Evaluation of the recombinant proteins RlpB and VacJ as a vaccine for protection against Glaesserella parasuis in pigs.


Journal

BMC veterinary research
ISSN: 1746-6148
Titre abrégé: BMC Vet Res
Pays: England
ID NLM: 101249759

Informations de publication

Date de publication:
27 May 2020
Historique:
received: 26 11 2019
accepted: 14 05 2020
entrez: 29 5 2020
pubmed: 29 5 2020
medline: 5 1 2021
Statut: epublish

Résumé

Glaesserella parasuis, the causative agent of Glӓsser's disease, is widespread in swine globally resulting in significant economic losses to the swine industry. Prevention of Glӓsser's disease in pigs has been plagued with an inability to design broadly protective vaccines, as many bacterin based platforms generate serovar or strain specific immunity. Subunit vaccines are of interest to provide protective immunity to multiple strains of G. parasuis. Selected proteins for subunit vaccination should be widespread, highly conserved, and surface exposed. Two candidate proteins for subunit vaccination (RlpB and VacJ) against G. parasuis were identified using random mutagenesis and an in vitro organ culture system. Pigs were vaccinated with recombinant RlpB and VacJ, outer membrane proteins with important contributions to cellular function and viability. Though high antibody titers to the recombinant proteins and increased interferon-γ producing cells were found in subunit vaccinated animals, the pigs were not protected from developing systemic disease. It appears there may be insufficient RlpB and VacJ exposed on the bacterial surface for antibody to bind, preventing high RlpB and VacJ specific antibody titers from protecting animals from G. parasuis. Additionally, this work confirms the importance of utilizing the natural host species when assessing the efficacy of vaccine candidates.

Sections du résumé

BACKGROUND BACKGROUND
Glaesserella parasuis, the causative agent of Glӓsser's disease, is widespread in swine globally resulting in significant economic losses to the swine industry. Prevention of Glӓsser's disease in pigs has been plagued with an inability to design broadly protective vaccines, as many bacterin based platforms generate serovar or strain specific immunity. Subunit vaccines are of interest to provide protective immunity to multiple strains of G. parasuis. Selected proteins for subunit vaccination should be widespread, highly conserved, and surface exposed.
RESULTS RESULTS
Two candidate proteins for subunit vaccination (RlpB and VacJ) against G. parasuis were identified using random mutagenesis and an in vitro organ culture system. Pigs were vaccinated with recombinant RlpB and VacJ, outer membrane proteins with important contributions to cellular function and viability. Though high antibody titers to the recombinant proteins and increased interferon-γ producing cells were found in subunit vaccinated animals, the pigs were not protected from developing systemic disease.
CONCLUSIONS CONCLUSIONS
It appears there may be insufficient RlpB and VacJ exposed on the bacterial surface for antibody to bind, preventing high RlpB and VacJ specific antibody titers from protecting animals from G. parasuis. Additionally, this work confirms the importance of utilizing the natural host species when assessing the efficacy of vaccine candidates.

Identifiants

pubmed: 32460764
doi: 10.1186/s12917-020-02377-5
pii: 10.1186/s12917-020-02377-5
pmc: PMC7252510
doi:

Substances chimiques

Antibodies, Bacterial 0
Bacterial Proteins 0
Bacterial Vaccines 0
Haemophilus Vaccines 0
Recombinant Proteins 0
Vaccines, Subunit 0

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

167

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/G019177/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/G020744/1, BB/G019177/1, BB/G019274/1 and BB/G018553/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/G020744/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/G019274/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/G018553/1
Pays : United Kingdom

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Auteurs

Samantha J Hau (SJ)

USDA, ARS, National Animal Disease Center, 1920 Dayton Ave, Ames, IA, 50010, USA.

Shi-Lu Luan (SL)

Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.

Crystal L Loving (CL)

USDA, ARS, National Animal Disease Center, 1920 Dayton Ave, Ames, IA, 50010, USA.

Tracy L Nicholson (TL)

USDA, ARS, National Animal Disease Center, 1920 Dayton Ave, Ames, IA, 50010, USA.

Jinhong Wang (J)

Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.

Sarah E Peters (SE)

Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.

David Seilly (D)

Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.

Lucy A Weinert (LA)

Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.

Paul R Langford (PR)

Section of Paediatric Infectious Diseases, Department of Infectious Disease, Imperial College London, St. Mary's Campus, London, UK.

Andrew N Rycroft (AN)

The Royal Veterinary College, Hawkshead Campus, Hatfield, UK.

Brendan W Wren (BW)

Faculty of Infectious & Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.

Duncan J Maskell (DJ)

Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Current address: The University of Melbourne, Level 9, Raymond Priestley Building, Melbourne, Victoria, 3010, Australia.

Alexander W Tucker (AW)

Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.

Susan L Brockmeier (SL)

USDA, ARS, National Animal Disease Center, 1920 Dayton Ave, Ames, IA, 50010, USA. Susan.Brockmeier@ars.usda.gov.

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Classifications MeSH