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Modular Combinatorial DNA Assembly of Group B Streptococcus Capsular Polysaccharide Biosynthesis Pathways to Expediate the Production of Novel Glycoconjugate Vaccines

Harrison, Mark A.; Atkins, Elizabeth; Faulds-Pain, Alexandra; Heap, John T.; Wren, Brendan W.; Passmore, Ian J.

Modular Combinatorial DNA Assembly of Group B Streptococcus Capsular Polysaccharide Biosynthesis Pathways to Expediate the Production of Novel Glycoconjugate Vaccines Thumbnail


Authors

Mark A. Harrison

Elizabeth Atkins

Brendan W. Wren

Ian J. Passmore



Abstract

Background/objectives: Streptococcus agalactiae (or Group B Streptococcus, GBS) is a major cause of neonatal meningitis globally. There are 10 serotypes of GBS, which are distinguished by their capsular polysaccharide (CPS) structure, with serotypes Ia, Ib, II, III, IV and V responsible for up to 99% of infections. Currently, there are no licensed vaccines against GBS. The most developed candidates are glycoconjugate vaccines, which can be highly effective but are also expensive to produce by existing approaches and unaffordable for many parts of the world. Biosynthesis of recombinant glycans and glycoconjugates in tractable strains of bacteria offers a low-cost alternative approach to current chemical conjugation methods. Methods: In this study, we apply combinatorial hierarchical DNA assembly to the heterologous biosynthesis of GBS III, IV and V CPSs in E. coli. Each gene was removed from its native regulation, paired with synthetic regulatory elements and rebuilt from the bottom up to generate libraries of reconstituted pathways. These pathways were screened for glycan biosynthesis using serotype-specific antisera. Results: We identified several configurations that successfully biosynthesised the GBS CPSs. Furthermore, we exploited the conserved nature of the GBS CPS biosynthesis loci and the flexibility of modular DNA assembly by constructing hybrid pathways from a minimal pool of glycosyltransferase genes. We show that transferase genes with homologous function can be used interchangeably between pathways, obviating the need to clone a complete locus for each new CPS assembly. Conclusions: In conclusion, we report the first demonstration of heterologous GBS CPS IV and V biosynthesis in E. coli, a key milestone towards the development of low-cost recombinant multivalent GBS glycoconjugate vaccines.

Citation

Harrison, M. A., Atkins, E., Faulds-Pain, A., Heap, J. T., Wren, B. W., & Passmore, I. J. (2025). Modular Combinatorial DNA Assembly of Group B Streptococcus Capsular Polysaccharide Biosynthesis Pathways to Expediate the Production of Novel Glycoconjugate Vaccines. Vaccines, 13(3), Article 279. https://doi.org/10.3390/vaccines13030279

Journal Article Type Article
Acceptance Date Feb 28, 2025
Online Publication Date Mar 6, 2025
Publication Date Mar 6, 2025
Deposit Date May 6, 2025
Publicly Available Date May 6, 2025
Journal Vaccines
Electronic ISSN 2076-393X
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 13
Issue 3
Article Number 279
DOI https://doi.org/10.3390/vaccines13030279
Public URL https://nottingham-repository.worktribe.com/output/48556544
Publisher URL https://www.mdpi.com/2076-393X/13/3/279

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