., Mrcarica, E., Dindic, B., 2004. Effect of chronic phenol intoxication on fertility and lifespan of Drosophila melanogaster. Arch. in Onco. 12, 17-18.
  • Podder, S., Roy, S., 2013. Study of the changes in life cycle parameters of Drosophila melanogaster exposed to fluorinated insecticide, cryolite. Toxicol. Ind. Health. DOI: 10.1177/0748233713493823.
  • Sarkar, S., Dutta, M., Roy, S., 2015. Potential toxicity of flubendiamide in Drosophila melanogaster and associated structural alterations of its compound eye. Toxicol. Environ. Chem. DOI: 10.1080/02772248.2014.997986
  • Rajak, P., Sahana, S., Roy, S., 2013. Acephate-induced shortening of developmental duration and early adult emergence in a nontarget insect Drosophila melanogaster. Toxicol. Environ. Chem. 95, 1369-1379.
  • Dutta, M., Sarkar, S., Roy, S., 2014. Sodium Fluoride Induced Alteration in Lifecycle Parameters and Compound Eye Morphology of Drosophila Melanogaster and Trans-generational Transmission of the Altered Eye Architecture. JIARM. 2,247-259.
  • Festing, M.F.H., Baumans, V., Combes, D.R., Halder, M., Hendricsen, F.M., Howard, B.R., 1998. Reducing the use of laboratory animals in biomedical research: problems and possible solutions. Altern. Lab. Anim. 26, 283–301.
  • Ashburner, M., Thompson, J.N., 1978. The laboratory culture of Drosophila In: The genetics and biology of Drosophila. (Ashburner M, Wright TRF (eds.). Academic Press 24, 1–81.
  • Podder, S.,Akbari, S., Roy, S., 2012. Cryolite Induced Morphological Change in the Compound Eye of Drosophila melanogaster. Fluoride. 45, 58-64.
  • Whitaker, R., Faulkner, S.,Miyokawa, R., Burhen, L.,Henriksen, M., Wood, J.G., Helfand, S.L., 2013. Increased expression of Drosophila Sir2 extends life span in a dose dependent manner. Ageing. 5(9), 681-692.
  • Bjedov, I., Toivonen, J.M., Kerr, F., Slack, C., Jacobson, J., Foley, A., Patridge, L., 2009. Mechanisms of Life Span Extension by Rapamycin in the Fruit Fly Drosophila melanogaster. Cell metab. 11(1), 35-36.
  • Das, S.K., Podder, S., Roy, S., 2010. Effect of fungicide, Thiovit ®Jet on several life history trait of Drosophila melanogaster (Diptera: Drosophilidae). JABS. 4, 31-36.
  • Cook, T., Zelhof, A., Mishra, M., Nie, J.,2011. 800 facets of retinal degeneration. Prog. Mol. Biol. Transl. Sci. 100, 331-368.
  • Sang, T.K., Jackson, G.R., 2005. Drosophila models of neurodegenerative disease. Neuro.Rx2. 438-446. http://dx.doi. org/10.1602/neurorx.2.3.438
  • Merzetti, E.M., Staveley, B.E., 2016. Altered expression of CG5961, a putative Drosophila melanogaster homologue of FBXO9, provides a new model of Parkinson disease. Genet. Mol. Res. 15 (2). doi: 10.4238/gmr.15028579.
  • Lindsay, L.L., Corces, V.G., 1997. The role of selectins in Drosophila eye and bristle development. Development. 124, 169-180.
  • Prober, D.A., Edgar, B.A., 2000. Ras1 Promotes Cellular Growth in the Drosophila Wing. Cell. 100, 435–446.
  • Alone, D.P., Tiwari, A.K., Mondal, L.,Li, M., Mechler, B.M., Roy, J.K., 2005. Rab11 is required during Drosophila eye development. Int. J. Dev. Biol. 49, 873-879.
  • Satoh, A.K., Tokunaga, F., Kawamura, S., Ozaki, K., In situ inhibition of vesicle transport and protein processing in the dominant negative Rab1 mutant of Drosophila. J. Cell. Sci. 110, 2943-2953.

Abstract Views: 529

PDF Views: 0




  • Rotenone Induced Alterations in Lifecycle Parameters and Compound Eye Morphology of Drosophila Melanogaster

Abstract Views: 529  |  PDF Views: 0

Authors

Arnab Roy
Toxicology Research Unit, Cytogenetics Laboratory, Department of Zoology, The University of Burdwan, Burdwan, West Bengal, India
Moutushi Mandi
Toxicology Research Unit, Cytogenetics Laboratory, Department of Zoology, The University of Burdwan, Burdwan, West Bengal, India
Sumedha Roy
Toxicology Research Unit, Cytogenetics Laboratory, Department of Zoology, The University of Burdwan, Burdwan, West Bengal, India

Abstract


Rotenone is a widely used natural pesticide and piscicide and a potent inhibitor of mitochondrial complex I (NADHquinone reductase) that elicits the degeneration of dopaminergic neurons. Present study explored the adverse effect of rotenone at concentrations far below the reported LC50 on several life cycle parameters and on the compound eye structure of a non-target insect, Drosophila melanogaster. Newly hatched first instar larvae were introduced in Drosophila food medium containing different concentrations (50, 100, 150, 200, 250 μg/L) of rotenone. Different life cycle parameters were recorded. Emerged adult flies were collected and studied under Scanning electron microscope. Student's t-test was performed to explore significant difference and changes in both life cycle parameter and eye architecture. Treated groups showed significant delay (p<0.05 level) in larval duration, pupal duration, and in emergence of flies when compared with the control groups. Delay in life cycle parameters significantly increased with increase of rotenone exposure. Interestingly, the compound eye structure of the treated flies was seen to be affected by rotenone. Thus these results clearly demonstrate that chronic exposure to rotenone can alter the structure and lifecycle of a non-target organism like Drosophila at sub-lethal concentrations. Thus rotenone in Drosophila at sub-lethal concentrations might be the reason for developmental toxicity.

Keywords


Rotenone, Drosophila, Ommatidia, SEM.

References





DOI: https://doi.org/10.22506/ti%2F2017%2Fv24%2Fi1%2F149034