Development of Primer-Probe Energy Transfer real-time PCR for the detection and quantification of porcine circovirus type 2

Author:

Bálint Ádám,Tenk Miklós1,Deim Zoltán2,Rasmussen Thomas3,Uttenthal Åse3,Cságola Attila4,Tuboly Tamás4,Farsang Attila5,Fossum Caroline6,Timmusk Sirje6,Berg Mikael,Belák Sándor

Affiliation:

1. 1 The National Veterinary Institute & The Swedish University of Agricultural Sciences Joint R&D Division, Departments of Virology Ulls väg 2B SE-751 89 Uppsala Sweden

2. 2 Central Agricultural Office Veterinary Diagnostic Directorate Budapest Hungary

3. 3 Technical University of Denmark National Veterinary Institute Lindholm, Kalvehave Denmark

4. 4 Szent István University Department of Microbiology and Infectious Diseases, Faculty of Veterinary Science Budapest Hungary

5. 5 Institute for Veterinary Medicinal Products Department of Virology Budapest Hungary

6. 6 Swedish University of Agricultural Sciences Department of Biomedical Sciences and Veterinary Public Health Uppsala Sweden

Abstract

A real-time PCR assay, based on Primer-Probe Energy Transfer (PriProET), was developed to improve the detection and quantification of porcine circovirus type 2 (PVC2). PCV2 is recognised as the essential infectious agent in post-weaning multisystemic wasting syndrome (PMWS) and has been associated with other disease syndromes such as porcine dermatitis and nephropathy syndrome (PDNS) and porcine respiratory disease complex (PRDC). Since circoviruses commonly occur in the pig populations and there is a correlation between the severity of the disease and the viral load in the organs and blood, it is important not only to detect PCV2 but also to determine the quantitative aspects of viral load. The PriProET real-time PCR assay described in this study was tested on various virus strains and clinical forms of PMWS in order to investigate any correlation between the clinical signs and viral loads in different organs. The data obtained in this study correlate with those described earlier; namely, the viral load in 1 ml plasma and in 500 ng tissue DNA exceeds 107copies in the case of PMWS. The results indicate that the new assay provides a specific, sensitive and robust tool for the improved detection and quantification of PCV2.

Publisher

Akademiai Kiado Zrt.

Subject

General Veterinary

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