A recombinant Helicoverpa armigera nucleopolyhedrovirus (HearNPV) expressing the insect-selective neurotoxin (RjAa17f) from Cuban scorpion Rhopalurus junceus was constructed by replacing the UDP-glucosyltransferase gene (egt) using λ-red homologous recombination system. Another egt deleted control HearNPV was constructed in a similar way by inserting egfp gene into the egt locus. One-step viral growth curve and viral DNA replication curve analysis confirmed that the recombination did not affect the viral growth and DNA replication in host cells. There is no discernable difference in occlusion-body morphogenesis between RjAa17f-HearNPV, Egfp-HearNPV and HZ8-HearNPV, which was confirmed by transmission electron microscopy analysis. However, the insecticidal activity of RjAa17f-HearNPV is enhanced against the third instar H. armigera larvae according to the bioassay on virulence comparison. There is a dramatic reduction (56.9%) in median lethal dose (LD ) and also a reduction (13.4%) in median survival time (ST ) for the recombinant RjAa17f-HearNPV compared to the HZ8-HearNPV, but only a 27.5% reduction in LD and 10.1% reduction in ST value when Egfp-HearNPV is compared with HZ8-HearNPV. The daily diet consumption analysis showed that the RjAa17f-HearNPV was able to inhibit the infected larvae feeding compared with the egt minus HearNPV. These results demonstrated that this novel recombinant RjAa17f-HearNPV could improve the insecticidal effect against its host insects and RjAa17f could be a considerable candidate for other recombinant baculovirus constructions.

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