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Molecular characterization of extraintestinal and diarrheagenic Escherichia coli blood isolates

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Pathogenic E. coli strains can be classified into two major groups, based on the presence of specific virulence factors: extraintestinal pathogenic E. coli (ExPEC) and diarrheagenic E. coli (DEC). Several case reports describe that DEC can cause bloodstream infections in some rare cases. This mainly concerns a few specific sequence types that express virulence factors from both ExPEC and DEC. In this study, we retrospectively analysed 234 E. coli blood isolates with whole genome sequencing (WGS). WGS was performed on an Illumina NovaSeq6000. Genotyping was performed using BioNumerics software. The presence of genes was determined with a minimum percentage sequence identity (ID) threshold of 95% and a minimum length for sequence coverage of 95%. Three of the 234 (1.28%) isolates were defined as DEC, 182 (77.78%) as ExPEC, and 49 (20.94%) did not carry pathotype-associated virulence genes. We identified 112 different virulence genes, 48 O-antigens, and 28 H-antigens 82 STs, among the 234 analyzed isolates. ST131 and ST88 were related to healthcare-associated infections. This study provides insight into the prevalence of virulence factors in a large set of E. coli blood isolates from the UZ Brussel. It illustrates high diversity in virulence profiles and highlights the potential of DEC to carry virulence factors associated with extraintestinal infections, making it possible for unusual pathotypes to invade and survive in the bloodstream causing bacteraemia. Diarrheagenic strains causing bacteremia are rare and presently underreported, but modern sequencing techniques will better underscore their importance.

Tijdschrift: Virulence
ISSN: 2150-5594
Issue: 1
Volume: 13
Pagina's: 2032-2041
Trefwoorden:Escherichia coli, virulence factors, pathotypes, sequence type, serotype, nosocomial, core genome sequencing, bacteremia, MLST, hybrid pathotype
  • ORCID: /0000-0002-7756-3691/work/123376571
  • ORCID: /0000-0002-6410-9246/work/123377018
  • ORCID: /0000-0002-6217-1695/work/123377071
  • PubMed Id: 36397646
  • Scopus Id: 85142755951
  • DOI: https://doi.org/10.1080/21505594.2022.2147735
  • ORCID: /0000-0002-5589-502X/work/125070438
  • WoS Id: 000898742100001
Toegankelijkheid:Open