Development of RT-LAMP and real-time RT-PCR assays for the rapid detection of the new duck Tembusu-like BYD virus

被引:36
作者
Jiang, Tao [1 ]
Liu, Juan [1 ,2 ]
Deng, Yong-Qiang [1 ]
Su, Jing-Liang [3 ]
Xu, Li-Juan [1 ]
Liu, Zhi-Hui [1 ,4 ]
Li, Xiao-Feng [1 ]
Yu, Xue-Dong [1 ]
Zhu, Shun-Ya [1 ]
Gao, George Fu [5 ]
Qin, E-De [1 ]
Qin, Cheng-Feng [1 ]
机构
[1] Beijing Inst Microbiol & Epidemiol, State Key Lab Pathogen & Biosecur, Dept Virol, Beijing 100071, Peoples R China
[2] PLA AF Gen Hosp, Dept Transfus Med, Beijing 100142, Peoples R China
[3] China Agr Univ, Key Lab Anim Epidemiol & Zoonosis, Minist Agr, Coll Vet Med, Beijing 100193, Peoples R China
[4] Xinjiang Agr Univ, Coll Vet Med, Urumqi 830052, Peoples R China
[5] Chinese Acad Sci, CAS Key Lab Pathogen Microbiol & Immunol, Inst Microbiol, Beijing 100101, Peoples R China
基金
中国国家自然科学基金;
关键词
MEDIATED ISOTHERMAL AMPLIFICATION;
D O I
10.1007/s00705-012-1431-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A new duck Tembusu virus (TMUV), also known as BYD virus, has been identified as the causative agent for the emerging duck egg-drop syndrome in mainland China. The rapid spread and wide distribution of the new TMUV in mainland China result in heavy loss to the poultry industry and pose great threats to public health. Rapid and sensitive detection methods are critical for prevention and control of TMUV infections. In this study, a reverse-transcription loop-mediated isothermal amplification assay (RT-LAMP) and an SYBR Green-I-based real-time RT-PCR assay specific for the duck TMUV were developed and validated with laboratory and field samples, respectively. The detection limits were 1 x 10(-4) and 1 x 10(-3) PFU per reaction for the RT-LAMP assay and real-time RT-PCR assay, respectively. The specificities were analyzed with other related members of the genus Flavivirus, and no cross-reaction was observed. Furthermore, both assays were evaluated with field samples, and they exhibited high sensitivity and specificity. In addition, the real-time RT-PCR assay worked well in viral load analysis, which revealed that the spleen may be the primary target for the replication of new duck TMUV in ducks. The TMUV-specific RT-LAMP and real-time RT-PCR assays will provide useful tools for the diagnosis and epidemiological surveillance of TMUV infection.
引用
收藏
页码:2273 / 2280
页数:8
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