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西瓜花叶病毒抗血清制备及其应用
引用本文:冀树娴,王姝雯,王健,李向东,朱天生,田延平.西瓜花叶病毒抗血清制备及其应用[J].植物病理学报,2018,48(6):833-837.
作者姓名:冀树娴  王姝雯  王健  李向东  朱天生  田延平
作者单位:山东农业大学植物保护学院植物病理学系,泰安 271018;
山东省农业微生物重点实验室,泰安 271018;
塔里木大学植物科学学院,阿拉尔 843300
基金项目:国家自然科学基金(31501612);国家重点研发计划(2017YFD0200900);山东省农业微生物重点实验室开放课题(SDKL2017015)
摘    要: 西瓜花叶病毒(Watermelon mosaic virus, WMV)是危害葫芦科作物的重要病毒。制备特异性强、效价高的抗血清对快速准确检测和鉴定WMV具有重要意义。本研究将WMV外壳蛋白(Coat protein,CP)基因克隆到原核表达载体pEHISTEV获得pEHISTEV-WMV-CP。将pEHISTEV-WMV-CP转化大肠杆菌Rosetta,经IPTG诱导,成功表达出分子量约为36 kDa的蛋白,与预期WMV CP大小一致。切胶回收WMV CP,与等体积弗氏不完全佐剂充分乳化后免疫健康新西兰大白兔。Western blotting结果表明,制备的抗血清与WMV CP有反应,与同属的番木瓜环斑病毒(Papaya ringspot virus,PRSV)、马铃薯Y病毒(Potato virus Y,PVY)、小西葫芦黄花叶病毒(Zucchini yellow mosaic virus, ZYMV)和烟草花叶病毒属的黄瓜绿斑驳花叶病毒(Cucumber green mottle mosaic virus,CGMMV)均无反应。酶联免疫吸附测定(PTA-ELISA)结果表明,本研究制备的WMV抗血清效价为1∶8 192,并且能够检测稀释512倍的病毒汁液。利用该抗血清对田间采集的10个RT-PCR检测为阳性的样品进行检测,全部呈现阳性。本研究利用大肠杆菌表达的CP制备的WMV抗血清具有较高的特异性和灵敏度。研究结果为WMV的快速检测和鉴定奠定了基础。

关 键 词:抗血清  外壳蛋白  原核表达  西瓜花叶病毒  
收稿时间:2018-01-11

Preparation and application of antiserum against Watermelon mosaic virus coat protein expressed in E. coli
JI Shu-xian,WANG Shu-wen,WANG Jian,LI Xiang-dong,ZHU Tian-sheng,TIAN Yan-ping.Preparation and application of antiserum against Watermelon mosaic virus coat protein expressed in E. coli[J].Acta Phytopathologica Sinica,2018,48(6):833-837.
Authors:JI Shu-xian  WANG Shu-wen  WANG Jian  LI Xiang-dong  ZHU Tian-sheng  TIAN Yan-ping
Institution:Department of Plant Pathology, College of Plant Protection, Shandong Agricultural University, Tai′an 271018, China;
Shandong Provincial Key Laboratory of Agricultural Microbiology, Tai′an 271018, China;
College of Plant Science, Tarim University, Alaer 843300, China
Abstract:Watermelon mosaic virus (WMV; genus Potyvirus) is an economically important virus infecting cucurbit crops. Preparation of antiserum with high specificity and sensitivity is essential for rapid and accurate detection and identification of WMV. In this study, WMV coat protein (CP) gene was cloned into E. coli expression vector pEHISTEV, named pEHISTEV-WMV-CP. pEHISTEV-WMV-CP was transformed and expressed into E. coli Rosetta. A protein with expected molecular weight of 36 kDa was obtained after IPTG induction. The band was cut and used to immune New Zealand white rabbit. Western blotting results showed that the antiserum could specifically recognize WMV CP expressed in E. coli and WMV from infected leaves. There was no cross reaction to closely related Papaya ringspot virus (PRSV), Potato virus Y (PVY), Zucchini yellow mosaic virus (ZYMV) from the genus Potyvirus, neither the Cucumber green mottle mosaic virus (CGMMV) of the genus Tobamovirus. The antiserum had a titer of 1∶8 192 in PTA-ELISA and could detect WMV infected samples diluted up to 512 times. Among the 10 samples showed positive reaction in RT-PCR, all of them were positive when detected with this antiserum via PTA-ELISA. These results indicated that the antiserum obtained in our study had high specificity and sensitivity and laid solid foundation for rapid and accurate detection and identification of WMV.
Keywords:antiserum  coat protein  prokaryotic expression  Watermelon mosaic virus  
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