Effect of Ionizing Radiation on Pheromone Biosynthesis Activating Neuropeptide (PBAN) Gene Expression and its Photosensitive Rhythm in Female Spodoptera litura (F.)

Authors

  • Madhumita Sengupta Applied Entomology and Radiation Biology Unit, Department of Zoology, University of Delhi, Delhi 110007
  • Nilza Angmo Applied Entomology and Radiation Biology Unit, Department of Zoology, University of Delhi, Delhi 110007
  • Neha Vimal Applied Entomology and Radiation Biology Unit, Department of Zoology, University of Delhi, Delhi 110007
  • R. K. Seth Applied Entomology and Radiation Biology Unit, Department of Zoology, University of Delhi, Delhi 110007

DOI:

https://doi.org/10.55446/IJE.2022.691

Keywords:

Spodoptera litura, F1 sterility, radiogenetic pest control, PBAN, gene expression, photosensitivity, diel rhythm, parabiological control, pheromone reduction, calling behaviour

Abstract

In this study, the effect of ionizing radiation was studied on the pheromone biosynthesis activating neuropeptide (PBAN) gene expression in female moths of a noctuid pest Spodoptera litura (F.), that would trigger pheromone production and its release needed for calling behaviour. The PBAN gene expression in the radiosterilized female moths (at 130 Gy) showed a decline with respect to control (unirradiated moths), and PBAN expression was drastically reduced at higher dose, 200 Gy. The photosensitivity and diel rhythm of PBAN gene expression, indicating higher expression during peak hours of scotophase and lowest expression during photophase was maintained at 130Gy, which deemed this gamma dose a suitable sterilizing dose for female moths which seemed to retain reproductive competence. This study might support the radiosterilized female moths for their combined release with substerilized males, using 130Gy to effectively operate the F1 sterility technique proposed to control S. litura.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Downloads

Published

2022-08-29

How to Cite

Sengupta, M., Angmo, N., Vimal, N., & Seth, R. K. (2022). Effect of Ionizing Radiation on Pheromone Biosynthesis Activating Neuropeptide (PBAN) Gene Expression and its Photosensitive Rhythm in Female <i>Spodoptera litura</i> (F.). Indian Journal of Entomology, 85(1), 109–114. https://doi.org/10.55446/IJE.2022.691

Issue

Section

Research Articles

References

Abernathy R L, Nachman R J, Teal P E A, Yamashita O, Tumlinson J H. 1995. Pheromonotropic activity of naturally occurring pyrokinin insect neuropeptides (FXPRLamide) in Helicoverpa zea. Peptides 16: 215-219.

Anisimov A I, Lazurkina N V, Shvedov A N. 1989. Influence of radiation induced genetic damage on the suppressive effect of inherited sterility in the codling moth (Lepidoptera: Tortricidae). Annals of the Entomological Society of America 82: 769-777.

Armes N J, Wightman J A, Jadhav D R, Ranga Rao G V. 1997. Status of insecticide resistance in Spodoptera litura in Andhra Pradesh, India. Pesticide Science 50: 240-248.

Babilis N A, Mazomenos B E. 1992. Pheromone production in Sesamia nonagrioides: diel periodicity and effect of age and mating. Journal of Insect Physiology 38(8): 561-564.

Bloch G, Hazan E, Rafaeli A. 2013. Circadian rhythms and endocrine functions in adult insects. Journal of Insect Physiology 59(1): 56-69.

Bragança M A, Zanuncio J, Picanço M, Laranjeiro A J. 1998. Effects of environmental heterogeneity on Lepidoptera and Hymenoptera populations in Eucalyptus plantations in Brazil. Forest Ecology and Management 103(2-3): 287-

Bughio A R. 1988. Parental and inherited sterility induced by gamma radiation in male moths of the maize borer, Chilo partellus (Swinhoe). Proceedings. Modern insect control: Nuclear techniques and biotechnology, Vienna, 1987. International Atomic Energy Agency, Vienna. pp. 413-421.

Carpenter J E, Young J R, Knipling E F, Sparks A N. 1983. Fall armyworm (Lepidoptera: Noctuidae): Inheritance of gamma-induced deleterious effects and potential for pest control. Journal of Economic Entomology 76: 378-382.

Carpenter J E, Young J R, Sparks A N, Cromroy H L, Chowdhury M A. 1987. Corn earworm (Lepidoptera: Noctuidae): Effects of substerilizing doses of radiation and inherited sterility on reproduction. Journal of Economic Entomology 80 (2): 483-489.

Carpenter J E, Young J R, Sparks A N, Cromroy H L, Chowdhury M A. 1987. Corn ear-worm (Lepidoptera: Noctuidae): effects of substerilizing doses of radiation and inherited sterility on reproduction. Journal of Economic Entomology 80: 483-489.

Carpenter J E, Young J R, Sparks A N. 1986. Fall armyworm (Lepidoptera: Noctuidae): Comparison of inherited deleterious effects in progeny from irradiated males and females. Journal of Economic Entomology 79: 46-49.

Carpenter, J E, Young J R, Knipling E F, Sparks A N. 1983. Fall armyworm (Lepidoptera: Noctuidae): Inheritance of gamma-induced deleterious effects and potential for pest control. Journal of Economic Entomology 76: 378-382.

Chang, J C, Ramasamy S. 2014. Identification and expression analysis of diapause hormone and pheromone biosynthesis activating neuropeptide (DH-PBAN) in the legume pod borer, Maruca vitrata Fabricius. PLoS ONE 9: e84916.

Choi M Y, Meer R K V. 2009. Identification of a new member of the PBAN family of neuropeptides from the fire ant, Solenopsis invicta. Insect Molecular Biology 18: 161-169.

Choi M Y, Vander Meer R K. 2012. Ant trail pheromone biosynthesis is triggered by a neuropeptide hormone. PLoS ONE 7: e50400.

Csiro R B. 1982. Mechanisms of communication disruption by pheromone in the control of Lepidoptera: a review. Physiological Entomology 7(4): 353-364.

Eliyahu D, Applebaum S, Rafaeli A. 2003. Moth sex-pheromone biosynthesis is inhibited by the herbicide diclofop. Pesticide Biochemistry and Physiology 77(2): 75-81.

Fabria ́ s G, Marco M P, Camps F. 1994. Effect of the pheromone biosynthesis activating neuropeptide on sex pheromone biosynthesis in Spodoptera littoralis isolated glands. Archives of Insect Biochemistry and Physiology 27: 77-87.

Flint H M, Merkle J R. 1983. Mating behaviour, sex pheromone responses, and radiation sterilization of the greater wax moth (Lepidoptera: Pyralidae). Journal of Economic Entomology 76(3): 467-472.

Hight S D, Bloem S, Bloem K A, Carpenter J E. 2005. Developing a sterile insect release program for Cactoblastis cactorum (Berg) (Lepidoptera: Pyralidae): Effective overflooding ratios and release-recapture field studies. Environmental Entomology 34(4): 850-856.

Iglesias F, Jacquin-Joly E, Marco M P, Camps F, Fabrias G. 1999. Temporal distribution of PBAN-like immunoreactivity in the hemolymph of Mamestra brassicae females in relation to sex pheromone production and calling behavior. Archives of Insect Biochemistry and Physiology: Published in collaboration with the Entomological Society of America 40(2): 80-87.

Iglesias F, Marco P, François M C, Camps F, Fabriàs G, Jacquin-Joly E. 2002. A new member of the PBAN family in Spodoptera littoralis: molecular cloning and immunovisualisation in scotophase hemolymph. Insect Biochemistry and Molecular Biology 32(8): 901-908.

Jurenka R. 2017. Regulation of pheromone biosynthesis in moths. Current opinion in insect science 24: 29-35.

Kittayapong P, Kaeothaisong N O, Ninphanomchai S, Limohpasmanee W. 2018. Combined sterile insect technique and incompatible insect technique: sex separation and quality of sterile Aedes aegypti male mosquitoes released in a pilot population suppression trial in Thailand. Parasites Vectors 11(2): 73-83.

Levi-Zada A, Byers J A. 2021. Circadian rhythms of insect pheromone titer, calling, emission, and response: a review. The Science of Nature 108(5): 1-20.

Livak K J, Schmittgen T D. 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2-DDCT method. Methods 25: 402-408.

Lu Q, Huang L Y, Chen P, Yu J F, Xu J, Deng J Y, Ye H. 2015. Identification and RNA interference of the pheromone biosynthesis activating neuropeptide (PBAN) in the common cutworm moth Spodoptera litura (Lepidoptera: Noctuidae). Journal of Economic Entomology 108(3): 1344-1353.

Masler E P, Raina A K, Wagner R M, Kochansky J P. 1994. Isolation and identification of a pheromonotropic neuropeptide from the brain-suboesophageal ganglion complex of Lymantria dispar: a new member of the PBAN family. Insect Biochemistry and Molecular Biology 24(8): 829-836.

Matsumoto S, Ozawa R, Uchiumi K, Kurihara M, Mitsui T. 1995. Intracellular signal transduction of PBAN action in the common cutworm, Spodoptera litura: effects of pharmacological agents on sex pheromone production in vitro. Insect Biochemistry and Molecular Biology 25(9): 1055-1059.

Moussa M A, Zaher M A, Kotby F. 1960. Abundance of cotton leafworm, Prodenia litura (F.) in relation to host plants. I. Host plants and their effect on biology. Bulletin de la Société entomologique d’Égypte 44: 241-251.

North D T, Holt G G. 1969. Population suppression by transmission of inherited sterility to progeny of irradiated cabbage loopers, Trichoplusia ni. The Canadian Entomologist 101: 513-520.

North D T. 1975. Inherited sterility in Lepidoptera. Annual Review of Entomology 20: 167-182.

Rafaeli A. 2009. Pheromone biosynthesis activating neuropeptide (PBAN): regulatory role and mode of action.

General and Comparative Endocrinology 162(1): 69-78.

Raina A K, Davis J C, Stadelbacher E A. 1991. Sex pheromone production and calling in Helicoverpa zea (Lepidoptera: Noctuidae): Effect of temperature and light. Environmental Entomology 20(5): 1451-1456.

Raina A K, Klun J A. 1984. Brain factor control of sex pheromone production in the female corn earworm moth. Science 225(4661): 531-533.

Seth R K, Sharma V P. 2001. Inherited sterility by substerilizing radiation in Spodoptera litura (Lepidoptera: Noctuidae): Bioefficacy and potential for pest suppression. Florida Entomologist. 84(2): 183-193.

Seth R K, Zarin M, Khan Z, Seth R. 2016. Ionizing radiation as a phytosanitary treatment against Phenacoccus solenopsis (Hemiptera: Pseudococcidae). Florida Entomologist. pp.76-87.

Seth R, Zarin M, Khan Z, Seth R K. 2016. Towards phytosanitary irradiation of Paracoccus marginatus (Hemiptera: Pseudococcidae): Ascertaining the radiosensitivities of all life stages. Florida Entomologist. pp. 88-101.

Traut W. 1977. A study of recombination, formation of chiasmata and synaptonemal complexes in female and male meiosis of Ephestia kuehniella (Lepidoptera). Genetica 47(2): 135-142.

Vreysen M. 2006. The sterile insect technique: as a component of sustainable area-wide integrated pest management of selected horticultural insect pests. Journal of Fruit and Ornamental Plant Research 14(3): 107-131.

Marec F, Vreysen M J. 2019. Advances and challenges of using the sterile insect technique for the management of pest Lepidoptera. Insects 10(11): 371.

White L D, Hutt R B, Moffitt H R, Winterfeld R G, Lydin L V, Clift A E, Schoenleber L G. 1976. Codling moth: Effects of releasing irradiated mixed sexes or females or males only on reproductive potential of a native population. Journal of Economic Entomology 69: 155-160.

Xu W H, Sato Y, Ikeda M, Yamashita O. 1995. Stage-dependent and Temperature-controlled Expression of the gene encoding the precursor protein of diapause hormone and pheromone biosynthesis activating neuropeptide in the silkworm, Bombyx mori(∗). Journal of Biological Chemistry 270(8): 3804-3808.

Zavodska R, von Wowern G, Löfstedt C, Rosen W, Sauman I. 2009. The release of a pheromonotropic neuropeptide, PBAN, in the turnip moth Agrotis segetum, exhibits a circadian rhythm. Journal of Insect Physiology 55(5): 435-440.