Staff Publications

Staff Publications

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    'Staff publications' is the digital repository of Wageningen University & Research

    'Staff publications' contains references to publications authored by Wageningen University staff from 1976 onward.

    Publications authored by the staff of the Research Institutes are available from 1995 onwards.

    Full text documents are added when available. The database is updated daily and currently holds about 240,000 items, of which 72,000 in open access.

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Record number 322395
Title Safety and protective efficacy of porcine reproductive and respiratory syndrome recombinant virus vaccines in young pigs.
Author(s) Verheije, M.H.; Kroese, M.V.; Linden, I.F.A. van der; Boer-Luijtze, E.A. de; Rijn, P.A. van; Pol, J.M.A.; Meulenberg, J.J.M.; Steverink, P.J.G.M.
Source Vaccine 21 (2003)19-20. - ISSN 0264-410X - p. 2556 - 2563.
DOI https://doi.org/10.1016/S0264-410X(03)00047-1
Department(s) ID - Infectieziekten
CIDC - Division Virology
Wageningen Business Generator B.V.
Publication type Refereed Article in a scientific journal
Publication year 2003
Keyword(s) nucleocapsid protein-n - syndrome prrs virus - lelystad virus - monoclonal-antibodies - structural proteins - north-american - strains - swine - genome - arteriviruses
Abstract Three porcine reproductive and respiratory syndrome virus (PRRSV) recombinants, generated by mutagenesis of an infectious cDNA clone of the Lelystad virus (LV) isolate, were tested for their safety and protective efficacy as potential PRRSV vaccines in pigs. Recombinant vABV688 contains two amino acid substitutions in the minor structural protein GP2 resulting in improved growth on cell line CL2621; in recombinant vABV707 the region encoding the ectodomain of the major unglycosylated membrane protein M has been replaced by that of the murine lactate dehydrogenase-elevating arterivirus; recombinant vABV746 lacks the six C-terminal amino acids of the nucleocapsid protein N. First, we determined the safety of these recombinant viruses by monitoring the stability of the introduced mutations in 8-week-old pigs. We showed that the introduced genomic mutations were maintained throughout the viraemic period. Second, the protective efficacy of immunization with the recombinant viruses against challenge with a homologous and a heterologous PRRSV strain was determined in two pigs and compared with the efficacy of vABV437, a virus derived from the parental LV cDNA. The viraemia in pigs immunized with the recombinant viruses was reduced compared to pigs immunized with vABV437. In addition, the length of viraemia was reduced in the sentinel pigs that were introduced into the groups immunized with vABV746, vABV688, and vABV707, however, all of the sentinel pigs became infected. Pigs immunized with vABV707 and vABV437 were protected against challenge with homologous virus LV-Ter Huurne and transmission of the latter virus. None of the immunized pigs were protected against heterologous challenge with the virulent US isolate SDSU#73, but the vABV707- and vABV746-immunized pigs were protected against transmission of this virus from challenged pigs. In conclusion, the obtained viral recombinants are interesting candidates to be further explored for their use as vaccines against PRRSV.
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