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小菜蛾Btk抗性品系对四种Bt杀虫晶体蛋白抗性发展的研究
引用本文:符伟,唐涛,王培,王勇,尹丽,马明勇,张政兵. 小菜蛾Btk抗性品系对四种Bt杀虫晶体蛋白抗性发展的研究[J]. 中国生物防治学报, 2022, 38(2): 328-332. DOI: 10.16409/j.cnki.2095-039x.2021.05.019
作者姓名:符伟  唐涛  王培  王勇  尹丽  马明勇  张政兵
作者单位:1. 湖南省农业科学院植物保护研究所,长沙 410125;2.湖南省植保植检站,长沙410005
基金项目:国家重点研发计划(2017YFD0201200);国家自然科学基金(31401775)
摘    要:使用苏云金芽胞杆菌库斯塔克亚种(Btk)可湿性粉剂对小菜蛾进行继代汰选获得F80代和F100代抗性品系。通过分别测定Cry1Ab、Cry1Ac、Cry1Ah和Cry1Ca四种杀虫晶体蛋白对小菜蛾Btk抗性品系F80代和F100代的室内毒力,明确了小菜蛾Btk抗性品系对四种Bt杀虫晶体蛋白抗性发展规律。研究结果表明,汰选至F80代时,Cry1Ca对小菜蛾的毒力最高,LC50约12.1mg/L,其次为Cry1Ac,LC50约47.7mg/L;而汰选至F100代时,仍以Cry1Ca对小菜蛾的毒力最高,LC50约21.4 mg/L,其次为Cry1Ab,LC50约72.2 mg/L。与相对敏感品系相比,小菜蛾抗性品系对Cry1Ac的抗性发展较快(抗性倍数高达67.3~106.8倍),对Cry1Ab的次之(抗性倍数高达60.0~66.1倍),而对Cry1Ca和Cry1Ah的抗性发展较慢(抗性倍数分别为3.4~6.0倍和1.6~2.5倍)。以上结果说明,在主效杀虫基因为Cry1Ac的Btk药剂选择压力下,小菜蛾对四种Bt杀虫晶体蛋白的抗性发展速度差异较大,且Cry1Ac和Cry1Ab存在交互抗性风险...

关 键 词:小菜蛾  苏云金芽胞杆菌  杀虫晶体蛋白  生物测定  抗药性
收稿时间:2020-12-17

Resistance Development of Four Bt Insecticidal Crystal Proteins against Btk-resistant Strain of Plutella xylostella in the Laboratory
FU Wei,TANG Tao,WANG Pei,WANG Yong,YIN Li,MA Mingyong,ZHANG Zhengbing. Resistance Development of Four Bt Insecticidal Crystal Proteins against Btk-resistant Strain of Plutella xylostella in the Laboratory[J]. Chinese Journal of Biological Control, 2022, 38(2): 328-332. DOI: 10.16409/j.cnki.2095-039x.2021.05.019
Authors:FU Wei  TANG Tao  WANG Pei  WANG Yong  YIN Li  MA Mingyong  ZHANG Zhengbing
Affiliation:1. Institue of Plant Protection, Hunan Academy of Agricultural Sciences, Changsha 410125, China; 2. Hunan Plant Protection and Quarantine Station, Changsha 410005, China
Abstract:The Bacillus thuringiensis (Bt)-resistant strains of Plutella xylostella (L.) were selected using a wettable powder formulation of Bt var. kurstaki (Btk) for 80 and 100 generations in the laboratory, respectively. The toxicities of four Bt-insecticidal crystal proteins (Cry1Ab, Cry1Ac, Cry1Ah, and Cry1Ca) against Btk-resistant and -susceptible strains of P. xylostella were determined using a standard leaf-dipping method. For the F80 generation of Btk-resistant strain, Cry1Ca had higher toxicity with a LC50value about 12.1 mg/Lthan the other three Cry proteins, followed by Cry1Ac with a LC50value about 47.7 mg/L. For the F100 generation of Btk-resistant strain, Cry1Ca still showed higher toxicity with a LC50 value about 21.4 mg/Lthan the other three Cry proteins, followed by Cry1Ab with a LC50 value about 72.2 mg/L. The Btk-resistant strains of P. xylostella showed quick development of resistance to Cry1Ac, with a resistance ratio (RR) increased from 67.3-fold to 106.8-fold when compared with the susceptible laboratory strain. The resistance to Cry1Ab was relatively low, with a RR value from 60.0-fold to 66.1-fold, and the resistance to Cry1Ca and Cry1Ah was even lower, with RR values of 3.4—6.0-fold and 1.6—2.5-fold, respectively. In conclusion, these results suggest that, under the selection pressure of Btk with a dominant gene of Cry1Ac, P. xylostella strains show significant differences in the development of resistance to four insecticidal crystal proteins, and that there is a potential risk of cross-resistance between Cry1Ac and Cry1Ab.
Keywords:Plutella xylostella  Bacillus thuringiensis  insecticidal crystal protein  bioassay  resistance  
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