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Resistance to BmNPV via Overexpression of an Exogenous Gene Controlled by an Inducible Promoter and Enhancer in Transgenic Silkworm Bombyx mori

机译:经由通过诱导型启动子和增强子在转基因家蚕所控制的外源基因的过表达抗性的BmNpV

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摘要

The hycu-ep32 gene of Hyphantria cunea NPV can inhibit Bombyx mori nucleopolyhedrovirus (BmNPV) multiplication in co-infected cells, but it is not known whether the overexpression of the hycu-ep32 gene has an antiviral effect in the silkworm, Bombyx mori. Thus, we constructed four transgenic vectors, which were under the control of the 39 K promoter of BmNPV (39 KP), Bombyx mori A4 promoter (A4P), hr3 enhancer of BmNPV combined with 39 KP, and hr3 combined with A4P. Transgenic lines were created via embryo microinjection using practical diapause silkworm. qPCR revealed that the expression level of hycu-ep32 could be induced effectively after BmNPV infection in transgenic lines where hycu-ep32 was controlled by hr3 combined with 39 KP (i.e., HEKG). After oral inoculation of BmNPV with 3 × 105 occlusion bodies per third instar, the mortality with HEKG-B was approximately 30% lower compared with the non-transgenic line. The economic characteristics of the transgenic lines remained unchanged. These results suggest that overexpression of an exogenous antiviral gene controlled by an inducible promoter and enhancer is a feasible method for breeding silkworms with a high antiviral capacity.
机译:豚鼠NPV的hycu-ep32基因可以抑制家蚕感染的多联体中的家蚕核多角体病毒(BmNPV)繁殖,但是尚不清楚hycu-ep32基因的过表达是否对家蚕Bombyx mori具有抗病毒作用。因此,我们构建了四个转基因载体,它们分别受BmNPV的39 K启动子(39 KP),家蚕A4启动子(A4P),BmNPV结合39 KP的hr3增强子和hr3与A4P结合的控制。使用实用的滞育蚕通过胚胎显微注射产生转基因品系。 qPCR显示在BmNPV感染后,在hr3和39 KP(即HEKG)结合控制hycu-ep32的转基因株系中,可以有效诱导hycu-ep32的表达水平。每三龄经3×10 5 闭塞体口服接种BmNPV后,HEKG-B的死亡率比非转基因株低约30%。转基因品系的经济特征保持不变。这些结果表明,由诱导型启动子和增强子控制的外源抗病毒基因的过表达是育种具有高抗病毒能力的家蚕的可行方法。

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