4.7 Article

Acetylcholinesterase point mutations putatively associated with monocrotophos resistance in the two-spotted spider mite

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PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY
卷 96, 期 1, 页码 36-42

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ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.pestbp.2009.08.013

关键词

Acaricide; Monocrotophos; Resistance; Tetranychus urticae; Acetylcholinesterase; Point mutation

资金

  1. Bio-Green 21 program [500-20060021]
  2. Brain Korea 21 program

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Molecular mechanisms of monocrotophos resistance in the two-spotted spider mite (TSSM), Tetranychus urticae Koch, were investigated. A monocrotophos-resistant strain (AD) showed ca. 3568- and 47.6-fold resistance compared to a susceptible strain (UD) and a moderately resistant strain (PyriF), respectively. No significant differences in detoxification enzyme activities, except for the cytochrome P450 monooxygenase activity, were found among the three strains. The sensitivity of acetylcholinesterase (AChE) to monocrotophos, however, was 90.6- and 41.9-fold less in AD strain compared to the UD and PyriF strains, respectively, indicating that AChE insensitivity mechanism plays a major role in monocrotophos resistance. When AChE gene (Tuace) sequences were compared, three point mutations (G228S, A391T and F439W) were identified in Tuace from the AD strain that likely contribute to the AChE insensitivity as predicted by structure analysis. Frequencies of the three mutations in field populations were predicted by quantitative sequencing (QS). Correlation analysis between the mutation frequency and actual resistance levels (LC50) of nine field populations suggested that the G228S mutation plays a more crucial role in resistance (r(2) = 0.712) compared to the F439W mutation (r(2) = 0.419). When correlated together, however, the correlation coefficient was substantially enhanced (r(2) = 0.865), indicating that both the F439W and G228S mutations may work synergistically. The A391T mutation was homogeneously present in all field populations examined, suggesting that it may confer a basal level of resistance. (c) 2009 Elsevier Inc. All rights reserved.

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