School of Life Sciences, Anhui Agricultural University, Hefei, People's Republic of China.
School of Life Sciences, Anhui Agricultural University, Hefei, People's Republic of China.
J Proteomics. 2017 Aug 8;165:35-50. doi: 10.1016/j.jprot.2017.06.007. Epub 2017 Jun 15.
Bombyx mori nucleopolyhedrovirus (BmNPV) has been identified as a major pathogen responsible for severe economic loss. Most silkworm strains are susceptible to BmNPV, with only a few highly resistant strains thus far identified. Here we investigated the molecular basis of silkworm resistance to BmNPV using susceptible (the recurrent parent P50) and resistant (near-isogenic line BC9) strains and a combination of iTRAQ-based quantitative proteomics, reverse-transcription quantitative PCR and Western blotting. By comparing the proteomes of infected and non-infected P50 and BC9 silkworms, we identified 793 differentially expressed proteins (DEPs). By gene ontology and KEGG enrichment analyses, we found that these DEPs are preferentially involved in metabolism, catalytic activity, amino sugar and nucleotide sugar metabolism and carbon metabolism. 114 (14.38%) DEPs were associated with the cytoskeleton, immune response, apoptosis, ubiquitination, translation, ion transport, endocytosis and endopeptidase activity. After removing the genetic background and individual immune stress response proteins, we identified 84 DEPs were found that are potentially involved in resistance to BmNPV. Further studies showed that a serine protease was down-regulated in P50 and up-regulated in BC9 after BmNPV infection. Taken together, these results provide insights into the molecular mechanism of silkworm response to BmNPV.
Bombyx mori nucleopolyhedrovirus (BmNPV) is highly pathogenic, causing serious losses in sericulture every year. However, the molecular mechanisms of BmNPV infection and host defence remain unclear. Here we combined quantitative proteomic, bioinformatics, RT-qPCR and Western blotting analyses and found that BmNPV invasion causes complex protein alterations in the larval midgut, and that these changes are related to cytoskeleton, immune response, apoptosis, ubiquitination, translation, ion transport, endocytosis and endopeptidase activity. Five important differentially expression proteins were validation by independent approaches. These finding will help address the molecular mechanisms of silkworm resistance to BmNPV and provide a molecular target for resisting BmNPV.
家蚕核型多角体病毒(BmNPV)已被确定为导致严重经济损失的主要病原体。大多数家蚕品种对 BmNPV 敏感,迄今为止仅发现少数高抗性品种。在这里,我们使用敏感(轮回亲本 P50)和抗性(近等基因系 BC9)品系以及基于 iTRAQ 的定量蛋白质组学、逆转录定量 PCR 和 Western blotting 的组合,研究了家蚕对 BmNPV 的抗性的分子基础。通过比较感染和未感染 P50 和 BC9 家蚕的蛋白质组,我们鉴定了 793 个差异表达蛋白(DEPs)。通过基因本体和 KEGG 富集分析,我们发现这些 DEPs 主要参与代谢、催化活性、氨基糖和核苷酸糖代谢以及碳代谢。114(14.38%)DEPs 与细胞骨架、免疫反应、细胞凋亡、泛素化、翻译、离子转运、内吞作用和内肽酶活性有关。去除遗传背景和个体免疫应激反应蛋白后,我们鉴定出 84 个 DEPs 可能参与对 BmNPV 的抗性。进一步的研究表明,一种丝氨酸蛋白酶在 P50 中下调,在 BC9 中上调。综上所述,这些结果为家蚕对 BmNPV 反应的分子机制提供了深入了解。
家蚕核型多角体病毒(BmNPV)高度致病,每年给养蚕业造成严重损失。然而,BmNPV 感染和宿主防御的分子机制仍不清楚。在这里,我们结合定量蛋白质组学、生物信息学、RT-qPCR 和 Western blotting 分析,发现 BmNPV 入侵导致幼虫中肠复杂的蛋白质改变,这些变化与细胞骨架、免疫反应、细胞凋亡、泛素化、翻译、离子转运、内吞作用和内肽酶活性有关。通过独立方法验证了 5 个重要的差异表达蛋白。这些发现将有助于解决家蚕对 BmNPV 抗性的分子机制,并为抵抗 BmNPV 提供分子靶标。