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Detection of blaOXA-23 in Acinetobacter spp. isolated from patients of a university hospital
Authors:Laís Lisboa Corrêa  Larissa Alvarenga Batista Botelho  Lívia Carvalho Barbosa  Claudio Simões Mattos  Jupira Miron Carballido  Carmem Lúcia Teixeira de Castro  Pedro Juan Jose Mondino  Geraldo Renato de Paula  Silvia Susana Bona de Mondino  Claudia Rezende Vieira de Mendonça-Souza
Affiliation:1. Postgraduate Program in Pathology, Medical School, Universidade Federal Fluminense (UFF), Niterói, RJ, Brazil;2. Department of Pathology, Medical School, UFF, Niterói, RJ, Brazil;3. Microbiology Laboratory, Pathology Service, Hospital Universitário Antônio Pedro, UFF, Niterói, RJ, Brazil;4. Laboratory of Microbiological Control, Department of Pharmaceutical Technology, Pharmacy School, UFF, Niterói, RJ, Brazil
Abstract:IntroductionAcinetobacter spp. have emerged as notorious pathogens involved in healthcare-associated infections. Carbapenems are important antimicrobial agents for treating infections due to multidrug resistant Acinetobacter spp. Different mechanisms may confer resistance to these drugs in the genus, particularly production of class D carbapenemases. OXA-23-like family has been pointed out as one of the predominant carbapenamases among Acinetobacter. The present work aimed to investigate the occurrence of OXA-23-like carbapenemases among Acinetobacter isolates recovered from patients of a university hospital in Niterói, RJ, Brazil.MethodsAntimicrobial susceptibility profiles were determined by disk-diffusion. Imipenem resistant isolates were submitted to Modified Hodge Test in order to screen for carbapenemase production, and later to polymerase chain reaction (PCR) to investigate the presence of blaOXA-23.ResultsImipenem and meropenem resistance rates were 71.4% and 69.7%, respectively. The Modified Hodge Test revealed carbapenemase production among 76 (89.4%) of the 85 imipenem resistant isolates analyzed; according to PCR results, 81 isolates (95.4%) carried the blaOXA-23 gene.ConclusionsOXA-23-like enzymes may be an important mechanism of carbapenem resistance among isolates present in the hospital studied.
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