Journal
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY
Volume 174, Issue -, Pages -Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.pestbp.2021.104798
Keywords
Insecticide mode of action; Ryanodine receptor; RyR; Diamide insecticides
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The Ryanodine receptor (RyR) is an intracellular calcium channel critical for regulating insect muscle contraction and is the target site of diamide insecticides. A new class of RyR activators, pyrrole-2carboxamides, has been discovered through target-based screening, showing comparable potency to commercial diamides against fruit fly RyR. However, poor insecticidal activity in whole-insect screens is attributed to differential selectivity among insect receptors and rapid detoxification.
The ryanodine receptor (RyR) is an intracellular calcium channel critical to the regulation of insect muscle contraction and the target site of diamide insecticides such as chlorantraniliprole, cyantraniliprole and flubendiamide. To-date, diamides are the only known class of synthetic molecules with high potency against insect RyRs. Target-based screening of an informer library led to discovery of a novel class of RyR activators, pyrrole-2carboxamides. Efforts to optimize receptor activity resulted in analogs with potency comparable to that of commercial diamides when tested against RyR of the fruit fly, Drosophila melanogaster. Surprisingly, testing of pyrrole-2-carboxamides in whole-insect screens showed poor insecticidal activity, which is partially attributed to differential selectivity among insect receptors and rapid detoxification. Among various lepidopteran species field resistance to diamide insecticides has been well documented and in many cases has been attributed to a single point mutation, G4946E, of the RyR gene. As with diamide insecticides, the G4946E mutation confers greatly reduced sensitivity to pyrrole-2-carboxamides. This, coupled with findings from radioligand binding studies, indicates a shared binding domain between anthranilic diamides and pyrrole-2-carboxamides.
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