Hostname: page-component-78c5997874-fbnjt Total loading time: 0 Render date: 2024-11-19T12:11:40.630Z Has data issue: false hasContentIssue false

A survey of insecticide resistance in Helicoverpa armigera in the Indian subcontinent

Published online by Cambridge University Press:  10 July 2009

Nigel J. Armes*
Affiliation:
Natural Resources Institute, Chatham Maritime, UK
Deepak R. Jadhav
Affiliation:
International Crops Research Institute for the Semi-Arid Tropics, Patancheru, India
Kenneth R. DeSouza
Affiliation:
Natural Resources Institute, Chatham Maritime, UK
*
N.J. Armes, Crop Protection Division, ICRISAT, Patancheru PO, Hyderabad, Andhra Pradesh 502 324, India.

Abstract

Helicoverpa armigera (Hübner) larvae were collected from field crops and wild hosts in India, Nepal and Pakistan from 1991 to 1995, and ninety eight laboratory cultures established. Cypermethrin, fenvalerate, endosulfan, quinalphos, monocrotophos and methomyl insecticides were topically applied to 30–40 mg, first laboratory generation larvae and resistance determined from log dose probit bioassays. Significant levels of cypermethrin and fenvalerate resistance were found in all field strains, demonstrating that resistance to at least some pyrethroids is now ubiquitous in H. armigera populations in the Indian subcontinent; cypermethrin and fenvalerate resistance levels ranged from 5– to 6500–fold and 16– to 3200–fold respectively. Pyrethroid resistance levels were highest in the intensive cotton and pulse growing regions of central and southern India where excessive application of insecticide is common. In all field strains assayed, pre-treatment with the metabolic synergist piperonyl butoxide (pbo), resulted in significant suppression of pyrethroid resistance. However, in nearly all cases, full suppression of resistance was not achieved. This residual non-pbo-suppressible resistance was most likely due to a nerve-insensitivity resistance mechanism. Pbo-insensitive resistance was highest in regions of India where insecticides were frequently applied to cotton and legume crops. In some regions where insecticides were heavily overused, a second high order nerve-insensitivity mechanism (possibly a Super -Kdr type mechanism), may have been present. Incipient endosulfan resistance (1–28-fold), was present throughout India, Nepal and Pakistan. Low to moderate levels of resistance (2–59–fold), were reported to the phosphorothionate group organophosphate, quinalphos, in India and Pakistan, but there was no evidence of significant resistance (0.4–3–fold), to the phosphate group organophosphate, monocrotophos, under our bioassay conditions between 1993 and 1994. H. armigera strains collected in Nepal in 1993 and 1994 were susceptible to quinalphos, but by 1995, 4–5–fold resistance was detected. It is probable that much of the resistance to pyrethroid, organophosphate and carbamate insecticides in the Indian subcontinent can be attributed to an inherited or inducible mixed function oxidase complex. Non-pbo-suppressible resistance becomes significant in regions and periods in the season when insecticide selection pressure on resistant H. armigera larvae on cotton and legume crops is very high.

Type
Review Article
Copyright
Copyright © Cambridge University Press 1996

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Abbott, W.S. (1925) A method of computing the effectiveness of an insecticide. Journal of Economic Entomology 18, 265267.CrossRefGoogle Scholar
Ahmad, M., Arif, M.I. & Ahmad, Z. (1995) Monitoring insecticide resistance of Helicoverpa armigera (Lepidoptera: Noctuidae) in Pakistan. Journal of Economic Entomology 88, 771776.CrossRefGoogle Scholar
Anon. (1970) Standard method for detection of insecticide resistance in Heliothis zea (Boddie) and H. virescens (F.). Bulletin of the Entomological Society of America 16, 147153.Google Scholar
Anon. (1995) Cotton estimates to be revised. The Hindu, Feb., 3 1995, p. 14.Google Scholar
Armes, N.J., Jadhav, D.R., Bond, G.S. & King, A.B.S. (1992) Insecticide resistance in Helicoverpa armigera in south India. Pesticide Science 34, 355364.CrossRefGoogle Scholar
Armes, N.J., Banerjee, S.K., DeSouza, K.R., Jadhav, D.R., King, A.B.S., Kranthi, K.R., Regupathy, A., Surulivelu, T. & Venugopal Rao, N. (1994) Insecticide resistance in Helicoverpa armigera in India: recent developments. pp. 437442 in Proceedings. Brighton Crop Protection Conference – Pests and Diseases 1994.Google Scholar
Caprio, M.A. & Tabashnik, B.E. (1992) Gene flow accelerates local adaptation among finite populations: simulating the evolution of insecticide resistance. Journal of Economic Entomology 85, 611620.CrossRefGoogle Scholar
Cheng, E.Y., Kao, C.H., & Chiu, C.S. (1992) Resistance, cross-resistance and chemical control of diamondback moth in Taiwan: recent developments. pp. 465475in Talekar, N.S. (Ed.) Diamondback moth and other crucifer pests: proceedings of the second international workshop, Tainan, Taiwan, 10–14 Dec. 1990. Asian Vegetable Research and Development Center, AVRDC Publication No. 92–368.Google Scholar
Daly, J.C. & Gregg, P. (1985) Genetic variation in Heliothis in Australia: species identification and gene flow in the two pest species H. armigera (Hübner) and H. punctigera Wallengren (Lepidoptera: Noctuidae). Bulletin of Entomological Research 75, 169184.CrossRefGoogle Scholar
Dhingra, S., Phokela, A. & Mehrotra, K.N. (1988) Cypermethrin resistance in the populations of Heliothis armigera Hübner. National Academy of Science Letters 2, 123125.Google Scholar
Eto, M. (1990) Biochemical mechanisms of insecticidal activities. Chemistry of Plant Protection 6, 65107. Springer-Verlag, Berlin.Google Scholar
Forrester, N.W., Cahill, M., Bird, L.J. & Layland, J.K. (1993) Management of pyrethroid and endosulfan resistance in Helicoverpa armigera (Lepidoptera: Noctuidae) in Australia. Bulletin of Entomological Research Supplement Series No. 1, 132 pp.Google Scholar
Geddes, A.M. & lles, M. (1991) The relative importance of crop pests in South Asia. Natural Resources Institute Bulletin No. 39, Natural Resources Institute, UK.Google Scholar
Gunning, R.V. & Easton, C.S. (1994) Endosulfan resistance in Helicoverpa armigera (Hübner) (Lepidoptera: Noctuidae) in Australia. Journal of the Australian Entomological Society 33, 912.CrossRefGoogle Scholar
Gunning, R.V., Easton, C.S., Balfe, M.E. & Ferris, I.G. (1991) Pyrethroid resistance mechanisms in Australian Helicoverpa armigera. Pesticide Science 33, 473490.CrossRefGoogle Scholar
Gunning, R.V., Balfe, M.E. & Easton, C.S. (1992) Carbamate resistance in Helicoverpa armigera (Hübner) (Lepidoptera: Noctuidae) in Australia. Journal of the Australian Entomological Society 31, 97103.CrossRefGoogle Scholar
Gunning, R.V., Devonshire, A.L. & Moores, G.D. (1995) Metabolism of esfenvalerate by pyrethroid-susceptible and resistant Australian Helicoverpa armigera (Lepidoptera: Noctuidae). Pesticide Biochemistry and Physiology 51, 205213.CrossRefGoogle Scholar
Ibrahim Ali, M. (1994) Circumstantial evidence supports insect resistance in Bangladesh. Resistant Pest Management 6, 5.Google Scholar
Kay, I.R. (1977) Insecticide resistance in Heliothis armigera (Hübner) (Lepidoptera: Noctuidae) in areas of Queensland, Australia. Journal of the Australian Entomological Society 16, 4345.CrossRefGoogle Scholar
McCaffery, A.R., King, A.B.S., Walker, A.J. & El-Nayir, H. (1989) Resistance to synthetic pyrethroids in the bollworm, Heliothis armigera from Andhra Pradesh, India. Pesticide Science 27, 6576.CrossRefGoogle Scholar
Mehrotra, K.N. (1990) Pyrethroid resistant insect pest management: Indian experience. Pesticide Research Journal 2, 4452.Google Scholar
Mehrotra, K.N. & Phokela, A. (1992) Pyrethroid resistance in Helicoverpa armigera Hübner V. Response of populations in Punjab in cotton. Pesticide Research Journal 4, 5961.Google Scholar
Oppenoorth, F.J. (1985) Biochemistry and genetics of insecticide resistance. pp. 731773in Kerkut, G.A. and Gilbert, L.I. (Eds.) Comprehensive insect physiology, biochemistry and pharmacology Vol 12 Insect control. Oxford, Pergamon Press.Google Scholar
Oppenoorth, F.J. & Welling, W. (1976) Biochemistry and physiology of resistance. pp. 507551in Wilkinson, C.F. (Ed.) Insecticide biochemistry and physiology. Plenum Press, New York.CrossRefGoogle Scholar
Padma Kumari, A.P., Phokela, A. & Mehrotra, K.N. (1995) Permeability of cuticle of Helicoverpa armigera (Hübner) larvae to deltamethrin. Current Science 69, 464466.Google Scholar
Pasupathy, S. & Regupathy, A. (1994) Status of insecticide resistance in the American bollworm Helicoverpa armigera Hübner in Tamil Nadu. Pesticide Research Journal 6, 117120.Google Scholar
Price, N.R. (1991) Insect resistance to insecticides: mechanisms and diagnosis. Comparative Biochemistry and Physiology 100C, 319326.Google Scholar
Ross, G.J.S. (1987) Maximum likelihood program. The Numerical Algorithms Group, Rothamsted Experimental Station, Harpenden, UK.Google Scholar
Sun, C.N. (1992) Insecticide resistance in diamondback moth. pp. 419426in Talekar, N.S. (Ed.) Diamondback moth and other crucifer pests: proceedings of the second international workshop, Tainan, Taiwan, 10–14 Dec. 1990. Asian Vegetable Research and Development Center, AVRDC Publication No. 92–368.Google Scholar
Tabashnik, B.E. & Croft, B.A. (1982) Managing pesticide resistance in crop-arthropod complexes: interactions between biological and operational factors. Environmental Entomology 11, 11371144.CrossRefGoogle Scholar
Welling, W., De Vries, A.W. and Voerman, S. (1974) Oxidative cleavage of a carboxyester bond as a mechanism of resistance to malaoxon in houseflies. Pesticide Biochemistry and Physiology 4, 3143.CrossRefGoogle Scholar
West, A.J. & McCaffery, A.R. (1992) Evidence of nerve insensitivity to cypermethrin from Indian strains of Helicoverpa armigera. pp. 233238 in Proceedings Brighton Crop Protection Conference – Pests and Diseases 1992.Google Scholar
Yu, S.J. (1991) Insecticide resistance in the fall armyworm, Spodoptera frugiperda (J.E. Smith). Pesticide Biochemistry and Physiology 39, 8491.CrossRefGoogle Scholar