All abuzz: Larvicidal flavonoids inhibit key enzyme in yellow fever mosquitoes
In a study published this month in BMC Biology, researchers from the University of Tsukuba have revealed that particular flavonoids inhibit an enzyme involved in the formation of a key insect hormone in the yellow fever mosquito, Aedes aegypti.
Mosquito-borne diseases are a major component of the worldwide burden of infectious disease in humans. Aedes aegypti is from a group of mosquitoes that can spread a number of viruses that cause infectious diseases in humans, including dengue fever, yellow fever, and Zika. In the wild, A. aegypti has begun to show resistance to insecticides, revealing a need for new types of pesticides for targeting this species.
“Flavonoids — a type of metabolic product from plants, fungi, and other organisms — can interfere with insect development and physiology, and have the ability to kill larvae of A. aegypti,” says senior author of the study, Professor Ryusuke Niwa. “Flavonoids are thought to be relatively safe for the environment, as well as human and animal health.”
To investigate how flavonoids can kill mosquito larvae, the researchers analyzed the activities of several flavonoids in A. aegypti, including daidzein, which has previously been identified as a larvicide for this species. The team found that the flavonoids inhibit the activity of glutathione S-transferase Noppera-bo (Nobo); in A. aegypti, Nobo is an enzyme involved in the biosynthesis of the hormone ecdysone.
Ecdysone is an insect steroid hormone, or ecdysteroid, required for the initiation of metamorphosis and regulation of molting. Because ecdysteroids are key to the life cycle of insects, chemical inhibitors of enzymes involved in making these hormones, including Nobo, are thought to be insect growth regulators (IGRs) that disrupt development in insects without affecting other organisms.
“We also discovered that, of the flavonoids we tested, desmethylglycitein (DMG) was the most efficient Nobo inhibitor in this species, even more so than daidzein,” says Professor Niwa. “DMG showed larvicidal activity against A. aegypti, and indicated promise for DMG-based insecticides in the future.”
The high prevalence of resistance in mosquitoes to current insecticides in some areas urgently requires the development of new insecticides with different chemical structures and targeting pathways from those currently in use. The results of this study offer a new avenue for developing new IGRs that are environmentally friendly and can be used for the control of mosquito populations by inhibiting the biosynthesis of ecdysteroids.