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一种用于广泛检测番茄褪绿斑驳病毒的一步免疫捕获实时TaqMan逆转录聚合酶链反应检测方法的开发。

Development of a one-step immunocapture real-time TaqMan RT-PCR assay for the broad spectrum detection of Pepino mosaic virus.

作者信息

Ling Kai-Shu, Wechter W Patrick, Jordan Ramon

机构信息

USDA-ARS, U.S. Vegetable Laboratory, 2700 Savannah Highway, Charleston, SC, USA.

出版信息

J Virol Methods. 2007 Sep;144(1-2):65-72. doi: 10.1016/j.jviromet.2007.03.022. Epub 2007 May 11.

Abstract

A real-time reverse-transcription polymerase chain reaction (RT-PCR) was developed for efficient detection of genetically diverse Pepino mosaic virus (PepMV) isolates. The novel detection system was designed to use a duo-primer system targeting the conserved region in the triple gene block 2 (TGB2) gene with a single conserved TaqMan probe to broaden its reaction to cover all available PepMV strains. This duo-primer real-time RT-PCR assay was evaluated against US1, US2, Ch1, Ch2 and 25 field isolates collected from six major commercial tomato greenhouse facilities in U.S. and Canada in 2006. Under optimum reaction conditions, sensitivity of the detection was as low as 100 fg of purified viral RNA. This assay was also evaluated for its efficiency in detecting PepMV in various levels of contaminated seed samples. Using immuno-capture sample preparation, real-time RT-PCR was able to detect PepMV in one infested seed in 1000. This level of sensitivity indicated that the one-step immuno-capture duo-primer TaqMan real-time RT-PCR developed in the present study could be used for routine seed health assays.

摘要

开发了一种实时逆转录聚合酶链反应(RT-PCR),用于高效检测基因多样的 Pepino 花叶病毒(PepMV)分离株。该新型检测系统设计使用双引物系统,靶向三重基因块 2(TGB2)基因中的保守区域,并使用单个保守的 TaqMan 探针,以扩大其反应范围,覆盖所有可用的 PepMV 菌株。针对 2006 年从美国和加拿大六个主要商业番茄温室设施收集的 US1、US2、Ch1、Ch2 和 25 个田间分离株,对这种双引物实时 RT-PCR 检测方法进行了评估。在最佳反应条件下,检测灵敏度低至 100 fg 的纯化病毒 RNA。还评估了该检测方法在检测不同污染水平种子样品中 PepMV 的效率。使用免疫捕获样品制备方法,实时 RT-PCR 能够检测出 1000 粒受侵染种子中的一粒 PepMV。这种灵敏度水平表明,本研究中开发的一步免疫捕获双引物 TaqMan 实时 RT-PCR 可用于常规种子健康检测。

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