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Inheritance of metabolic resistance to the synthetic pyrethroids in Australian Helicoverpa armigera(Lepidoptera: Noctuidae)

Published online by Cambridge University Press:  10 July 2009

Joanne C. Daly  and
Jennifer H. Fisk
Joanne C. Daly*
Affiliation:
CSIRO Division of Entomology, GPO Box 1700 Canberra, Australia
Jennifer H. Fisk
Affiliation:
CSIRO Division of Entomology, GPO Box 1700 Canberra, Australia
*
Dr J.C. Daly, CSIRO Division of Entomology, GPO Box 1700, Canberra, Act 2601, Australia.
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Abstract

Two strains of Helicoverpa armigera (Hübner), resistant to synthetic pyrethroids, were isolated from field populations collected in the irrigated cotton growing areas of northern New South Wales: an isofemale strain, Mfo, and a composite field strain, Field. A series of crosses were undertaken between the Mfo and susceptible strains to determine the genetic basis of the resistance. Dose-responses were obtained by bioassay using topical application of fenvalerate in acetone. Considerable variation in tolerance was observed in both resistant and susceptible strains. In the Mfo strain, the major shift in resistance phenotype (33-fold resistance) was due to a single major gene with incomplete dominance. The resistance phenotype was not diluted by 23 generations of backcrossing. The major resistance phenotype could be eliminated almost completely by the addition of piperonyl butoxide which affects oxidative breakdown of the pyrethroids by mixed function oxidase (mfo) enzymes. Similar results were observed in the Field strain. Monitoring for resistance in field populations will be imprecise because a true discriminating dose does not exist for susceptible and heterozygous resistant individuals.

Type
Research Paper
Information
Bulletin of Entomological Research , Volume 82 , Issue 1 , March 1992 , pp. 5 - 12
Copyright
Copyright © Cambridge University Press 1992

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References

Ahmad, M. & McCaffery, A.R. (1988) Resistance to insecticides in a Thailand strain of Heliothis armigera (Hübner) (Lepidoptera: Noctuidae). Journal of Economic Entomology 81, 45–48.CrossRefGoogle Scholar
Anon. (1970) Standard method of detection of insecticide resistance in Heliothis zea (Boddie) and H. virescens (F.). Bulletin of the Entomological Society of America 16, 147–153.Google Scholar
Brattsten, L.B. (1987) Sublethal virus infection depresses cytochrome P-450 in an insect. Experientia 43, 451–454.CrossRefGoogle Scholar
Campanhola, C. & Plapp, F.W. (1989) Toxicity and synergism of insecticides against susceptible and pyrethroid-resistant third instars of the tobacco budworm (Lepidoptera: Noctuidae). Journal of Economic Entomology 82, 1495–1501.CrossRefGoogle Scholar
Corbett, J.R., Wright, K. & Baillie, A.C. (1984) The biochemical mode of action of pesticides. 2nd edn.382 pp. London, Academic Press.Google Scholar
Daly, J.C., Fisk, J.H. & Forrester, N.W. (1988a) Selective mortality in field trials between strains of Heliothis armigera (Hübner) (Lepidoptera: Noctuidae) resistant and susceptible to synthetic pyrethroids: functional dominance of resistance and age-class. Journal of Economic Entomology 81, 1000–1007.CrossRefGoogle Scholar
Daly, J.C., Fitt, G.P. & Fisk, J.H. (1988b) Pyrethroid resistance in pupae and adult Heliothis armigera. Australian Cotton Growers Research Association, (5th Conference), Surfers Paradise, August 1988, pp 73–78.Google Scholar
Firko, M.J. & Hayes, J.L. (1991) Quantitative genetic analysis of larval resistance to cypermethrin in tobacco budworm (Lepidoptera: Noctuidae). Journal of Economic Entomology 84, 34–40.CrossRefGoogle Scholar
Forrester, N.W. (1989) Updated insecticide resistance levels. Australian Cotton Grower 10(1), 30–32.Google Scholar
Forrester, N.W. & Cahill, M. (1987) Management of insecticide resistance in Heliothis armigera (Hübner) in Australia, pp. 127–137in Ford, M., Khambay, B.P.S., Holloman, D.W., & Sawicki, R.M. (Eds) Combating resistance in xenobiotics: biological and chemical approaches. Chichester, Ellis Horwood.Google Scholar
Georghiou, G.P. (1969) Genetics of resistance to insecticides in houseflies and mosquitoes. Experimental Parasitology 26, 224–255.Google Scholar
Gunderson, C.A., Brattsten, L.B. & Fleming, J.T. (1986) MIcrosomal oxidase and glutathione transferase as factors influencing the effects of pulegone in southern and fall ar-myworm larvae. Pesticide Biochemistry and Physiology 26, 238–249.Google Scholar
Gunning, R.V. & Easton, C.S. (1987) Inheritance of resistance to fenvalerate in Heliothis armigera (Hübner) (Lepidoptera: Noctuidae). Journal of the Australian Entomological Society 26, 249–250.CrossRefGoogle Scholar
Gunning, R.V. & Easton, C.S. (1989) Pyrethroid resistance in Heliothis armigera (Hübner) collected from unsprayed maize crops in New South Wales 1983–1987. Journal of the Australian Entomological Society 28, 57–61.CrossRefGoogle Scholar
Gunning, R.V., Easton, C.S., Greenup, L.R. & Edge, V.E. (1984) Pyrethroid resistance in Heliothis armigera (Hübner) (Lepidoptera: Noctuidae) in Australia. Journal of Economic Entomology 77, 1283–1287.CrossRefGoogle Scholar
Gunning, R.V., Easton, C.S., Balfe, M.E., & Ferris, I.G., (1991) Pyrethroid resistance mechanisms in Australian Heliothis armigera. Pesticide Science 33, 473–490.CrossRefGoogle Scholar
Holloway, G.J. (1986) A theoretical examination of the classical theory of inheritance of insecticide resistance and the genetics of time to knockdown and dry body weight in Sitophilus oryzae (L.P (Coleoptera Curculionidae)). Bulletin of Entomological Research 76, 661–670.CrossRefGoogle Scholar
Little, E.J., McCaffery, A.R., Walker, C.H. & Parker, T. (1989) Evidence for an enhanced metabolism of cypermethrin by a monooxygenase in a pyrethroid-resistant strain of the tobacco budworm (Heliothis viresciens F.). Pesticide Biochemistry and Physiology 34, 58–68.Google 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, 65–75.Google Scholar
McKenzie, J.A., Whitten, M.J. & Adena, M.A. (1982) The effect of genetic background on the fitness of diazinon resistance genotypes of the Australian sheep blowfly, Lucilia cuprina. Heredity 49, 1–9.Google Scholar
Neal, J.J. (1987) Metabolic costs of mixed-function oxidase induction in Heliothis zea. Entomologia Experimentalis et Applicata 43, 175–179.Google Scholar
Payne, CD. (1985) The GLIM system release 3.77 manual. Oxford, Numerical Algorithms Group.Google Scholar
Ross, G.J.S. (1980) MLP maximum likelihood program. Rothamsted, The Statistics Department.Google Scholar
Roush, R.T. & Daly, J.C. (1990) The role of population genetics in resistance research and management, pp 97–153in Roush, R.T. & Tabashni, B. (Eds) Pesticide resistance in arthropods. New York, Chapman and Hall.Google Scholar
Roush, R.T. & McKenzie, J.A. (1987) Ecological genetics of insecticide and acaricide resistance. Annual Review of Entomology 32, 361–380.Google Scholar
Roush, R.T. & Miller, G.L. (1986) Considerations for design of insecticide resistance monitoring programs. Journal of Economic Entomology 79, 293–298.Google Scholar
Scott, J.G. (1990) Investigating mechanisms of insecticide resistance: methods, strategies, and pitfalls, pp 39–57in Roush, R.T. & Tabashnik, B. (Eds) Pesticide resistance in arthropods. New York, Chapman and Hall.CrossRefGoogle Scholar
Sundseth, S.S., Kennel, S.J. & Waters, L.C. (1989) Monoclonal antibodies to resistance-related forms of cytochrome P450 in Drosophila melanogaster. Pesticide Biochemistry and Physiology 33, 176–188.CrossRefGoogle Scholar
Tabashnik, B.E. & Cushing, N.L. (1989) Quantitative genetic analysis of insecticide resistance: variation in fenvalerate tolerance in a diamondback moth (Lepidoptera: Plutelli-dae) population. Journal of Economic Entomology 82, 5–10.Google Scholar
Teakle, R.E. & Jensen, J.M. (1985) Heliothis punctiger. pp. 312–322. in Singh, R. & Moore, R.F. (Eds) Handbook of insect rearing. Vol 2. Amsterdam, Elsevier.Google Scholar
Tsukamoto, M. (1963) The log dosage-probit mortality curve in genetic researches of insect resistance to insecticides. Botyu-Kagaku 28, 91–98.Google Scholar