首页> 外文期刊>Proteomics >Quantitative proteomics by 2-DE, 16O/18O labelling and linear ion trap mass spectrometry analysis of lymph nodes from piglets inoculated by porcine circovirus type 2.
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Quantitative proteomics by 2-DE, 16O/18O labelling and linear ion trap mass spectrometry analysis of lymph nodes from piglets inoculated by porcine circovirus type 2.

机译:通过2-DE,16O / 18O标记和线性离子阱质谱分析法对2型猪圆环病毒接种的仔猪的淋巴结进行定量蛋白质组学分析。

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Porcine circovirus type 2 (PCV2) has been identified as the essential causal agent of postweaning multisystemic wasting syndrome. However, little is known regarding the mechanism(s) underlying the pathogenesis of PCV2-induced disease and the interaction of the virus with the host immune system. Here, we present a proteomics study on inguinal lymph nodes of piglets inoculated with PCV2, in order to better understand the pathogenesis of postweaning multisystemic wasting syndrome and the pathways might be affected after infection. We used two proteomics strategies, 2-DE and 1-DE followed by (16)O/(18)O peptide labelling and peptide identification and quantification by MS. More than 100 proteins were found to be differentially regulated and the results obtained by the two strategies were fairly concordant but also complementary, the (18)O labelling approach being a more robust alternative. Analysis of these proteins by systems biology tools revealed the implication of acute phase response and NrF2-mediated oxidative stress, suggesting a putative role for these pathways in the pig immune response. Besides, CD81 was found to be up-regulated, suggesting a possible role in the internalization of the virus. The use of proteomics technologies together with biology analysis systems opens up the way to gain more exhaustive and systematic knowledge of virus-pathogen interactions.
机译:猪圆环病毒2型(PCV2)已被确定为断奶后多系统消耗综合症的必要病因。然而,关于PCV2诱导的疾病的发病机理以及病毒与宿主免疫系统相互作用的基本机制还知之甚少。在这里,我们对接种PCV2的仔猪腹股沟淋巴结进行蛋白质组学研究,以更好地了解断奶后多系统消耗综合症的发病机理,并且感染后的途径可能受到影响。我们使用了两种蛋白质组学策略:2-DE和1-DE,然后进行了(16)O /(18)O肽标记以及通过MS进行肽鉴定和定量分析。发现有100多种蛋白质受到差异调节,并且通过两种策略获得的结果相当一致,而且是互补的,(18)O标记方法是更可靠的选择。通过系统生物学工具对这些蛋白质的分析揭示了急性期反应和NrF2介导的氧化应激的暗示,暗示了这些途径在猪免疫反应中的假定作用。此外,发现CD81被上调,提示可能在病毒的内在化中起作用。蛋白质组学技术与生物学分析系统的结合使用为获取病毒与病原体相互作用的更详尽和系统的知识开辟了道路。

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