Rapid preclinical detection of Sheeppox virus by a real-time PCR assay

被引:83
|
作者
Balinsky, C. A. [1 ,3 ,4 ]
Delhon, G. [1 ,5 ,6 ]
Smoliga, G. [1 ]
Prarat, M. [1 ,2 ]
French, R. A. [4 ]
Geary, S. J. [3 ,4 ]
Rock, D. L. [1 ,6 ]
Rodriguez, L. L. [1 ]
机构
[1] USDA ARS, Plum Isl Anim Dis Ctr, Greenport, NY 11944 USA
[2] USDA, Anim & Plant Hlth Inspect Serv, Plum Isl Anim Dis Ctr, Greenport, NY 11944 USA
[3] Univ Connecticut, Ctr Excellence Vaccine Res, Storrs, CT 06269 USA
[4] Univ Connecticut, Dept Pathobiol & Vet Sci, Storrs, CT 06269 USA
[5] Univ Buenos Aires, Sch Vet Sci, Area Virol, Buenos Aires, DF, Argentina
[6] Univ Illinois, Coll Vet Med, Dept Pathobiol, Urbana, IL 61802 USA
关键词
D O I
10.1128/JCM.01953-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sheeppox virus (SPPV) is a member of the Capripoxvirus (CaPV) genus of the Poxviridae family. Members of this genus, which also include goatpox and lumpy skin disease viruses, cause economically significant disease in sheep, goats, and cattle. A rapid diagnostic assay for CaPV would be useful for disease surveillance as well as for detection of CaPV in clinical samples and for outbreak management. Here we describe a fluorogenic probe hydrolysis (TaqMan) PCR assay designed for rapid detection of CaPV and tested on sheep experimentally infected with a virulent strain of SPPV. This assay can detect SPPV in huffy coats, nasal swabs, oral swabs, scabs, and skin lesions as well as in lung and lymph nodes collected at necropsy. This single-tube diagnostic assay can be performed in 2 h or less and can detect viral DNA in preclinical, clinical, and postmortem samples.
引用
收藏
页码:438 / 442
页数:5
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