Advanced target‐specific probe‐based real‐time loop‐mediated isothermal amplification assay for the rapid and specific detection of porcine circovirus 3. Issue 6 (6th July 2020)

• Record Type: Journal Article
• Authors: Kim, Hye‐Ryung; Lim, Da‐Rae; Chae, Ha‐Gyeong; Park, Ji‐Young; Kim, Seong‐Hee; Lee, Kyoung‐Ki; Lee, Changhee; Lyoo, Young S.; Park, Choi‐Kyu
• Is Part Of: Transboundary and emerging diseases. Volume 67:Issue 6(2020)
• Page Start: 2336
• Page End: 2344
• Publication Date: 2020-07-06
• Subjects: assimilating probe -- porcine circovirus 3 -- real‐time LAMP -- swarm primer; Veterinary medicine -- Periodicals; 636.089
• DOI: 10.1111/tbed.13671
• Languages: English
• ISSNs: 1865-1674

Abstract

Abstract: Porcine circovirus type 3 (PCV3) is an emerging viral pathogen that has been identified in pigs with various clinical signs. For rapid and specific detection of PCV3, an advanced real‐time loop‐mediated isothermal amplification (rLAMP) assay that uses both assimilating probes and swarm primers were developed and evaluated in this study. The assay specifically amplified PCV3 DNA, but it did not amplify other porcine viral nucleic acids. The limit of detection of rLAMP with swarm primers was 50 PCV3 DNA copies/reaction, which was comparable to that of the real‐time quantitative polymerase chain reaction (qPCR) and 10 times more sensitive than rLAMP without swarm primers. In an evaluation of clinical samples, the rLAMP assay was able to detect PCV3 DNA within 17.34 ± 4.45 min, which is more rapid than what has been previously reported for the standard qPCR assay (31.78 ± 4.60 min). Detection with rLAMP was largely in agreement with that of the qPCR with a kappa value (95% confidence interval) of 0.98 (0.95–1.00). Taken together, these results suggest that the rLAMP assay presented will be a valuable tool for rapid, specific and reliable diagnosis of PCV3 in clinical samples.