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Time to acquire and lose carriership of ESBL/pAmpC producing E. coli in humans in the Netherlands.
Teunis, Peter F M; Evers, Eric G; Hengeveld, Paul D; Dierikx, Cindy M; Wielders, Cornelia C H; van Duijkeren, Engeline.
Afiliação
  • Teunis PFM; Centre for Infectious Disease control, RIVM, Bilthoven, The Netherlands.
  • Evers EG; Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta GA, United States of America.
  • Hengeveld PD; Centre for Infectious Disease control, RIVM, Bilthoven, The Netherlands.
  • Dierikx CM; Centre for Infectious Disease control, RIVM, Bilthoven, The Netherlands.
  • Wielders CCH; Centre for Infectious Disease control, RIVM, Bilthoven, The Netherlands.
  • van Duijkeren E; Centre for Infectious Disease control, RIVM, Bilthoven, The Netherlands.
PLoS One ; 13(3): e0193834, 2018.
Article em En | MEDLINE | ID: mdl-29561861
ABSTRACT
A subset of the study population from a cross-sectional study of carriership of ESBL/pAmpC-producing E. coli (ESBL-E) in the general population was followed up by five successive samples over an approximate half year period, leading to six samples in 333 persons. Fecal samples were cultured and analyzed for the presence of E. coli types as characterized by MLST, and ESBL/pAmpC genes were analysed by PCR and sequencing. The study included 255 persons who had a negative first sample, to allow observations of acquiring carriership of ESBL-E. Any individual record thus consisted of a series of snapshots of episodes of presence and absence of ESBL-E carriage. A survival model was built to estimate times to acquire or lose carriership, allowing for any combination of ESBL/pAmpC gene and E. coli MLST type. In carriers, the mean time to lose carriership was 1.1 (95% range 0.8-1.6) years. The estimated mean time to acquire carriership was 3.0 (95% range 1.6-6.3) years. Analysis of these times by ESBL/pAmpC gene found substantial variation among resistance genes both in persistence of carriership and in rates of acquiring carriership blaCTX-M-1, blaCTX-M-14, blaCTX-M-15, blaCTX-M-27 and blaSHV-12 were easily acquired, but blaCTX-M-1 and blaSHV-12 were also easily lost, while blaCTX-M-15, blaCTX-M-27 and blaCMY-2 were more likely to persist. When in addition bacterial host types were included, some combinations appeared more persistent than others (blaCTX-M-1 in ST10 and ST58; blaCTX-M-14, blaCMY-2, and blaSHV-12 in ST69), or were acquired with higher frequency (blaCTX-M-14 in ST38, ST69, and ST131; blaCTX-M-15 and blaCTX-M-27 in ST131; blaSHV-12 in ST69). The relatively short duration of carriership means that when an intervention drastically reduces the exposure of humans to ESBL-E, the prevalence will be halved in 0.66 years. The observed differences between carriage rates of ESBL/pAmpC genes and E. coli strains need further investigation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Beta-Lactamases / Portador Sadio / Escherichia coli / Infecções por Escherichia coli Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Beta-Lactamases / Portador Sadio / Escherichia coli / Infecções por Escherichia coli Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article