The red imported fire ant (Solenopsis invicta), a worldwide invasive and polyphagous pest, and often nests in residential areas. Finding an alternative pesticide that is both effective on S. invicta and environmentally friendly is urgent and crucial. Fluralaner, a novel isoxazoline insecticide, has been proven to possess selective toxicity for insects versus mammals and has been safe for mammals and non-target organisms, suggesting its potential in pest management. However, little toxicity information is available for the controlment of S. invicta. In this article, we studied the toxicity of fluralaner against S. invicta systematically, and the roles of metabolism-related enzymes in the metabolism process of fluralaner. The toxicity results showed that the topical application and feeding application were all effective for S. invicta. Moreover, fluralaner can be transmitted among workers by contacting and feeding which leads to a toxic reaction among nestmates. By exploring the biochemistry change, we found cytochrome P450 monooxygenase (P450) may be involved in the detoxification of fluralaner as well as carboxylesterase (CarE), but not glutathione S-transferase (GST). Synergism assays gave solid evidence in which piperonyl butoxide, an activity inhibitor of P450, increased the toxicity of fluralaner to S. invicta. Importantly, with the RNAi treatment, four of S.invicta P450 genes were significantly inhibited and showed more sensitivity to fluralaner at LC50 concentration. Our result indicated that fluralaner could be a potential alternative pesticide in S. invicta control. And CYP9AS16, CYP6AS161, CYP6SQ20, and CYP336A45 genes were closely associated with the metabolism process of fluralaner.
Keywords: Cytochrome P450 enzyme; Fluralaner; Solenopsis invicta; Toxicity.
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