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Virulence factors profiles and ESBL production in Escherichia coli causing bacteremia in Peruvian children

  • Noemí Palma
    ,
  • Cláudia Gomes
    ,
  • Maribel Riveros
    ,
  • Wilfredo García
    ,
  • Sandra Martínez-Puchol
    ,
  • Lidia Ruiz-Roldán
  • Hospital Clínic – Universitat de Barcelona
    ,
  • Universidad Peruana Cayetano Heredia, Instituto de Medicina Tropical Alexander von Humboldt
    ,
  • CIBIR
    ,
  • University of Leuven
    ,
  • Prins Leopold Instituut voor Tropische Geneeskunde
    ,
  • School of Public Health, University of Texas
Research Output:
Contribution to journal
Article
Peer-review

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 70-75 (6 pages)

Journal (Volume, Issue Number)

Diagnostic Microbiology and Infectious Disease (Volume 86, Issue 1)

Publication milestones

  • Published - 01/09/2016

Publication status

Published - 01/09/2016

ISSN

0732-8893

Publication IDs

  • Scopus: 84977555553
  • PubMed: 27345125

Abstract

The presence of 25 virulence genes (VGs), genetic phylogroups, quinolone-resistance and Extended Spectrum β-lactamase (ESBL)-production was assessed in 65 Escherichia coli isolates from blood cultures in children <5 years in Peru. The most frequent VGs were fimA (89.2%), iutA (83.1%), agn43 (72.3%), iucA (67.7%), and fyuA (49.2%). The isolates belonged to D (47.7%), A (26.1%), B1 (21.5%), and B2 (4.6%) phylogroups. D + B2 isolates presented a high number of fimA, hly, papC, sat, and fyuA genes. Quinolone-susceptible (22 isolates – 33.8%) and ESBL-negative (31 isolates – 47.7%) isolates carried more VGs that their respective counterparts (5.7 vs. 4.7 and 5.3 vs. 4.4 respectively); the frequency of the fyuA, aat, aap, and hly genes significantly differed between quinolone-resistant and quinolone-susceptible isolates. Neonatal sepsis isolates tended to be more quinolone-resistant (P = 0.0697) and ESBL-producers (P = 0.0776). Early-onset neonatal sepsis isolates possessed a high number of VGs (5.2 VGs), especially in neonates of ≤1 day (5.9 VGs).

Funding Details

JR has a fellowship from the program I3SNS of the ISCIII (grant number: CES11/012), and CG has a predoctoral grant from the ISCIII (FI12/00561). This work was supported by Agencia Española de Cooperación Internacional para el Desarrollo (AECID), Spain, Programa de Cooperación Interuniversitaria e Investigación Científica con Iberoamérica (D/019499/08, D/024648/09, D/030509/10, and A1/035720/11) (J.R and T.J.O) by the Spanish Network for the Research in Infectious Diseases (REIPI RD12/0015) and Generalitat de Catalunya, Departament d’Universitats, Recerca i Societat de la Informació (2014 SGR 26) (JR) and Directorate General for Development Cooperation (DGCD) of the Belgian Government (framework agreement 3, project 95502).
FundersFunding numbers
DGCD
95502
Directorate General for Development Cooperation
-
Programa de Cooperación Interuniversitaria e Investigación Científica con Iberoamérica
A1/035720/11, D/030509/10, D/019499/08, D/024648/09
Spanish Network for the Research in Infectious Diseases
REIPI RD12/0015
ISCIII
CES11/012, FI12/00561
AECID
-
DURSI
2014 SGR 26

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