Escherichia coli O25b-ST131: a pandemic, multiresistant, community-associated strain

被引:583
作者
Rogers, Benjamin A. [1 ]
Sidjabat, Hanna E. [1 ]
Paterson, David L. [1 ]
机构
[1] Univ Queensland, UQ Ctr Clin Res, Brisbane, Qld 4006, Australia
关键词
beta-lactamases; molecular epidemiology; bacterial infections; SPECTRUM-BETA-LACTAMASES; URINARY-TRACT-INFECTIONS; BLOOD-STREAM INFECTIONS; ST131 PRODUCING CTX-M-15; SEQUENCE TYPE ST131; CTX-M ENZYMES; KLEBSIELLA-PNEUMONIAE; CIPROFLOXACIN-RESISTANT; MOLECULAR EPIDEMIOLOGY; HIGH PREVALENCE;
D O I
10.1093/jac/dkq415
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Escherichia coli sequence type 131 (ST131) is a worldwide pandemic clone, causing predominantly community-onset antimicrobial-resistant infection. Its pandemic spread was identified in 2008 by utilizing multilocus sequence typing (MLST) of CTX-M-15 extended-spectrum beta-lactamase-producing E. coli from three continents. Subsequent research has confirmed the worldwide prevalence of ST131 harbouring a broad range of virulence and resistance genes on a transferable plasmid. A high prevalence of the clone (similar to 30%-60%) has been identified amongst fluoroquinolone-resistant E. coli. In addition, it potentially harbours a variety of beta-lactamase genes; most often, these include CTX-M family beta-lactamases, and, less frequently, TEM, SHV and CMY beta-lactamases. Our knowledge of ST131's geographical distribution is incomplete. A broad distribution has been demonstrated amongst antimicrobial-resistant E. coli from human infection in Europe (particularly the UK), North America, Canada, Japan and Korea. High rates are suggested from limited data in Asia, the Middle East and Africa. The clone has also been detected in companion animals, non-companion animals and foods. The clinical spectrum of disease described is similar to that for other E. coli, with urinary tract infection predominant. This can range from cystitis to life-threatening sepsis. Infection occurs in humans of all ages. Therapy must be tailored to the antimicrobial resistance phenotype of the infecting isolate and the site of infection. Phenotypic detection of the ST131 clone is not possible and DNA-based techniques, including MLST and PCR, are described.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 109 条
[61]   CTX-M enzymes are the predominant extended-spectrum β-lactamases produced by Enterobacteriaceae in Ireland [J].
Morris, Dearbhaile ;
Boyle, Fiona ;
Buckley, Victoria ;
Xu, Li ;
Hanahoe, Belinda ;
Hawkey, Peter ;
Cormican, Martin .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2009, 64 (04) :864-866
[62]   Sporadic occurrence of CMY-2-producing multidrug-resistant Escherichia coli of ST-complexes 38 and 448, and ST131 in Norway [J].
Naseer, U. ;
Haldorsen, B. ;
Simonsen, G. S. ;
Sundsfjord, A. .
CLINICAL MICROBIOLOGY AND INFECTION, 2010, 16 (02) :171-178
[63]   Molecular characterization of CTX-M-15-producing clinical isolates of Escherichia coli reveals the spread of multidrug-resistant ST131 (O25:H4) and ST964 (O102:H6) strains in Norway [J].
Naseer, Umaer ;
Haldorsen, Bjorg ;
Tofteland, Stale ;
Hegstad, Kristin ;
Scheutz, Flemming ;
Simonsen, Gunnar Skov ;
Sundsfjord, Arnfinn .
APMIS, 2009, 117 (07) :526-536
[64]   Intercontinental emergence of Escherichia coli clone O25:H4-ST131 producing CTX-M-15 [J].
Nicolas-Chanoine, Marie-Helene ;
Blanco, Jorge ;
Leflon-Guibout, Veronique ;
Demarty, Raphael ;
Alonso, Maria Pilar ;
Canica, Maria Manuela ;
Park, Yeon-Joon ;
Lavigne, Jean-Philippe ;
Pitout, Johann ;
Johnson, James R. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2008, 61 (02) :273-281
[65]   Should tigecycline be considered for urinary tract infections? A pharmacokinetic re-evaluation [J].
Nix, David E. ;
Matthias, Kathryn R. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2010, 65 (06) :1311-1312
[66]   Identification of a progenitor of the CTX-M-9 group of extended-spectrum β-lactamases from Kluyvera georgiana isolated in Guyana [J].
Olson, AB ;
Silverman, M ;
Boyd, DA ;
McGeer, A ;
Willey, BM ;
Pong-Porter, V ;
Daneman, N ;
Mulvey, MR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (05) :2112-2115
[67]   Emergence of imipenem resistance in clinical Escherichia coli during therapy [J].
Oteo, Jesus ;
Delgado-Iribarren, Alberto ;
Vega, Dolores ;
Bautista, Veronica ;
Cruz Rodriguez, Maria ;
Velasco, Maria ;
Maria Saavedra, Jose ;
Perez-Vazquez, Maria ;
Garcia-Cobos, Silvia ;
Martinez-Martinez, Luis ;
Campos, Jose .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2008, 32 (06) :534-537
[68]   AmpC β-lactamases in Escherichia coli: emergence of CMY-2-producing virulent phylogroup D isolates belonging mainly to STs 57, 115, 354, 393, and 420, and phylogroup B2 isolates belonging to the international clone O25b-ST131 [J].
Oteo, Jesus ;
Cercenado, Emilia ;
Cuevas, Oscar ;
Bautista, Veronica ;
Delgado-Iribarren, Alberto ;
Orden, Beatriz ;
Perez-Vazquez, Maria ;
Garcia-Cobos, Silvia ;
Campos, Jose .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2010, 67 (03) :270-276
[69]   CTX-M-15-producing urinary Escherichia coli O25b-ST131-phylogroup B2 has acquired resistance to fosfomycin [J].
Oteo, Jesus ;
Orden, Beatriz ;
Bautista, Veronica ;
Cuevas, Oscar ;
Arroyo, Margarita ;
Martinez-Ruiz, Rocio ;
Perez-Vazquez, Maria ;
Alcaraz, Marta ;
Garcia-Cobos, Silvia ;
Campos, Jose .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2009, 64 (04) :712-717
[70]   Extended-spectrum β-lactamase-producing Escherichia coli in Spain belong to a large variety of multilocus sequence typing types, including ST10 complex/A, ST23 complex/A and ST131/B2 [J].
Oteo, Jesus ;
Diestra, Karol ;
Juan, Carlos ;
Bautista, Veronica ;
Novais, Angela ;
Perez-Vazquez, Maria ;
Moya, Bartolome ;
Miro, Elisenda ;
Coque, Teresa M. ;
Oliver, Antonio ;
Canton, Rafael ;
Navarro, Ferran ;
Campos, Jose .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2009, 34 (02) :173-176