Skip to main content
Log in

The biochemical genetics of permethrin resistance in the Learn-PyR strain of house fly

  • Published:
Biochemical Genetics Aims and scope Submit manuscript

Abstract

Permethrin resistance in the Learn-PyR strain of house fly was examined in four genetically derived substrains, each being homozygous for a different “resistant” autosome of the Learn-PyR strain. The resistance of these derivative strains was characterized toxicologically and biochemically. The relative levels of resistance to permethrin conferred by each autosome were 5>3>1>2. Three factors were associated with resistance: (1) increased mixed-function oxidase (MFO) activity associated with elevated levels of cytochrome P-450, cytochrome b5, and NADPH-cytochrome c reductase (P-450 reductase) activity; (2) target-site insensitivity (kdr); and (3) decreased cuticular penetration. Permethrin resistance factors on chromosome 1 consisted of a piperonyl butoxide (PB)-suppressible mechanism correlated with increased levels of cytochromes P-450 and b5; on chromosome 2, a PB-suppressible mechanism associated with elevated amounts of cytochrome P-450; on chromosome 3, decreased cuticular penetration, kdr, and increased amounts of P-450 reductase activity; and on chromosome 5, a largely PB-suppressible mechanism correlated with elevated levels of cytochrome P-450 and P-450 reductase activity.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Adams, M. E., and Miller, T. A. (1979). Site of action of pyrethroids: Repetitive “backfiring” in flight motor units of house fly. Pestic. Biochem. Physiol. 11218.

    Google Scholar 

  • Anonymous (1984). Pyrethroid sales. Calif. Ariz. Press 23:2.

  • Farnham, A. W. (1973). Genetics of resistance of pyrethroid-selected houseflies, Musca domestica L. Pest. Sci. 4513.

    Google Scholar 

  • Fine, B. C., Goodin, P. J., and Thain, E. M. (1963). Penetration of pyrethrin I labelled with carbon-14 into susceptible and pyrethroid resistant houseflies. Nature 199927.

    Google Scholar 

  • Finney, D. J. (1952). Probit Analysis 2nd ed., Cambridge University Press, Cambridge.

    Google Scholar 

  • Georghiou, G. P. (1969). Genetics of resistance to insecticides in houseflies and mosquitoes. Exp. Parisitol. 26224.

    Google Scholar 

  • Hodgson, E. (1983). The significance of cytochrome P-450 in insects. Insect Biochem. 13237.

    Google Scholar 

  • MacDonald, R. S., Solomon, K. R., Surgeoner, G. A., and Harris, C. R. (1985). Laboratory studies on the mechanisms of resistance to permethrin in a field-selected strain of house flies. Pest. Sci. 1610.

    Google Scholar 

  • Motoyama, N. (1984). Pyrethroid resistance in a Japanese colony of the housefly. J. Pest. Sci. 9523.

    Google Scholar 

  • Murray, D., and Cull, P. (1984). Resistance strategy works at Emerald. Austral. Cottongrower Feb.–Apr.:22.

  • Omura, T., and Sato, R. (1964). The carbon monoxide-binding pigment of liver microsomes. J. Biol. Chem. 2392370.

    Google Scholar 

  • Plapp, F. W., Jr. (1984). The genetic basis of insecticide resistance in the house fly: Evidence that a single locus plays a major role in metabolic resistance to insecticides. Pest. Biochem. Physiol. 22194.

    Google Scholar 

  • Plapp, F. W., Jr., and Casida, J. E. (1969). Genetic control of house fly NADPH-dependent oxidases: Relation to insecticide chemical metabolism and resistance. J. Econ. Entomol. 621174.

    Google Scholar 

  • Plapp, F. W., Jr., and Hoyer, R. F. (1968). Possible pleiotropism of a gene conferring resistance to DDT, DDT analogs, and pyrethrins in the house fly and Culex tarsalis. J. Econ. Entomol. 61761.

    Google Scholar 

  • Sawicki, R. M., and Farnham, A. W. (1967). The use of visible mutant markers in the study of resistance of house flies to insecticides. Proc. Fourth Brit. Insect. Fung. Conf. 1355.

    Google Scholar 

  • Sawicki, R. M., Devonshire, A. L., Farnham, A. W., O'Dell, K., and Morres, G. D. (1984). Factors affecting resistance to insecticides in house-flies, Musca domestica L. II. Close linkage on autosome 2 between an esterase and resistance to trichlorphon and pyrethroids. Bull. Entomol. Res. 74197.

    Google Scholar 

  • Scott, J. G., and Georghiou, G. P. (1984). Influence of temperature on knockdown, toxicity, and resistance to pyrethroids in the house fly, Musca domestica. Pest. Biochem. Physiol. 2153.

    Google Scholar 

  • Scott, J. G., and Georghiou, G. P. (1985a). Rapid development of high-level permethrin resistance in a field collected strain of house fly under laboratory selection. J. Econ. Entomol. 78 316.

    Google Scholar 

  • Scott, J. G., and Georghiou, G. P. (1985b). Mechanisms responsible for high levels of permethrin resistance in the house fly. Pest. Sci. (in press).

  • Scott, J. G., Shono, T., and Georghiou, G. P. (1984). Genetic analysis of permethrin resistance in the house fly, Musca domestica L. Experientia 40416.

    Google Scholar 

  • Tsukamoto, M. (1983). Methods of genetic analysis of insecticide resistance. In Georghiou, G. P., and Saito, T. (eds.), Pest Resistance to Pesticides Plenum Press, New York, p. 71.

    Google Scholar 

  • Yu, S. J., and Terriere, L. C. (1979). Cytochrome P-450 in insects. 1. Differences in the forms present in insecticide resistant and susceptible house flies. Pest. Biochem. Physiol. 12239.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Scott, J.G., Georghiou, G.P. The biochemical genetics of permethrin resistance in the Learn-PyR strain of house fly. Biochem Genet 24, 25–37 (1986). https://doi.org/10.1007/BF00502976

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00502976

Key words

Navigation