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238 Biotechnological Approaches for Pest Management and Ecological Sustainability<br />

and L235-4 (glandular trichomes), along with the cryV-Bt-transgenic lines of each genotype,<br />

were tested for resistance to potato tuber moth, P. operculella. Nearly 54% mortality<br />

was observed when fi rst-instar larvae were fed on the leaves of USDA8380-1. High levels<br />

of expression occurred in cryV-Bt transgenic lines, with up to 96% mortality. Walker et al.<br />

(2002) combined a QTL conditioning corn earworm resistance in soybean PI 229358, and<br />

cry1Ac transgene from the recurrent parent Jack-Bt into BC 2F 3 plants by marker-assisted<br />

selection. The segregating individuals were genotyped and SSR markers linked to an<br />

antibiosis/antixenosis QTL on linkage group M, and were tested for the presence of<br />

Cry1Ac. Few larvae of corn earworm and soybean looper survived on leaves expressing<br />

the Cry1Ac protein. Though not as great as the effect of Cry1Ac, the PI 229358-derived LG<br />

M QTL also had a detrimental effect on larval weights of both species, and on defoliation<br />

by corn earworm, but did not reduce defoliation by soybean looper, indicating that combining<br />

transgene- and QTL-mediated resistance to lepidopteran pests may be a viable<br />

strategy for insect control.<br />

Transgenic plants of cotton with Bt GNA conferred resistance to bollworm, H. armigera<br />

and the cotton aphid, A. gossypii (Z. Liu et al., 2003). Segregation of resistant and susceptible<br />

plants in F 2 and BC 1 populations fi tted the 3:1 and 1:1 ratios, respectively, indicating<br />

that resistance to bollworm was controlled by one pair of dominant genes and inherited in<br />

Mendelian manner with no cytoplasmic effects. Allelic tests showed that the resistance<br />

gene in transgenic line TBG and that of insect-resistant transgenic cotton strains Zhongxin<br />

94, R 19, Shanxi 94-24, Shuangkang 1, and Xinmian 33B might be inserted in different chromosomes.<br />

The Bt gene and OC gene have been co-transformed to tobacco chloroplast with<br />

the particle bombardment method. Transgenic tobacco containing both genes had enhanced<br />

toxicity to the larvae of corn earworm, H. zea, as compared to plants containing only the<br />

Bt or OC gene alone. The Bt and OC genes were inherited maternally (Su et al., 2002).<br />

Sugarcane plants transformed with both the GNA and a proteinase inhibitor from Nicotiana<br />

alata Link and Oho. caused a signifi cant negative effect on the weight gain of Dermolepida<br />

albohirtum (Waterhouse) larvae (Nutt et al., 2001). Transformed entomopathogenic virus<br />

that produces chitinase displayed enhanced insecticidal activity (Chit Kramer and<br />

Muthukrishnan, 1997). Chitinase also potentiates the effi cacy of the toxin from B. thuringiensis.<br />

Gahakwa et al. (2000) studied the stability of transgene expression in 40 independent<br />

rice plants representing 11 diverse cultivated varieties. Each line contained three or four<br />

different transgenes delivered by particle bombardment, either by co-transformation, or in<br />

the form of a co-integrate vector. Approximately 75% of the lines showed Mendelian inheritance<br />

of all transgenes, suggesting integration at a single locus. The levels of transgene<br />

expression varied among different lines, but primary transformants showing high-level<br />

expression of the GNA, gusA, hpt, and bar genes were transmitted to the progeny. Six transgenes<br />

(three markers and three insect resistance genes) were stably expressed over four<br />

generations of transgenic rice plants. Transgene expression was stable, and this represented<br />

a step toward genetic engineering from model varieties to elite breeding lines grown in<br />

different parts of the world.<br />

Conclusions<br />

The ideal transgenic technology should be commercially viable, environmentally benign<br />

(biodegradable), easy to use in diverse agroecosystems, and have a wide spectrum of

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