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Esterase activity in populations of the whitefly, Bemisia tabaci (Homoptera: Aleyrodidae): heritability and associated organophosphorus insecticide resistance

Published online by Cambridge University Press:  10 July 2009

Guy Bloch
Affiliation:
Department of Zoology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Israel
David Wool*
Affiliation:
Department of Zoology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Israel
*
Prof. David Wool, Department of Zoology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Ramat Aviv 69978, Israel.

Abstract

The association of esterase (EST) activity with resistance to the organophosphorus (OP) insecticide methidathion was investigated in field-collected populations of whitefly (Bemisia tabaci (Gennadius)) in Israel. The inheritance of EST activity was studied by controlled crosses in the laboratory. Among-family variance of EST activity was highly significant although all families were maintained in the same rearing room. This indicates that genetic or common environmental effects due to rearing each family on a different caged plant must have been important. Heritability estimated from son-mother regression was h2=0.98, but this estimate seems to be unrealistically high. Daughter-mother and daughter-mid-parent regressions produced lower heritability estimates (as expected). None of the regression coefficients of daughters on mother, however, were significantly different from zero and the regression on parent explained only very small amounts of the activity variation in the offspring. Estimates obtained from intraclass correlations among offspring were higher and outside the acceptable range, reflecting the variance component due to the common environment. The predictive value of the heritability estimates appears to be very low. The frequency distribution of activity among individuals sampled from one insecticide treated site (AM) was skewed to the right, as previously reported. But samples from another site (TZ) showed a symmetrical distribution, unlike the previous pattern. When field collected individuals from AM were released on clean plants in the laboratory, samples taken from the plants one or more days later showed symmetrical EST distribution. Electro-phoretic paterns of field and laboratory samples were the same, but band intensity was stronger in samples from laboratory populations. Differences in mean EST activity between populations and sampling years were unrelated to methidathion resistance.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1995

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References

Anber, H.A.I. & Oppenoorth, F.J. (1989) A mutant esterase degrading organophosphates in a resistant strain of the predacious mite Amblyseius potentillae (Garman). Pesticide Biochemistry and Physiology 33, 283297.CrossRefGoogle Scholar
Bloch, G. & Wool, D. (1994) Methidathion resistance in the sweetpotato whitefly (Aleyrodidae, Homoptera) in Israel: selection, heritability, and correlated changes in esterase activity. Journal of Economic Entomology 87, 11471156.CrossRefGoogle Scholar
Brewer, M.J. & Trumble, J.T. (1991) Classifying resistance severity in field populations: sampling inspection plans for an insecticide resistance monitoring program. journal of Economic Entomology 84, 379389.CrossRefGoogle Scholar
Brown, T.M. & Brogdon, W.G. (1987) Improved detection of insecticide resistance through conventional and molecular techniques. Annual Review of Entomology 32, 145162.CrossRefGoogle ScholarPubMed
Byrne, D.N. & Bellows, T.M, (1991) Whitefly biology. Annual Review of Entomology 36, 431457.CrossRefGoogle Scholar
Byrne, D.N., Bellows, T.S. & Parella, M.P. (1990) Whiteflies in agricultural systems. In Gerling, D. (Ed.) Whiteflies, their bionomics, pest status and management. Andover, UK, Intercept.Google Scholar
Byrne, F.J. & Devonshire, A.L. (1991) In vivo inhibition of esterase and acetylcholinesterase activities by profenofos treatment in the tobacco whitefly Bemisia tabaci (Genn.) Implications for routine biochemical monitoring of these enzymes. Pesticide Biochemistry and Physiology 40, 198204.CrossRefGoogle Scholar
Clark, A.G. (1990) Genetic components of variation in energy storage in Drosophila melanogaster. Evolution 44, 637650.CrossRefGoogle ScholarPubMed
Devonshire, A.L. (1989) Insecticide resistance in Myzus persicae: from field to gene and back again. Pesticide Science 26, 375382.CrossRefGoogle Scholar
Devonshire, A.L. & Sawicki, R.M. (1979) Insecticide-resistant Myzus persicae as an example of evolution by gene duplication. Nature 280, 140141.CrossRefGoogle Scholar
Dittrich, V., Ernst, G.H., Ruesch, O. & Uk, S. (1990) Resistance mechanisms in sweetpotato whitefly (Homoptera: Aleyrodidae) populations from Sudan, Turkey, Guatemala, and Nicaragua. Journal of Economic Entomology 83, 16651670.CrossRefGoogle Scholar
Falconer, D.S. (1989) Introduction to quantitative genetics, 3rd ed. New York, Longman.Google Scholar
Ferrari, J.A. & Georghiou, G.P. (1991) Quantitative genetic variation of esterase activity associated with a gene amplification in Culex quinquefasciatus. Heredity 66, 265272.CrossRefGoogle ScholarPubMed
Harlow, C.D. & Lampert, E.P. (1990) Resistance mechanisms in two color forms of the tobacco aphid (Homoptera: Aphidi-dae). journal of Economic Entomology 83, 21302135.CrossRefGoogle Scholar
Hemingway, J., Small, G.J. & Monro, A.G. (1993) Possible mechanisms of organophosphorous and carbamate insecticide resistance in German cockroaches (Dictyoptera: Blattellidae) from different geographical areas. journal of Economic Entomology 86, 16231630.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.) (Coleoptera: Curculionidae). Bulletin of Entomological Research 76, 661670.CrossRefGoogle Scholar
Horowitz, A.R. (1986) Population dynamics of Bemisia tabaci (Gennadius): with special emphasis on cotton fields. Agriculture, Ecosystems and Environment 17, 3747.CrossRefGoogle Scholar
Horowitz, A.R., Toscano, N.C., Youngman, R.R. & Georghiou, G.P. (1988) Synergism of insecticides with DEF in sweetpotato whitefly (Homoptera: Aleyrodidae). Journal of Economic Entomology 81, 110114.CrossRefGoogle Scholar
Ishaaya, I., Mendelson, Z., Asher, K.R.S. & Casida, J.E. (1987) Cypermethrin synergism by pyrethroid esterase inhibitors in adults of the whitefly Bemisia tabaci. Pesticide Biochemistry and Physiology 28, 155162.CrossRefGoogle Scholar
Jayaraj, S., Rangarajan, A.V., Murugesan, S., Santharamj, G., Jayaraghavan, S.V. & Thangaraj, D. (1986) Studies on the outbreak of whitefly, Bemisia tabaci (Gennadius) on cotton in Tamil Nadu. In Jayaraj, S. (Ed.) Resurgence of sucking pests. Proceedings of National Symposium. Coimbatore, India, Tamil Nadu Agricultural University.Google Scholar
Laurie-Ahlberg, C.C., Wilton, A.N., Curtsinger, J.W. & Emigh, T.H. (1982) Naturally occurring enzyme activity variation in Drosophila melanogaster. I. Sources of variation for 23 enzymes. Genetics 102, 191206.CrossRefGoogle ScholarPubMed
Lewis, G.A. & Madge, D.S. (1984) Esterase activity and associated insecticide resistance in the damson-hop aphid, Phorodon humuli (Schrank) (Hemiptera: Aphididae). Bulletin of Entomological Research 74, 227238.CrossRefGoogle Scholar
McKenzie, J.A., Parker, A.G. & Yen, J.L. (1992) Polygeneic and single gene responses to selection for resistance to diazinon in Lucilia cuprina. Genetics 130, 613620.CrossRefGoogle Scholar
Margolies, D.C. & Cox, T.S. (1993) Quantitative genetics applied to haplodiploid insects and mites. pp. 549559 in Wrensch, D.L. & Ebbert, M.A. (Eds) Evolution and diversity of sex ratio in insects and mites. New York, Chapman & Hall.Google Scholar
Mouches, C., Pasteur, N., Berge, J.B., Hyrien, O., Raymond, M., Saint Vincent, B.R., Silvestri, M. & Georghiou, G.P. (1986) Amplification of an esterase gene is responsible for insecticide resistance in California Culex mosquito. Science 233, 778780.CrossRefGoogle ScholarPubMed
Oppenoorth, F.J. & Van Asperen, K. (1960) Allelic genes in the housefly producing modified enzymes that cause organophos-phate resistance. Science 132, 298299.CrossRefGoogle ScholarPubMed
Owen, R.E. (1989) Differential size variation of male and female bumblebees. Journal of Heredity 80, 3943.CrossRefGoogle Scholar
Prabhaker, N., Courdriet, D.L. & Meyerdirk, D.E. (1985) Insecticide resistance in the sweetpotato whitefly, Bemisia tabaci (Homoptera: Aleyrodidae). Journal of Economic Entomology 78, 748752.CrossRefGoogle Scholar
Prabhaker, N., Courdriet, D.L. & Toscano, N.C. (1988) Effect of synergists on organophosphate and permethrin resistance in sweetpotato whitefly (Homoptera: Aleyrodidae). Journal of Economic Entomology 81, 3439.CrossRefGoogle Scholar
Roush, R.T. & Daly, J.C. (1990) The role of population genetics in resistance research and management. pp. 97152 in Roush, R.T. & Tabashnik, B.E. (Eds) Pesticide resistance in arthropods. New York and London, Chapman & Hall.CrossRefGoogle Scholar
Roush, R.T. & McKenzie, J.A. (1987) Ecological genetics of insecticide resistance. Annual Review of Entomology 32, 361380.CrossRefGoogle Scholar
Soderlund, D.M. & Bloomquist, J.R. (1990) Molecular mechanisms of insecticide resistance. pp. 5896 in Roush, R.T. & Tabashnik, B.E. (Eds) Pesticide resistance in arthropods. New York and London, Chapman & Hall.CrossRefGoogle Scholar
Sokal, R.R., & Rohlf, F.J. (1981) Biometry. 2nd ed. New York, Freeman.Google Scholar
Tabashnik, B.E. & Cushing, N.L. (1989) Quantitative genetic analysis of insecticide resistance: variation in fenvalerate tolerance in a diamondback moth (Lepidoptera: Plutellidae) population. Journal of Economic Entomology 82, 510.CrossRefGoogle Scholar
Tabashnik, B.E. (1992) Resistance risk assessment: realized herita-bility of resistance to Bacillus thuringiensis in diamondback moth (Lepidoptera: Plutellidae), tobacco budworm (Lepidoptera: Noctuidae) and Colorado potato beetle (Coleoptera: Chrysomelidae). Journal of Economic Entomology 85, 15511559.CrossRefGoogle Scholar
Takada, H. & Murakami, Y. (1988) Esterase variation and insecticide resistance in Japanese Aphis gossypii. Entomologia Experimentalis et Applicata 48, 3741.CrossRefGoogle Scholar
Wool, D. & Greenberg, S. (1990) Esterase activity in whiteflies (Bemisia tabaci) in Israel in relation to insecticide resistance. Entomologia Experimentalis et Applicata 57, 251258.CrossRefGoogle Scholar
Wool, D., Gerling, D., Bellotti, A.C., Morales, F.J. & Nolt, B. (1991) Spatial and temporal genetic variation in populations of the whitefly Bemisia tabaci (Genn.) in Israel and Colombia: an interim report. Insect Science and its Application 12, 225230.Google Scholar
Wool, D., Gerling, D., Bellotti, A.C. & Morales, F.J. (1993) Esterase electrophoretic variation in Bemisia tabaci (Genn.) (Horn., Aleyrodidae) among host plants and localities in Israel. Journal of Applied Entomology 115, 185196.CrossRefGoogle Scholar