Semiquantitative dot-blot immunogold assay for specific detection of white spot syndrome virus

被引:4
作者
Bunsanong, Nittaya [1 ]
Chotigeat, Wilaiwan [1 ,2 ]
Deachamag, Panchalika [1 ,2 ]
Thananimit, Suchera [1 ,2 ]
机构
[1] Prince Songkla Univ, Fac Sci, Dept Mol Biotechnol & Bioinformat, Hat Yai, Songkhla, Thailand
[2] Prince Songkla Univ, Fac Sci, Ctr Genom & Bioinformat Res, Hat Yai 90112, Songkhla, Thailand
关键词
dot-blot immunogold assay; nitrocellulose membrane; polyclonal antibody; shrimp farming; white spot syndrome virus; POLYMERASE-CHAIN-REACTION; ENZYME IMMUNOASSAYS; PENAEID SHRIMP; SYNDROME WSBV; WSSV; ELIMINATION; PROTEINS; VP26;
D O I
10.1002/bab.1640
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A dot-blot immunogold assay (DBIA) was developed to detect white spot syndrome virus (WSSV) using the polyclonal antibody VP26 (anti-VP26). The anti-VP26 was immobilized on gold nanoparticles (Ab-AuNPs), and a nitrocellulose membrane was used as a detection pad. When the target WSSV bound to the Ab-AuNPs a reddish dot appeared on the surface of the membrane used within 2-5 Min, which could be seen with the naked eye. The test was able to detect WSSV at concentrations as low as 10(5) copies L-1 of WSSV. The DBIA developed had good specificity, and the colloidal gold probe can be applied within 2-3 days when stored at 4 degrees C. For real sample analysis, the DBIA was applied to samples of seawater used for shrimp cultivation without sample preparation. The results indicate that sample 1 showed a positive result, whereas samples 2 and 3 produced negative results. Then, samples 2 and 3 were spiked with WSSV for method validation. To confirm the performance of the DBIA developed, polymerase chain reaction (PCR) was conducted and the PCR results were the same as those found by the DBIA. Therefore, the DBIA developed could be applied for WSSV detection in real water samples.
引用
收藏
页码:586 / 593
页数:8
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