2009
DOI: 10.1111/j.1440-6055.2009.00723.x
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Biochemical mechanisms of insecticide resistance in the diamondback moth (DBM), Plutella xylostella L. (Lepidopterata: Yponomeutidae), in the Sydney region, Australia

Abstract: Following the detection of resistant diamondback moth (DBM) populations to synthetic pyrethroid, organophosphorus and indoxacarb insecticides in the Sydney Basin, a study of the major biochemical mechanisms was conducted to determine the type of resistance in these populations. The activity of cytochrome P450 monooxygenases increased two-to sixfold when compared with the susceptible strain. Up to a 1.9-fold increase in esterase activity in resistant strains compared with the susceptible strain was observed. In… Show more

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Cited by 17 publications
(17 citation statements)
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“…8 DBM resistance to acephate, indoxacarb, beta-cypermethrin and spinosad has been reported. 13,16,52,53 In this work, these insecticides were used to challenge the expression of DBM GST genes.…”
Section: Effect Of Insecticide Exposure On Dbm Gst Gene Expressionmentioning
confidence: 99%
“…8 DBM resistance to acephate, indoxacarb, beta-cypermethrin and spinosad has been reported. 13,16,52,53 In this work, these insecticides were used to challenge the expression of DBM GST genes.…”
Section: Effect Of Insecticide Exposure On Dbm Gst Gene Expressionmentioning
confidence: 99%
“…Metabolic capacity is strongly related to the activities of the enzymes carboxylesterase (CarE), glutathione S-transferase (GST) Kao and Sun 1991), and cytochrome P450 monooxygenases (MFO) (Li et al 2007;Eziah et al 2009). Insensitivity of the target site to organophosphates and pyrethroids is usually related to the activity of acetylcholine esterase (AChE) (Baek et al 2005;Lee et al 2007).…”
Section: Introductionmentioning
confidence: 99%
“…Field‐evolved pyrethroid‐resistance in DBM collected from 16 field sites in southern Australia was related to at least three different mutations (L1014F, T929I and F1020S) in the para sodium channel gene (Endersby et al ., ). Metabolic mechanisms of pyrethroid resistance, which may involve detoxification by the microsomal P450‐dependent monooxygenase system, esterases or glutathione S‐transferases, have also been reported in DBM (Sun et al ., ; Eziah et al ., ). It is possible that the resistance in any one individual comprises more than one mechanism (Schuler et al ., ; Lambkin & Furlong, ).…”
Section: Introductionmentioning
confidence: 97%