Your browser doesn't support javascript.
loading
Within-Host and Population Transmission of blaOXA-48 in K. pneumoniae and E. coli.
Haverkate, Manon R; Dautzenberg, Mirjam J D; Ossewaarde, Tjaco J M; van der Zee, Anneke; den Hollander, Jan G; Troelstra, Annet; Bonten, Marc J M; Bootsma, Martin C J.
  • Haverkate MR; Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Dautzenberg MJ; Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands; Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands; Department of Medical Microbiology, Maasstad Ziekenhuis, Rotterdam, the Netherlands.
  • Ossewaarde TJ; Department of Medical Microbiology, Maasstad Ziekenhuis, Rotterdam, the Netherlands.
  • van der Zee A; Department of Medical Microbiology, Maasstad Ziekenhuis, Rotterdam, the Netherlands.
  • den Hollander JG; Department of Internal Medicine, Maasstad Ziekenhuis, Rotterdam, the Netherlands.
  • Troelstra A; Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Bonten MJ; Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands; Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Bootsma MC; Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands; Department of Mathematics, Utrecht University, Utrecht, the Netherlands.
PLoS One ; 10(10): e0140960, 2015.
Article en En | MEDLINE | ID: mdl-26485437
During a large hospital outbreak of OXA-48 producing bacteria, most K. pneumoniaeOXA-48 isolates were phenotypically resistant to meropenem or imipenem, whereas most E. coliOXA-48 isolates were phenotypically susceptible to these antibiotics. In the absence of molecular gene-detection E. coliOXA-48 could remain undetected, facilitating cross-transmission and horizontal gene transfer of blaOXA-48. Based on 868 longitudinal molecular microbiological screening results from patients carrying K. pneumoniaeOXA-48 (n = 24), E. coliOXA-48 (n = 17), or both (n = 40) and mathematical modelling we determined mean durations of colonisation (278 and 225 days for K. pneumoniaeOXA-48 and E. coliOXA-48, respectively), and horizontal gene transfer rates (0.0091/day from K. pneumoniae to E. coli and 0.0015/day vice versa). Based on these findings the maximum effect of horizontal gene transfer of blaOXA-48 originating from E. coliOXA-48 on the basic reproduction number (R0) is 1.9%, and it is, therefore, unlikely that phenotypically susceptible E. coliOXA-48 will contribute significantly to the spread of blaOXA-48.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Beta-Lactamasas / Transferencia de Gen Horizontal / Proteínas de Escherichia coli / Farmacorresistencia Bacteriana / Escherichia coli / Klebsiella pneumoniae Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Beta-Lactamasas / Transferencia de Gen Horizontal / Proteínas de Escherichia coli / Farmacorresistencia Bacteriana / Escherichia coli / Klebsiella pneumoniae Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2015 Tipo del documento: Article