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Toxicity and binding analyses of Bacillus thuringiensis toxin Vip3A in Cry1Ac-resistant and-susceptible strains of Helicoverpa armigera (Hübner)
  • ISSN号:2095-1353
  • 期刊名称:《应用昆虫学报》
  • 时间:0
  • 分类:S476.11[农业科学—农业昆虫与害虫防治;农业科学—植物保护] TQ453.401[化学工程—农药化工]
  • 作者机构:[1]State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, 100193 Beijing, P.R. China, [2]Institute of Cotton Research, Hebei Academy of Agriculture and Forestry Sciences, Shijiazhuang 050051, P.R. China, [3]College of Plant Science and Technology, Huazhong Agricultural University, 430070 Wuhan, P.R.China
  • 相关基金:This research was supported by the Key Project for Breeding Genetically Modified Organisms, China (2014ZX08011-002) and the National Natural Science Foundation of China (30971921, 31321004).
中文摘要:

The Bacillus thuringiensis vegetative insecticidal protein, Vip3 A, represents a new family of Bt toxin and is currently applied to commercial transgenic cotton. To determine whether the Cry1Ac-resistant Helicoverpa armigera is cross-resistant to Vip3 Aa protein, insecticidal activities, proteolytic activations and binding properties of Vip3 Aa toxin were investigated using Cry1Ac-susceptible(96S) and Cry1Ac-resistant H. armigera strain(Cry1Ac-R). The toxicity of Vip3 Aa in Cry1Ac-R slightly reduced compared with 96 S, the resistance ratio was only 1.7-fold. The digestion rate of full-length Vip3 Aa by gut juice extracts from 96 S was little faster than that from Cry1Ac-R. Surface plasmon resonance(SPR) showed there was no significant difference between the binding affinity of Vip3 Aa and BBMVs between 96 S and Cry1Ac-R strains, and there was no significant competitive binding between Vip3 Aa and Cry1 Ac in susceptible or resistant strains. So there had little cross-resistance between Vip3 Aa and Cry1 Ac,Vip3A+Cry proteins maybe the suitable pyramid strategy to control H. armigera in China in the future.

英文摘要:

The Bacillus thuringiensis vegetative insecticidal protein, Vip3 A, represents a new family of Bt toxin and is currently applied to commercial transgenic cotton. To determine whether the Cry1Ac-resistant Helicoverpa armigera is cross-resistant to Vip3 Aa protein, insecticidal activities, proteolytic activations and binding properties of Vip3 Aa toxin were investigated using Cry1Ac-susceptible(96S) and Cry1Ac-resistant H. armigera strain(Cry1Ac-R). The toxicity of Vip3 Aa in Cry1Ac-R slightly reduced compared with 96 S, the resistance ratio was only 1.7-fold. The digestion rate of full-length Vip3 Aa by gut juice extracts from 96 S was little faster than that from Cry1Ac-R. Surface plasmon resonance(SPR) showed there was no significant difference between the binding affinity of Vip3 Aa and BBMVs between 96 S and Cry1Ac-R strains, and there was no significant competitive binding between Vip3 Aa and Cry1 Ac in susceptible or resistant strains. So there had little cross-resistance between Vip3 Aa and Cry1 Ac,Vip3A+Cry proteins maybe the suitable pyramid strategy to control H. armigera in China in the future.

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期刊信息
  • 《应用昆虫学报》
  • 中国科技核心期刊
  • 主管单位:中国科学院
  • 主办单位:中国昆虫学会 中国科学院动物研究所
  • 主编:戈峰
  • 地址:北京朝阳区北辰西路1号院5号中科院动物所
  • 邮编:100101
  • 邮箱:entom@ioz.ac.cn
  • 电话:010-64807137
  • 国际标准刊号:ISSN:2095-1353
  • 国内统一刊号:ISSN:11-6020/Q
  • 邮发代号:2-151
  • 获奖情况:
  • 96、2000年获中科院《优秀期刊三等奖》,92年获中国科协《优秀学术期刊一等奖》,2001进入“中国期刊”方阵,“双百”期刊,排名第96位
  • 国内外数据库收录:
  • 俄罗斯文摘杂志,美国化学文摘(网络版),英国农业与生物科学研究中心文摘,美国剑桥科学文摘,美国生物科学数据库,英国动物学记录,日本日本科学技术振兴机构数据库,中国中国科技核心期刊,中国北大核心期刊(2011版),中国北大核心期刊(2014版)
  • 被引量:3170