Literature DB >> 28216097

Epidemiology and resistance characteristics of Pseudomonas aeruginosa isolates from the respiratory department of a hospital in China.

Wei Feng1, Fengjun Sun1, Qian Wang1, Wei Xiong2, Xuewen Qiu1, Xiaotian Dai3, Peiyuan Xia4.   

Abstract

OBJECTIVES: Pseudomonas aeruginosa is one of the most common pathogens causing nosocomial pneumonia. The aim of this study was to investigate the epidemiology and resistance of P. aeruginosa isolated from hospitalised patients in the respiratory department of a hospital in China.
METHODS: Clinical isolates were collected from the respiratory department of Southwest Hospital (Chongqing, China) from January 2013 to December 2014. Patients' social and demographic information was obtained from the hospital's information system. Antimicrobial susceptibility was assessed using the agar dilution method. Screening for carbapenemase production among carbapenem-resistant P. aeruginosa was performed using the modified Hodge test and MBL Etest, and carbapenemase-encoding genes were amplified by PCR. Amplification and sequencing of the oprD gene were performed for carbapenem-resistant P. aeruginosa. Sequence types were determined by multilocus sequence typing (MLST).
RESULTS: A total of 92 P. aeruginosa isolates were collected from patients in the respiratory department, and piperacillin/tazobactam was the most effective antibiotic against these isolates. Multivariate analysis revealed that antibiotic use prior to admission was an independent risk factor for P. aeruginosa infection. The isolates comprised 25 genotypes, the most common of which were ST235 and ST111. The blaIMP-4 gene was present in 4 isolates and blaVIM-2 in 1 isolate among the 24 carbapenem-resistant isolates. Most of the carbapenem-resistant isolates contained mutational inactivation of the oprD gene.
CONCLUSIONS: These results suggested that patients and the hospital environment were sources of P. aeruginosa in nosocomial infections. Mutational inactivation of the oprD gene might be the main mechanism of carbapenem resistance.
Copyright © 2017 International Society for Chemotherapy of Infection and Cancer. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Epidemiology; Multilocus sequence typing; Nosocomial infection; Pseudomonas aeruginosa; Resistance

Mesh:

Year:  2017        PMID: 28216097     DOI: 10.1016/j.jgar.2016.11.012

Source DB:  PubMed          Journal:  J Glob Antimicrob Resist        ISSN: 2213-7165            Impact factor:   4.035


  8 in total

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Journal:  Antimicrob Agents Chemother       Date:  2017-10-24       Impact factor: 5.191

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3.  Antibiotic-Resistant Bacteria in Clams-A Study on Mussels in the River Rhine.

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4.  Screening of Antimicrobial Resistance Genes and Epidemiological Features in Hospital and Community-Associated Carbapenem-Resistant Pseudomonas aeruginosa Infections.

Authors:  Ayşegül Çopur Çiçek; Ayşe Ertürk; Nebahat Ejder; Erva Rakici; Uğur Kostakoğlu; İlknur Esen Yıldız; Songül Özyurt; Emine Sönmez
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5.  Multilocus sequence typing and variations in the oprD gene of Pseudomonas aeruginosa isolated from a hospital in China.

Authors:  Huiqin Liu; Weina Kong; Weina Yang; Gukui Chen; Haihua Liang; Yani Zhang
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6.  Successful control of resistance in Pseudomonas aeruginosa using antibiotic stewardship and infection control programs at a Chinese university hospital: a 6-year prospective study.

Authors:  Lei Liu; Bin Liu; Yu Li; Wei Zhang
Journal:  Infect Drug Resist       Date:  2018-05-01       Impact factor: 4.003

Review 7.  The Building Blocks of Antimicrobial Resistance in Pseudomonas aeruginosa: Implications for Current Resistance-Breaking Therapies.

Authors:  R Frèdi Langendonk; Daniel R Neill; Joanne L Fothergill
Journal:  Front Cell Infect Microbiol       Date:  2021-04-16       Impact factor: 5.293

8.  Emergence of Carbapenem-Resistant ST244, ST292, and ST2446 Pseudomonas aeruginosa Clones in Burn Patients in Yunnan Province.

Authors:  Yue Fang; Zulqarnain Baloch; Wei Zhang; Ying Hu; Rui Zheng; Yuzhu Song; Wenlin Tai; Xueshan Xia
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  8 in total

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