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Co-existence of blaOXA-23 with armA in quinolone-resistant Acinet | 17684
Journal of Drug Metabolism & Toxicology

Journal of Drug Metabolism & Toxicology
Open Access

ISSN: 2157-7609

+44-20-4587-4809

Co-existence of blaOXA-23 with armA in quinolone-resistant Acinetobacter baumannii from a Chinese University Hospital


2nd World Congress and Exhibition on Antibiotics and Antibiotic Resistance

October 13-15, 2016 Manchester, UK

Baodong Ling, Min Shen, Guangxin Luan, Yanhong Wang, Yaowen Chang, Chi Zhang, Jingni Yang and Shanshan Deng and Xu Jia

Chengdu Medical College, China

Posters & Accepted Abstracts: J Drug Metab Toxicol

Abstract :

Nosocomial infections caused by Quinolone-Resistant Acinetobacter Baumannii (QRAB) have been increasing in recent years, posing a threat to public health. In this study, we aimed to determine the mechanisms of quinolone resistance in A. baumannii isolates and investigate the occurrence of carbapenem resistance gene blaOXA-23 and aminoglycoside resistance gene armA among these QRAB. Totally, 101 A. baumannii isolates were collected from one university hospital in western China between 2011 and 2012. All isolates were identified and confirmed by sequencing analysis of 16S rRNA internal transcribed spacer and recA. The Minimal Inhibitory Concentrations (MICs) of ciprofloxacin and levofloxacin were determined by agar dilution. Plasmid-Mediated Quinolone Resistance Determinants (PMQRs) were performed with PCR assay, whilst gyrA and parC genes of QRAB were amplified and sequenced. The results showed that 77 QRAB harbored mutations of gyrA and parC, whereas PMQRs were not detected. Additionally, 41 isolates had resistance to aminoglycosides and carbapenems due to the expression of a 16S rRNA methylase armA (with high level resistance) and acquisition of OXA-type carbapenemase OXA-23. Obviously, most of sequence types belonged to clonal complex 92 in these 41 isolates, which demonstrated that these isolates had a common origin and caused nosocomial infection. An A. baumannii clone producing OXA-23, armA along with mutations of Quinolone Resistance-Determining Regions (QRDRs) has been identified as an emerging and rapidly spreading pathogen. To our knowledge, this is the first report of hospital dissemination of A. baumannii carrying blaOXA-23, armA and mutations of QRDRs in QRAB in western China.

Biography :

Baodong Ling has completed his MD from West China Medical University and worked as a Visiting Scholar in University of Zurich in 1996. He is a Distinguished Professor of Pharmacology. He is also the Director of Small Molecule Drugs Key Laboratory of Sichuan Province and Institute of Materia Medica. He has published more than 60 papers in reputed journals and has been serving as an Editorial Board Member of Chinese Journal of Antibiotics and World Notes on Antibiotics.

Email: lingbaodong@cmc.edu.cn

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