Reverse transcription loop-mediated isothermal amplification for rapid detection of the newly emerged poultry Flavivirus

被引:1
|
作者
Li, Zhaolong [1 ,2 ]
Chen, Shaoying [1 ,2 ]
Wang, Shao [1 ,2 ]
Chen, Shilong [1 ,2 ]
Lin, Fengqian [1 ,2 ]
机构
[1] Fujian Acad Agr Sci, Dept Anim Husb & Vet Med, Fuzhou 350013, Peoples R China
[2] Fujian Acad Agr Sci, Dept Fujian Anim Dis Control Technol Dev Ctr, Fuzhou 350013, Peoples R China
基金
中国国家自然科学基金;
关键词
DIFFERENTIAL DETECTION; DISEASE VIRUS; TEMBUSU VIRUS; WEST-NILE; DIAGNOSIS; INFECTION; ASSAY; PCR;
D O I
10.1007/s12223-012-0204-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Poultry Flavivirus (PF) was a recently emerged virus with high morbidity rates and mortality rates in China. It is the causative agent of egg drop syndrome at present. Development of the reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay was the most efficient way to prevent and control the PF disease. The assay was performed at 64 degrees C for 45 min, using six specific primers that recognized eight targets of the PF E gene. The RT-LAMP assay, compared to conventional reverse transcription polymerase chain reaction, has 100-fold-greater sensitivity, with a detection limit of 1 x 10(-3) copies per mu L RNA and no cross-reaction with poultry other viruses. The RT-LAMP assay is a valuable tool for detected PF without requiring any sophisticated equipment, and the detection has potential usefulness for clinical diagnosis in the field.
引用
收藏
页码:277 / 282
页数:6
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