1. Sequential outbreaks in a Spanish hospital caused by multiresistant OXA-58-producing Acinetobacter baumannii ST92.
- Author
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Alvargonzalez JJC, Hernando AV, Martín MDR, Casas CM, Iglesias JO, Marín MFB, Alvarez MLA, Sanchez VB, and Marí JMN
- Subjects
- Acinetobacter Infections genetics, Acinetobacter baumannii genetics, Acinetobacter baumannii metabolism, Gene Expression Regulation, Bacterial physiology, Gene Expression Regulation, Enzymologic, Humans, Spain epidemiology, Time Factors, beta-Lactamases genetics, Acinetobacter Infections metabolism, Acinetobacter baumannii classification, Acinetobacter baumannii drug effects, Anti-Bacterial Agents pharmacology, Disease Outbreaks statistics & numerical data, Drug Resistance, Multiple, Bacterial, beta-Lactamases metabolism
- Abstract
The aim of this study was to assess the epidemiology and molecular basis of the infection and dissemination of multidrug-resistant Acinetobacter baumannii (MDRAB) in three sequential outbreaks at the intensive care units (ICUs) of a tertiary university hospital in Granada, Spain, between 2009 and 2011. Strains from all patients infected and/or colonized by MDRAB during outbreak periods were characterized using PFGE and multilocus sequence typing (MLST). The first outbreak appeared in the summer of 2009 involving 38 ICU patients: 25 from a Traumatology-Rehabilitation hospital (TRH) and 13 from a Medical-Surgery hospital (MSH). Between 2010 and 2011, outbreaks were limited to the MSH-ICU, affecting 9 and 11 patients, respectively. Two PFGE types were detected. In the 2009 outbreak, two clones were identified: profile 1 strains were isolated at the TRH, whilst profile 2 was isolated at the MSH. Only one clone was identified in the 2010 and 2011 outbreaks: the profile 2 clone detected at the MSH in 2009. After MLST analysis, a single sequence type (ST92) was identified. This suggested that an endemic strain could evolve and cause localized outbreaks in vulnerable patients. Multiplex PCR for OXA group enzymes yielded a positive result for blaOXA-58-like and blaOXA-51-like genes, and gene sequencing showed the presence of blaOXA-58. However, the absence of ISAba1 upstream of the blaOXA-51-like gene suggested the absence of OXA-51 expression. The susceptibility pattern was not an appropriate method for MDRAB surveillance, as several susceptibility patterns were identified in a single clone. Consequently, molecular methods of characterization are recommended for epidemiological surveillance of MDRAB., (© 2014 The Authors.)
- Published
- 2014
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