| 感染新型鸭呼肠孤病毒的番鸭肝脏蛋白质组双向电泳方法的建立 |
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| 引用本文： | 黄梅清,朱果真,陈仕龙,郑敏,程晓霞,陈少莺.感染新型鸭呼肠孤病毒的番鸭肝脏蛋白质组双向电泳方法的建立[J].中国农学通报,2013,29(26):19-24. |
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| 作者姓名： | 黄梅清 朱果真 陈仕龙 郑敏 程晓霞 陈少莺 |
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| 作者单位： | [1]福建省畜禽疫病防治工程技术研究中心,福州350013 [2]福建省农业科学院畜牧兽医研究所,福州350013 [3]福建农林大学动物科学学院,福州350007 |
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| 基金项目： | 国家自然科学基金项目“水禽呼肠孤病毒致病性差异的机理研究”（31172334）; 国家863项目“家禽病毒病基因工程疫苗创制”（2011AA10A209） |
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| 摘 要： | 为建立感染新型鸭呼肠孤病毒（NDRV）的番鸭肝脏蛋白质组双向电泳（2-DE）方法。本研究通过对人工感染NDRV的雏番鸭肝脏病变的观察,对肝脏蛋白质提取裂解液的配方、样品上样量、一向等电聚焦（IEF）参数等条件的对比和优化,建立了有效的番鸭肝脏2-DE方法。结果表明：采用攻毒后病变最典型的第5天的番鸭肝脏作为研究样品;采用研磨-超声-裂解液（7 mol/L尿素、2 mol/L硫脲、4%CHAPS、65 mmol/L DTT、40 mmol/L Tris-base、0.5%IPG buffer）法提取肝脏蛋白质,结合2D clean-up kit以及去拖尾DeStreak试剂纯化蛋白,按1100μg上样,设置IEF参数为：50 V 12 h、200 V 1.5 h、500 V 1 h、1000 V 1 h、8000 V 3 h、8000 V 60000 V h、500 V维持,采用胶体考马斯亮蓝染色,能获得分辨率高、重复性好的2-DE图谱。应用建立的2-DE方法和PDQest 8.0分析软件,发现26个与正常番鸭肝脏蛋白表达水平超过3倍的差异蛋白点。该方法的建立为进一步寻找NDRV感染宿主组织相关蛋白以及水禽呼肠孤病毒差异蛋白质组学研究提供了技术支持。
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| 关 键 词： | 番鸭 肝脏 蛋白质组 新型鸭呼肠孤病毒 |
| 收稿时间： | 2013/5/13 0:00:00 |
| 修稿时间： | 2013/7/11 0:00:00 |
Establishment of Two-dimensional Electrophoresis for Proteme of Liver from Muscovy Duck Experimentally Infected with Norvel Duck Reovirus |
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| Huang Meiqing,Zhu Guozhen,Chen Shilong,Zheng Min,Cheng Xiaoxia,Chen Shaoying.Establishment of Two-dimensional Electrophoresis for Proteme of Liver from Muscovy Duck Experimentally Infected with Norvel Duck Reovirus[J].Chinese Agricultural Science Bulletin,2013,29(26):19-24. |
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| Authors: | Huang Meiqing Zhu Guozhen Chen Shilong Zheng Min Cheng Xiaoxia Chen Shaoying |
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| Institution: | 1Fujian Animal Diseases Control Technology Development Center, Fuzhou 350013; 2Institute of Animal Husbandry and Veterinary Medicine, Fujian Academy of Agricultural Sciences, Fuzhou 350013; 3College of Animal Science, Fujian Agricultural and Forestry University, Fuzhou 350002) |
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| Abstract: | The aim was to establish an efficient Two-Dimensional Electrophoresis （2-DE） ptotocol for proteomic method of livers from muscovy ducks which were experimentally infected with Norvel Duck Reovirus （NDRV）. The conditions which included the reagent of Lysis buffer, amount of loaded protein and parameters of Isoelectric Focusing （IEF） were compared and optimized. The pathological changes in livers were simultaneously observed. The results showed that the livers with characteristic pathology were chosen to be the samples, which were from muscovy ducks at the fifth day after inoculated with NDRV. The high-resolution and good-repeatability 2-DE images were obtained with 1100 Ixg of liver protein samples which were extracted by Lysis-buffer, purified by 2D clean-up kit, separated by 2-DE under suitable electrophoresis parameters, and stained with colloidal Coomassie brilliant blue G-250 solution. Analyzed with the software PDQest 8.0, 26differentially expressed proteins spots were detected between the NDRV-NP03 infected group and the mock-infected group, of which the expression levels were more than 3 times in expression level. The established 2-DE method would pave the way for the further study on the host cell protein and differential proteomic analysis of waterfowl reovirus. |
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| Keywords: | Muscovy Duck liver proteomic Norvel Duck Reovirus |
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