Abstract
Organophosphorus and carbamate insecticide resistance in Nilaparvata lugens is based on amplification of a carboxylesterase gene, NI-EST1. An identical gene occurs in susceptible insects. Quantitative real-time PCR was used to demonstrate that NI-EST1 is amplified 37-fold in the genome of resistant compared to susceptible planthoppers. Expression levels were similar to amplification levels, with 1-15-fold more NI-EST1 mRNA in individual insects and 5-11-fold more NI-EST1 mRNA in mass whole body homogenates of resistant females compared to susceptibles. These values corresponded to an 8-10-fold increase in esterase activity in the head and thorax of individual resistant insects. Although amplification, expression and activity levels of NI-EST1 in resistant N. lugens were similar, the correlation between esterase activity and NI-EST1 mRNA levels in resistant individuals was not linear.
| Original language | English |
|---|---|
| Pages (from-to) | 655-660 |
| Number of pages | 6 |
| Journal | Insect Molecular Biology |
| Volume | 9 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 1 Jan 2000 |
| Externally published | Yes |
Keywords
- Carboxylesterase
- Gene amplification
- Nilaparvata lugens
- Quantitative PCR
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