An Outbreak of NDM-1-Producing Klebsiella pneumoniae, Associated with OmpK35 and OmpK36 Porin Loss in Tunisia

被引:39
作者
Hamzaoui, Zaineb [1 ,2 ]
Ocampo-Sosa, Alain [3 ]
Maamar, Elaa [1 ]
Fernandez Martinez, Marta [3 ]
Ferjani, Sana [1 ,2 ]
Hammami, Samia [1 ,2 ]
Harbaoui, Sarra [1 ]
Genel, Nathalie [4 ]
Arlet, Guillaume [4 ]
Saidani, Mabrouka [1 ,5 ]
Slim, Amine [1 ,5 ]
Boutiba-Ben Boubaker, Ilhem [1 ,5 ]
Martinez-Martinez, Luis [3 ,6 ]
机构
[1] Univ Tunis El Manar, Fac Med Tunis LR99ES09, Res Lab Antimicrobial Resistance, Tunis 1007, Tunisia
[2] Univ Carthage, Fac Sci Bizerte, Tunis, Tunisia
[3] Univ Hosp Marques de Valdecilla, Microbiol Serv, IDIVAL, Santander, Spain
[4] Univ Paris 06, Sch Med, Dept Bacteriol, Paris, France
[5] Charles Nicolle Hosp, Microbiol Lab, Tunis, Tunisia
[6] Univ Cantabria, Sch Med, Dept Mol Biol, Santander, Spain
关键词
Klebsiella pneumoniae; carbapenemases; New Delhi metallo-beta-lactamase; carbapenem-resistant Enterobacteriaceae; outer membrane porin; epidemiology; CARBAPENEMASE-PRODUCING ENTEROBACTERIACEAE; BETA-LACTAMASE; IMIPENEM RESISTANCE; VIRULENCE FACTORS; MULTIPLEX PCR; EMERGENCE; IDENTIFICATION; OXA-48; NDM-1; CEPHALOSPORINS;
D O I
10.1089/mdr.2017.0165
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To describe clinical and molecular characteristics of an outbreak due to metallo--lactamases (MBLs) producing Klebsiella pneumoniae collected at Charles Nicolle Hospital of Tunis and to analyze the impact of outer membrane porin (OMP) loss on carbapenem resistance levels. Methods: Between 2010 and 2015, 178 carbapenem-resistant Enterobacteriaceae were isolated. Screening for MBL production was performed using combined disk diffusion method, with imipenem and ethylene diamine tetraacetic acid (EDTA) as inhibitors. Resistance genes and virulence factors were identified by polymerase chain reaction (PCR) and sequencing. Genotyping was performed by pulsed-field gel electrophoresis and multilocus sequence typing. Genetic environment of carbapenemase genes was determined by PCR mapping. Conjugation assays were performed, and plasmids were assigned to incompatibility groups by PCR-based replicon typing. OMPs were profiled by sodium dodecyl sulfate-polyacrilamide gel electrophoresis, and porin genes were sequenced. Results: Nineteen K. pneumoniae (10.6%) showing MBL activity were isolated from patients hospitalized on four different wards. NDM-1 was the only MBL identified, in association with bla(OXA-48). All strains lacked at least one OMP, and carbapenem resistance levels were remarkably elevated in strains lacking OmpK35 and OmpK36. bla(NDM-1) was located in IncFIA-type conjugative plasmid, with the same genetic context in all strains. The epidemiological diffusion of bla(NDM-1) was due to two clones, one major clone belonging to sequence type (ST) 147 (n = 16) and the other clone belonging to ST307 (n = 3). Conclusions: This study describes an outbreak of NDM-1-producing K. pneumoniae strains, isolated from a Tunisian hospital, caused by two clones belonging to ST147 and ST307; and highlights the role of OMPs loss, in combination with beta-lactamase expression, in conferring high carbapenem resistance.
引用
收藏
页码:1137 / 1147
页数:11
相关论文
共 45 条
[1]   OXA-163-Producing Klebsiella pneumoniae in Cairo, Egypt, in 2009 and 2010 [J].
Abdelaziz, Mohammed O. ;
Bonura, Celestino ;
Aleo, Aurora ;
El-Domany, Ramadan A. ;
Fasciana, Teresa ;
Mammina, Caterina .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (07) :2489-2491
[2]  
[Anonymous], ANT SUSC TEST EUCAST
[3]   MOLECULAR EPIDEMIOLOGY OF KLEBSIELLA-PNEUMONIAE STRAINS THAT PRODUCE SHV-4 BETA-LACTAMASE AND WHICH WERE ISOLATED IN 14 FRENCH HOSPITALS [J].
ARLET, G ;
ROUVEAU, M ;
CASIN, I ;
BOUVET, PJM ;
LAGRANGE, PH ;
PHILIPPON, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (10) :2553-2558
[4]   Emergence of NDM-1 in Association with OXA-48 in Klebsiella pneumoniae from Tunisia [J].
Ben Nasr, Adam ;
Decre, Dominique ;
Compain, Fabrice ;
Genel, Nathalie ;
Barguellil, Farouk ;
Arlet, Guillaume .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2013, 57 (08) :4089-4090
[5]   Imipenem resistance of Enterobacter aerogenes mediated by outer membrane permeability [J].
Bornet, C ;
Davin-Regli, A ;
Bosi, C ;
Pages, JM ;
Bollet, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (03) :1048-1052
[6]   Imipenem resistance in Klebsiella pneumoniae is associated with the combination of ACT-1, a plasmid-mediated AmpC beta-lactamase, and the loss of an outer membrane protein [J].
Bradford, PA ;
Urban, C ;
Mariano, N ;
Projan, SJ ;
Rahal, JJ ;
Bush, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (03) :563-569
[7]   Resistance Plasmid Families in Enterobacteriaceae [J].
Carattoli, Alessandra .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (06) :2227-2238
[8]   Early Dissemination of NDM-1-and OXA-181-Producing Enterobacteriaceae in Indian Hospitals: Report from the SENTRY Antimicrobial Surveillance Program, 2006-2007 [J].
Castanheira, Mariana ;
Deshpande, Lalitagauri M. ;
Mathai, Dilip ;
Bell, Jan M. ;
Jones, Ronald N. ;
Mendes, Rodrigo E. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (03) :1274-1278
[9]   Epidemiology and Virulence of Klebsiella pneumoniae [J].
Clegg, Steven ;
Murphy, Caitlin N. .
MICROBIOLOGY SPECTRUM, 2016, 4 (01)
[10]  
Clinical and Laboratory Standards Institute (CLSI), M100S23 CLSI