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利用实时荧光定量PCR和高分辨率熔解曲线分析同时检测樱桃坏死锈斑病毒和樱桃绿环斑驳病毒

Simultaneous detection of Cherry necrotic rusty mottle virus and Cherry green ring mottle virus using real-time PCR and high resolution melting analysis.

作者信息

Komorowska Beata, Fiore Nicola, Zamorano Alan, Li Ruhui

机构信息

Research Institute of Horticulture, Department of Plant Protection, Konstytucji 3 Maja 1/3, 96-100 Skierniewice, Poland.

Universidad de Chile, Facultad de Ciencias Agronómicas, Av. Santa Rosa 11315, La Pintana, Santiago, Chile.

出版信息

Mol Cell Probes. 2014 Aug;28(4):186-91. doi: 10.1016/j.mcp.2014.03.002. Epub 2014 Mar 24.

Abstract

In this study, the real-time PCR assays were combined with high resolution melting (HRM) analysis for the simultaneous detection of Cherry necrotic rusty mottle virus (CNRMV) and Cherry green ring mottle virus (CGRMV) infection in sweet cherry trees. Detection of CNRMV and CGRMV was performed in a real-time PCR using a primer set for both of them or duplex real-time PCR that included one specific primer set for each virus. These two strategies allowed us to confirmed virus infection in all tested samples. In 17 field samples the technique revealed samples positive for CNRMV or CGRMV as well as positive for both viruses. In addition, the HRM analysis made it possible to differentiate clearly between CNRMV and CGRMV. Sequence variations among CNRMV and CGRMV isolates observed from the HRM peaks were confirmed by sequencing. To test the capability to use this method in field, forty one sweet cherry samples were examined by HRM analysis. The HRM data showed that seven samples were positive for CNRMV and three were infected with CGRMV. The results presented in this study indicated that real-time PCR followed by HRM analysis provides sensitive, automated and rapid tool to detect and differentiate between CNRMV and CGRMV isolates.

摘要

在本研究中,实时荧光定量PCR检测与高分辨率熔解曲线(HRM)分析相结合,用于同时检测甜樱桃树中樱桃坏死锈斑驳病毒(CNRMV)和樱桃绿环斑驳病毒(CGRMV)的感染情况。使用针对这两种病毒的引物对,通过实时荧光定量PCR检测CNRMV和CGRMV,或者采用双链实时荧光定量PCR,其中包含针对每种病毒的一个特异性引物对。这两种策略使我们能够在所有测试样品中确认病毒感染情况。在17个田间样品中,该技术检测出CNRMV或CGRMV呈阳性的样品,以及两种病毒均呈阳性的样品。此外,HRM分析能够清晰地区分CNRMV和CGRMV。通过测序证实了从HRM峰观察到的CNRMV和CGRMV分离株之间的序列差异。为了测试该方法在田间的应用能力,通过HRM分析检测了41个甜樱桃样品。HRM数据显示,7个样品CNRMV呈阳性,3个样品感染了CGRMV。本研究结果表明,实时荧光定量PCR结合HRM分析为检测和区分CNRMV和CGRMV分离株提供了一种灵敏、自动化且快速的工具。

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