Human extraintestinal pathogenic Escherichia coli strains differ in prevalence of virulence factors, phylogroups, and bacteriocin determinants
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
27646192
PubMed Central
PMC5028950
DOI
10.1186/s12866-016-0835-z
PII: 10.1186/s12866-016-0835-z
Knihovny.cz E-zdroje
- Klíčová slova
- Bacteriocinogeny, Colicin, Escherichia coli, ExPEC, Microcin, Virulence factor,
- MeSH
- bakteriální geny MeSH
- bakteriociny klasifikace genetika metabolismus MeSH
- dítě MeSH
- DNA bakterií genetika MeSH
- dospělí MeSH
- dýchací soustava mikrobiologie MeSH
- extraintestinální patogenní Escherichia coli genetika izolace a purifikace metabolismus patogenita MeSH
- faktory virulence genetika metabolismus MeSH
- feces mikrobiologie MeSH
- fylogeneze * MeSH
- gastrointestinální trakt mikrobiologie MeSH
- infekce reprodukčního traktu mikrobiologie MeSH
- infekce vyvolané Escherichia coli mikrobiologie MeSH
- kojenec MeSH
- koliciny metabolismus MeSH
- kůže mikrobiologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- předškolní dítě MeSH
- prevalence * MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- kojenec MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Česká republika MeSH
- Názvy látek
- bakteriociny MeSH
- DNA bakterií MeSH
- faktory virulence MeSH
- koliciny MeSH
- microcin MeSH Prohlížeč
BACKGROUND: The study used a set of 407 human extraintestinal pathogenic E. coli strains (ExPEC) isolated from (1) skin and soft tissue infections, (2) respiratory infections, (3) intra-abdominal infections, and (4) genital smears. The set was tested for bacteriocin production, for prevalence of bacteriocin and virulence determinants, and for phylogenetic typing. Results obtained from the group of ExPEC strains were compared to data from our previously published analyses of 1283 fecal commensal E. coli strains. RESULTS: The frequency of bacteriocinogeny was significantly higher in the set of ExPEC strains (63.1 %), compared to fecal E. coli (54.2 %; p < 0.01). Microcin producers and microcin determinants dominated in ExPEC strains, while colicin producers and colicin determinants were more frequent in fecal E. coli (p < 0.01). Higher production of microcin M and lower production of microcin B17, colicin Ib, and Js was detected in the set of ExPEC strains. ExPEC strains had a significantly higher prevalence of phylogenetic group B2 (52.6 %) compared to fecal E. coli strains (38.3 %; p < 0.01). CONCLUSIONS: Human ExPEC strains were shown to differ from human fecal strains in a number of parameters including bacteriocin production, prevalence of several bacteriocin and virulence determinants, and prevalence of phylogenetic groups. Differences in these parameters were also identified within subgroups of ExPEC strains of diverse origin. While some microcin determinants (mM, mH47) were associated with virulent strains, other bacteriocin types (mB17, Ib, and Js) were associated with fecal flora.
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