Evidence map›Paper›PMID 42092774›Full record

ArticleBMC microbiology2026

Flagellar glycosylation with pseudaminic acids is widespread in the genus Clostridium.

Orlagh H Anderson, Jay M Johnson, Emily K P Flack, Martin A Fascione, James P J Chong, Gavin H Thomas

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Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Orlagh H AndersonDepartment of Biology, University of York, Wentworth Way, York, YO10 5DD, UK.
Jay M JohnsonDepartment of Biology, University of York, Wentworth Way, York, YO10 5DD, UK.
Emily K P FlackDepartment of Biology, University of York, Wentworth Way, York, YO10 5DD, UK.
Martin A FascioneDepartment of Chemistry, Green Chemistry Centre of Excellence, University of York, Heslington, York, YO10 5DD, UK.
James P J ChongDepartment of Biology, University of York, Wentworth Way, York, YO10 5DD, UK.
Gavin H ThomasDepartment of Biology, University of York, Wentworth Way, York, YO10 5DD, UK. gavin.thomas@york.ac.uk.

Funding

BBSRC BB/M011151/1
6 · The paper itself

Abstract

backgroundThe ability of bacteria to chemically modify their cell surfaces through O-linked glycosylation is well characterised in Gram-negative bacteria and includes the modification of flagellin proteins with nonulosonic acids (NulOs). These modifications are widespread and have established roles in flagellar assembly, motility and virulence in various pathogens. However, there are limited documented examples of similar modifications in Gram-positive bacteria, and the significance of these is less well understood. In this study, we expand upon our previous findings that the flagellar biosynthetic locus of several pathogenic Clostridium butyricum strains contains a cluster of genes predicted to be involved in the biosynthesis of NulOs, and examine similar clusters across the whole genus Clostridium to assess the wider occurrence of NulO-mediated flagellin modification.

resultsUsing orthologues of the components of the biosynthetic pathways for the NulOs pseudaminic acid (Pse) and legionaminic acid (Leg) in the pathogenic species Campylobacter jejuni, we predict that the flagellar biosynthetic loci of several pathogenic C. butyricum strains also encode genes for these modifications. To verify this, we demonstrate that the predicted PseB orthologue encoded in the flagellar biosynthesis locus of the pathogenic strain C. butyricum 5521 is able to catalyse the first step of Pse biosynthesis. Furthermore, we show that across the genus Clostridium, genes involved in flagellar glycosylation are located in a hypervariable region (HVR) of the flagellar biosynthetic locus, which is flanked by the flagellar structural genes flgB and fliD. The content of this region differs considerably across strains and species, but remarkably over half of the Clostridium genomes encode NulO biosynthesis genes in these regions. Finally, we present evidence that suggests that this flagellar HVR has evolved independently from the rest of the genome.

conclusionsWe show that genes required for NulO-mediated flagellar glycosylation are widespread across the genus Clostridium. Our findings have potential applications in the characterisation of pathogenic strains within these species and in the engineering of strains used in industrial biotechnology.

Indexed as

ClostridiumClostridium butyricumFlagellaFlagellinSialic AcidsSugar AcidsBiosynthetic PathwaysGlycosylationMultigene Family5,7-diacetamido-3,5,7,9-tetradeoxynonulosonic acid5,7-diacetamido-8-O-acetyl-3,5,7,9-tetradeoxy-glycero-talo-nonulosonic acidFlagellinSialic AcidsSugar AcidsClostridium butyricumFlagellar glycosylationHypervariable regionLegionaminic acidPseudaminic acid

Identifiers

PMID42092774
PMCPMC13317340

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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.