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Mechanisms and Inheritance of Resistance to Insect Pests 135<br />

has been stopped because of its susceptibility to southern corn leaf blight, Bipolaris maydis<br />

(Nisikado and Miyake), which severely damaged maize crop in the United States in the<br />

1970s (Tatum, 1971). In pearl millet, most of the hybrids are based on A 1 cytoplasm (Burton<br />

and Athwal, 1967), and the hybrids based on 111A CMS line are less susceptible to the<br />

Oriental armyworm, Mythimna separata (Walker) than those based on 5141A and 5054A<br />

(H.C. Sharma, Bhatnagar, and Davies, 1982). Most of the sorghum hybrids are based on<br />

Milo (A 1) cytoplasm (Stephens and Holland, 1954), and a large number of these hybrids are<br />

highly susceptible to insect pests. Sorghum lines KS 34 to 39 are as susceptible as CKA<br />

(Combine Kafi r-based CMS lines) to greenbug, S. graminum (Ross and Kofoid, 1979).<br />

Cytoplasmic male-sterile lines are more susceptible to insects than the corresponding<br />

maintainer lines, suggesting that resistance to insects is infl uenced by the interaction of<br />

factors in the cytoplasm of the maintainer lines and the nuclear genes (H.C. Sharma, 2001;<br />

H.C. Sharma et al., 1994, 2004). Resistance to sorghum shoot fl y, A. soccata, sorghum midge,<br />

S. sorghicola, sugarcane aphid, Melanaphis sacchari (Zehntner), and shoot bug, Peregrinus<br />

maidis Ashmead, in F 1 hybrids of sorghum is infl uenced by CMS lines, while resistance to<br />

spotted stem borer, C. partellus is infl uenced by the restorer lines (H.C. Sharma et al., 2004;<br />

Dhillon et al., 2006a, 2006b). Hybrids based on insect-resistant male-sterile and restorer<br />

lines are resistant, while those based on insect susceptible CMS, and resistant, or susceptible<br />

restorer lines are susceptible to shoot fl y, sugarcane aphid, shoot bug, head bug, and<br />

midge (H.C. Sharma et al., 1996, 2000a; Dhillon et al., 2006a, 2006b). A 4M and A 4VzM cytoplasms<br />

in sorghum are less susceptible to shoot fl y than the A 1, A 2, and A 3 cytoplasms<br />

(Dhillon, Sharma, and Reddy, 2005; Dhillon et al., 2005; H.C. Sharma et al., 2005c). To overcome<br />

the problem of a narrow genetic base based on a single source of male sterility, efforts<br />

should be made to transfer the insect resistance genes into diverse genetic backgrounds or<br />

discover new sources of male-sterility that are less susceptible to insect pests.<br />

Genetics and Inheritance of Resistance to Insect Pests<br />

Information on genetics and inheritance of resistance to insect pests is important in crop<br />

improvement, which indicates the degree of ease or diffi culty involved in incorporating<br />

the resistance genes into the improved cultivars. Resistance to insects may be dominant or<br />

recessive. The general combining ability (GCA) of a cultivar to transmit resistance to the<br />

progeny is determined from the average resistance levels of the F 1 and F 2 plants in all<br />

crosses involving a particular genotype, while the specifi c combining ability (SCA) is a<br />

measure of the amount of resistance transferred by a genotype in a single cross to a<br />

particular parent. Heritability or variation observed in the progeny of a cross is another<br />

measure of inheritance of resistance, which may be affected by several factors. When several<br />

different alleles from genes in resistant plants contribute to variation for resistance to<br />

an insect species, these are called additive effects. Epistatic effects of alleles may also<br />

contribute to variation. The genetics and inheritance of resistance to insects has been discussed<br />

by Khush and Brar (1991), Panda and Khush (1995), and Smith (2005). Information<br />

on inheritance of resistance to insects in different crops is discussed below.<br />

Rice<br />

Many genes have been identifi ed in rice that contribute for resistance to brown planthopper,<br />

N. lugens, green leafhoppers, Nephotettix cincticeps Uhler and N. virescens, gall midge,

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