A reverse transcription loop-mediated isothermal amplification method for rapid detection of bovine viral diarrhea virus

被引:24
|
作者
Fan, Qing [1 ,2 ]
Xie, Zhixun [1 ,2 ]
Xie, Liji [1 ,2 ]
Liu, Jiabo [1 ,2 ]
Pang, Yaoshan [1 ,2 ]
Deng, Xianwen [1 ,2 ]
Xie, Zhiqin [1 ,2 ]
Peng, Yi [1 ,2 ]
Wang, Xiuqing [3 ]
机构
[1] Guangxi Vet Res Inst, Dept Biotechnol, Nanning 530001, Guangxi, Peoples R China
[2] Guangxi Key Lab Anim Vaccines & Diagnost, Nanning 530001, Guangxi, Peoples R China
[3] S Dakota State Univ, Dept Biol & Microbiol, Brookings, SD 57007 USA
关键词
Bovine viral diarrhea virus (BVDV); 5 ' untranslated region (5 ' UTR); Reverse transcription loop-mediated isothermal amplification (RT-LAMP); INFECTION; DIAGNOSIS; SAMPLES; ASSAY; DNA;
D O I
10.1016/j.jviromet.2012.08.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay was developed and optimized to detect bovine viral diarrhea viral (BVDV) RNA. The RI-LAMP assay is highly sensitive and able to detect 4.67 x 10(0) copies of BVDV RNA. Additionally, the RI-LAMP method is capable of detecting both genotypes of BVDV. No cross-reaction with other bovine viruses was observed. The ability of RT-LAMP to detect BVDV RNA from bovine fecal swabs was also evaluated. Of the 88 fecal swabs, 38 were found to be positive by RT-LAMP assay, whereas 39 were positive by real-time RT-PCR Taken together, the BVDV specific RT-LAMP method is highly specific and sensitive and can be used as a rapid and direct diagnostic assay for testing clinical samples. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 48
页数:6
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