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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

A PCV2 vaccine based on genotype 2b is more effective than a 2a-based vaccine to protect against PCV2b or combined PCV2a/2b viremia in pigs with concurrent PCV2, PRRSV and PPV infection

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Author(s):
Opriessnig, Tanja [1] ; O'Neill, Kevin [1] ; Gerber, Priscilla F. [1] ; de Castro, Alessandra M. M. G. [1, 2] ; Gimenez-Lirola, Luis G. [1] ; Beach, Nathan M. [3] ; Zhou, Lei [3] ; Meng, Xiang-Jin [3] ; Wang, Chong [1, 4] ; Halbur, Patrick G. [1]
Total Authors: 10
Affiliation:
[1] Iowa State Univ, Dept Vet Diagnost & Prod Anim Med, Coll Vet Med, Ames, IA 50011 - USA
[2] Univ Sao Paulo, Coll Vet Med, Dept Prevent Vet Med & Anim Hlth, BR-05508270 Sao Paulo - Brazil
[3] Virginia Polytech Inst & State Univ, Coll Vet Med, Dept Biomed Sci & Pathobiol, Ctr Mol Med & Infect Dis, Blacksburg, VA 24061 - USA
[4] Iowa State Univ, Dept Stat, Coll Liberal Arts & Sci, Ames, IA - USA
Total Affiliations: 4
Document type: Journal article
Source: Vaccine; v. 31, n. 3, p. 487-494, JAN 7 2013.
Web of Science Citations: 33
Abstract

The predominant genotype of porcine circovirus (PCV) in the pig population today is PCV2b yet PCV2a-based commercial vaccines are considered effective in protecting against porcine circovirus associated disease. The objective of this study was to compare the ability of PCV2a- and PCV2b-based vaccines to control PCV2b viremia in a challenge model that mimics the U.S. field situation. Sixty-three pigs were randomly assigned to one of eight groups. Sixteen pigs were vaccinated with an experimental live-attenuated chimeric PCV1-2a vaccine based on genotype 2a and another 16 pigs with a chimeric PCV1-2b vaccine based on genotype 2b. Challenge was done 28 days post vaccination (dpv) using PCV2b (or a combination of PCV2a and PCV2b), porcine reproductive and respiratory syndrome virus (PRRSV), and porcine parvvirus (PPV) to mimic what commonly occurs in the field. The experiment was terminated 21 days post challenge (dpc) or 49 dpv. Pigs vaccinated with the chimeric PCV1-2b vaccine had significantly higher levels of PCV1-2b viremia and shedding of the PCV1-2b vaccine virus in feces and nasal secretions but also a more robust humoral immune response as evidenced by significantly higher ELISA S/P ratios compared to the PCV1-2a vaccination. Regardless of challenge, the PCV1-2b vaccination significantly reduced the prevalence and amount of PCV2 viremia compared to the PCV1-2a vaccination. Interestingly, in the non-vaccinated pigs concurrent PCV2a infection resulted in clinical disease and increased macroscopic lung lesions compared to pigs challenged with PCV2b alone, further supporting the idea that concurrent PCV2a/PCV2b infection is necessary for optimal PCV2 replication. (C) 2012 Elsevier Ltd. All rights reserved. (AU)