Development of a real-time loop-mediated isothermal amplification method for the detection of severe fever with thrombocytopenia syndrome virus

被引:12
|
作者
Lee, Jae Woong [1 ]
Won, Yu-Jung [1 ]
Kang, Lae Hyung [1 ]
Lee, Sung-Geun [2 ]
Park, Seung-Won [3 ]
Paik, Soon-Young [1 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Microbiol, Seoul 06591, South Korea
[2] Jeonbuk Natl Univ, Korea Zoonosis Res Inst, Iksan 54596, South Korea
[3] Daegu Catholic Univ, Dept Biotechnol, Gyongsan 38430, South Korea
关键词
severe fever with thrombocytopenia syndrome (STFS); reverse transcription loop-mediated isothermal amplification (LAMP); molecular diagnostics; virus detection; NUCLEOCAPSID PROTEIN; SYNDROME BUNYAVIRUS; SOUTH-KOREA; INFECTION; PCR; STRAINS; SFTS;
D O I
10.1007/s12275-020-0109-1
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Severe fever with thrombocytopenia syndrome (SFTS) is being reported annually in South Korea since its first detection there in 2010. The causal agent is a negative-strand RNA virus 80-100 nm in diameter. It causes fever, thrombocytopenia, leukocytopenia, gastrointestinal symptoms, and neural symptoms. The mortality rate of SFTS was 32.6% among 172 cases reported from 2012 to 2015 in South Korea. Thus, is necessary to develop an effective diagnostic method that selectively identifies the isolates circulating in South Korea. The real-time reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay is a simple, rapid, and sensitive approach for molecular diagnosis. Here, we designed novel primers for this assay and found that the technique had very high specificity, sensitivity, and efficiency. This real-time RT-LAMP approach using the novel primers developed herein can be applied for early diagnosis of SFTSV strains in South Korea to reduce the mortality rate of SFTS.
引用
收藏
页码:711 / 715
页数:5
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