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Modification of avian pathogenic Escherichia coli χ7122 lipopolysaccharide increases accessibility to glycoconjugate antigens.

Published version
Peer-reviewed

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Authors

Smith, Alexander A 
Corona-Torres, Ricardo 
Hewitt, Rachel E 
Stevens, Mark P 
Grant, Andrew J 

Abstract

BACKGROUND: Worldwide, an estimated 70.7 billion broilers were produced in 2020. With the reduction in use of prophylactic antibiotics as a result of consumer pressure and regulatory oversight alternative approaches, such as vaccination, are required to control bacterial infections. A potential way to produce a multivalent vaccine is via the generation of a glycoconjugate vaccine which consists of an antigenic protein covalently linked to an immunogenic carbohydrate. Protein-glycan coupling technology (PGCT) is an approach to generate glycoconjugates using enzymes that can couple proteins and glycan when produced in bacterial cells. Previous studies have used PGCT to generate a live-attenuated avian pathogenic Escherichia coli (APEC) strain capable of N-glycosylation of target proteins using a chromosomally integrated Campylobacter jejuni pgl locus. However, this proved ineffective against C. jejuni challenge. RESULTS: In this study we demonstrate the lack of surface exposure of glycosylated protein in APEC strain χ7122 carrying the pgl locus. Furthermore, we hypothesise that this may be due to the complex cell-surface architecture of E. coli. To this end, we removed the lipopolysaccharide O-antigen of APEC χ7122 pgl+ via deletion of the wecA gene and demonstrate increased surface exposure of glycosylated antigens (NetB and FlpA) in this strain. We hypothesise that increasing the surface expression of the glycosylated protein would increase the chance of host immune cells being exposed to the glycoconjugate, and therefore the generation of an efficacious immune response would be more likely. CONCLUSIONS: Our results demonstrate an increase in cell surface exposure and therefore accessibility of glycosylated antigens upon removal of lipopolysaccharide antigen from the APEC cell surface.

Description

Keywords

Glycoconjugate lipopolysaccharide, Poultry, Protein glycan coupling technology, Vaccine, Animals, Chickens, Escherichia coli, Escherichia coli Infections, Glycoconjugates, Lipopolysaccharides

Journal Title

Microb Cell Fact

Conference Name

Journal ISSN

1475-2859
1475-2859

Volume Title

Publisher

BioMed Central
Sponsorship
Biotechnology and Biological Sciences Research Council (BB/N001591/1)
The authors gratefully acknowledge funding from the Biotechnology & Biological Sciences Research Council (BBSRC; grant references BB/N001591/1 and BBS/E/D/20002174).