Plutella xylostella is a major global pest with increasing resistance to insecticides. ATP-binding cassette (ABC) transporters are implicated in the metabolism of insecticides, but their molecular mechanisms remain poorly understood. Here, we identified and characterized the role of P. xylostella ABCC3 (PxABCC3) in mediating the metabolism of chemical insecticides and its function as a receptor for Bacillus thuringiensis (Bt) toxins. PxABCC3 and its mutant variants were cloned, expressed, and purified, followed by biochemical and structural analyses. Our results showed that PxABCC3 exhibits typical ABC transporter structural features and its ATPase activity is significantly modulated by chlorpyrifos and pyripro... More
Plutella xylostella is a major global pest with increasing resistance to insecticides. ATP-binding cassette (ABC) transporters are implicated in the metabolism of insecticides, but their molecular mechanisms remain poorly understood. Here, we identified and characterized the role of P. xylostella ABCC3 (PxABCC3) in mediating the metabolism of chemical insecticides and its function as a receptor for Bacillus thuringiensis (Bt) toxins. PxABCC3 and its mutant variants were cloned, expressed, and purified, followed by biochemical and structural analyses. Our results showed that PxABCC3 exhibits typical ABC transporter structural features and its ATPase activity is significantly modulated by chlorpyrifos and pyriproxyfen, and other insecticides. Surface plasmon resonance confirmed direct insecticide binding. Overexpression of PxABCC3 in insect cells enhanced survival under chlorpyrifos and pyriproxyfen exposure, suggesting an efflux-mediated detoxification mechanism. The analysis of predicted complex structures of PxABCC3 with chlorpyrifos or pyriproxyfen identified overlapping substrate-binding pockets within the transmembrane channel. Furthermore, PxABCC3 functions as a receptor for Bt toxins Cry1Ac and Cry1Ab, as evidenced by toxin-induced ATPase activation, binding affinity, and cellular swelling in transfected cells. We further predicted the complex structure of PxABCC3-Cry1Ab, revealing that Cry1Ab binds to the extracellular side of PxABCC3 via domain II through electrostatic complementarity and hydrogen-bond networks. These findings provide novel insights into mechanistic understanding at the protein level, especially with respect to structural characteristics and substrate-binding specificity, and highlight PxABCC3 as a potential target for pest control.
