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Development of Resistance to Transgenic Plants 373<br />

were 16.9 to 39.9 ng cm 2 , and the LC 90 values were 40.3 to 157 ng cm 2 . The most sensitive<br />

Southwestern corn borer colony was collected from the Mississippi delta exhibiting an<br />

LC 50 value of 22.6 ng cm 2 , which displayed the widest LC 90 confi dence limits of 40.3 to 94.8<br />

ng cm 2 . This baseline data can be used for monitoring of resistance to Cry9C in the future.<br />

Baseline susceptibility studies have also been carried out for Cry1Ab to fall armyworm,<br />

Spodoptera frugiperda ( J.E. Smith) (Lynch et al., 2003). Comparison of LC 50 values for various<br />

colonies did not indicate an appreciable change in susceptibility of this insect from 1998<br />

to 2000.<br />

The LC 50 for diamondback moth, Plutella xylostella (L.), larvae from different locations in<br />

India varied from 1.0 to 10.97 mg per liter. Nine generations of selection for resistance<br />

resulted in an increase in LC 50 from 2.76 to 5.28 mg per liter (using a selection pressure of<br />

6.4 mg per liter), indicating that there is a possibility of developing resistance to Bt in this<br />

insect in India (Mohan and Gujar, 2000). The susceptibility to different toxin proteins of Bt<br />

ranged from 0.14 to 3.74 μg mL 1 for Cry1Aa, 0.007 to 1.25 for Cry1Ab, 0.18 to 2.47 for Cry1Ac,<br />

and 0.12 to 3.0 μg for Cry1C (Mohan and Gujar, 2002). There were small differences in<br />

susceptibility of Sesamia nonagrioides (Lefebre) populations, but no differences were observed<br />

in two populations of O. nubilalis in Spain. In another study, differences in fi ve populations<br />

of O. nubilalis from the United States were fi ve-fold in susceptibility to Dipel, but the populations<br />

responded quite rapidly for resistance to Bt, indicating that low levels of susceptibility<br />

do not necessarily imply low potential to respond to selection pressure. Very high differences<br />

in susceptibility to Bt products and Cry1Ab and Cry1Ac have been found in the case<br />

of H. virescens and H. zea (Stone and Sims, 1993; Zhao et al., 1996; Wu, Gou, and Nan, 1999).<br />

Effect of Host Plant on Insect Susceptibility to Cry Proteins<br />

The susceptibility of neonates of H. armigera to B. thuringiensis ssp. kurstaki (HD-73)<br />

ranged from twofold (LC50 84.5 to 164.2 μg per liter) for insects collected from chickpea<br />

to about fi ve-fold (LC50 51.1 to 247.7 μg per liter) for insects collected from cotton (Gujar<br />

et al., 2004) (Figure 12.2). The insects collected from pearl millet were twice as tolerant as<br />

those collected from cotton and sunfl ower at Sirsa, Haryana, India. Host-specifi c colonies<br />

raised from insects collected from cotton in Bhatinda, Punjab, India (by incorporating<br />

cabbage, caulifl ower, chickpea, green pea, pearl millet, and pigeonpea into the artifi cial<br />

diet) indicated that insects reared on cabbage-, caulifl ower-, and pearl millet-based diets<br />

% mortality/100 ppm<br />

80<br />

70<br />

60<br />

50<br />

40<br />

30<br />

20<br />

10<br />

0<br />

Pigeonpea Lady's finger Tomato<br />

Delhi Madurai Vijayawada<br />

Population and Host crop<br />

FIGURE 12.2 Variation in susceptibility of Helicoverpa armigera to Bacillus thuringiensis across host plants.<br />

(From Gujar, G.T. et al., 2004. Entomologia Experimentalis et Applicata 113: 165–172. With permission.)

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