State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China.
Environment and Plant Protection Institute of Chinese Academy of Tropical Agricultural Sciences, Haikou, Hainan, China.
Lett Appl Microbiol. 2019 Nov;69(5):318-324. doi: 10.1111/lam.13220.
Peach is a major crop in China, and like any other stone fruit, virus and virus-like diseases can reduce the yield and quality of the fruit. Herein, we developed a multiplex RT-PCR (mRT-PCR) assay for simultaneously detecting three viruses known to infect peach: peach-associated luteovirus (PaLV), peach virus D (PeVD) and nectarine stem-pitting-associated virus (NSPaV). Plant nad5 mRNA was used as the internal control. Field samples that were co-infected with PaLV, PeVD and NSPaV were used; we identified three primer pairs to be the most specific for detecting these viruses, followed by determining the ideal concentration of each primer pair and optimizing the annealing temperature for mRT-PCR. We also assessed the detection limit using serial dilutions of RNA and cDNA. The newly developed mRT-PCR assay could simultaneously detect PaLV, PeVD and NSPaV. To validate the reliability of mRT-PCR for virus detection, mRT-PCR was used to detect viruses in the leaves of 21 peach plants collected in Liaoning Province, China. The obtained results revealed the presence of single and co-infections. To conclude, the mRT-PCR assay developed herein is sensitive, reliable and economical, and we believe that it can thus be used for large-scale surveys of PaLV, PeVD and NSPaV. SIGNIFICANCE AND IMPACT OF THE STUDY: In this study, we developed a multiplex reverse transcriptase PCR (mRT-PCR) assay for simultaneously detecting three viruses that infect peach: peach-associated luteovirus (PaLV), peach virus D (PeVD) and nectarine stem-pitting-associated virus (NSPaV). This assay is simple, easy to perform, reliable and cost-effective, and can thus be applied for large-scale surveys of PaLV, PeVD and NSPaV.
桃是中国的主要作物之一,与其他核果一样,病毒和类病毒病害会降低果实的产量和品质。在此,我们开发了一种多重 RT-PCR(mRT-PCR)检测方法,用于同时检测三种已知感染桃的病毒:李痘病毒(PaLV)、李痘病毒 D(PeVD)和油桃茎陷点状病毒(NSPaV)。以植物 nad5mRNA 为内参。使用同时感染 PaLV、PeVD 和 NSPaV 的田间样本;我们鉴定了三个最特异的引物对来检测这些病毒,随后确定了每个引物对的最佳浓度,并优化了 mRT-PCR 的退火温度。我们还通过 RNA 和 cDNA 的系列稀释来评估检测限。新开发的 mRT-PCR 检测方法可同时检测 PaLV、PeVD 和 NSPaV。为验证 mRT-PCR 检测病毒的可靠性,我们使用 mRT-PCR 检测了在中国辽宁省采集的 21 株桃叶中的病毒。获得的结果显示存在单重和多重感染。综上所述,本研究中开发的 mRT-PCR 检测方法灵敏、可靠、经济,我们相信它可用于大规模调查 PaLV、PeVD 和 NSPaV。研究的意义和影响:在本研究中,我们开发了一种多重逆转录 PCR(mRT-PCR)检测方法,用于同时检测三种感染桃的病毒:李痘病毒(PaLV)、李痘病毒 D(PeVD)和油桃茎陷点状病毒(NSPaV)。该检测方法简单、易于操作、可靠且具有成本效益,因此可用于大规模调查 PaLV、PeVD 和 NSPaV。