Mark A. Harrison
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.
Authors
Elizabeth Atkins
Dr ALEXANDRA FAULDS-PAIN Alexandra.Faulds-Pain1@nottingham.ac.uk
SENIOR RESEARCH FELLOW
Professor JOHN HEAP JOHN.HEAP@NOTTINGHAM.AC.UK
Professor of Engineering Biology
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 |
Files
Vaccines-13-00279
(2.1 Mb)
PDF
Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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