Rapid and sensitive detection of white spot syndrome virus by loop-mediated isothermal amplification combined with a lateral flow dipstick

被引:127
作者
Jaroenrama, Wansadaj [1 ,2 ]
Kiatpathomchai, Wansika [1 ,3 ]
Flegel, Timothy W. [1 ]
机构
[1] Mahidol Univ, CENTEX Shrimp, Fac Sci, Bangkok 10700, Thailand
[2] Mahidol Univ, Dept Biotechnol, Fac Sci, Bangkok 10700, Thailand
[3] Natl Ctr Genet Engn & Biotechnol BIOTEC, Pathum Thani 12120, Thailand
关键词
WSSV; White spot syndrome virus; Penaeus monodon; Shrimp; Loop-mediated isothermal amplification; LAMP; Nested PCR; Lateral flow dipstick; LFD; POLYMERASE-CHAIN-REACTION; TAURA-SYNDROME VIRUS; SHRIMP PENAEUS-MONODON; CRAB SCYLLA-SERRATA; MACROBRACHIUM-ROSENBERGII; BACULOVIRUS WSBV; WSSV; PCR; INFECTION; DISEASE;
D O I
10.1016/j.mcp.2008.12.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Loop-mediated isothermal amplification (LAMP) allows rapid amplification of nucleic acids under isothermal conditions using a set of four specifically designed primers that recognize six distinct target sequences. It can be combined with a chromatographic lateral flow dipstick (LFD) for highly specific, rapid and simple visual detection of WSSV-specific amplicons. Using this protocol, a 30-min amplification followed by 5 min hybridization with an FITC-labeled DNA probe and 5 min LFD resulted in visualization of DNA amplicons trapped at the LFD test line. Thus, 10 min for rapid DNA extraction followed by LAMP combined with LFD detection resulted in a total assay time of approximately 50 min. Detection sensitivity was comparable to other commonly-used methods for nested PCR detection of WSSV but had the additional advantages of reduced assay time, confirmation of amplicon identity by hybridization and elimination of electrophoresis with carcinogenic ethidium bromide. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:65 / 70
页数:6
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