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European monitoring of resistance to insecticides in Myzus persicae and Aphis gossypii (Hemiptera: Aphididae) with special reference to imidacloprid

Published online by Cambridge University Press:  09 March 2007

R. Nauen*
Affiliation:
Bayer CropScience AG, Global Biology Insecticides, Alfred Nobel Str. 50, D-40789 Monheim, Germany
A. Elbert
Affiliation:
Bayer CropScience AG, Agronomic Development Insecticides, Alfred Nobel Str. 50, D-40789 Monheim, Germany
*
*Fax: +49 (0)2173 384932 E-mail: ralf.nauen@bayercropscience.com

Abstract

The susceptibility to several insecticides of 16 and 8 strains of Myzus persicae Sulzer and Aphis gossypii Glover, respectively, received from different European countries in 2001 was investigated. Most of the strains were derived from places known for their aphid resistance problems to conventional insecticides before imidacloprid was introduced. In many regions and agronomic cropping systems imidacloprid has been an essential part of aphid control strategies for a decade, and therefore the susceptibility of aphid populations to imidacloprid using FAO-dip tests and diagnostic concentrations in a leaf-dip bioassay was checked. Additional insecticides tested were cyfluthrin (chemical class: pyrethroid), pirimicarb (carbamate), methamidophos and oxydemeton-methyl (organophosphates). Diagnostic concentrations (LC99-values of reference strains) for each insecticide were established by dose response analysis using a new leaf-disc dip bioassay format in 6-well tissue culture plates. Virtually no resistance to imidacloprid in any of the field-derived populations of M. persicae and A. gossypii was detected. In contrast, strong resistance was found to pirimicarb and oxydemeton-methyl, and to a lesser extent also to cyfluthrin. Two strains of A. gossypii exhibited reduced susceptibility to imidacloprid when tested directly after collection. However, after maintaining them for six weeks in the laboratory, the aphids were as susceptible as the reference strain. The diagnostic concentration of methamidophos did not reveal any resistance in M. persicae, but did so in four strains of A. gossypii.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2003

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References

Abbott, W.S. (1925) A method of computing the effectiveness of an insecticide. Journal of Economic Entomology 18, 265267.CrossRefGoogle Scholar
Buchholz, A. & Nauen, R. (2001) Organophosphate and carbamate resistance in Myzus persicae Sulzer and Phorodon humuli Schrank (Homopetra: Aphididae): biological and biochemical considerations. Mitteilungen der Deutschen Gesellschaft für Allgemeine und Angewandte Entomologie 13, 227233.Google Scholar
Casida, J.E. & Quistad, G.B. (1998) Golden age of insecticide research: Past, present, or future?. Annual Review of Entomology 43, 116.CrossRefGoogle ScholarPubMed
Devine, G.J., Harling, Z.K., Scarr, A.W. & Devonshire, A.L. (1996) Resistance to lethal and sublethal effects of imidacloprid in nicotine tolerant Myzus nicotianae and Myzus persicae. Pesticide Science 48, 5762.3.0.CO;2-9>CrossRefGoogle Scholar
Devonshire, A.L. & Moores, G.D. (1982) A carboxylesterase with broad substrate specificity causes organophosphorus, carbamate and pyrethroid resistance in peach–potato aphids (Myzus persicae). Pesticide Biochemistry and Physiology 18, 235246.CrossRefGoogle Scholar
Devonshire, A.L. (1989) Insecticide resistance in Myzus persicae: from field to gene and back again. Pesticide Science 26, 375382.CrossRefGoogle Scholar
Elbert, A., Becker, B., Hartwig, J. & Erdelen, C. (1991) Imidacloprid – a new systemic insecticide. Pflanzenschutz-Nachrichten Bayer 44, 113136.Google Scholar
Elbert, A., Nauen, R., Cahill, M., Devonshire, A., Scarr, A., Sone, S. & Steffens, R. (1996) Resistance management for chloronicotinyls using imidacloprid as an example. Pflanzenschutz-Nachrichten Bayer 49, 554.Google Scholar
Elbert, A., Nauen, R. & Leicht, W. (1998) Imidacloprid, a novel chloronicotinyl insecticide, biological activity and agricultural importance. pp 5073. in Ishaaya, I. & Degheele, D. (Eds) Insecticides with novel modes of action, mechanism and application. Heidelberg, Springer Verlag.CrossRefGoogle Scholar
Eto, M. (1974) Organophosphorus pesticides: organic and biological chemistry. Boca Raton, Florida, CRC Press.Google Scholar
FAO (1979) Recommended methods for the detection and measurement of resistance of agricultural pests to pesticides: method for adult aphids – FAO method No. 17. FAO Plant Protection Bulletin FAO method No. 17. 18, 6.Google Scholar
Field, L.M., Devonshire, A.L. & Forde, B.G. (1988) Molecular evidence that insecticide resistance in peach–potato aphids, Myzus persicae (Sulz), results from amplification of an esterase gene. Biochemical Journal 251, 309315.CrossRefGoogle ScholarPubMed
Field, L.M., Blackmann, R.L. & Devonshire, A.L. (2001) Evolution of amplified esterase genes as a mode of insecticide resistance in aphids. pp 209219. in Ishaaya, I. (Ed.) Biochemical sites important in insecticide action and resistance. Berlin, Heidelberg: Springer Verlag.CrossRefGoogle Scholar
Flückiger, C.R., Kristinsson, H., Senn, R., Rindlisbacher, A., Buholzer, H. & Voss, G. (1992) CGA 215'944 – a novel agent to control aphids and whiteflies. Proceedings of the Brighton Crop Protection Conference – Pests and Diseases 2–3, 4350.Google Scholar
Foster, S.P., Denholm, I., Harling, Z.K., Moores, G.D. & Devonshire, A.L. (1998) Intensification of resistance in UK field populations of the peach–potato aphid, Myzus persicae (Homoptera: Aphididae) in 1996. Bulletin of Entomological Research 88, 127130.CrossRefGoogle Scholar
Foster, S.P. & Devonshire, A.L. (1999) Field-simulator study of insecticide resistance conferred by esterase-, MACE- and kdr-based mechanisms in the peach–potato aphid, Myzus persicae (Sulzer). Pesticide Science 55, 810814.3.0.CO;2-#>CrossRefGoogle Scholar
Foster, S.P., Denholm, I. & Devonshire, A.L. (2000) The ups and downs of insecticide resistance in peach–potato aphids (Myzus persicae) in the UK. Crop Protection 19, 873879.CrossRefGoogle Scholar
Han, Z., Moores, G.D., Denholm, I. & Devonshire, A.L. (1998) Association between biochemical markers and insecticide resistance in the cotton aphid, Aphis gossypii Glover. Pesticide Biochemistry and Physiology 62, 164171.CrossRefGoogle Scholar
Horowitz, A.R. & Denholm, I. (2001) Impact of insecticide resistance mechanisms on management strategies. pp 323328. in Ishaaya, I. (Ed.) Biochemical sites important in insecticide action and resistance. Berlin, Heidelberg, Springer Verlag.CrossRefGoogle Scholar
Ishaaya, I. (2001) Biochemical processes related to insecticide action: an overview. pp 116. in Ishaaya, I. (Ed.) Biochemical sites simportant in insecticide action and resistance. Berlin, Heidelberg, Springer Verlag.CrossRefGoogle Scholar
Martinez-Torres, D., Foster, S.P., Field, L.M., Devonshire, A.L. & Williamson, M.S. (1998) A sodium channel point mutation is associated with resistance to DDT and pyrethroid insecticides in the peach–potato aphid, Myzus persicae (Sulzer) (Hemiptera: Aphididae). Insect Molecular Biology 8, 18.Google Scholar
Moores, G.D., Devine, G.J. & Devonshire, A.L. (1994) Insecticide-insensitive acetylcholinesterase can enhance esterase-based resistance in Myzus persicae and Myzus nicotianae. Pesticide Biochemistry and Physiology 49, 114120.CrossRefGoogle Scholar
Moores, G.D., Devine, G.J. & Devonshire, A.L. (1994) Insecticide resistance due to insensitive acetylcholinesterase in Myzus persicae and Myzus nicotianae. In Proceedings of the Brighton Crop Protection Conference – Pests and Diseases. pp 413418.Google Scholar
Nauen, R. & Elbert, A. (1997) Apparent tolerance of a field-collected strain of Myzus nicotianae to imidacloprid due to strong antifeeding response. Pesticide Science 49, 252258.3.0.CO;2-2>CrossRefGoogle Scholar
Nauen, R., Strobel, J., Otsu, K., Tietjen, K., Erdelen, C. & Elbert, A. (1996) Aphicidal activity of imidacloprid against a carbamate and organophosphate resistant Japanese strain of the tobacco feeding form of Myzus persicae (Homoptera: Aphididae) closely related to Myzus nicotianae. Bulletin of Entomological Research 86, 165171.CrossRefGoogle Scholar
Nauen, R., Hungenberg, H., Tollo, B., Tietjen, K. & Elbert, A. (1998) Antifeedant effect, biological efficacy and high affinity binding of imidacloprid to acetylcholine receptors in Myzus persicae and Myzus nicotianae. Pesticide Science 53, 133140.3.0.CO;2-D>CrossRefGoogle Scholar
Nauen, R., Ebbinghaus-Kintscher, U., Elbert, A., Jeschke, P. & Tietjen, K. (2001) Acetylcholine receptors as sites for developing neonicotinoid insecticides. pp 77105. in Ishaaya, I. (Ed.) Biochemical sites simportant in insecticide action and resistance. Berlin, Heidelberg, Springer Verlag.CrossRefGoogle Scholar
Silver, A.R.J., van Emden, H.F. & Battersby, M. (1995) A biochemical mechanism of resistance to pirimicarb in two glasshouse clones of Aphis gossypii. Pesticide Science 43, 2129.CrossRefGoogle Scholar
Wang, K.Y., Liu, T.X., Jiang, X.Y. & Yi, M.Q. (2001) Cross-resistance of Aphis gossypii to selected insecticides on cotton and cucumber. Phytoparasitica 29, 393399.CrossRefGoogle Scholar
Wellings, P.W., Ward, S.A., Dixon, A.F.G. & Rabbinge, R. (1989) Crop loss assessment. pp 4964. in Minks, A.K. and Harrewijn, P. (Eds) Aphids: their biology, natural enemies and control Volume 2, Amsterdam, Elsevier.Google Scholar
Wenliang, P., Zhihong, D., Zhanlin, G., Haimin, J. & Kejin, Z. (2000) Resistance of three species of aphids to imidacloprid. Nongyaoxue Xuebao 2, 8587.Google Scholar
Zhaojun, H., Moores, G.D., Denholm, I. & Devonshire, A.L. (1998) Association between biochemical markers and insecticide resistance in the cotton aphid, Aphis gossypii Glover. Pesticide Biochemistry and Physiology 62, 164171.Google Scholar