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

机译:敏感和近等基因抗家蚕(鳞翅目)幼虫中肠对BmNPV感染的反应的比较亚细胞蛋白质组学分析。

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摘要

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.
机译:蚕抗家蚕核多角体病毒(BmNPV)感染的分子机制仍不清楚。越来越多的证据表明,结合蛋白质组学的亚细胞分级分离是分析宿主抗病毒机制的理想技术。为了阐明家蚕的抗BmNPV机制,在比较的亚细胞蛋白质组学研究中使用了近等基因系BC9(抗性品系)和复发亲本P50(易感品系)。对从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)与质谱(MS)结合。从三个亚细胞部分中成功鉴定出总共87种蛋白质。这些蛋白质主要参与能量代谢,蛋白质代谢,信号传导途径,疾病和运输。特别是,与疾病相关的蛋白质在微粒体中尤其发生了变化。用BmNPV感染后,差异表达蛋白(DEP)主要出现在胞质和微粒体组分中,这表明这两个组分可能在对BmNPV感染的应答中起更重要的作用。去除遗传背景和个体免疫应激反应蛋白后,鉴定出16种蛋白可能与抑制BmNPV感染有关。在这些蛋白质中,根据逆转录定量PCR(RT-qPCR)分析的8种蛋白质的差异表达模式与2-DE结果一致。

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