Community and hospital spread of Escherichia coli producing CTX-M extended-spectrum β-lactamases in the UK

被引:408
|
作者
Woodford, N
Ward, ME
Kaufmann, ME
Turton, J
Fagan, EJ
James, D
Johnson, AP
Pike, R
Warner, M
Cheasty, T
Pearson, A
Harry, S
Leach, JB
Loughrey, A
Lowes, JA
Warren, RE
Livermore, DM
机构
[1] Hlth Protect Agcy, Antibiot Resistance Monitoring & Reference Lab, Specialist & Refrence Microbiol Div Colindale, London NW9 5HT, England
[2] Hlth Protect Agcy, Lab Healthcare Associated Infect, Specialist & Refrence Microbiol Div Colindale, London NW9 5HT, England
[3] Hlth Protect Agcy, Lab Enter Pathogens, Specialist & Refrence Microbiol Div Colindale, London NW9 5HT, England
[4] Hlth Protect Agcy, Communicable Dis Surveillance Ctr, London, England
[5] Hlth Protect Agcy, Local & Reg Serv, London, England
[6] Kingston Hosp NHS Trust, Kingston, Surrey, England
[7] Belfast City Hosp, Belfast BT9 7AD, Antrim, North Ireland
[8] HPA SE, Southampton Lab, Southampton, Hants, England
[9] Shrewsbury & Telford Hosp NHS Trust, Shrewsbury, Salop, England
关键词
ESBLs; CTX-M beta-lactamases; community infections; molecular epidemiology;
D O I
10.1093/jac/dkh424
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: During 2003, the Health Protection Agency's Antibiotic Resistance Monitoring and Reference Laboratory began to receive isolates of Escherichia coli for confirmation of extended-spectrum beta-lactamase production with a phenotype implying a CTX-M-type beta-lactamase, i.e. MICs of cefotaxime greater than or equal to8-fold higher than MICs of ceftazidime. Many were referred as being from community patients. We examined 291 CTX-M-producing isolates from the UK and investigated the genetic basis of their phenotype. Methods: PCR was used to detect alleles encoding CTX-M enzymes and to assign these to their bla(CTX-M) phylogenetic groups. Selected alleles were sequenced. Producers were compared by analysis of banding patterns generated by pulsed-field gel electrophoresis of XbaI-digested genomic DNA. MICs were determined by an agar dilution method or by Etest. Results: Of 291 CTX-M-producing E. coli isolates studied from 42 UK centres, 70 (24%) were reportedly from community patients, many of whom had only limited recent hospital contact. Community isolates were referred by 12 centres. Two hundred and seventy-nine (95.9%) producers contained genes encoding group 1 CTX-M enzymes and 12 contained bla(CTX-M-9)-like alleles. An epidemic CTX-M-15-producing strain was identified, with 110 community and inpatient isolates referred from six centres. Representatives of four other major strains also produced CTX-M-15, as did several sporadic isolates examined. Most producers were multi-resistant to fluoroquinolones, trimethoprim, tetracycline and aminoglycosides as well as to non-carbapenem beta-lactams. Conclusions: CTX-M-producing E. coli are a rapidly developing problem in the UK, with CTX-M-15 particularly common. The diversity of producers and geographical scatter of referring laboratories indicates wide dissemination of bla(CTX-M) genes. Because of the public health implications, including for the treatment of community-acquired urinary tract infections, the spread of these strains-and CTX-M-15 beta-lactamase in particular-merits close monitoring.
引用
收藏
页码:735 / 743
页数:9
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