RNA interference-mediated knockdown of three putative aminopeptidases N affects susceptibility of Spodoptera exigua larvae to Bacillus thuringiensis Cry1Ca

被引:20
|
作者
Ren, Xiang-Liang [1 ]
Ma, Yan [2 ]
Cui, Jin-Jie [2 ]
Li, Guo-Qing [1 ]
机构
[1] Nanjing Agr Univ, Coll Plant Protect, Educ Minist Key Lab Integrated Management Crop Di, Nanjing 210095, Jiangsu, Peoples R China
[2] CAAS, Inst Cotton Res, State Key Lab Cotton Biol, Anyang 455000, Henan, Peoples R China
关键词
S; exigua; Aminopeptidase N; Crystal toxin; Bacillus thuringiensis; RNA interference; Candidate receptor; DELTA-ENDOTOXIN BINDING; SEXTA BT-R-1 RECEPTOR; HELICOVERPA-ARMIGERA; TOXIN-BINDING; GENE-EXPRESSION; DOMAIN-II; MIDGUT; MOTH; PROTEINS; IDENTIFICATION;
D O I
10.1016/j.jinsphys.2014.06.002
中图分类号
Q96 [昆虫学];
学科分类号
摘要
Aminopeptidase N (APN) isoforms in insects have been documented to be involved in the mode of action of insecticidal crystal proteins (Cry) from Bacillus thuringiensis. Here we cloned two novel Seapns from the larval midgut of Spodoptera exigua, a major pest of many crops of economic importance in China. According to a phylogenetic analysis, these two novel SeAPNs, along with the four SeAPN isoforms already described, belong to six different clades. All the six SeAPNs share similar structural features. From N- to C-terminus a signal peptide, a gluzincin aminopeptidase motif, a zinc binding/gluzincin motif, and a glycosylphosphatidylinositol-anchor sequence are located. The six Seapn genes were highly expressed at the larval stage, especially in the larval gut. Ingestion during four consecutive days of double-stranded RNAs (dsRNAs) targeting Seapn1, Seapn2, Seapn3, Seapn4, Seapn5 and Segn6 significantly reduced corresponding mRNA levels by 55.6%, 45.5%, 43.2%, 56.8%, 45.4%, and 46.0% respectively, compared with those recorded in control larvae fed on non-specific dsRNA (dsegfp). When the larvae that previously ingested phosphate buffered saline (PBS)-, dsegfp-, or six dsSeapns-overlaid diets were then exposed to a diet containing Cry1Ca, the larval mortalities were 71.2%, 69.3%, 52.0%, 77.2%, 43.3%, 62.0%, 65.4% and 53.8% respectively recorded after 6 days. ANOVA analysis revealed that the larvae previously fed on dsSeapn1-, dsSeapn3-, and dsSeapn6-overlaid diets had significantly lower mortalities than those previously ingested PBS-, dsegfp-, dsSeapn2-, dsSeapn4- and dsSeapn5-overlaid diets. Thus, these results suggest that SeAPN1, SeAPN3 and SeAPN6 may be candidate receptors for Cry1Ca in S. exigua. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:28 / 36
页数:9
相关论文
共 15 条
  • [11] RNA interference knockdown of aminopeptidase N genes decrease the susceptibility of Chilo suppressalis larvae to Cry1Ab/Cry1Ac and Cry1Ca-expressing transgenic rice
    Qiu, Lin
    Fan, Jinxing
    Zhang, Boyao
    Liu, Lang
    Wang, Xiaoping
    Lei, Chaoliang
    Lin, Yongjun
    Ma, Weihua
    JOURNAL OF INVERTEBRATE PATHOLOGY, 2017, 145 : 9 - 12
  • [12] Bacillus thuringiensis Cry1Ca-resistant Spodoptera exigua lacks expression of one of four Aminopeptidase N genes -: art. no. 96
    Herrero, S
    Gechev, T
    Bakker, PL
    Moar, WJ
    de Maagd, RA
    BMC GENOMICS, 2005, 6 (1)
  • [13] Knockout of three aminopeptidase N genes does not affect susceptibility of Helicoverpa armigera larvae to Bacillus thuringiensis Cry1A and Cry2A toxins
    Wang, Jing
    Zuo, Ya-Yun
    Li, Ling-Li
    Wang, Hui
    Liu, Shao-Yan
    Yang, Yi-Hua
    Wu, Yi-Dong
    INSECT SCIENCE, 2020, 27 (03) : 440 - 448
  • [14] In vivo identification of Bacillus thuringiensis Cry4Ba toxin receptors by RNA interference knockdown of glycosylphosphatidylinositol-linked aminopeptidase N transcripts in Aedes aegypti larvae
    Saengwiman, Suchada
    Aroonkesorn, Aratee
    Dedvisitsakul, Plaipol
    Sakdee, Somsri
    Leetachewa, Somphob
    Angsuthanasombat, Chanan
    Pootanakit, Kusol
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2011, 407 (04) : 708 - 713
  • [15] Knockdown of aminopeptidase-N from Helicoverpla armigera larvae and in transfected Sf21 cells by RNA interference reveals its functional interaction with Bacillus thuringiensis insecticidal protein Cry1Ac
    Sivakumar, Swaminathan
    Rajagopal, Raman
    Venkatesh, G. Raja
    Srivastava, Anand
    Bhatnagar, Raj K.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (10) : 7312 - 7319