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Reconstruction of HaSNPV with helicoverpa hormone receptor 3
作者姓名:扈进冬  Shao  Honglian  Zhang  Yubao  Fu  Qiang  Sun  Chen  Wang  Jinxing  Zhao  Xiaofan
作者单位:[1]School of Life Sciences, Shandong University, Jinan 250100, P.R. China [2]School of Meclicine, Shangdong University, Jinan 250100, P.R. China
基金项目:国家自然科学基金 , 国家高技术研究发展计划(863计划) , 山东省自然科学基金
摘    要:In order to develop a more efficient virus for controlling the cotton bollworm Helicoverpa armigera, Helicoverpa hormone receptor 3 (HHR3), which is involved in the ecdysteroid regulatory pathway, was used to genetically modify wild HaSNPV. HaSNPV-HHR3 budded virus and occlusion body virus were constructed in three steps: preparation of pFastBacHaPhpP10-HHR3 donor plasmid, transposition of HHR3 into the HaBacHZ8 bacmid, and transfection of HzAM1 cells to get HaSNPV-HHR3 virus.HHR3 was proved to be expressed in the HaSNPV-HHR3 virus infected HzAM1 cells by immunoblotting. Results of bioassay indicated that the body weight of the HaSNPV-HHR3 infected larvae was lower than the larvae infected with wild virus and uninfected normal larvae, which suggests that HaSNPV-HHR3 delayed larval growth.

关 键 词:HaSNPV  激素受体  棉铃虫  鳞翅类
修稿时间:2006-06-13

Reconstruction of HaSNPV with helicoverpa hormone receptor 3
Hu Jindong,Shao Honglian,Zhang Yubao,Fu Qiang,Sun Chen,Wang Jinxing,Zhao Xiaofan.Reconstruction of HaSNPV with helicoverpa hormone receptor 3[J].High Technology Letters,2007,13(3):327-331.
Authors:Hu Jindong  Shao Honglian  Zhang Yubao  Fu Qiang  Sun Chen  Wang Jinxing  Zhao Xiaofan
Institution:1. School of Life Sciences, Shandong University, Jinan 250100, P.R. China
2. School of Life Sciences, Shandong University, Jinan 250100, P.R. China;School of Meclicine, Shangdong University, Jinan 250100, P.R.China
Abstract:In order to develop a more efficient virus for controlling the cotton bollworm Helicoverpa armigera,Helicoverpa hormone receptor 3 (HHR3), which is involved in the ecdysteroid regulatory pathway, was used to genetically modify wild HaSNPV. HaSNPV-HHR3 budded virus and occlusion body virus were constructed in three steps: preparation of pFastBacHaPhpP10-HHR3 donor plasmid, transposition of HHR3 into the HaBacHZ8 bacmid, and transfection of HzAM1 cells to get HaSNPV-HHR3 virus. HHR3was proved to be expressed in the HaSNPV-HHR3 virus infected HzAM1 cells by immunoblotting. Results of bioassay indicated that the body weight of the HaSNPV-HHR3 infected larvae was lower than the larvae infected with wild virus and uninfected normal larvae, which suggests that HaSNPV-HHR3 delayed larval growth.
Keywords:lepidoptera  noctuidae  Helicoverpa armigera  Helicoverpa armigera single nucleocapsid nucleopolyhedrovirus (HaSNPV)  Helicoverpa hormone receptor 3 (HHR3)  genetical manipulation  bioassay
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