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

Mechanisms of Resistance to Insects<br />

Knowledge of insect-plant relationships and the mechanisms that contribute to insect<br />

resistance is critical for developing germplasm with high yield and durable resistance<br />

(H.C. Sharma, 1994). In view of limited success in the past in developing crop cultivars<br />

with resistance to insect pests by using known sources of resistance, there is a need to<br />

identify genotypes with diverse mechanisms (genes), and pyramid the resistance genes<br />

to increase the levels and diversify the bases of resistance. Information on different mechanisms<br />

of resistance to insects, such as antixenosis or nonpreference, antibiosis, and tolerance<br />

is discussed below.<br />

Antixenosis<br />

Antixenosis or nonpreference is expressed in terms of unsuitability of the host plant for<br />

oviposition or feeding. The word antixenosis is derived from the Greek, xeno, meaning<br />

“guest.” It describes the inability of a plant to serve as a host to a herbivore insect, and<br />

forces the insect to change its host plant for feeding and oviposition. Antixenotic (nonpreference)<br />

resistance reduces the rate of both initial and successive insect population buildup.<br />

Antixenotic resistance may also shift the insect population to other fi elds of the same crop<br />

or to other host plants of the insect. It is due to physico-chemical characteristics of the host<br />

plant that affect insect behavior adversely, resulting in selection of an alternative host<br />

plant. Absence of physico chemical stimuli that are involved in selection of the host plant<br />

or presence of repellents, deterrents, and antifeedants contribute to the antixenosis mechanism<br />

of resistance. Sensory cues that mediate host selection for oviposition include visual,<br />

tactile, and chemical stimuli (Thompson and Pellmyr, 1991). Antixenosis is an important<br />

component of resistance to the Hessian fl y, Mayetiola destructor (Say) in wheat (Roberts<br />

et al., 1979), the onion fl y, Hylemyia antiqua (Meigen) in onion, the carrot fl y, Psila rosae (Fab.)<br />

in carrot (Stadler and Buser, 1984), and the Asiatic stem borer, Chilo suppressalis (Walker)<br />

in rice (Saxena, 1986). Antixenosis for oviposition is a major component of resistance to the<br />

shoot fl y, Atherigona soccata (Rondani) and midge, Stenodiplosis sorghicola (Coquillett) in<br />

sorghum (Figure 5.1) (H.C. Sharma and Vidyasagar, 1994; H.C. Sharma and Nwanze, 1997;<br />

H.C. Sharma, Franzmann, and Henzell, 2002). Cotton genotypes with red and okra leaf<br />

No. of eggs/100 spikelets<br />

180<br />

160<br />

140<br />

120<br />

100<br />

80<br />

60<br />

40<br />

20<br />

0<br />

DJ 6514<br />

AF 28<br />

TAM 2566<br />

IS 15107<br />

FIGURE 5.1 Oviposition by the females of sorghum midge, Stenodiplosis sorghicola, on different sorghum genotypes<br />

under no-choice conditions in the headcage.<br />

CSH 1<br />

Swarna

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