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Emergence of Enteroaggregative Escherichia coli within the ST131 Lineage as a Cause of Extraintestinal Infections
Erik J Boll1, Søren Overballe-Petersen1, Henrik Hasman1
1Department of Bacteria, Parasites and Fungi, Statens Serum Institut, Copenhagen, Denmark.
Abstract:
Escherichia coli sequence type 131 (ST131) is a major cause of urinary and bloodstream infections. Its association with extended-spectrum β-lactamases (ESBLs) significantly complicates treatment. Its best-described component is the rapidly expanding H30Rx clade, containing allele 30 of the type 1 fimbrial adhesin gene fimH This lineage appears to have emerged in the United States and spread around the world in part due to the acquisition of the ESBL-encoding blaCTX-M-15 gene and resistance to fluoroquinolones. However, non-H30 ST131 sublineages with other acquired CTX-M-type resistance genes are also emerging. Based on whole-genome analyses, we describe here the presence of an (fimH) H27 E. coli ST131 sublineage that has recently caused an outbreak of community-acquired bacteremia and recurrent urinary tract infections (UTIs) in Denmark. This sublineage has acquired both a virulence plasmid (pAA) that defines the enteroaggregative E. coli (EAEC) diarrheagenic pathotype and multiple genes associated with extraintestinal E. coli (ExPEC); combined, these traits have made this particular ST131 sublineage successful at colonizing its human host and causing recurrent UTI. Moreover, using a historic World Health Organization (WHO) E. coli collection and publicly available genome sequences, we identified a global H27 EAEC ST131 sublineage that dates back as far as 1998. Most H27 EAEC ST131 isolates harbor pAA or pAA-like plasmids, and our analysis strongly implies a single ancestral acquisition among these isolates. These findings illustrate both the profound plasticity of this important pathogenic E. coli ST131 H27 sublineage and genetic acquisitions of EAEC-specific virulence traits that likely confer an enhanced ability to cause intestinal colonization.IMPORTANCEE. coli ST131 is an important extraintestinal pathogenic lineage. A signature characteristic of ST131 is its ability to asymptomatically colonize the gastrointestinal tract and then opportunistically cause extraintestinal infections, such as cystitis, pyelonephritis, and urosepsis. In this study, we identified an ST131 H27 sublineage that has acquired the enteroaggregative diarrheagenic phenotype, spread across multiple continents, and caused multiple outbreaks of community-acquired ESBL-associated bloodstream infections in Denmark. The strain's ability to both cause diarrhea and innocuously colonize the human gastrointestinal tract may facilitate its dissemination and establishment in the community.
Insights
A new Escherichia coli ST131 H27 sublineage has emerged, causing infections and carrying virulence genes. This adaptable strain can colonize the gut and cause recurrent urinary tract infections and bacteremia globally.
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Escherichia coli sequence type 131 (ST131) is a significant cause of urinary tract infections (UTIs) and bloodstream infections, often associated with antimicrobial resistance.
- The H30Rx clade is a well-known, globally spreading ST131 sublineage characterized by the fimH allele 30 and acquisition of resistance genes like blaCTX-M-15.
- Emerging non-H30 ST131 sublineages with different resistance profiles and virulence factors are increasingly recognized.
Purpose of the Study:
- To characterize a novel fimH H27 Escherichia coli ST131 sublineage identified during an outbreak of community-acquired bacteremia and recurrent UTIs in Denmark.
- To investigate the genetic basis of virulence and global distribution of this H27 ST131 sublineage, including its association with enteroaggregative E. coli (EAEC) pathotype traits.
- To understand the evolutionary plasticity and acquisition of virulence factors contributing to the success of this ST131 sublineage.
Main Methods:
- Whole-genome sequencing and phylogenetic analysis of E. coli isolates.
- Comparative genomics to identify virulence genes, plasmids (e.g., pAA), and antimicrobial resistance determinants.
- Analysis of historical E. coli collections and publicly available genome sequences to trace the lineage's origin and spread.
Main Results:
- Identification of an Escherichia coli ST131 H27 sublineage causing recurrent UTIs and bacteremia in Denmark, linked to the acquisition of the pAA virulence plasmid.
- This H27 sublineage possesses genes associated with both the EAEC pathotype and extraintestinal pathogenic E. coli (ExPEC), enhancing host colonization and infection.
- A global H27 EAEC ST131 sublineage, dating back to at least 1998, was identified, with most isolates harboring pAA or similar plasmids, suggesting a single ancestral acquisition event.
Conclusions:
- The H27 EAEC ST131 sublineage demonstrates significant genetic adaptability, acquiring virulence plasmids that enhance its ability to cause intestinal colonization and extraintestinal infections.
- This adaptable lineage poses a growing threat, capable of causing outbreaks of community-acquired infections, including ESBL-associated bloodstream infections.
- The findings highlight the dynamic evolution of E. coli ST131 and the critical role of acquired virulence traits in driving the emergence and spread of successful pathogenic clones.
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