Institute of Microbiology, Chinese Academy of Sciences, No 1 West Beichen Road, Chaoyang District, Beijing 100101, China.
J Virol Methods. 2013 Oct;193(1):177-83. doi: 10.1016/j.jviromet.2013.06.013. Epub 2013 Jun 14.
Banana bunchy top virus (BBTV) is the causal agent of banana bunchy top disease. Current diagnostic methods for BBTV are laborious and prone to generate false-negative results. A simple, reliable, and high-throughput method for detecting BBTV in plants and aphids has been developed, which involves tissues disruption from banana plants and viruliferous aphids followed by real-time TaqMan(®) PCR. Extraction of BBTV single-stranded DNA using this method is simple and less prone to contamination than using the CTAB (hexadecyltrimethylammonium bromide) method. The high throughput TaqMan(®) PCR system was highly sensitive, detecting as few as 2.76 copies of BBTV genomic DNA or 1.0 ng-1.0mg of infected banana leaves. The entire assay could be completed within 2h. Regression analysis showed that the quantitative results of TaqMan(®) PCR and copies of the virus have good correlation for plasmids (R(2)=0.966) and for infected leaves (R(2)=0.979). The method developed in this study can quantify BBTV in aphids and plants, even before the appearance of symptoms of banana bunchy top disease.
香蕉束顶病毒(BBTV)是香蕉束顶病的病原体。目前用于检测 BBTV 的方法繁琐,容易产生假阴性结果。本研究建立了一种简单、可靠、高通量的检测植物和蚜虫中 BBTV 的方法,该方法涉及从感染 BBTV 的香蕉植物和蚜虫组织中提取病毒 RNA,然后使用实时 TaqMan(®)PCR 进行检测。与使用 CTAB(十六烷基三甲基溴化铵)法相比,该方法提取 BBTV 单链 DNA 更简单,不易污染。高通量 TaqMan(®)PCR 系统具有高度的敏感性,能够检测到低至 2.76 个 BBTV 基因组 DNA 拷贝或 1.0ng-1.0mg 的感染香蕉叶片。整个检测过程可以在 2 小时内完成。回归分析表明,TaqMan(®)PCR 的定量结果与质粒(R(2)=0.966)和感染叶片(R(2)=0.979)的病毒拷贝数之间具有良好的相关性。本研究建立的方法可用于定量检测蚜虫和植物中的 BBTV,甚至在香蕉束顶病症状出现之前。