Journal article
Multilocus Sequence Typing versus Pulsed-Field Gel Electrophoresis for Characterization of Extended-Spectrum Beta-Lactamase-Producing Escherichia coli Isolates
Journal of clinical microbiology, Vol.43(4), pp.1776-1781
04/2005
DOI: 10.1128/JCM.43.4.1776-1781.2005
PMCID: PMC1081380
PMID: 15814998
Abstract
Extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli strains are emerging pathogens. Molecular typing of ESBL-producing E. coli is useful for surveillance purposes, to monitor outbreaks and track nosocomial spread. Although pulsed-field gel electrophoresis (PFGE) is the current "gold standard" for bacterial molecular typing, multilocus sequence typing (MLST) may offer advantages. Forty ESBL-producing E. coli isolates were selected at random from a cohort of intensive care unit patients who had active surveillance perirectal cultures done. PFGE identified 19 unique PFGE types (PT) among the 40 isolates; MLST identified 22 unique sequence types. MLST had greater discriminatory ability than PFGE for ESBL-producing E. coli. Simpson's indices of diversity for PFGE and MLST were 0.895 and 0.956, respectively. There were five clonal complexes (CCs) (isolates with differences of no more than two loci) that each contained multiple PT, but each PT was found in only one CC, indicating genetic consistency within a CC. MLST has clear utility in studies of ESBL-producing E. coli, based on a greater discriminatory ability and reproducibility than PFGE and the ability to a priori define genetically related bacterial strains.
Details
- Title: Subtitle
- Multilocus Sequence Typing versus Pulsed-Field Gel Electrophoresis for Characterization of Extended-Spectrum Beta-Lactamase-Producing Escherichia coli Isolates
- Creators
- Lucia L Nemoy - University of Maryland, BaltimoreMamuka KotetishviliJustine TignoAnanda Keefer-NorrisAnthony D HarrisEli N PerencevichJudith A JohnsonDave TorpeyAlexander SulakvelidzeJ Glenn Morris JrO Colin Stine
- Resource Type
- Journal article
- Publication Details
- Journal of clinical microbiology, Vol.43(4), pp.1776-1781
- DOI
- 10.1128/JCM.43.4.1776-1781.2005
- PMID
- 15814998
- PMCID
- PMC1081380
- NLM abbreviation
- J Clin Microbiol
- ISSN
- 0095-1137
- eISSN
- 1098-660X
- Publisher
- United States
- Grant note
- 5K23AI001752-02 / NIAID NIH HHS K23 AI001752 / NIAID NIH HHS
- Language
- English
- Date published
- 04/2005
- Academic Unit
- Epidemiology; Internal Medicine
- Record Identifier
- 9983779295002771
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