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Evaluation of Glycosylated FlpA and SodB as Subunit Vaccines Against Campylobacter jejuni Colonisation in Chickens

Campylobacter jejuni is the leading bacterial cause of human gastroenteritis worldwide and the handling or consumption of contaminated poultry meat is the key source of infection. C. jejuni proteins FlpA and SodB and glycoconjugates containing the C. jejuni N-glycan have been separately reported to...

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Autores principales: Vohra, Prerna, Chintoan-Uta, Cosmin, Terra, Vanessa S., Bremner, Abi, Cuccui, Jon, Wren, Brendan W., Vervelde, Lonneke, Stevens, Mark P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564835/
https://www.ncbi.nlm.nih.gov/pubmed/32932979
http://dx.doi.org/10.3390/vaccines8030520
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author Vohra, Prerna
Chintoan-Uta, Cosmin
Terra, Vanessa S.
Bremner, Abi
Cuccui, Jon
Wren, Brendan W.
Vervelde, Lonneke
Stevens, Mark P.
author_facet Vohra, Prerna
Chintoan-Uta, Cosmin
Terra, Vanessa S.
Bremner, Abi
Cuccui, Jon
Wren, Brendan W.
Vervelde, Lonneke
Stevens, Mark P.
author_sort Vohra, Prerna
collection PubMed
description Campylobacter jejuni is the leading bacterial cause of human gastroenteritis worldwide and the handling or consumption of contaminated poultry meat is the key source of infection. C. jejuni proteins FlpA and SodB and glycoconjugates containing the C. jejuni N-glycan have been separately reported to be partially protective vaccines in chickens. In this study, two novel glycoproteins generated by protein glycan coupling technology—G-FlpA and G-SodB (with two and three N-glycosylation sites, respectively)—were evaluated for efficacy against intestinal colonisation of chickens by C. jejuni strain M1 relative to their unglycosylated variants. Two independent trials of the same design were performed with either a high challenge dose of 10(7) colony-forming units (CFU) or a minimum challenge dose of 10(2) CFU of C. jejuni M1. While antigen-specific serum IgY was detected in both trials, no reduction in caecal colonisation by C. jejuni M1 was observed and glycosylation of vaccine antigens had no effect on the outcome. Our data highlight inconsistencies in the outcome of C. jejuni vaccination trials that may reflect antigen-, challenge strain-, vaccine administration-, adjuvant- and chicken line-specific differences from previously published studies. Refinement of glycoconjugate vaccines by increasing glycosylation levels or using highly immunogenic protein carriers could improve their efficacy.
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spelling pubmed-75648352020-10-26 Evaluation of Glycosylated FlpA and SodB as Subunit Vaccines Against Campylobacter jejuni Colonisation in Chickens Vohra, Prerna Chintoan-Uta, Cosmin Terra, Vanessa S. Bremner, Abi Cuccui, Jon Wren, Brendan W. Vervelde, Lonneke Stevens, Mark P. Vaccines (Basel) Article Campylobacter jejuni is the leading bacterial cause of human gastroenteritis worldwide and the handling or consumption of contaminated poultry meat is the key source of infection. C. jejuni proteins FlpA and SodB and glycoconjugates containing the C. jejuni N-glycan have been separately reported to be partially protective vaccines in chickens. In this study, two novel glycoproteins generated by protein glycan coupling technology—G-FlpA and G-SodB (with two and three N-glycosylation sites, respectively)—were evaluated for efficacy against intestinal colonisation of chickens by C. jejuni strain M1 relative to their unglycosylated variants. Two independent trials of the same design were performed with either a high challenge dose of 10(7) colony-forming units (CFU) or a minimum challenge dose of 10(2) CFU of C. jejuni M1. While antigen-specific serum IgY was detected in both trials, no reduction in caecal colonisation by C. jejuni M1 was observed and glycosylation of vaccine antigens had no effect on the outcome. Our data highlight inconsistencies in the outcome of C. jejuni vaccination trials that may reflect antigen-, challenge strain-, vaccine administration-, adjuvant- and chicken line-specific differences from previously published studies. Refinement of glycoconjugate vaccines by increasing glycosylation levels or using highly immunogenic protein carriers could improve their efficacy. MDPI 2020-09-11 /pmc/articles/PMC7564835/ /pubmed/32932979 http://dx.doi.org/10.3390/vaccines8030520 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vohra, Prerna
Chintoan-Uta, Cosmin
Terra, Vanessa S.
Bremner, Abi
Cuccui, Jon
Wren, Brendan W.
Vervelde, Lonneke
Stevens, Mark P.
Evaluation of Glycosylated FlpA and SodB as Subunit Vaccines Against Campylobacter jejuni Colonisation in Chickens
title Evaluation of Glycosylated FlpA and SodB as Subunit Vaccines Against Campylobacter jejuni Colonisation in Chickens
title_full Evaluation of Glycosylated FlpA and SodB as Subunit Vaccines Against Campylobacter jejuni Colonisation in Chickens
title_fullStr Evaluation of Glycosylated FlpA and SodB as Subunit Vaccines Against Campylobacter jejuni Colonisation in Chickens
title_full_unstemmed Evaluation of Glycosylated FlpA and SodB as Subunit Vaccines Against Campylobacter jejuni Colonisation in Chickens
title_short Evaluation of Glycosylated FlpA and SodB as Subunit Vaccines Against Campylobacter jejuni Colonisation in Chickens
title_sort evaluation of glycosylated flpa and sodb as subunit vaccines against campylobacter jejuni colonisation in chickens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564835/
https://www.ncbi.nlm.nih.gov/pubmed/32932979
http://dx.doi.org/10.3390/vaccines8030520
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