Suppr超能文献

用于灵敏检测桃潜隐花叶类病毒的逆转录液滴数字PCR检测方法的开发

Development of a reverse transcription droplet digital PCR assay for sensitive detection of peach latent mosaic viroid.

作者信息

Lee Hyo-Jeong, Cho In-Sook, Ju Ho-Jong, Jeong Rae-Dong

机构信息

Department of Applied Biology, Institute of Environmentally Friendly Agriculture, Chonnam National University, Gwangju, 61185, Republic of Korea.

Horticultural and Herbal Crop Environment Division, National Institute of Horticultural and Herbal Science, RDA, Wanju, 55365, Republic of Korea.

出版信息

Mol Cell Probes. 2021 Aug;58:101746. doi: 10.1016/j.mcp.2021.101746. Epub 2021 Jun 5.

Abstract

Peach latent mosaic viroid (PLMVd) represents a continuing threat to peach tree production worldwide. In this study, a sensitive and accurate quantification of PLMVd in peach leaves was established using a reverse transcription droplet digital polymerase chain reaction (RT-ddPCR) assay. The quantitative linearity, accuracy, and sensitivity of RT-ddPCR for the detection of PLMVd were comparatively assessed to those of reverse-transcription real-time quantitative polymerase chain reaction (RT-qPCR) assay. The specificity assay shows no amplification in major peach viruses, apple chlorotic leaf spot virus and prunus necrotic ring spot virus and negative control. Furthermore, the levels of PLMVd transcripts determined using RT-ddPCR and RT-qPCR showed a high degree of linearity and quantitative correlation. Our results also indicated that the RT-ddPCR assay is at least two-fold more sensitive than qPCR and could therefore, be used to detect PLMVd in field samples. Moreover, optimization of RT-ddPCR was found to enhance the sensitivity of PLMVd detection in the peach leaf samples with low viral loads. In summary, the established RT-ddPCR assay represents a promising alternative method for the precise quantitative detection of PLMVd; it would be particularly applicable for diagnosing PLMVd infections in plant quarantine inspection and PLMVd-free certification program.

摘要

桃潜隐花叶类病毒(PLMVd)对全球桃树生产持续构成威胁。在本研究中,利用逆转录液滴数字聚合酶链反应(RT-ddPCR)检测法建立了桃叶片中PLMVd灵敏且准确的定量检测方法。将RT-ddPCR检测PLMVd的定量线性、准确性和灵敏度与逆转录实时定量聚合酶链反应(RT-qPCR)检测法进行了比较评估。特异性检测表明,在主要的桃病毒、苹果褪绿叶斑病毒和李坏死环斑病毒以及阴性对照中均无扩增。此外,使用RT-ddPCR和RT-qPCR测定的PLMVd转录本水平显示出高度的线性和定量相关性。我们的结果还表明,RT-ddPCR检测法的灵敏度至少比qPCR高两倍,因此可用于检测田间样本中的PLMVd。此外,发现RT-ddPCR的优化提高了低病毒载量桃叶样本中PLMVd检测的灵敏度。总之,所建立的RT-ddPCR检测法是一种用于精确定量检测PLMVd的有前景的替代方法;它特别适用于植物检疫检查中PLMVd感染的诊断以及无PLMVd认证项目。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验