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Adaptation of Escherichia coli traversing from the faecal environment to the urinary tract.
Nielsen, Karen L; Stegger, Marc; Godfrey, Paul A; Feldgarden, Michael; Andersen, Paal S; Frimodt-Møller, Niels.
Afiliación
  • Nielsen KL; Microbiology and Infection Control, Statens Serum Institut, Copenhagen, Denmark; Department of Clinical Microbiology, Hvidovre Hospital, Hvidovre, Denmark. Electronic address: Karen.Leth.Nielsen.01@regionh.dk.
  • Stegger M; Microbiology and Infection Control, Statens Serum Institut, Copenhagen, Denmark.
  • Godfrey PA; Genome Sequencing and Analysis Program, Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Feldgarden M; Genome Sequencing and Analysis Program, Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Andersen PS; Microbiology and Infection Control, Statens Serum Institut, Copenhagen, Denmark; Veterinary Disease Biology, University of Copenhagen, Copenhagen, Denmark.
  • Frimodt-Møller N; Department of Clinical Microbiology, Hvidovre Hospital, Hvidovre, Denmark.
Int J Med Microbiol ; 306(8): 595-603, 2016 Dec.
Article en En | MEDLINE | ID: mdl-27825516
ABSTRACT
The majority of extraintestinal pathogenic Escherichia coli (ExPEC) causing urinary tract infections (UTI) are found in the patient's own gut flora, but only limited knowledge is available on the potential adaptation that may occur in the bacteria in order to traverse the perineum and successfully infect the urinary tract. Here, matching pairs of faecal and UTI isolates from 42 patients were compared pairwise using in-depth whole-genome sequencing to investigate whether genetic changes were evident for successful colonization in these two different environments. The identified non-synonymous mutations (0-12 substitutions in each pair) were primarily associated to genes encoding virulence factors and nutrient metabolism; and indications of parallel evolution were observed in genes encoding the major phase-variable protein antigen 43, a toxin/antitoxin locus and haemolysin B. No differences in virulence potential were observed in a mouse UTI model for five matching faecal and UTI isolates with or without mutations in antigen 43 and haemolysin B. Variations in plasmid content were observed in only four of the 42 pairs. Although, we observed mutations in known UTI virulence genes for a few pairs, the majority showed no detectable differences with respect to mutations or mobilome when compared to their faecal counterpart. The results show that UPECs are successful in colonizing both the bladder and gut without adaptation.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Sistema Urinario / Escherichia coli / Heces Tipo de estudio: Prognostic_studies Límite: Adult / Animals / Female / Humans Idioma: En Revista: Int J Med Microbiol Asunto de la revista: MICROBIOLOGIA Año: 2016 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Sistema Urinario / Escherichia coli / Heces Tipo de estudio: Prognostic_studies Límite: Adult / Animals / Female / Humans Idioma: En Revista: Int J Med Microbiol Asunto de la revista: MICROBIOLOGIA Año: 2016 Tipo del documento: Article