This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zsak, L.
Right arrow Articles by Rock, D. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zsak, L.
Right arrow Articles by Rock, D. L.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, January 2005, p. 112-119, Vol. 43, No. 1
0095-1137/05/$08.00+0     doi:10.1128/JCM.43.1.112-119.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Preclinical Diagnosis of African Swine Fever in Contact-Exposed Swine by a Real-Time PCR Assay

L. Zsak,1* M. V. Borca,1 G. R. Risatti,1 A. Zsak,1 R. A. French,2 Z. Lu,1 G. F. Kutish,1 J. G. Neilan,1 J. D. Callahan,3 W. M. Nelson,3 and D. L. Rock1

Plum Island Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, Greenport, New York,1 Department of Pathobiology, University of Connecticut, Storrs, Connecticut,2 Tetracore Inc., Gaithersburg, Maryland3

Received 2 March 2004/ Returned for modification 26 July 2004/ Accepted 6 September 2004

A fluorogenic probe hydrolysis (TaqMan) PCR assay for African swine fever virus (ASFV) was developed and evaluated in experimentally infected swine. This sensitive and specific one-step single-tube assay, which can be performed in 2 h or less, detected viral DNA in tonsil scraping samples 2 to 4 days prior to onset of clinical disease. Thus, the assay would have application for preclinical diagnosis of African swine fever and surveillance and/or emergency management of a disease outbreak.


* Corresponding author. Mailing address: Plum Island Animal Disease Center, P.O. Box 848, Greenport, NY 11944-0848. Phone: (631) 323-3023. Fax: (631) 323-2507. E-mail: lzsak{at}piadc.ars.usda.gov.


Journal of Clinical Microbiology, January 2005, p. 112-119, Vol. 43, No. 1
0095-1137/05/$08.00+0     doi:10.1128/JCM.43.1.112-119.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Chapman, D. A. G., Tcherepanov, V., Upton, C., Dixon, L. K. (2008). Comparison of the genome sequences of non-pathogenic and pathogenic African swine fever virus isolates. J. Gen. Virol. 89: 397-408 [Abstract] [Full Text]  
  • Reis, A. L., Parkhouse, R. M. E., Penedos, A. R., Martins, C., Leitao, A. (2007). Systematic analysis of longitudinal serological responses of pigs infected experimentally with African swine fever virus. J. Gen. Virol. 88: 2426-2434 [Abstract] [Full Text]  
  • Perez-Filgueira, D. M., Gonzalez-Camacho, F., Gallardo, C., Resino-Talavan, P., Blanco, E., Gomez-Casado, E., Alonso, C., Escribano, J. M. (2006). Optimization and Validation of Recombinant Serological Tests for African Swine Fever Diagnosis Based on Detection of the p30 Protein Produced in Trichoplusia ni Larvae.. J. Clin. Microbiol. 44: 3114-3121 [Abstract] [Full Text]