Escherichia coli ST131 isolates are rare in human meningitis but belong to a distinct O25b-fimH22 clade B lineage shared with avian pathogenic Escherichia coli

Escherichia coli ST131 is a globally disseminated extraintestinal lineage best known for its resistance-driven expansion, yet it is rarely reported as a cause of neonatal meningitis. Whether specific ST131 sublineages retain neuroinvasive potential remains poorly understood. We analysed a 25-year nationwide French collection of 355 neonatal meningitis E. coli isolates recovered between 2000 and 2024. ST131 isolates were characterized by whole-genome sequencing, and ST131-O25b- fim H22 genomes were contextualized in a phylogeny including human-associated genomes and selected animal- and food-associated references. An extended dataset of 623 animal- and food-associated ST131-O25b- fim H22 genomes was analysed separately to assess the distribution of virulence-associated lineages across non-human reservoirs. Nine neonatal meningitis isolates belonged to ST131. Six were O25b:H4- fim H22 clade B isolates carrying K1, invasion of brain endothelium A ( ibe A) and pS88-like markers; non- fim H22 isolates had heterogeneous virulence/resistance profiles, including two with sen B -cjr ABC-positive pRS218-like signatures. Phylogenomic analysis placed French ST131-O25b- fim H22 meningitis isolates within a conserved 85-genome lineage spanning 1995–2024 and comprising meningitis, bloodstream, urinary and avian-source isolates. This lineage was enriched in K1, ibe A, pS88-like signatures and virotype D/D4, with most isolates sharing HC100 assignment (≤100 core-genome allelic differences). The extended animal- and food-associated dataset identified a large poultry-associated HC100 population with the same K1/ ibe A/pS88-like profile, whereas pRS218-like signatures were uncommon and mainly canine or feline. Although ST131 rarely causes neonatal meningitis, the isolates identified belong to a conserved ancestral ST131-O25b- fim H22 clade B lineage combining the major determinants of neonatal meningitis E. coli pathogenicity and are closely related to poultry-associated populations. Together with previous observations in ST95, these findings support a shared avian reservoir for highly pathogenic extraintestinal pathogenic E. coli lineages, distinct from the resistance-driven expansion of ST131-H30 and highlight the importance of One Health genomic surveillance.

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Journal
Microbial Genomics
Published
2026-10-07
DOI
https://doi.org/10.1099/mgen.0.001857
Primary Topic
Escherichia coli research studies
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article
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article

Escherichia coli ST131 isolates are rare in human meningitis but belong to a distinct O25b-fimH22 clade B lineage shared with avian pathogenic Escherichia coli

Céline Courroux, Philippe Bidet, Guillaume Geslain, Kévin La et al.
Microbial Genomics
Escherichia coli research studies
article

Escherichia coli ST131 isolates are rare in human meningitis but belong to a distinct O25b-fimH22 clade B lineage shared with avian pathogenic Escherichia coli

Céline Courroux, Philippe Bidet, Guillaume Geslain, Kévin La, André Birgy, Érick Denamur, Stéphane Bonacorsi, Yasmine Benhadid-Brahmi
article en

Abstract

Escherichia coli ST131 is a globally disseminated extraintestinal lineage best known for its resistance-driven expansion, yet it is rarely reported as a cause of neonatal meningitis. Whether specific ST131 sublineages retain neuroinvasive potential remains poorly understood. We analysed a 25-year nationwide French collection of 355 neonatal meningitis E. coli isolates recovered between 2000 and 2024. ST131 isolates were characterized by whole-genome sequencing, and ST131-O25b- fim H22 genomes were contextualized in a phylogeny including human-associated genomes and selected animal- and food-associated references. An extended dataset of 623 animal- and food-associated ST131-O25b- fim H22 genomes was analysed separately to assess the distribution of virulence-associated lineages across non-human reservoirs. Nine neonatal meningitis isolates belonged to ST131. Six were O25b:H4- fim H22 clade B isolates carrying K1, invasion of brain endothelium A ( ibe A) and pS88-like markers; non- fim H22 isolates had heterogeneous virulence/resistance profiles, including two with sen B -cjr ABC-positive pRS218-like signatures. Phylogenomic analysis placed French ST131-O25b- fim H22 meningitis isolates within a conserved 85-genome lineage spanning 1995–2024 and comprising meningitis, bloodstream, urinary and avian-source isolates. This lineage was enriched in K1, ibe A, pS88-like signatures and virotype D/D4, with most isolates sharing HC100 assignment (≤100 core-genome allelic differences). The extended animal- and food-associated dataset identified a large poultry-associated HC100 population with the same K1/ ibe A/pS88-like profile, whereas pRS218-like signatures were uncommon and mainly canine or feline. Although ST131 rarely causes neonatal meningitis, the isolates identified belong to a conserved ancestral ST131-O25b- fim H22 clade B lineage combining the major determinants of neonatal meningitis E. coli pathogenicity and are closely related to poultry-associated populations. Together with previous observations in ST95, these findings support a shared avian reservoir for highly pathogenic extraintestinal pathogenic E. coli lineages, distinct from the resistance-driven expansion of ST131-H30 and highlight the importance of One Health genomic surveillance.

Microbial GenomicsVol. 12(10)
Inserm (FR), Université Paris Cité (FR), Université Sorbonne Paris Nord (FR), Assistance Publique – Hôpitaux de Paris (FR), Hôpital Robert-Debré (FR), Infection, Anti-microbiens, Modélisation, Evolution (FR)
Openalex Percentile: Top 14%
Escherichia coli research studies
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