ABCC2 is a functional receptor of Bacillus thuringiensis Cry1Ca in Spodoptera litura

被引:9
|
作者
Yao, Xue [1 ]
Liu, Chen [2 ]
Duan, Yunpeng [1 ]
An, Shiheng [1 ]
Wei, Jizhen [1 ]
Liang, Gemei [2 ]
机构
[1] Henan Agr Univ, Coll Plant Protect, State Key Lab Wheat & Maize Crop Sci, Zhengzhou 450002, Peoples R China
[2] Chinese Acad Agr Sci, Inst Plant Protect, State Key Lab Biol Plant Dis & Insect Pests, Beijing 100193, Peoples R China
基金
中国国家自然科学基金;
关键词
Cry1Ca; Spodoptera litura; ABCC2; BORDER MEMBRANE-VESICLES; EXIGUA LEPIDOPTERA-NOCTUIDAE; FIELD EVOLVED RESISTANCE; DELTA-ENDOTOXIN CRY1C; HELICOVERPA-ARMIGERA; AMINOPEPTIDASE-N; BINDING-PROTEINS; CHEMISTRY INSECTICIDES; DIAMONDBACK MOTH; CROSS-RESISTANCE;
D O I
10.1016/j.ijbiomac.2021.11.174
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Spodoptera litura is a serious polyphagous pest in the whole world, which has developed resistance to most conventional insecticides and even some Bacillus thuringiensis (Bt) toxins. Cry1Ca has excellent insecticide activity against S. litura with potential application to control S. litura and delay the development of insect resistance. However, the mode of action of Cry1Ca in S. litura is poorly understood. Here, Cry1Ca-binding proteins were identified from S. litura by using pull down assays and liquid chromatography-tandem mass spectrometry (LC-MS/MS). The results indicated that aminopeptidase-N (APN), ATP binding cassette subfamily C member 2 (ABCC2), polycalin, actin and V-type proton ATPase subunit A may bind with Cry1Ca. Further study confirmed that ABCC2 fragment expressed in vitro can bind to Cry1Ca as demonstrated by Ligand blot and homologous competition experiments. The over-expression of endogenous SlABCC2 in Sf9 cells increased Cry1Ca cytotoxicity. Correspondingly, the vivo loss of function analyses by SlABCC2 small interfering RNAs (siRNAs) in S. litura larvae decreased the toxicity of Cry1Ca to larvae. Altogether, these results show that ABCC2 of S. litura is a functional receptor that is involved in the action mode of Cry1Ca.
引用
收藏
页码:9 / 16
页数:8
相关论文
共 50 条
  • [1] Molecular characterization of Spodoptera frugiperda Bacillus thuringiensis Cry1Ca toxin interaction
    Rodriguez-Cabrera, Lianet
    Trujillo-Bacallao, Damian
    Borras-Hidalgo, Orlando
    Wright, Denis J.
    Ayra-Pardo, Camilo
    TOXICON, 2008, 51 (04) : 681 - 692
  • [2] A Spodoptera exigua Cadherin Serves as a Putative Receptor for Bacillus thuringiensis Cry1Ca Toxin and Shows Differential Enhancement of Cry1Ca and Cry1Ac Toxicity
    Ren, Xiang-Liang
    Chen, Rui-Rui
    Zhang, Ying
    Ma, Yan
    Cui, Jin-Jie
    Han, Zhao-Jun
    Mu, Li-Li
    Li, Guo-Qing
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2013, 79 (18) : 5576 - 5583
  • [3] Spodoptera frugiperda (J. E. Smith) Aminopeptidase N1 Is a Functional Receptor of the Bacillus thuringiensis Cry1Ca Toxin
    Gomez, Isabel
    Rodriguez-Chamorro, Daniel E.
    Flores-Ramirez, Gabriela
    Grande, Ricardo
    Zuniga, Fernando
    Portugal, Francisco J.
    Sanchez, Jorge
    Pacheco, Sabino
    Bravo, Alejandra
    Soberon, Mario
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2018, 84 (17)
  • [4] Hetero-oligomerization of Bacillus thuringiensis Cry1A proteins enhance binding to the ABCC2 transporter of Spodoptera exigua
    Pinos, Daniel
    Joya, Noelia
    Herrero, Salvador
    Ferre, Juan
    Hernandez-Martinez, Patricia
    BIOCHEMICAL JOURNAL, 2021, 478 (13) : 2589 - 2600
  • [5] Role of Bacillus thuringiensis CrylA toxins domains in the binding to the ABCC2 receptor from Spodoptera exigua
    Martinez-Solis, Maria
    Pinos, Daniel
    Endo, Haruka
    Portugal, Leivi
    Sato, Ryoichi
    Ferre, Juan
    Herrero, Salvador
    Hernandez-Martinez, Patricia
    INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2018, 101 : 47 - 56
  • [6] The Spodoptera exigua (Lepidoptera: Noctuidae) ABCC2 Mediates Cry1Ac Cytotoxicity and, in Conjunction with Cadherin, Contributes to Enhance Cry1Ca Toxicity in Sf9 Cells
    Ren, Xiang-Liang
    Jiang, Wei-Li
    Ma, Ya-Jie
    Hu, Hong-Yan
    Ma, Xiao-Yan
    Ma, Yan
    Li, Guo-Qing
    JOURNAL OF ECONOMIC ENTOMOLOGY, 2016, 109 (06) : 2281 - 2289
  • [7] Mutations in the Bacillus thuringiensis Cry1Ca toxin demonstrate the role of domains II and III in specificity towards Spodoptera exigua larvae
    Herrero, S
    González-Cabrera, J
    Ferré, J
    Bakker, PL
    De Maagd, RA
    BIOCHEMICAL JOURNAL, 2004, 384 : 507 - 513
  • [8] ABCC2 is associated with Bacillus thuringiensis Cry1Ac toxin oligomerization and membrane insertion in diamondback moth
    Josue Ocelotl
    Jorge Sánchez
    Isabel Gómez
    Bruce E. Tabashnik
    Alejandra Bravo
    Mario Soberón
    Scientific Reports, 7
  • [9] ABCC2 is associated with Bacillus thuringiensis Cry1Ac toxin oligomerization and membrane insertion in diamondback moth
    Ocelotl, Josue
    Sanchez, Jorge
    Gomez, Isabel
    Tabashnik, Bruce E.
    Bravo, Alejandra
    Soberon, Mario
    SCIENTIFIC REPORTS, 2017, 7
  • [10] Expression and Crystallization of an N-Terminally Activated Form of the Bacillus thuringiensis Cry1Ca Toxin
    Thaleia Kouskoura
    Candy Tickner
    Neil Crickmore
    Current Microbiology, 2001, 43 : 371 - 373