Dr. Rod Mahon, Ms. Karen Olsen, Ms. Su Young, and Dr. Sharon Downes. CSIRO Entomology, GPO Box 1700, Canberra, ACT 2601, Canberra, Australia
From 1996 - 2004 Australia deployed the Cry1Ac expressing Ingard® (elsewhere Bollgard®) variety of Bt-cotton under a conservative resistance management plan whereby the transgenic crop was limited to 30% of the area planted to cotton. In 2002 Ingard® was replaced with the two gene (cry1Ac and cry2Ab) variety of Bt-cotton, Bollgard II®. Prior to the widespread use of Bollgard II® F2 screens were employed to detect alleles that conferred resistance to Cry1Ac or Cry2Ab. No alleles conferring resistance to Cry1Ac were discovered, however alleles that conferred resistance to Cry2Ab were found at a frequency of 0.003 (R. Mahon, K. Olsen S. Downes and S. Addison, 2007). Resistance in the first isolate (SP15) resulted from a single autosomal gene and was recessive (Mahon et al. 2007). Four of the 10 isolations of Cry2Ab resistance were examined through complementation tests and are allelic, and like SP15, recessive. Here we summarise our current knowledge of Cry2Ab resistance in H. armigera and present data from population cage experiments that test for fitness costs associated with this trait.