ArticleGenome medicine2026
Global survey of extraintestinal pathogenic Escherichia coli identifies stable serogroup-virulence-resistance linkages.
Article in Genome medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Diversity and Antimicrobial Resistance Profiles of ESBL-ProducingPathogens (Basel, Switzerland) · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
13 authors.
Funding
Abstract
backgroundExtraintestinal pathogenic Escherichia coli (ExPEC) is a leading cause of urinary tract infections, sepsis, and neonatal meningitis globally. However, global patterns linking O-serogroups, sequence types (STs), virulence, and antimicrobial resistance (AMR) remain poorly resolved.
methodsWe analyzed 12,220 ExPEC genomes, including 12,160 publicly available genomes retrieved from the NCBI database and 60 representative isolates collected and sequenced in this study. Serogroups were assigned by in silico wzm/wzt/wzx/wzy and fliC gene analysis, and phylogenies constructed using maximum likelihood methods. Virulence and antibiotic resistance genes were annotated with the Virulence Factor Database and the Comprehensive Antibiotic Resistance Database. A set of ExPEC isolates collected from China was tested phenotypically for motility, iron acquisition and growth assays under standardized conditions.
resultsWe identified 199 O-serogroups from the 12,220 genomes, with 17 dominant types accounting for 83% of isolates. O25 (30.75%) was globally prevalent, while O101 was more prevalent than O25 in China and India. Most of the isolates were from urine (44.49%) and blood (26.80%) as primary sources. Phylogenetic analysis revealed 52 clusters with stable serogroup-ST associations (e.g., O25-ST131, O2/O6-ST73). Virulence analysis uncovered 383 genes, with a conserved 24-gene core encoding adhesion and iron uptake genes. Resistance profiling revealed 308 genes, dominated by β-lactamases and efflux regulators. Integrated analysis identified iron acquisition (Vir_2) and efflux-mediated resistance (Res_5) as key genomic traits of high-risk serogroups, supported by phenotypic assays showing correlated motility and iron uptake patterns.
conclusionsWe propose a genomic survey that integrates serogroup profiling with virulence-resistance gene-content clusters to resolve ExPEC population structure and functional convergence. These insights may guide the rational development of next-generation ExPEC vaccines and precision surveillance strategies.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.