Transgenic Bt maize expressing the Cry1Ab toxin is poorly effective for suppressing populations of two non-target Lepidoptera, Mythimna unipuncta and Helicoverpa armigera. In order to determine the mechanisms that may be involved in this poor effectiveness, last instar larvae of the two Lepidoptera were fed with a diet containing lyophilized leaves with Bt vs non-Bt toxin for different periods; additionally, some larvae fed on Bt diet were transferred to non-Bt diet for an additional period. In the experimental larvae, we measured the growth (weight) gain from just before treatment to after the end of the treatment, and the Cry1Ab contents in the hemolymph, the peritrophic membrane and its contents and midgut epithelium. Effects of the treatments on the midgut epithelium were observed by light and transmission electron microscopy. It was seen that multiple mechanisms can be involved in the low susceptibility of the two Lepidoptera. The low content of the toxin within the peritrophic membrane 48h after ingestion indicates a high rate of toxin elimination in this space. Moreover, M. unipuncta larvae fed on the Bt diet displayed a similar growth gain index to those fed on the non-Bt diet, and showed an increasing elimination rate during the experiment. Little toxin reached the midgut epithelium, indicating a low permeability of the peritrophic membrane or a low affinity at the binding sites. Larvae fed on the Bt toxin showed rapid recovery in weight gain and in the midgut epithelium, and also showed overcompensation mechanisms.

Three transgenic maize hybrids, viz. Prabal YG, Hishell YG and Double YG, producing Bacillus thuringiensis (Bt) Cry1Ab protein (event Mon 810), were evaluated under field and laboratory conditions for their resistance to spotted stemborer Chilo partellus (Swinhoe). The Bt maize hybrids suffered less damage than their non-Bt iso-hybrids with respect to per cent plant infestation (0.0–0.6), leaf injury rating (1.0–1.1) and per cent stem tunnelling. These hybrids also resulted in significantly higher larval mortality (79.4–100.0%) in laboratory bioassays. The toxin protein produced in leaves was equally effective against neonates and 15-day-old larvae. Neonate larvae consumed less leaf area (5.0–13.8%) in case of Bt hybrids than their non-Bt iso-hybrids.

Various insect pests, of which stemborers are the most widely distributed and damaging, affect about 30 out of the 35 million hectares planted with maize in developing countries. Chemical control, biological control; cultural methods and host plant resistance constitute the four general approaches to stemborer control. The use of stemborer-resistant maize increases farming efficiency by both reducing yield losses from stemborer damage and reducing or eliminating the cost of insecticides and other inputs. In the past, CIMMYT followed conventional breeding methods to develop germplasm resistant to stemborers and molecular technology, quantitative trait loci (QTL) in marker-assisted selection (MAS) to select for improved stemborer resistance in elite lines. More recently, CIMMYT has developed the capacity to produce transgenic maize with resistance factor(s) derived from genes that encode delta-endotoxins derived from the soil bacterium Bacillus thuringiensis (Bt). A sub-tropical source population with multiple borer resistance (MBR population) was developed by recombination and recurrent selection under infestation with four stemborer species. Marker-assisted selection is being used in two African countries to promote the transfer of resistance into elite and adapted germplasm. The Insect Resistant Maize for Africa (IRMA) project is pursuing the transfer of Bt-based resistance to adapted maize germplasm, initially in Kenya, but later to other interested African countries. CIMMYT's varietal release strategy is to pyramid Bt genes into maize populations with existing multigenic pest resistance, in order to enhance both the levels and durability of plant resistance to maize pests. This paper discusses the various approaches used at CIMMYT to develop stemborer-resistant maize germplasm.