Selection, mechanism, cross resistance and stability of spinosad resistance in Spodoptera litura (Fabricius) (Lepidoptera: Noctuidae)

Spodoptera litura is one of the most destructive pests in Pakistan and in many other regions of the world. A field collected population of S. litura was selected with spinosad for eleven generations under controlled laboratory conditions to study the cross resistance, mechanism and stability of spinosad resistance in S. litura. The resistance to spinosad in S. litura increased 3921-fold (after eleven generations of selection with spinosad) as compared to a susceptible population of S. litura. No cross resistance between spinosad and ernamectin benzoate, methoxyfenozide, fipronil, indoxacarb, profenofos, lufenuron or deltamethrin was found in the spinosad-selected population of S. litura. To find the possible mechanism of spinosad resistance in S. litura two synergists, Piperonyl butoxide (PBO), S, S, S-tributyl phosphorotrithioate (DEF) were tested on the susceptible and resistant strains and on the un-selected field population. The values of the synergism ratios of PBO and DEF were 2.33 and 1.06 for the spinosad-selected strain, 1.36 and 1.06 for the un-selected field population and 1.14 and 1.00 for the susceptible strain, respectively. As high PBO ratio indicates the role of microsomal O-demethylase in causing spinosad resistance in S. litura. The spinosad-resistant and field populations of S. litura were reared without any selection pressure from the 12th to the 16th generation (G(12)-G(16)). The spinosad resistance decreased from 3921 to 678-fold in the spinosad-resistant population and from 31.1 to 15.1-fold in the un-selected population of S. litura as compared to the susceptible strain. Spinosad resistance in S. litura has a high reversion rate (-0.15) which indicates that spinosad resistance in S. litura is unstable and can be easily managed by switching off the selection pressure for a few generations or alternating with insecticides having different modes of action. (C) 2013 Elsevier Ltd. All rights reserved.