Gadiou S, Kundu J K
Division of Plant Health, Department of Virology, Crop Research Institute, 16106 Prague, Czech Republic.
Indian J Virol. 2012 Jun;23(1):39-41. doi: 10.1007/s13337-012-0065-4. Epub 2012 Mar 25.
A SYBR Green(®)-based one step RT-qPCR assay was developed for the detection and quantification of Apple stem grooving virus (ASGV) and Apple mosaic virus (ApMV). The RT-qPCR assay employed seven plant-expressed genes-glyceraldehyde 3-phosphate dehydrogenase (GAPDH), 18S ribosomal RNA, ubiquitin, ribosomal protein S19, Rubisco, RNA polymerase subunit II and β-actin-as internal reference housekeeping genes in a relative quantification system in three apple cultivars (i.e. Idared, Champion, Fragrance). The average expression stability (M) found by GeNorm software suggest that GAPDH and S19 were the most stable reference genes. We propose employing GAPDH and S19 as housekeeping genes for accurate quantification of ASGV and ApMV in apple leaf samples. The detection limit for both viruses was found around 70 copies of viral genome by one-step RT-qPCR.
开发了一种基于SYBR Green(®)的一步法RT-qPCR检测方法,用于检测和定量苹果茎沟病毒(ASGV)和苹果花叶病毒(ApMV)。该RT-qPCR检测方法在三个苹果品种(即Idared、Champion、Fragrance)的相对定量系统中,采用了七个植物表达基因——甘油醛-3-磷酸脱氢酶(GAPDH)、18S核糖体RNA、泛素、核糖体蛋白S19、核酮糖-1,5-二磷酸羧化酶/加氧酶(Rubisco)、RNA聚合酶亚基II和β-肌动蛋白——作为内参管家基因。GeNorm软件得出的平均表达稳定性(M)表明,GAPDH和S19是最稳定的参考基因。我们建议使用GAPDH和S19作为管家基因,以准确定量苹果叶片样本中的ASGV和ApMV。通过一步法RT-qPCR发现,两种病毒的检测限约为70个病毒基因组拷贝。