De novo transcriptome and expression profile analyses of the Asian corn borer (Ostrinia furnacalis) reveals relevant flubendiamide response genes

被引:33
作者
Cui, Li [1 ]
Rui, Changhui [1 ]
Yang, Daibin [1 ]
Wang, Zhenying [2 ]
Yuan, Huizhu [1 ]
机构
[1] Chinese Acad Agr Sci, Inst Plant Protect, Minist Agr, Key Lab Integrated Pest Management Crops, Beijing 100193, 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
RYANODINE RECEPTOR; DROSOPHILA-MELANOGASTER; POLLEN BEETLE; BOMBYX-MORI; RNA-SEQ; RESISTANCE; SILKWORM; FAMILY; L; LEPIDOPTERA;
D O I
10.1186/s12864-016-3431-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The Asian corn borer (ACB), Ostrinia furnacalis (Guenee), has become the most damaging insect pest of corn in Asia. However, the lack of genome or transcriptome information heavily hinders our further understanding of ACB in every aspect at a molecular level and on a genome-wide scale. Here, we used the Ion Torrent Personal Genome Machine (PGM) Sequencer to explore the ACB transcriptome and to identify relevant genes in response to flubendiamide, showing high selective activity against ACB. Results: We obtained 35,430 unigenes, with an average length of 716 bp, representing a dramatic expansion of existing cDNA sequences available for ACB. These sequences were annotated with Non-redundant Protein (Nr), Gene Ontology (GO), Clusters of Orthologous Groups (COG) and Kyoto Encyclopedia of Genes and Genomes (KEGG) to better understand their functions. A total of 31 cytochrome P450 monooxygenases (P450s), 27 carboxyl/cholinesterases (CCEs) and 19 glutathione S-transferases (GSTs) were manually curated to construct phylogenetic trees, and 25 unigenes encoding target proteins (acetylcholinesterase, nicotinic acetylcholine receptor, gamma-aminobutyric acid receptor, glutamategated chloride channel, voltage-gated sodium channel and ryanodine receptor) were identified. In addition, we compared and validated the differentially expressed unigenes upon flubendiamide treatment, revealing that the genes for detoxification enzymes (P450s and esterase), calcium signaling pathways and muscle control pathways (twitchin and tropomyosin), immunoglobulin (hemolin), chemosensory protein and heat shock protein 70 were significantly overexpressed in response to flubendiamide, while the genes for cuticular protein, protease and oxidoreductase showed much lower expression levels. Conclusion: The obtained transcriptome information provides large genomic resources available for further studies of ACB. The differentially expressed gene data will elucidate the molecular mechanisms of ACB in response to the novel diamide insecticide, flubendiamide. In particular, these findings will facilitate the identification of the genes involved in insecticide resistance and the development of new compounds to control the ACB.
引用
收藏
页数:14
相关论文
共 46 条
[1]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[2]   The significance of digital gene expression profiles [J].
Audic, S ;
Claverie, JM .
GENOME RESEARCH, 1997, 7 (10) :986-995
[3]   RNA interference-mediated knockdown of a cytochrome P450, CYP6BG1, from the diamondback moth, Plutella xylostella, reduces larval resistance to permethrin [J].
Bautista, Ma. Anita M. ;
Miyata, Tadashi ;
Miura, Ken ;
Tanaka, Toshiharu .
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2009, 39 (01) :38-46
[4]   Using the miraEST assembler for reliable and automated mRNA transcript assembly and SNP detection in sequenced ESTs [J].
Chevreux, B ;
Pfisterer, T ;
Drescher, B ;
Driesel, AJ ;
Müller, WEG ;
Wetter, T ;
Suhai, S .
GENOME RESEARCH, 2004, 14 (06) :1147-1159
[5]   A deficit of detoxification enzymes: pesticide sensitivity and environmental response in the honeybee [J].
Claudianos, C. ;
Ranson, H. ;
Johnson, R. M. ;
Biswas, S. ;
Schuler, M. A. ;
Berenbaum, M. R. ;
Feyereisen, R. ;
Oakeshott, J. G. .
INSECT MOLECULAR BIOLOGY, 2006, 15 (05) :615-636
[6]   Anthranilic diamides: A new class of insecticides with a novel mode of action, ryanodine receptor activation [J].
Cordova, D ;
Benner, EA ;
Sacher, MD ;
Rauh, JJ ;
Sopa, JS ;
Lahm, GP ;
Selby, TP ;
Stevenson, TM ;
Flexner, L ;
Gutteridge, S ;
Rhoades, DF ;
Wu, L ;
Smith, RM ;
Tao, Y .
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 2006, 84 (03) :196-214
[7]   Molecular Cloning, Characterization and Expression Profiling of a Ryanodine Receptor Gene in Asian Corn Borer, Ostrinia furnacalis (Guenee) [J].
Cui, Li ;
Yang, Daibin ;
Yan, Xiaojing ;
Rui, Changhui ;
Wang, Zhenying ;
Yuan, Huizhu .
PLOS ONE, 2013, 8 (10)
[8]   Mining Genes Involved in Insecticide Resistance of Liposcelis bostrychophila Badonnel by Transcriptome and Expression Profile Analysis [J].
Dou, Wei ;
Shen, Guang-Mao ;
Niu, Jin-Zhi ;
Ding, Tian-Bo ;
Wei, Dan-Dan ;
Wang, Jin-Jun .
PLOS ONE, 2013, 8 (11)
[9]   Phthalic acid diamides activate ryanodine-sensitive Ca2+ release channels in insects [J].
Ebbinghaus-Kintscher, U ;
Luemmen, P ;
Lobitz, N ;
Schulte, T ;
Funke, C ;
Fischer, R ;
Masaki, T ;
Yasokawa, N ;
Tohnishi, M .
CELL CALCIUM, 2006, 39 (01) :21-33
[10]  
Feyereisen R, 2012, INSECT MOLECULAR BIOLOGY AND BIOCHEMISTRY, P236, DOI 10.1016/B978-0-12-384747-8.10008-X