Nosocomial outbreak of imipenem-resistant Pseudomonas aeruginosa producing VIM-2 metallo-β-lactamase in a kidney transplantation unit

被引:46
作者
Hammami, S. [1 ]
Boutiba-Ben Boubaker, I. [1 ,2 ]
Ghozzi, R. [1 ,2 ]
Saidani, M. [1 ,2 ]
Amine, S. [1 ,2 ]
Ben Redjeb, S. [1 ]
机构
[1] Tunis Univ Elmanar, Lab Resistance Antimicrobiens, Fac Med, Tunis 1007, Tunisia
[2] Hop Charles Nicolle, Microbiol Lab, Tunis 1006, Tunisia
关键词
pulsed-field gel electrophoresis; carbapenem; P; aeruginosa; epidemiology; RISK-FACTORS; ACINETOBACTER-BAUMANNII; GENE; IDENTIFICATION; CARBAPENEMASES; EMERGENCE; INTEGRONS; PATTERNS; REGION;
D O I
10.1186/1746-1596-6-106
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background: Twenty four non replicate imipenem resistant P. aeruginosa were isolated between January and November 2008, in the kidney transplantation unit of Charles Nicolle Hospital of Tunis (Tunisia). This study was conducted in order to establish epidemiological relationship among them and to identify the enzymatic mechanism involved in imipenem resistance. Methods: Analysis included antimicrobial susceptibility profile, phenotypic (imipenem-EDTA synergy test) and genotypic detection of metallo-beta-lactamase (MBL) (PCR), O-serotyping and pulsed-field gel electrophoresis. Results: All strains showed a high level of resistance to all antimicrobials tested except to colistin. The presence of MBL showed concordance between phenotypic and genotypic methods. Sixteen isolates were identified as VIM-2 MBL-producers and 13 of them were serotype O4 and belonged to a single pulsotype (A). Conclusions: This study describes an outbreak of VIM-2-producing P. aeruginosa in a kidney transplantation unit. Clinical spread of bla(VIM-2) gene is a matter of great concern for carbapenem resistance in Tunisia.
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共 39 条
[1]   Multidrug-resistant Pseudomonas aeruginosa: Risk factors and clinical impact [J].
Aloush, V ;
Navon-Venezia, S ;
Seigman-Igra, Y ;
Cabili, S ;
Carmeli, Y .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (01) :43-48
[2]   Susceptibility patterns of Pseudomonas aeruginosa strains isolated in the Monastir region, Tunisia [J].
Ben Abdallah, H. ;
Noomen, S. ;
Khelifa, A. Ben Elhadj ;
Sahnoun, O. ;
Elargoubi, A. ;
Mastouri, M. .
MEDECINE ET MALADIES INFECTIEUSES, 2008, 38 (10) :554-556
[3]   Molecular characterization of a β-lactamase gene, blaGIM-1, encoding a new subclass of metallo-β-lactamase [J].
Castanheira, M ;
Toleman, MA ;
Jones, RN ;
Schmidt, FJ ;
Walsh, TR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (12) :4654-4661
[4]   Nosocomial outbreak by imipenem-resistant metallo-β-lactamase-producing Pseudomonas aeruginosa in an adult intensive care unit in a Brazilian teaching hospital [J].
Cezario, Renata Cristina ;
De Morais, Lea Duarte ;
Ferreira, Joseane Cristina ;
Costa-Pinto, Rogerio M. ;
da Costa Darini, Ana Lucia ;
Gontijo-Filho, Paulo P. .
ENFERMEDADES INFECCIOSAS Y MICROBIOLOGIA CLINICA, 2009, 27 (05) :269-274
[5]  
Clinical and Laboratory Standards Institute, 2006, M100S16 CLSI
[6]   Hospital outbreak of carbapenem-resistant Pseudomonas aeruginosa producing VIM-1, a novel transferable metallo-β-lactamase [J].
Cornaglia, G ;
Mazzariol, A ;
Lauretti, L ;
Rossolini, GM ;
Fontana, R .
CLINICAL INFECTIOUS DISEASES, 2000, 31 (05) :1119-1125
[7]   Polymyxin B sulfate and colistin: Old antibiotics for emerging multiresistant gram-negative bacteria [J].
Evans, ME ;
Feola, DJ ;
Rapp, RP .
ANNALS OF PHARMACOTHERAPY, 1999, 33 (09) :960-967
[8]   Risk factors for the isolation of multi-drug-resistant Acinetobacter baumannii and Pseudomonas aeruginosa:: a systematic review of the literature [J].
Falagas, M. E. ;
Kopterides, P. .
JOURNAL OF HOSPITAL INFECTION, 2006, 64 (01) :7-15
[9]   Metallo beta lactamases in Pseudomonas aeruginosa and Acinetobacter species [J].
Gupta, Varsha .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2008, 17 (02) :131-143
[10]   Diversity in VIM-2-encoding class 1 integrons and occasional blaSHV2a carriage in isolates of a persistent, multidrug-resistant Pseudomonas aeruginosa clone from Tunis [J].
Hammami, S. ;
Gautier, V. ;
Ghozzi, R. ;
Da Costa, A. ;
Ben-Redjeb, S. ;
Arlet, G. .
CLINICAL MICROBIOLOGY AND INFECTION, 2010, 16 (02) :189-193