Exploring the function of the host immune system can help to understand the host-parasitoid interaction. Prophenoloxidase (PPO) is crucial in defensive melanization during the encapsulation of wasp eggs. However, the existence of multiple PPO sequences increases the difficulty of exploring the specific functions of individual PPOs. We previously identified three PPOs in the nipa palm hispid beetle, Octodonta nipae. Our current work showed that OnPPO1 and OnPPO2 possessed the typical characteristics of the type III copper family, but OnPPO3 lacked the conserved histidine residues, and its active sites were substituted with Gln. OnPPOs showed the highest expression in hemocytes, but OnPPO3 presented extremely low abundance compared with that of OnPPO1 and OnPPO2, and only OnPPO1 showed a quick response after wasp infection. OnPPO1 knockdown decreased the encapsulation index and inhibited melanization, whereas silencing of OnPPO3 appeared to have no adverse effect on encapsulation and melanization, and silencing of OnPPO2 presented low RNAi efficiency. Moreover, the cleavage of recombinant OnPPO1 produced a 62 kDa fragment with high PO activity. OnPPO1 could be produced by oenocytoids, granulocytes and plasmatocytes, and was distributed around wasp eggs during capsule formation. Overall, our results indicate that proteolytic cleavage of OnPPO1 plays key roles in the melanized encapsulation of wasp eggs. This finding illuminates the mechanism of PPO activation in this invasive beetle and provides guidance for its biological control.
Keywords: Encapsulation; Melanization; Octodonta nipae; Parasitoid; Prophenoloxidase.
Copyright © 2023. Published by Elsevier Ltd.