首页 | 本学科首页   官方微博 | 高级检索  
     

甘蔗黄叶病毒的RT-PCR检测技术
引用本文:高三基,郭晋隆,孟岩,黄振瑞,陈如凯,刘文荣,MICHAEL S Irey. 甘蔗黄叶病毒的RT-PCR检测技术[J]. 福建农林大学学报(自然科学版), 2006, 35(5): 466-470
作者姓名:高三基  郭晋隆  孟岩  黄振瑞  陈如凯  刘文荣  MICHAEL S Irey
作者单位:1. 福建农林大学农业部甘蔗生理生态与遗传改良重点开放实验室,福建,福州,350002
2. 美国农业部农业研究服务中心,美国园艺研究实验室,弗罗里达,34945
基金项目:引进国际先进农业科技计划(948计划);福建省自然科学基金
摘    要:以甘蔗黄叶病毒(ScYLV)特异性引物YLSF111和YLSR462为引物,对福建蔗区8个罹病品种的疑似病株进行RT-PCR检测,扩增出352 bp特异性片段.将PCR产物克隆后测序,序列分析表明,该片段是ScYLV外壳蛋白(CP)基因的一部分,核苷酸和氨基酸序列同源性达95%以上,与美国、印度、巴西等国家ScYLV分离物(GeneBank登录号分别为AF157029、AY236971、AF141385)CP基因同源性达100%,证实我国福建地区甘蔗黄叶综合症的病原体为ScYLV.本研究同时建立了ScYLV的RT-PCR检测技术.

关 键 词:甘蔗  甘蔗黄叶病毒  RT-PCR  分子鉴定
文章编号:1671-5470(2006)05-0466-05
收稿时间:2006-05-09
修稿时间:2006-07-09

Detection of sugarcane yellow leaf virus by RT-PCR
GAO San-ji,GUO Jin-long,MENG Yan,HUANG Zhen-rui,CHEN Ru-kai,LIU Wen-rong,MICHAEL S Irey. Detection of sugarcane yellow leaf virus by RT-PCR[J]. Journal of Fujian Agricultural and Forestry University, 2006, 35(5): 466-470
Authors:GAO San-ji  GUO Jin-long  MENG Yan  HUANG Zhen-rui  CHEN Ru-kai  LIU Wen-rong  MICHAEL S Irey
Abstract:Using primers YLSF111 and YLSR462,a 352 bp fragment was amplified by RT-PCR in total RNA extracted from leaves of eight infected sugarcane varieties in Fujian,P.R.China.The PCR product was cloned and sequenced.Nucleotide and deduced amino acid sequences were greater than 95% homologus with ScYLV isolates from other countries and were 100% homologus with ScYLV isolates from America,India and Brazil(GenBank accession numbers AF157029,AY236971 and AF141385 respectively).The results confirmed that the causal organism of YLS of sugarcane in China was ScYLV.The protocol for the use of RT-PCR to detect ScYLV was described in the paper.
Keywords:RT-PCR
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号