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柑橘衰退病毒多克隆和单克隆抗体的制备及检测效果分析
引用本文:王彩霞 王国平 洪霓 姜波 刘辉 吴康为. 柑橘衰退病毒多克隆和单克隆抗体的制备及检测效果分析[J]. 生物工程学报, 2006, 22(4): 629-634
作者姓名:王彩霞 王国平 洪霓 姜波 刘辉 吴康为
作者单位:1. 华中农业大学植物科学技术学院,武汉,430070;华中农业大学国家农业微生物重点实验室,武汉,430070
2. 华中农业大学植物科学技术学院,武汉,430070;华中农业大学国家果树脱毒种质资源室内保存中心,武汉,430070
3. 华中农业大学植物科学技术学院,武汉,430070;华中农业大学国家果树脱毒种质资源室内保存中心,武汉,430070;华中农业大学国家农业微生物重点实验室,武汉,430070
4. 华中农业大学植物科学技术学院,武汉,430070
基金项目:国家高技术研究发展计划(863)基金资助项目(No.2001AA241142)。~~
摘    要:通过改进提纯方法获得了柑橘衰退病毒(Citrustristezavirus,CTV)的提纯液,其产量为1mg/100g植物组织。用CTV免疫大耳白兔,获得多克隆抗体,间接ELISA效价为1∶25600。用CTV免疫小鼠,经细胞融合、ELISA筛选和克隆化培养,获得18株能稳定分泌抗CTV单克隆抗体的杂交瘤单细胞株。对其中4株单克隆腹水抗体进行分析的结果表明,这些抗体的ELISA效价为1∶51200~1∶204800,其中2G和3H的抗体类型及亚类为IgG2a,1E和4H为IgG2b。用所制备抗体对不同来源柑橘样品的CTV检测结果显示,单克隆和多克隆抗体结合使用,采用三抗体夹心ELISA(TAS-ELISA)可以获得理想的检测效果,其特异性强、灵敏度高。同时发现所分析4株单克隆抗体对不同的CTV分离物鉴别能力存在差异,但有关这些CTV分离物的特性及其血清学关系还需进一步研究。

关 键 词:柑橘衰退病毒  多克隆抗体  单克隆抗体  三抗体夹心ELISA
文章编号:1000-3061(2006)04-0629-06
收稿时间:2005-11-11
修稿时间:2006-03-14

Production of Polyclonal and Monoclonal Antibodies Against Citrus Tristeza Virus and Their Efficiency for the Detection of the Virus
WANG Cai-Xia,WANG Guo-Ping,HONG Ni,JIANG Bo,LIU Hui,WU Kang-Wei. Production of Polyclonal and Monoclonal Antibodies Against Citrus Tristeza Virus and Their Efficiency for the Detection of the Virus[J]. Chinese journal of biotechnology, 2006, 22(4): 629-634
Authors:WANG Cai-Xia  WANG Guo-Ping  HONG Ni  JIANG Bo  LIU Hui  WU Kang-Wei
Affiliation:1 College of Plant Science and Technology, Wuhan 430070, China; 2 National Indoor Conservation Center of Virus-free Gemplasms of Fruit Crops, Wuhan 430070, China ;3 State Key Laboratory of Agromicrobiology, Huazhong Agricultural University, Wuhan, 430070, China
Abstract:Citrus tristeza virus (CTV) was purified from a citrus sample by a modified protocol, and the yield was about 1 mg from 100 g citrus tissues. Polyclonal antibody was prepared by immunizing rabbits with the purified CTV preparation with a titer 1:25600 in indirect ELISA test. Eighteen hybridoma-cell lines secreting monoclonal antibodies (MAbs) against CTV were screened after the fusion of mouse myeloma cells (SP2/0) with spleen cells from BALB/c immunized with the virus preparation. Four hybridoma-cell lines were selected randomly for later analysis. The results indicated that the titers of ascetic fluids against these hybridoma cell lines ranged from 1:51200 to 1:204800 in indirect ELISA, and their isotypes and subclasses were IgG2a for 2G and 3H and IgG2b for IE and 4H. These four Mabs were used to detect CTV in citrus samples in different sources. Results showed that TAS-ELISA with polyclonal antibody as trapping antibody and monoclonal antibody as testing antibody had a higher specificity and sensitivity than PAS-ELISA. Four Mabs showed different intensities of serological reaction with different CTV isolates. However, much work remains for realizing the characteristics and the serological relationships among these isolates.
Keywords:Citrus tristeza virus (CTV)   polyclonal antibody   monoclonal antibody   TAS-ELISA
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