Real-time target-specific detection of loop-mediated isothermal amplification for white spot syndrome virus using fluorescence energy transfer-based probes

被引:73
作者
Chou, Pin-Hsing [2 ]
Lin, Yu-Chan [2 ]
Teng, Ping-Hua [2 ]
Chen, Chu-Liang [3 ]
Lee, Pei-Yu [1 ]
机构
[1] Cent Taiwan Univ Sci & Technol, Inst Med Biotechnol, Taichung 406, Taiwan
[2] GeneReach Technol Corp, Taichung 407, Taiwan
[3] Tunghai Univ, Dept Anim Sci & Biotechnol, Taichung 407, Taiwan
关键词
LAMP; FRET hybridization probe; Isothermal amplification; WSSV; Amplicon-specific detection; POLYMERASE-CHAIN-REACTION; LATERAL FLOW DIPSTICK; TAURA-SYNDROME VIRUS; IN-SITU HYBRIDIZATION; SYNDROME BACULOVIRUS WSBV; CULTURED PENAEID SHRIMP; YELLOW-HEAD VIRUS; SENSITIVE DETECTION; MONOCLONAL-ANTIBODIES; VISUAL DETECTION;
D O I
10.1016/j.jviromet.2011.01.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Aiming to establish a target amplicon-specific detection system for loop-mediated isothermal amplification (LAMP), the fluorescent resonance energy transfer (FRET) probe technology was applied to develop the FRET LAMP platform. This report describes the development of the first FRET LAMP assay targeting white spot syndrome virus (WSSV) of penaeid shrimp. A successful accelerated WSSV LAMP was assembled first in a conventional oven and confirmed by gel electrophoresis and dot-blot hybridization. Subsequently, two additional FRET probes designed to target one loop region within WSSV LAMP amplicons were added to the same LAMP reaction. The reactions were carried out in a LightCycler (Roche) and significant FRET signals were detected in real time. Optimization of the reaction using plasmid DNA shortened the time for the detection of 102 copies of the target DNA to less than 70 min. Cross reactivity was absent with WSSV-free or infectious hypodermal and hematopoietic necrosis virus-infected Penaeus vannamei samples. The performance of this system was comparable with that of a nested PCR assay from 21 WSSV-infected shrimp. Specifically detecting target amplicons and requiring no post-amplification manipulation, the novel FRET LAMP assay should allow indisputable detection of pathogens with minimized risks of amplicon contamination. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:67 / 74
页数:8
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