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Molecular epidemiology,resistance profiles and clinical features in clinical plasmid-mediated AmpC-producing Enterobacteriaceae
Authors:   Jose Gude,Cristina Seral,Yolanda Sá  enz,Rocí  o Cebollada,Marí  a Gonzá  lez-Domí  nguez,Carmen Torres,F. Javier Castillo
Affiliation:1. Servicio de Microbiología. Hospital Clínico Universitario Lozano Blesa, Zaragoza, Spain;2. Departamento de Microbiología. Universidad de Zaragoza, Zaragoza, Spain;3. Área de Microbiología Molecular. Centro de Investigación Biomédica de La Rioja (CIBIR), Logroño, Spain;4. Área de Bioquímica y Biología Molecular, Universidad de La Rioja, Logroño, Spain
Abstract:
During the 30 months of surveillance period, 85 pAmpC-producing isolates were detected (prevalence 0.56% overall): blaCMY-2 gene in 70 E. coli, 2 K. pneumoniae and 6 P. mirabilis isolates; and the blaDHA-1 gene in 4 E. coli and 3 K. pneumoniae. In 8.23% of them, other β-lactamases (predominantly OXA-1) were identified. All pAmpC-producing isolates were susceptible to carbapenems, whereas high resistance to nalidixic acid, ciprofloxacin and trimethoprim-sulfamethoxazole was observed among pAmpC-producing isolates (80%, 60%, and 44.7%, respectively). In hospital patients, predisposing factors such as prior antibiotic use, previous hospitalization, presence of an indwelling device, invasive urinary tract procedures and mechanical ventilation were observed. In the community setting, urinary tract infection was the most common type of infection related to pAmpC-producing isolates. A wide heterogeneity of clones was found among our E. coli isolates by PFGE, suggesting that this mechanism of resistance is not due to the dissemination of a clonal strain. Surveillance of these resistance mechanisms in the community is thus needed. Awareness of pAmpC dynamic is required to prevent introduction into hospitals and to control the spread of this emerging resistance within the community.
Keywords:Plasmid-mediated AmpC   CMY-2   PFGE   Clinical features   Prevalence   Molecular epidemiology
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