Biochemical and Biophysical Research Communications 2007-02-16

Mutations of acetylcholinesterase1 contribute to prothiofos-resistance in Plutella xylostella (L.).

Dae-Weon Lee, Jae Young Choi, Won Tae Kim, Yeon Ho Je, Jong Tae Song, Bu Keun Chung, Kyung Saeng Boo, Young Ho Koh

Index: Biochem. Biophys. Res. Commun. 353(3) , 591-7, (2007)

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Abstract

Insensitive acetylcholinesterase (AChE) is involved in the resistance of organophosphorous and carbamate insecticides. We cloned a novel full-length AChE cDNA encoding ace1 gene from adult heads of the diamondback moth (DBM, Plutella xylostella). The ace1 gene encoding 679 amino acids has conserved motifs including catalytic triad, choline-binding site and acyl pocket. Northern blot analysis revealed that the ace1 gene was expressed much higher than the ace2 in all examined body parts. The biochemical properties of expressed AChEs showed substrate specificity for acetylthiocholine iodide and inhibitor specificity for BW284C51 and eserine. Three mutations of AChE1 (D229G, A298S, and G324A) were identified in the prothiofos-resistant strain, two of which (A298S and G324A) were expected to be involved in the prothiofos-resistance through three-dimensional modeling. In vitro functional expression of AChEs in Sf9 cells revealed that only resistant AChE1 is less inhibited with paraoxon, suggesting that resistant AChE1 is responsible for prothiofos-resistance.