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Transgenic Res. 2013 Dec;22(6):1207-22. doi: 10.1007/s11248-013-9716-5. Epub 2013 Jun 8.
The sequence specificity of the endogenous RNA interference pathway allows targeted suppression of genes essential for insect survival and enables the development of durable and efficacious insecticidal products having a low likelihood to adversely impact non-target organisms. The spectrum of insecticidal activity of a 240 nucleotide (nt) dsRNA targeting the Snf7 ortholog in Western Corn Rootworm (WCR; Diabrotica virgifera virgifera) was characterized by selecting and testing insects based upon their phylogenetic relatedness to WCR. Insect species, representing 10 families and 4 Orders, were evaluated in subchronic or chronic diet bioassays that measured potential lethal and sublethal effects. When a specific species could not be tested in diet bioassays, the ortholog to the WCR Snf7 gene (DvSnf7) was cloned and corresponding dsRNAs were tested against WCR and Colorado potato beetle (Leptinotarsa decemlineata); model systems known to be sensitive to ingested dsRNA. Bioassay results demonstrate that the spectrum of activity for DvSnf7 is narrow and activity is only evident in a subset of beetles within the Galerucinae subfamily of Chrysomelidae (>90% identity with WCR Snf7 240 nt). This approach allowed for evaluating the relationship between minimum shared nt sequence length and activity. A shared sequence length of ≥ 21 nt was required for efficacy against WCR (containing 221 potential 21-nt matches) and all active orthologs contained at least three 21 nt matches. These results also suggest that WCR resistance to DvSnf7 dsRNA due to single nucleotide polymorphisms in the target sequence of 240 nt is highly unlikely.
内源性 RNA 干扰途径的序列特异性允许靶向抑制对昆虫生存至关重要的基因,并能够开发出具有持久和有效的杀虫作用的产品,而这些产品不太可能对非目标生物产生不利影响。针对西方玉米根虫(WCR;Diabrotica virgifera virgifera)的 Snf7 同源物的 240 个核苷酸(nt)dsRNA 的杀虫活性谱通过基于与 WCR 的系统发育关系选择和测试昆虫来表征。评估了代表 10 个科和 4 个目昆虫的亚慢性或慢性饮食生物测定,以测量潜在的致死和亚致死作用。当特定物种无法在饮食生物测定中进行测试时,克隆了 WCR Snf7 基因(DvSnf7)的同源物,并针对 WCR 和科罗拉多马铃薯甲虫(Leptinotarsa decemlineata)测试了相应的 dsRNA;这些模型系统已知对摄入的 dsRNA 敏感。生物测定结果表明,DvSnf7 的活性谱很窄,仅在 Chrysomelidae 类的 Galerucinae 亚科中的一部分甲虫中表现出活性(与 WCR Snf7 240 nt 的同一性> 90%)。这种方法允许评估最小共享 nt 序列长度与活性之间的关系。需要至少 21 个 nt 的共享序列长度才能对 WCR 有效(包含 221 个潜在的 21-nt 匹配),所有活性同源物都至少包含三个 21-nt 匹配。这些结果还表明,由于 240 nt 靶序列中的单核苷酸多态性,WCR 对 DvSnf7 dsRNA 的抗性极不可能。