甘蔗黄叶病毒外壳蛋白基因克隆及其实时荧光RT-PCR检测  被引量:4

Cloning and detection of coat protein gene of Sugarcane yellow leaf virus by real-time fluorescent RT-PCR

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作  者:高三基[1] 杨帆[1] 陈平华[1] 王恒波[1] 徐景升[1] 陈如凯[1] 

机构地区:[1]福建农林大学农业部甘蔗遗传改良重点开放实验室,福州350002

出  处:《植物病理学报》2011年第3期262-269,共8页Acta Phytopathologica Sinica

基  金:现代农业产业技术体系建设专项资金项目(nycytx-024);公益性行业(农业)科研专项(nyhyzx07-019);福建省自然科学基金资助项目(2008J0048)

摘  要:甘蔗黄叶病毒(Sugarcane yellow leaf virus,SCYLV)引起的甘蔗黄叶病是一种新的全球性病毒病害。本文以YLSCPF1和YLSCPR591为引物,采用RT-PCR方法克隆了甘蔗黄叶病毒福建分离物(CHN-FJ1)外壳蛋白(CP)基因,编码196个氨基酸。分析不同地理来源的SCYLV病毒分离物cp基因核苷酸及其推导编码的氨基酸序列,同源性达95%以上。根据cp基因的保守序列,设计1对特异性引物和TaqMan探针,建立了SCYLV的TaqMan实时荧光RT-PCR方法。结果表明,检测下限为初始质粒模板DNA 1 000拷贝/μL(约3.61 fg/μL),比常规PCR方法的灵敏度提高100倍。检测甘蔗花叶病毒、宿根矮化病菌和黑穗病菌,没有典型的扩增曲线和无Ct值。应用实时荧光RT-PCR、常规RT-PCR和组织印迹免疫杂交(TBIA)对田间甘蔗叶片样品进行检测,阳性检出率分别为100%、61.5%和69.2%,表明该方法比常规RT-PCR和TBIA具有更高的灵敏度,适合于对SCYLV的检测。Sugarcane yellow leaf disease induced by Sugarcane yellow leaf virus(SCYLV) is a global viral disease.The coat protein gene(cp) that deduced 196 amino acids from CHN-FJ1 isolate was cloned by RT-PCR with the primers YLSCPF1and YLSCPR591.Sequence analysis showed that identity of nucleotides and deduced amino acids shared above 95% among the isolates from different geographical origins.The primers and TaqMan probe located on the conservative sequence of cp were designed for real-time fluorescent RT-PCR.The studies demonstrated that the detection limit was 1 000 copies/μL(3.61 fg/μL) of positive cloning plasmid,was 100-fold higher than that of regular RT-PCR.Typical amplification curve and Ct value did not appear in detection of Sugarcane mosaic virus(SCMV),the pathogens of sugarcane ratoon stunning di-sease(Leifsonia xyli subsp.xyli) and sugarcane smut(Ustilago scitaminea Syd.).The detection of leaf samples from field were conducted by real-time fluorescent RT-PCR,regular RT-PCR as well as tissue blot immunoassay(TBIA) and positive results reached 100%,61.5% and 69.2%,respectively.The real-time fluorescent RT-PCR was more sensitive and reliable method for detection of SCYLV as compared with regular RT-PCR and TBIA.

关 键 词:甘蔗黄叶病毒 外壳蛋白 序列分析 实时荧光RT-PCR 

分 类 号:S432.41[农业科学—植物病理学] S435.661[农业科学—农业昆虫与害虫防治]

 

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