Truncated transcripts of nicotinic acetylcholine subunit gene Bdα6 are associated with spinosad resistance in Bactrocera dorsalis

被引:92
作者
Hsu, Ju-Chun [1 ]
Feng, Hai-Tung [2 ]
Wu, Wen-Jer [1 ,3 ]
Geib, Scott M. [4 ]
Mao, Ching-hua [1 ]
Vontas, John [5 ]
机构
[1] Natl Taiwan Univ, Dept Entomol, Taipei 106, Taiwan
[2] Taiwan Agr Chem & Tox Subst Res Inst, Council Agr, Taichung, Taiwan
[3] Natl Taiwan Univ, Res Ctr Plant Med, Taipei 106, Taiwan
[4] ARS, Trop Crop & Commod Protect Res Unit, USDA, Pacific Basin Agr Res Ctr, Hilo, HI 96720 USA
[5] Univ Crete, Dept Biol, Fac Appl Biol & Biotechnol, Iraklion 71409, Greece
关键词
Spinosad; RNA editing; Bactrocera dorsalis; nAChRs; Insecticide resistance; Deletion; HELIOTHIS-VIRESCENS LEPIDOPTERA; FRUIT-FLY DIPTERA; INSECTICIDE RESISTANCE; LABORATORY STRAIN; DIAMONDBACK MOTH; TOBACCO BUDWORM; MUSCA-DOMESTICA; PROTEIN BAITS; RECEPTOR; TEPHRITIDAE;
D O I
10.1016/j.ibmb.2012.07.010
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
Spinosad-resistance mechanisms of Bactrocera dorsalis, one of the most important agricultural pests worldwide, were investigated. Resistance levels to spinosad in a B. dorsalis strain from Taiwan were more than 2000-fold, but showed no cross resistance to imidacloprid or fipronil. Combined biochemical and synergistic data indicated that target-site insensitivity is the major resistance component. The gene encoding the nAChR subunit alpha 6 (Bd alpha 6), the putative molecular target of spinosad, was isolated using PCR and RACE techniques. The full-length cDNA of Bd alpha 6 from spinosad-susceptible strains had an open reading frame of 1467 bp and codes for a typical nAChR subunit. Two isoforms of exon 3 (3a and 3b) and exon 8 (8a and 8b), and four full-length splicing variants were found in the susceptible strain. All transcripts from the spinosad-resistant strain were truncated and coded for apparently non-functional Bd alpha 6. Genetic linkage analysis further associated spinosad-resistance phenotype with the truncated Bd alpha 6 forms. This finding is consistent with a previous study in Plutella xylostella. Small deletions and insertions and consequent premature stop codons in exon 7 were associated with the truncated transcripts at the cDNA level. Analysis of genomic DNA sequences (intron 2 and exons 3-6) failed to detect exon 5 in resistant flies. In addition, a mutation in Bd alpha 6 intron 2, just before the truncated/mis-splicing region and in same location with a mutation previously reported in the Pxyl alpha 6 gene, was identified in the resistant flies. RNA editing was investigated but was not found to be associated with resistance. While the demonstration of truncated transcripts causing resistance was outlined, the mechanism responsible for generating truncated transcripts remains unknown. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:806 / 815
页数:10
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