Cong Lin, Chen Fei, Yu Shijiang, Ding Lili, Yang Juan, Luo Ren, Tian Huixia, Li Hongjun, Liu Haoqiang, Ran Chun
Citrus Research Institute, Southwest University/Chinese Academy of Agricultural Sciences, Chongqing 400712, China.
Sinofert Holdings Limited, Henan Branch, Zhengzhou 450000, China.
Int J Mol Sci. 2016 May 27;17(6):704. doi: 10.3390/ijms17060704.
Several fenpropathrin-resistant predatory mites have been reported. However, the molecular mechanism of the resistance remains unknown. In the present study, the Neoseiulus barkeri (N. barkeri) transcriptome was generated using the Illumina sequencing platform, 34,211 unigenes were obtained, and 15,987 were manually annotated. After manual annotation, attentions were attracted to resistance-related genes, such as voltage-gated sodium channel (VGSC), cytochrome P450s (P450s), and glutathione S-transferases (GSTs). A polymorphism analysis detected two point mutations (E1233G and S1282G) in the linker region between VGSC domain II and III. In addition, 43 putative P450 genes and 10 putative GST genes were identified from the transcriptome. Among them, two P450 genes, NbCYP4EV2 and NbCYP4EZ1, and four GST genes, NbGSTd01, NbGSTd02, NbGSTd03 and NbGSTm03, were remarkably overexpressed 3.64-46.69-fold in the fenpropathrin resistant strain compared to that in the susceptible strain. These results suggest that fenpropathrin resistance in N. barkeri is a complex biological process involving many genetic changes and provide new insight into the N. barkeri resistance mechanism.
已有报道称几种抗甲氰菊酯的捕食螨。然而,其抗性的分子机制仍不清楚。在本研究中,利用Illumina测序平台构建了巴氏新小绥螨(N. barkeri)转录组,获得了34,211个单基因,其中15,987个进行了人工注释。人工注释后,抗性相关基因受到关注,如电压门控钠通道(VGSC)、细胞色素P450(P450s)和谷胱甘肽S-转移酶(GSTs)。多态性分析在VGSC结构域II和III之间的连接区域检测到两个点突变(E1233G和S1282G)。此外,从转录组中鉴定出43个假定的P450基因和10个假定的GST基因。其中,两个P450基因NbCYP4EV2和NbCYP4EZ1,以及四个GST基因NbGSTd01、NbGSTd02、NbGSTd03和NbGSTm03,在抗甲氰菊酯品系中相对于敏感品系显著过表达3.64至46.69倍。这些结果表明,巴氏新小绥螨对甲氰菊酯的抗性是一个涉及许多基因变化的复杂生物学过程,并为巴氏新小绥螨的抗性机制提供了新的见解。