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对易感性和近等基因抗性家蚕(鳞翅目)幼虫中肠对 BmNPV 感染的亚细胞蛋白质组学比较分析。

Comparative Subcellular Proteomics Analysis of Susceptible and Near-isogenic Resistant Bombyx mori (Lepidoptera) Larval Midgut Response to BmNPV infection.

机构信息

School of Life Sciences, Anhui Agricultural University, Hefei, 230036, People's Republic of China.

Institute of Sericulture, Anhui Academy of Agricultural Sciences, Hefei, 230061, People's Republic of China.

出版信息

Sci Rep. 2017 Mar 31;7:45690. doi: 10.1038/srep45690.

Abstract

The molecular mechanism of silkworm resistance to Bombyx mori nucleopolyhedrovirus (BmNPV) infection remains largely unclear. Accumulating evidence suggests that subcellular fractionation combined with proteomics is an ideal technique to analyse host antiviral mechanisms. To clarify the anti-BmNPV mechanism of the silkworm, the near-isogenic line BC9 (resistant strain) and the recurrent parent P50 (susceptible strain) were used in a comparative subcellular proteomics study. Two-dimensional gel electrophoresis (2-DE) combined with mass spectrometry (MS) was conducted on proteins extracted from the cytosol, mitochondria, and microsomes of BmNPV-infected and control larval midguts. A total of 87 proteins were successfully identified from the three subcellular fractions. These proteins were primarily involved in energy metabolism, protein metabolism, signalling pathways, disease, and transport. In particular, disease-relevant proteins were especially changed in microsomes. After infection with BmNPV, differentially expressed proteins (DEPs) primarily appeared in the cytosolic and microsomal fractions, which indicated that these two fractions might play a more important role in the response to BmNPV infection. After removing genetic background and individual immune stress response proteins, 16 proteins were identified as potentially involved in repressing BmNPV infection. Of these proteins, the differential expression patterns of 8 proteins according to reverse transcription quantitative PCR (RT-qPCR) analyses were consistent with the 2-DE results.

摘要

家蚕对家蚕核型多角体病毒(BmNPV)感染的分子机制在很大程度上仍不清楚。越来越多的证据表明,亚细胞组分分离与蛋白质组学相结合是分析宿主抗病毒机制的理想技术。为了阐明家蚕抗 BmNPV 的机制,本研究使用近等基因系 BC9(抗性品系)和轮回亲本 P50(敏感品系)进行了亚细胞蛋白质组学比较研究。对 BmNPV 感染和对照幼虫中肠的细胞质、线粒体和微粒体中提取的蛋白质进行了二维凝胶电泳(2-DE)结合质谱(MS)分析。从三个亚细胞部分成功鉴定了 87 种蛋白质。这些蛋白质主要参与能量代谢、蛋白质代谢、信号通路、疾病和运输。特别是,与疾病相关的蛋白质在微粒体中发生了特别变化。感染 BmNPV 后,差异表达蛋白(DEPs)主要出现在细胞质和微粒体部分,这表明这两个部分可能在家蚕对 BmNPV 感染的反应中发挥更重要的作用。在去除遗传背景和个体免疫应激反应蛋白后,鉴定出 16 种可能参与抑制 BmNPV 感染的蛋白。其中,8 种蛋白根据反转录定量 PCR(RT-qPCR)分析的差异表达模式与 2-DE 结果一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c8c/5374506/72c55b9cddc8/srep45690-f1.jpg

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