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Comparison of the efficacy of autogenous inactivated Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) vaccines with that of commercial vaccines against homologous and heterologous challenges

Marc Geldhof, Merijn Vanhee UGent, Wander Van Breedam UGent, Jan Van Doorsselaere UGent, Uladzimir Karniychuk and Hans Nauwynck UGent (2012) BMC VETERINARY RESEARCH. 8.
abstract
Background: The porcine reproductive and respiratory syndrome virus (PRRSV) is a rapidly evolving pathogen of swine. At present, there is a high demand for safe and more effective vaccines that can be adapted regularly to emerging virus variants. A recent study showed that, by the use of a controlled inactivation procedure, an experimental BEI-inactivated PRRSV vaccine can be developed that offers partial protection against homologous challenge with the prototype strain LV. At present, it is however not known if this vaccine can be adapted to currently circulating virus variants. In this study, two recent PRRSV field isolates (07 V063 and 08 V194) were used for BEI-inactivated vaccine production. The main objective of this study was to assess the efficacy of these experimental BEI-inactivated vaccines against homologous and heterologous challenge and to compare it with an experimental LV-based BEI-inactivated vaccine and commercial inactivated and attenuated vaccines. In addition, the induction of challenge virus-specific (neutralizing) antibodies by the different vaccines was assessed. Results: In a first experiment (challenge with 07 V063), vaccination with the experimental homologous (07 V063) inactivated vaccine shortened the viremic phase upon challenge with approximately 2 weeks compared to the mock-vaccinated control group. Vaccination with the commercial attenuated vaccines reduced the duration of viremia with approximately one week compared to the mock-vaccinated control group. In contrast, the experimental heterologous (LV) inactivated vaccine and the commercial inactivated vaccine did not influence viremia. Interestingly, both the homologous and the heterologous experimental inactivated vaccine induced 07 V063-specific neutralizing antibodies upon vaccination, while the commercial inactivated and attenuated vaccines failed to do so. In the second experiment (challenge with 08 V194), use of the experimental homologous (08 V194) inactivated vaccine shortened viremia upon challenge with approximately 3 weeks compared to the mock-vaccinated control group. Similar results were obtained with the commercial attenuated vaccine. The experimental heterologous (07 V063 and LV) inactivated vaccines did not significantly alter viremia. In this experiment, 08 V194-specific neutralizing antibodies were induced by the experimental homologous and heterologous inactivated vaccines and a faster appearance post challenge was observed with the commercial attenuated vaccine. Conclusions: The experimental homologous inactivated vaccines significantly shortened viremia upon challenge. Despite the concerns regarding the efficacy of the commercial attenuated vaccines used on the farms where the field isolates were obtained, use of commercial attenuated vaccines clearly shortened the viremic phase upon challenge. In contrast, the experimental heterologous inactivated vaccines and the commercial inactivated vaccine had no or only a limited influence on viremia. The observation that homologous BEI-inactivated vaccines can provide a more or less standardized, predictable degree of protection against a specific virus variant suggests that such vaccines may prove useful in case virus variants emerge that escape the immunity induced by the attenuated vaccines.
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
MYSTERY SWINE DISEASE, NEUTRALIZING ANTIBODIES, FETAL IMPLANTATION SITES, GENETIC DIVERSITY, IMMUNE-RESPONSES, PASSIVE TRANSFER, LELYSTAD VIRUS, NORTH-AMERICAN, INFECTION, PIGS
journal title
BMC VETERINARY RESEARCH
BMC Vet. Res.
volume
8
article number
182
pages
16 pages
Web of Science type
Article
Web of Science id
000312223200001
JCR category
VETERINARY SCIENCES
JCR impact factor
1.861 (2012)
JCR rank
18/142 (2012)
JCR quartile
1 (2012)
ISSN
1746-6148
DOI
10.1186/1746-6148-8-182
language
English
UGent publication?
yes
classification
A1
copyright statement
I have retained and own the full copyright for this publication
id
3237501
handle
http://hdl.handle.net/1854/LU-3237501
date created
2013-06-07 09:55:21
date last changed
2017-04-13 14:08:33
@article{3237501,
  abstract     = {Background: The porcine reproductive and respiratory syndrome virus (PRRSV) is a rapidly evolving pathogen of swine. At present, there is a high demand for safe and more effective vaccines that can be adapted regularly to emerging virus variants. A recent study showed that, by the use of a controlled inactivation procedure, an experimental BEI-inactivated PRRSV vaccine can be developed that offers partial protection against homologous challenge with the prototype strain LV. At present, it is however not known if this vaccine can be adapted to currently circulating virus variants. In this study, two recent PRRSV field isolates (07 V063 and 08 V194) were used for BEI-inactivated vaccine production. The main objective of this study was to assess the efficacy of these experimental BEI-inactivated vaccines against homologous and heterologous challenge and to compare it with an experimental LV-based BEI-inactivated vaccine and commercial inactivated and attenuated vaccines. In addition, the induction of challenge virus-specific (neutralizing) antibodies by the different vaccines was assessed.
Results: In a first experiment (challenge with 07 V063), vaccination with the experimental homologous (07 V063) inactivated vaccine shortened the viremic phase upon challenge with approximately 2 weeks compared to the mock-vaccinated control group. Vaccination with the commercial attenuated vaccines reduced the duration of viremia with approximately one week compared to the mock-vaccinated control group. In contrast, the experimental heterologous (LV) inactivated vaccine and the commercial inactivated vaccine did not influence viremia. Interestingly, both the homologous and the heterologous experimental inactivated vaccine induced 07 V063-specific neutralizing antibodies upon vaccination, while the commercial inactivated and attenuated vaccines failed to do so.
In the second experiment (challenge with 08 V194), use of the experimental homologous (08 V194) inactivated vaccine shortened viremia upon challenge with approximately 3 weeks compared to the mock-vaccinated control group. Similar results were obtained with the commercial attenuated vaccine. The experimental heterologous (07 V063 and LV) inactivated vaccines did not significantly alter viremia. In this experiment, 08 V194-specific neutralizing antibodies were induced by the experimental homologous and heterologous inactivated vaccines and a faster appearance post challenge was observed with the commercial attenuated vaccine.
Conclusions: The experimental homologous inactivated vaccines significantly shortened viremia upon challenge. Despite the concerns regarding the efficacy of the commercial attenuated vaccines used on the farms where the field isolates were obtained, use of commercial attenuated vaccines clearly shortened the viremic phase upon challenge. In contrast, the experimental heterologous inactivated vaccines and the commercial inactivated vaccine had no or only a limited influence on viremia. The observation that homologous BEI-inactivated vaccines can provide a more or less standardized, predictable degree of protection against a specific virus variant suggests that such vaccines may prove useful in case virus variants emerge that escape the immunity induced by the attenuated vaccines.},
  articleno    = {182},
  author       = {Geldhof, Marc and Vanhee, Merijn and Van Breedam, Wander and Van Doorsselaere, Jan and Karniychuk, Uladzimir and Nauwynck, Hans},
  issn         = {1746-6148},
  journal      = {BMC VETERINARY RESEARCH},
  keyword      = {MYSTERY SWINE DISEASE,NEUTRALIZING ANTIBODIES,FETAL IMPLANTATION SITES,GENETIC DIVERSITY,IMMUNE-RESPONSES,PASSIVE TRANSFER,LELYSTAD VIRUS,NORTH-AMERICAN,INFECTION,PIGS},
  language     = {eng},
  pages        = {16},
  title        = {Comparison of the efficacy of autogenous inactivated Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) vaccines with that of commercial vaccines against homologous and heterologous challenges},
  url          = {http://dx.doi.org/10.1186/1746-6148-8-182},
  volume       = {8},
  year         = {2012},
}

Chicago
Geldhof, Marc, Merijn Vanhee, Wander Van Breedam, Jan Van Doorsselaere, Uladzimir Karniychuk, and Hans Nauwynck. 2012. “Comparison of the Efficacy of Autogenous Inactivated Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) Vaccines with That of Commercial Vaccines Against Homologous and Heterologous Challenges.” Bmc Veterinary Research 8.
APA
Geldhof, M., Vanhee, M., Van Breedam, W., Van Doorsselaere, J., Karniychuk, U., & Nauwynck, H. (2012). Comparison of the efficacy of autogenous inactivated Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) vaccines with that of commercial vaccines against homologous and heterologous challenges. BMC VETERINARY RESEARCH, 8.
Vancouver
1.
Geldhof M, Vanhee M, Van Breedam W, Van Doorsselaere J, Karniychuk U, Nauwynck H. Comparison of the efficacy of autogenous inactivated Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) vaccines with that of commercial vaccines against homologous and heterologous challenges. BMC VETERINARY RESEARCH. 2012;8.
MLA
Geldhof, Marc, Merijn Vanhee, Wander Van Breedam, et al. “Comparison of the Efficacy of Autogenous Inactivated Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) Vaccines with That of Commercial Vaccines Against Homologous and Heterologous Challenges.” BMC VETERINARY RESEARCH 8 (2012): n. pag. Print.