Development of a novel real-time RT-PCR assay with LUX primer for the detection of swine transmissible gastroenteritis virus

被引:36
作者
Chen, R [1 ]
Huang, WM [1 ]
Lin, ZX [1 ]
Zhou, ZF [1 ]
Yu, HQ [1 ]
Zhu, DZ [1 ]
机构
[1] Guangdong Entry Exit Inspect & Quarantine Bur, Anim Quarantine Lab, Guangzhou 510623, Peoples R China
关键词
LUX fluorogenic primers; transmissible gastroenteritis virus; real-time RT-PCR; rapid detection;
D O I
10.1016/j.jviromet.2004.08.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Real-time RT-PCR assay, based on light upon extension (LUX) fluorogenic primer and LightCycle technology, was developed for rapid detection of transmissible gastroenteritis virus (TGEV). Viral RNA from different TGEV isolates and clinical specimens was detected. To evaluate the sensitivity of the assay, a gel-based RT-PCR method targeted at the same 101 bp sequence was also developed. Serial 10-fold dilutions of TGEV RNA were detected by the two methods. Although the real time method used only 2 mul RNA for each reaction, a 10-fold increase of sensitivity over that of the gel-based method, which used 10 mul RNA was demonstrated. The study indicates that the LUX assay reported below is rapid, reliable and sensitive and it has the potential for use as an alternative molecular method for TGEV diagnosis. (C) 2004 Elsevier B.V. All rights reserved.
引用
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页码:57 / 61
页数:5
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