論文

査読有り 国際誌
2019年3月12日

Genome-wide Identification of Tebufenozide Resistant Genes in the smaller tea tortrix, Adoxophyes honmai (Lepidoptera: Tortricidae).

Scientific reports
  • Miwa Uchibori-Asano
  • Akiya Jouraku
  • Toru Uchiyama
  • Kakeru Yokoi
  • Gaku Akiduki
  • Yoshitaka Suetsugu
  • Tetsuya Kobayashi
  • Akihito Ozawa
  • Saki Minami
  • Chiharu Ishizuka
  • Yoshiaki Nakagawa
  • Takaaki Daimon
  • Tetsuro Shinoda
  • 全て表示

9
1
開始ページ
4203
終了ページ
4203
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1038/s41598-019-40863-5

The smaller tea tortrix, Adoxophyes honmai, has developed strong resistance to tebufenozide, a diacylhydrazine-type (DAH) insecticide. Here, we investigated its mechanism by identifying genes responsible for the tebufenozide resistance using various next generation sequencing techniques. First, double-digest restriction site-associated DNA sequencing (ddRAD-seq) identified two candidate loci. Then, synteny analyses using A. honmai draft genome sequences revealed that one locus contained the ecdysone receptor gene (EcR) and the other multiple CYP9A subfamily P450 genes. RNA-seq and direct sequencing of EcR cDNAs found a single nucleotide polymorphism (SNP), which was tightly linked to tebufenozide resistance and generated an amino acid substitution in the ligand-binding domain. The binding affinity to tebufenozide was about 4 times lower in in vitro translated EcR of the resistant strain than in the susceptible strain. RNA-seq analyses identified commonly up-regulated genes in resistant strains, including CYP9A and choline/carboxylesterase (CCE) genes. RT-qPCR analysis and bioassays showed that the expression levels of several CYP9A and CCE genes were moderately correlated with tebufenozide resistance. Collectively, these results suggest that the reduced binding affinity of EcR is the main factor and the enhanced detoxification activity by some CYP9As and CCEs plays a supplementary role in tebufenozide resistance in A. honmai.

リンク情報
DOI
https://doi.org/10.1038/s41598-019-40863-5
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/30862839
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414682
ID情報
  • DOI : 10.1038/s41598-019-40863-5
  • PubMed ID : 30862839
  • PubMed Central 記事ID : PMC6414682

エクスポート
BibTeX RIS