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Journal of Clinical Microbiology, February 2008, p. 438-442, Vol. 46, No. 2
0095-1137/08/$08.00+0 doi:10.1128/JCM.01953-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Plum Island Animal Disease Center, Agricultural Research Service, United States Department of Agriculture, Greenport, New York 11944,1 Plum Island Animal Disease Center, Animal and Plant Health Inspection Service, United States Department of Agriculture, Greenport, New York 11944,2 Center of Excellence for Vaccine Research, University of Connecticut, Storrs, Connecticut 06269,3 Department of Pathobiology and Veterinary Science, University of Connecticut, Storrs, Connecticut 06269,4 Area of Virology, School of Veterinary Sciences, University of Buenos Aires, 1427 Buenos Aires, Argentina,5 Department of Pathobiology, College of Veterinary Medicine, University of Illinois, Urbana, Illinois 618026
Received 3 October 2007/ Returned for modification 21 October 2007/ Accepted 11 November 2007
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 buffy 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.
Published ahead of print on 21 November 2007.
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