Redefining enteroaggregative Escherichia coli (EAEC): Genomic characterization of epidemiological EAEC strains

PLoS Negl Trop Dis. 2020 Sep 8;14(9):e0008613. doi: 10.1371/journal.pntd.0008613. eCollection 2020 Sep.

Abstract

Although enteroaggregative E. coli (EAEC) has been implicated as a common cause of diarrhea in multiple settings, neither its essential genomic nature nor its role as an enteric pathogen are fully understood. The current definition of this pathotype requires demonstration of cellular adherence; a working molecular definition encompasses E. coli which do not harbor the heat-stable or heat-labile toxins of enterotoxigenic E. coli (ETEC) and harbor the genes aaiC, aggR, and/or aatA. In an effort to improve the definition of this pathotype, we report the most definitive characterization of the pan-genome of EAEC to date, applying comparative genomics and functional characterization on a collection of 97 EAEC strains isolated in the course of a multicenter case-control diarrhea study (Global Enteric Multi-Center Study, GEMS). Genomic analysis revealed that the EAEC strains mapped to all phylogenomic groups of E. coli. Circa 70% of strains harbored one of the five described AAF variants; there were no additional AAF variants identified, and strains that lacked an identifiable AAF generally did not have an otherwise complete AggR regulon. An exception was strains that harbored an ETEC colonization factor (CF) CS22, like AAF a member of the chaperone-usher family of adhesins, but not phylogenetically related to the AAF family. Of all genes scored, sepA yielded the strongest association with diarrhea (P = 0.002) followed by the increased serum survival gene, iss (p = 0.026), and the outer membrane protease gene ompT (p = 0.046). Notably, the EAEC genomes harbored several genes characteristically associated with other E. coli pathotypes. Our data suggest that a molecular definition of EAEC could comprise E. coli strains harboring AggR and a complete AAF(I-V) or CS22 gene cluster. Further, it is possible that strains meeting this definition could be both enteric bacteria and urinary/systemic pathogens.

Publication types

  • Multicenter Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adhesins, Bacterial / genetics
  • Bacterial Adhesion / genetics*
  • Bacterial Adhesion / physiology
  • Case-Control Studies
  • Cell Line
  • Child, Preschool
  • Diarrhea / microbiology
  • Escherichia coli / classification
  • Escherichia coli / genetics*
  • Escherichia coli / isolation & purification
  • Escherichia coli / pathogenicity*
  • Escherichia coli Infections / epidemiology*
  • Escherichia coli Proteins / genetics*
  • Fimbriae Proteins / genetics*
  • Fimbriae, Bacterial / genetics*
  • Genome, Bacterial / genetics
  • Genomics
  • Humans
  • Infant
  • Infant, Newborn
  • Trans-Activators / genetics
  • Virulence / genetics
  • Virulence Factors / genetics
  • Whole Genome Sequencing

Substances

  • Adhesins, Bacterial
  • AggA protein, E coli
  • AggR protein, E coli
  • CSEA protein, E coli
  • Escherichia coli Proteins
  • Trans-Activators
  • Virulence Factors
  • Fimbriae Proteins

Grants and funding

This study was supported by DFF1333-00156 to N.B.O and The National Institutes of Health grants AI-033096 and AI-125181 to J. P. N. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.