Key result
TaqMan real-time PCR improves PCV2 detection by ~18% over conventional PCR.
Why the study?
Rapid detection of porcine circovirus type 2 is important for effective prophylaxis and treatment of postweaning multisystemic wasting syndrome.
Absolute Event Rate: 97.3% vs 78.3%
A newly developed TaqMan-based real-time PCR assay provides a highly sensitive and specific method for the rapid detection and quantitation of porcine circovirus type 2.
May aid rapid PCV2 detection in swine; leaves open prospective validation before routine diagnostic use.
Porcine circovirus type 2 (PCV2) and the associated disease postweaning multisystemic wasting syndrome (PMWS) have caused heavy losses in global agriculture in recent decades. Rapid detection of PCV2 is very important for the effective prophylaxis and treatment of PMWS. To establish a sensitive, specific assay for the detection and quantitation of PCV2, we designed and synthesized specific primers and a probe in the open reading frame 2. The assay had a wide dynamic range with excellent linearity and reliable reproducibility, and detected between 102 and 1010 copies of the genomic DNA per reaction. The coefficient of variation for Ct values varied from 0.59% to 1.05% in the same assay and from 1.9% to 4.2% in 10 different assays. The assay did not cross-react with porcine circovirus type 1, porcine reproductive and respiratory, porcine epidemic diarrhea, transmissible gastroenteritis of pigs and rotavirus. The limits of detection and quantitation were 10 and 100 copies, respectively. Using the established real-time PCR system, 39 of the 40 samples we tested were detected as positive.
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Zhao et al. (2010) studied Porcine circovirus type 2 (PCV2) infection (n=40). TaqMan-based real-time PCR vs. Conventional PCR was evaluated on Detection rate of PCV2 in unknown clinical samples. The TaqMan-based real-time PCR assay detected PCV2 in 97.3% of unknown clinical samples, increasing the detection rate by 18% compared to conventional PCR.
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