Evidence map›Paper›PMID 37596672›Full record

ArticleMicrobial cell factories2023

Development of a novel glycoengineering platform for the rapid production of conjugate vaccines.

Sherif Abouelhadid, Elizabeth R Atkins, Emily J Kay, Ian J Passmore, Simon J North, Burhan Lehri, Paul Hitchen, Eirik Bakke, Mohammed Rahman, Janine T Bossé and 6 more

Open access · goldAbstract read
In one paragraph

Article in Microbial cell factories, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 2 institutions in 1 country.

Sherif AbouelhadidDepartment of Infection Biology, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Elizabeth R AtkinsDepartment of Infection Biology, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Emily J KayDepartment of Infection Biology, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Ian J PassmoreDepartment of Infection Biology, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Simon J NorthDepartment of Life Sciences, Imperial College London, London, SW7 2AZ, UK.
Burhan LehriDepartment of Infection Biology, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Paul HitchenDepartment of Life Sciences, Imperial College London, London, SW7 2AZ, UK.
Eirik BakkeDepartment of Infection Biology, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Mohammed RahmanDepartment of Infection Biology, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Janine T BosséDepartment of Infectious Diseases, Imperial College London, London, W2 1NY, UK.
Yanwen LiDepartment of Infectious Diseases, Imperial College London, London, W2 1NY, UK.
Vanessa S TerraDepartment of Infection Biology, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Paul R LangfordDepartment of Infectious Diseases, Imperial College London, London, W2 1NY, UK.
Anne DellDepartment of Life Sciences, Imperial College London, London, SW7 2AZ, UK.
Brendan W WrenDepartment of Infection Biology, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
Jon CuccuiDepartment of Infection Biology, London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK. jon.cuccui@lshtm.ac.uk.
London School of Hygiene & Tropical Medicine · GBImperial College London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/F009321/1Biotechnology and Biological Sciences Research Council BB/G018553/1Biotechnology and Biological Sciences Research Council BBSRC BB/H017437/1
6 · The paper itself

Abstract

Conjugate vaccines produced either by chemical or biologically conjugation have been demonstrated to be safe and efficacious in protection against several deadly bacterial diseases. However, conjugate vaccine assembly and production have several shortcomings which hinders their wider availability. Here, we developed a tool, Mobile-element Assisted Glycoconjugation by Insertion on Chromosome, MAGIC, a novel biotechnological platform that overcomes the limitations of the current conjugate vaccine design method(s). As a model, we focused our design on a leading bioconjugation method using N-oligosaccharyltransferase (OTase), PglB. The installation of MAGIC led to at least twofold increase in glycoconjugate yield via MAGIC when compared to conventional N-OTase based bioconjugation method(s). Then, we improved MAGIC to (a) allow rapid installation of glycoengineering component(s), (b) omit the usage of antibiotics, (c) reduce the dependence on protein induction agents. Furthermore, we show the modularity of the MAGIC platform in performing glycoengineering in bacterial species that are less genetically tractable than the commonly used Escherichia coli. The MAGIC system promises a rapid, robust and versatile method to develop vaccines against serious bacterial pathogens. We anticipate the utility of the MAGIC platform could enhance vaccines production due to its compatibility with virtually any bioconjugation method, thus expanding vaccine biopreparedness toolbox.

Indexed as

Anti-Bacterial AgentsBiotechnologyEscherichia coliVaccine DevelopmentVaccines, ConjugateAnti-Bacterial AgentsVaccines, ConjugateBacterial vaccinesBioconjugationConjugate vaccinesGlycoengineering

Identifiers

PMID37596672
PMCPMC10436394
OpenAlexW4385996361

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.