A synthetic laboratory population of the diamondback moth, Plutella xylostella, was used to validate the F2 screen developed for detecting the frequency of rare resistance alleles to Cry1Ac and Cry1C toxins of Bacillus thuringiensis (Bt). We made 106 F2 families for screening of Cry1Ac or Cry1C resistance alleles using both transgenic broccoli and an artificial diet overlay assay with a diagnostic dose. When using Bt broccoli plants as the F2 screen method, only one F2 family was detected for Cry1Ac resistance and no family was detected for Cry1C resistance. Six families were detected for either Cry1Ac or Cry1C resistance using the diet assay. Four F2 families were confirmed to contain one copy of an allele resistant to Cry1Ac in the original single-pairs and four other F2 families contained an allele resistant to Cry1C. Our results suggest that using transgenic plants expressing a high level of a Bt toxin in an F2 screen may underestimate the frequency of resistance alleles with high false negatives, or fail to detect true resistance alleles. The diagnostic diet assay was a better F2 screen method to detect alleles, especially for the Cry1Ac resistance with monogenic inheritance in the diamondback moth. Careful validation of the screen method for each insect-crop system is necessary before the F2 screen can be used to detect rare Bt resistance alleles in field populations.
Species 1: Lepidoptera Plutellidae Plutella xylostella (diamondback moth)
Keywords: Bacillus thuringiensis, transgenic crops
The ESA 2001 Annual Meeting - 2001: An Entomological Odyssey of ESA