Abstract:
:The aim of this study was to establish a method that could differentiate antibodies against live and inactivated vaccines of porcine reproductive and respiratory syndrome virus (PRRSV). A blocking ELISA (b-ELISA) was established using the PRRSV non-structural protein, Nsp9, as the antigen and a monoclonal antibody, 2D6, against the Nsp9 protein as the capture antibody. The test was validated by using 415 clinical sera in the b-ELISA compared to a commercial kit based on the indirect ELISA using the nucleocapsid (N) protein as antigen. Significant differences were observed for the data obtained by the two detection methods. This may be due to the commercial kit detecting antibodies elicited by live and inactivated virus, whereas the b-ELISA only detects antibodies produced by any active viral replication, such as natural infection or live vaccination. Therefore, the b-ELISA in this study is able to distinguish between antibodies against live and inactivated viruses in pigs.
journal_name
Virologyjournal_title
Virologyauthors
Cong Y,Huang Z,Sun Y,Ran W,Zhu L,Yang G,Ding X,Yang Z,Huang X,Wang C,Ding Zdoi
10.1016/j.virol.2013.06.027subject
Has Abstractpub_date
2013-09-01 00:00:00pages
310-6issue
1-2eissn
0042-6822issn
1096-0341pii
S0042-6822(13)00397-8journal_volume
444pub_type
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