Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6134185 | Journal of Virological Methods | 2013 | 7 Pages |
Abstract
The purpose of this study was to develop a rapid, sensitive and easy quantitative immunofluorescence assay (QIFA) using the recombinant PCV2 nucleocapsid protein (NCP) for the detection of PCV2-specific antibodies in pig sera. The recombinant PCV2 NCP was expressed in Vero cells by a lentivirus system. The performance of QIFA using these Vero cells as a diagnostic antigen was compared with currently available C-ELISA and I-ELISA; the relative sensitivity turned out to range from 92.5% up to 99.3%. The relative specificity was 93.3% when compared to C-ELISA as the gold standard. The serological experiment also indicated the inverse relationship between QIFA and the viral load in serum, semen, feces samples from 7 PCV2-positive boars. In addition, the PCV2 sequence detected from bone marrow cells shows 99% of sequence identity with PCV2 genome, confirming the infectivity of PCV2.
Related Topics
Life Sciences
Immunology and Microbiology
Virology
Authors
Yeon-Hee Kim, Chang-Hee Kweon, Seung-Won Kang, Yoon I Oh, Jae Young Song, Kyoung Ki Lee, Se Chang Park,