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1.
Insect Mol Biol ; 8(4): 539-44, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10620049

ABSTRACT

A novel concept applying baculovirus-mediated gene silencing to study insect gene function and regulation is described in this paper. A recombinant baculovirus, Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV), was constructed with the juvenile hormone esterase (JHE) gene from the tobacco budworm Heliothis virescens in the antisense orientation, driven by the viral p10 promoter. Infection with this recombinant greatly reduced the haemolymph JHE level and resulted in aberrant morphogenesis of final-instar H. virescens larvae. The body organization remained larval, although the cuticle became hard and brown, similar to pupal cuticle. These results demonstrated that baculovirus-mediated gene silencing can be accomplished and utilized to dissect insect development and to design a new class of baculovirus insecticides.


Subject(s)
Gene Silencing , Moths/growth & development , Nucleopolyhedroviruses , Animals , Carboxylic Ester Hydrolases/genetics , DNA, Antisense , Developmental Biology/methods , Larva/growth & development , Moths/genetics , Moths/virology
2.
Arch Insect Biochem Physiol ; 32(3-4): 659-69, 1996.
Article in English | MEDLINE | ID: mdl-8756313

ABSTRACT

Applying the proinsecticide principle developed earlier for neurotoxic carbamate insecticides, a series of new N-sulfenylated, N-sulfinylated, and N-sulfonylated derivatives of fenoxycarb were synthesized and evaluated for juvenile hormone mimicking activity. Laboratory evaluations of the compounds using Pieris brassicae and Sitophilus oryzae, as well as field experiments using Bemisia tabaci, showed that several symmetrical biscarbamates with either a sulfenyl or sulfinyl bridge possessed higher activity than the parent carbamate. From the unsymmetrical compounds containing biologically inert derivatizing moieties, one of the sulfenylated biscarbamates also showed improved activity against P. brassicae. The changes in the biological activity of the sulfur-containing derivatives compared to that of the parent compound are attributed to the modified physicochemical characteristics, i.e., increased lipophilicity facilitating penetration, transport, as well as protection of the compound from metabolism.


Subject(s)
Carbamates/pharmacology , Insecticides/pharmacology , Phenylcarbamates , Animals , Biological Assay , Butterflies , Carbamates/chemical synthesis , Carbamates/chemistry , Coleoptera , Insecta , Insecticides/chemical synthesis , Insecticides/chemistry , Juvenile Hormones/pharmacology , Molecular Mimicry , Molecular Structure , Prodrugs/chemical synthesis , Prodrugs/chemistry , Prodrugs/pharmacology , Sulfur/chemistry
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