Liu Yingjie, Wang Yingli, Wang Qin, Zhang Yanhui, Shen Wanxia, Li Ruhui, Cao Mengji, Chen Lei, Li Xue, Zhou Changyong, Zhou Yan
National Citrus Engineering Research Center, Citrus Research Institute, Southwest University, Chongqing, 400712, China.
Academy of Agricultural Sciences, Southwest University, Chongqing, 400712, China.
Arch Virol. 2019 Mar;164(3):691-697. doi: 10.1007/s00705-018-04123-7. Epub 2018 Dec 11.
In 2009, a new viral disease of citrus caused by citrus yellow vein clearing virus (CYVCV) was first discovered in China. CYVCV is considered to be the most serious pathogen affecting lemon production. In this study, a sensitive and reliable reverse transcription droplet digital polymerase chain reaction (RT-ddPCR) assay was developed to detect and quantify CYVCV without references. The specificity of the assay was demonstrated by its failure to amplify other relevant citrus viruses. The quantitative linearity, sensitivity and accuracy of RT-ddPCR for detecting CYVCV were compared to those of real-time RT-PCR. The results showed that both methods had a high degree of linearity (R = 0.9776) and quantitative correlation. Furthermore, RT-ddPCR was found to be 100 times more sensitive than real-time RT-PCR, and it can therefore be used to detect CYVCV in individual arthropods. In summary, the results demonstrated that the RT-ddPCR assay is a promising approach for quantitative detection of CYVCV with high precision and accuracy.
2009年,在中国首次发现了由柑橘黄脉明病毒(CYVCV)引起的一种新的柑橘病毒性病害。CYVCV被认为是影响柠檬生产的最严重病原体。在本研究中,开发了一种灵敏且可靠的逆转录液滴数字聚合酶链反应(RT-ddPCR)检测方法,用于在无参照的情况下检测和定量CYVCV。该检测方法的特异性通过其未能扩增其他相关柑橘病毒得以证明。将RT-ddPCR检测CYVCV的定量线性、灵敏度和准确性与实时RT-PCR的进行了比较。结果表明,两种方法均具有高度线性(R = 0.9776)和定量相关性。此外,发现RT-ddPCR比实时RT-PCR灵敏100倍,因此可用于检测单个节肢动物中的CYVCV。总之,结果表明RT-ddPCR检测方法是一种用于高精度和准确地定量检测CYVCV的有前景的方法。