Li Xu , Yin Huang , Zezheng Liu , Qi Zuo , Minghui Long , Yichen Fu , Runqiang Liu , Yunchao Kan , Dongzhi Li
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引用次数: 0
Abstract
Ribavirin is a nucleoside analog used to control virus disease clinically. In this study, toxicity determination, transcriptome analysis and ELISA were employed to explore its toxicity and potential mechanism on Helicoverpa armigera larvae. Results suggested that ribavirin showed stomach toxicity to H. armigera, but low contact toxicity. Chemicals 1,2,4-triazole and 1,2,4-triazole-3-carboxamide showed low stomach toxicity to H. armigera, indicating 1,2,4-triazole and furanose were both the key chemical structure to ensure the larvicidal activity of ribavirin. Transcriptome and qRT-PCR results validated that ribavirin treatment inhibited the expression of genes in chitin biosynthesis, lipid biosynthesis and cuticle protein genes. Ribavirin treatment also decreased the Juvenile Hormone (JH) titer, but showed no influence to ecdysone titer. These results indicated that ribavirin treatment inhibited JH biosynthesis and interfered new cuticle formation, which resulted to the failure of H. armigera larvae molting and normal pupation. These results provided a novel lead compound for IGR development to control H. armigera.
期刊介绍:
The journal publishes original research papers, review articles and short communications in the basic and applied area concerning insects, mites or other arthropods and nematodes of economic importance in agriculture, forestry, industry, human and animal health, and natural resource and environment management, and is the official journal of the Korean Society of Applied Entomology and the Taiwan Entomological Society.