Abstract

The aim of this study was to identify the presence of group CTX-M-9 extended spectrum beta-lactamases (ESBL) in clinical Escherichia coli isolates from pediatric patients. A total of 404 non-repeated positive ESBL E. coli isolates were collected from documented clinical infections in pediatric patients over a 2-year period. The identification and susceptibility profiles were determined using an automated system. Isolates that suggested ESBL production based on their resistance profiles to third and fourth generation cephalosporin and monobactam were selected. ESBL production was phenotypically confirmed using a diffusion method with cefotaxime and ceftazidime discs alone and in combination with clavulanic acid. blaESBL gene identification was performed through PCR amplification and sequencing. Pulsed Field Gel Electrophoresis (PFGE) and Multilocus Sequence Typing (MLST) were performed to establish the clonal relationships of the E. coli isolates. CTX-M-9-type ESBLs were detected in 2.5% of the isolates. The subtypes corresponded to blaCTX-M-14 (n = 4) and blaCTX-M-27 (n = 6). Additionally, coexistence with other beta-lactamases was observed. A clonal relationship was established in three isolates; the rest were classified as non-related. We found seven different sequence type (ST) in CTX-M-9- producing E. coli isolates. ST38 was the most frequent. This study is the first report in Mexico to document the presence of group CTX-M-9 ESBLs in E. coli isolates from pediatric patients.

Highlights

  • Nosocomial infections constitute one the most important problems of medical care, which do increase morbidity-mortality indices, and the total cost of healthcare

  • The 404 E. coli isolates with extended spectrum beta-lactamases (ESBL) patterns were positive for the phenotypic confirmatory test

  • Group CTX-M-9 ESBLs were detected in 2.5% of these isolates (n = 10)

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Summary

Introduction

Nosocomial infections constitute one the most important problems of medical care, which do increase morbidity-mortality indices, and the total cost of healthcare. Hospitalized patients in the intensive care units (ICU) are usually more susceptible to these kinds of infections. A prolonged hospital stay, invasive procedures and total parenteral nutrition are some of the principal risk factors for the development of nosocomial infections in pediatric patients [1]. The prevalence of nosocomial infections in pediatric intensive care units (PICUs) has been reported to be 6–12% and 10–25% in neonatal intensive care units (NICUs) [2]. PLOS ONE | DOI:10.1371/journal.pone.0168608 December 19, 2016

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