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Enzymes mediating resistance to lambda-cyhalothrin in Eriopis connexa (Coleoptera: Coccinellidae).
Rodrigues, Agna R S; Siqueira, Herbert A A; Torres, Jorge B.
Afiliação
  • Rodrigues AR; Departamento de Agronomia/Entomologia, Universidade Federal Rural de Pernambuco, Av. Dom Manoel de Medeiros S/N, Dois Irmãos, Recife, PE 52171-900, Brazil. Electronic address: agnarodrigues@yahoo.com.br.
  • Siqueira HA; Departamento de Agronomia/Entomologia, Universidade Federal Rural de Pernambuco, Av. Dom Manoel de Medeiros S/N, Dois Irmãos, Recife, PE 52171-900, Brazil.
  • Torres JB; Departamento de Agronomia/Entomologia, Universidade Federal Rural de Pernambuco, Av. Dom Manoel de Medeiros S/N, Dois Irmãos, Recife, PE 52171-900, Brazil.
Pestic Biochem Physiol ; 110: 36-43, 2014 Mar.
Article em En | MEDLINE | ID: mdl-24759049
ABSTRACT
Resistance to widely used insecticide, lambda-cyhalothrin, was recently reported in the predatory lady beetle Eriopis connexa (Germar) (Coleoptera Coccinellidae). However, to understand whether metabolic mechanisms underlie such resistance, synergism bioassays and in vitro studies were carried out by using inhibitors and model substrates for enzymatic assays, respectively. The LD50s estimated for susceptible and resistant populations ηg of lambda-cyhalothrin/insect, and thus, a 22-fold difference in resistance ratio. Synergism ratios for the susceptible population with piperonyl butoxide (PBO), diethyl maleate (DEM), triphenyl phosphate (TPP), and S,S,S-tributylphosphorotrithioate (DEF) were respectively 33.8-, 0.24-, 0.35-, and 4.25-fold, while for the resistant population, they were 1463.0-, 0.79-, 0.85-, and 282.6-fold, respectively. The synergized resistance ratios were 0.50-, 2.00-, 6.75-, and 8.77-fold with PBO, DEF, DEM, and TPP, respectively, while resistance was virtually suppressed with DEF. The esterase exhibited 4.16-, 4.03-, and 5.38-fold greater activity towards formation of α-naphthol, ß-naphthol, and 4-nitrophenol in the resistant population of E. connexa than in the susceptible population. The activity of esterase depended on concentrations of DEF applied, either using α-naphthol or ß-naphthol, which completely inhibited the activity at 636 ηM. The PBO inhibited the ß-naphthol formation in approximately 50%, suggesting it as inhibitor of esterases. The activities of glutathione-S-transferase were similar and corresponded to 0.36-0.47 ηmol(-1) min(-1)µg of protein, for S and R populations, respectively. Similarly, the activities of cytochrome P450-dependent microsomal monooxygenases were 0.04 and 0.05 ηmol(-1) min(-1)µg of protein. The native gel indicated that the formation of ß-naphthol was completely inhibited by methyl-paraoxon, but only partially inhibited by eserine, TPP, and PBO. Although other studies with DEF and PBO have demonstrated strong inhibition of type B carboxylesterase associated with insecticide resistance, the results reported here do not rule out metabolism by cytochrome P450-dependent microsomal monooxygenases as a factor conferring E. connexa resistance to lambda-cyhalothrin and confirmed that PBO may also act by inhibiting esterases of insects.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piretrinas / Besouros / Proteínas de Insetos / Esterases / Inseticidas / Nitrilas Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Piretrinas / Besouros / Proteínas de Insetos / Esterases / Inseticidas / Nitrilas Idioma: En Ano de publicação: 2014 Tipo de documento: Article