Toga Kouhei, Kimoto Fumiko, Fujii Hiroki, Bono Hidemasa
Laboratory of BioDX, PtBio Co-Creation Research Center, Genome Editing Innovation Center, Hiroshima University, 3-10-23 Kagamiyama, Higashi-Hiroshima City, Hiroshima 739-0046, Japan.
Laboratory of Genome Informatics, Graduate School of Integrated Sciences for Life, Hiroshima University, 3-10-23 Kagamiyama, Higashi-Hiroshima City, Hiroshima 739-0046, Japan.
Insects. 2024 Sep 24;15(10):737. doi: 10.3390/insects15100737.
Insecticide resistance in the bed bug is poorly understood due to the lack of genome sequences for resistant strains. In Japan, we identified a resistant strain of that exhibits a higher pyrethroid resistance ratio compared to many previously discovered strains. We sequenced the genomes of the pyrethroid-resistant and susceptible strains using long-read sequencing, resulting in the construction of highly contiguous genomes (N50 of the resistant strain: 2.1 Mb and N50 of the susceptible strain: 1.5 Mb). Gene prediction was performed by BRAKER3, and the functional annotation was performed by the Fanflow4insects workflow. Next, we compared their amino acid sequences to identify gene mutations, identifying 729 mutated transcripts that were specific to the resistant strain. Among them, those defined previously as resistance genes were included. Additionally, enrichment analysis implicated DNA damage response, cell cycle regulation, insulin metabolism, and lysosomes in the development of pyrethroid resistance. Genome editing of these genes can provide insights into the evolution and mechanisms of insecticide resistance. This study expanded the target genes to monitor allele distribution and frequency changes, which will likely contribute to the assessment of resistance levels. These findings highlight the potential of genome-wide approaches to understand insecticide resistance in bed bugs.
由于缺乏抗性品系的基因组序列,人们对臭虫的抗药性了解甚少。在日本,我们鉴定出了一个抗性品系,与许多先前发现的品系相比,该品系对拟除虫菊酯的抗性比率更高。我们使用长读长测序技术对拟除虫菊酯抗性品系和敏感品系的基因组进行了测序,构建了高度连续的基因组(抗性品系的N50:2.1 Mb,敏感品系的N50:1.5 Mb)。通过BRAKER3进行基因预测,并通过Fanflow4insects工作流程进行功能注释。接下来,我们比较了它们的氨基酸序列以鉴定基因突变,鉴定出729个抗性品系特有的突变转录本。其中包括那些先前被定义为抗性基因的转录本。此外,富集分析表明DNA损伤反应、细胞周期调控、胰岛素代谢和溶酶体与拟除虫菊酯抗性的发展有关。对这些基因进行基因组编辑可以深入了解抗药性的进化和机制。本研究扩展了用于监测等位基因分布和频率变化的靶基因,这可能有助于评估抗性水平。这些发现凸显了全基因组方法在理解臭虫抗药性方面的潜力。