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毒力和非毒力病毒的感染差异影响了地熊蜂中 dicer-1、ago-1 和 microRNAs 的表达。

Infections of virulent and avirulent viruses differentially influenced the expression of dicer-1, ago-1, and microRNAs in Bombus terrestris.

机构信息

Key Laboratory of Entomology and Pest Control Engineering, College of Plant Protection, Southwest University, Chongqing 400716, China.

Department of Crop Protection, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, B-9000 Ghent, Belgium.

出版信息

Sci Rep. 2017 Apr 4;7:45620. doi: 10.1038/srep45620.

Abstract

The microRNA (miRNA) pathway is well established to be involved in host-pathogen interactions. As key insect pollinators, bees are suffering from widely spreading viruses, especially honeybees and bumblebees. In order to better understand bee-virus interaction, we comparatively analyzed the involvement of the bumblebee miRNA pathway upon infection by two different viruses. In our setup, an avirulent infection is induced by slow bee paralysis virus (SBPV) and a virulent infection is induced by Israeli acute paralysis virus (IAPV). Our results showed the increased expressions of dicer-1 and ago-1 upon SBPV infection. There were 17 and 12 bumblebee miRNAs differentially expressed upon SBPV and IAPV infections, respectively. These results may indicate the involvement of the host miRNA pathway in bumblebee-virus interaction. However, silencing of dicer-1 did not influence the genome copy number of SBPV. Target prediction for these differentially expressed miRNAs showed their possible involvement in targeting viral genomic RNA and in the regulation of networks in bumblebee. Our study opens a new insight into bee-virus interaction meditated by host miRNAs.

摘要

微小 RNA(miRNA)途径被广泛认为参与了宿主-病原体的相互作用。作为重要的昆虫传粉媒介,蜜蜂正遭受着广泛传播的病毒的侵袭,尤其是蜜蜂和大黄蜂。为了更好地理解蜜蜂-病毒的相互作用,我们比较分析了两种不同病毒感染对大黄蜂 miRNA 途径的影响。在我们的实验中,通过慢速麻痹病毒(SBPV)诱导非致命性感染,而通过以色列急性麻痹病毒(IAPV)诱导致命性感染。我们的结果显示,在 SBPV 感染后,dicer-1 和 ago-1 的表达增加。在 SBPV 和 IAPV 感染后,分别有 17 个和 12 个大黄蜂 miRNAs 差异表达。这些结果可能表明宿主 miRNA 途径参与了大黄蜂-病毒的相互作用。然而,dicer-1 的沉默并没有影响 SBPV 的基因组拷贝数。对这些差异表达的 miRNA 的靶标预测表明,它们可能参与了靶向病毒基因组 RNA 以及调节大黄蜂网络的作用。我们的研究为宿主 miRNAs 介导的蜜蜂-病毒相互作用提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3236/5379481/0384a1005460/srep45620-f1.jpg

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