Journal of Clinical Microbiology, December 2003, p. 5389-5397, Vol. 41, No. 12
0095-1137/03/$08.00+0 DOI: 10.1128/JCM.41.12.5389-5397.2003
Copyright © 2003, American
Society for
Microbiology. All Rights Reserved.
Multilocus Variable-Number Tandem Repeat Analysis Distinguishes Outbreak and Sporadic Escherichia coli O157:H7 Isolates
Anna C. Noller,1,2 M. Catherine McEllistrem,1 Antonio G. F. Pacheco,3,4 David J. Boxrud,5 and Lee H. Harrison1*
Infectious
Diseases Epidemiology Research Unit, University of Pittsburgh Graduate
School of Public Health and School of
Medicine,1
Department of Infectious
Diseases and Microbiology,2
Department of
Epidemiology, University of Pittsburgh Graduate
School of Public HealthSchool of Medicine,
Pittsburgh, Pennsylvania,3
Departamento de
Epidemiologia e Métodos Quantitativos em Saúde, Escola
Nacional de Saúde Pública, FIOCRUZ, Rio de
Janeiro, Brazil,4
Microbiology Laboratory,
Minnesota Department of Health, Minneapolis,
Minnesota5
Received 16 April 2003/
Returned for modification 7 July 2003/
Accepted 11 September 2003
Escherichia
coli O157:H7 is a major cause of food-borne illness in the United
States. Outbreak detection involves traditional epidemiological methods
and routine molecular subtyping by pulsed-field gel electrophoresis
(PFGE). PFGE is labor-intensive, and the results are difficult to
analyze and not easily transferable between laboratories. Multilocus
variable-number tandem repeat (VNTR) analysis (MLVA) is a fast,
portable method that analyzes multiple VNTR loci, which are areas of
the bacterial genome that evolve quickly. Eighty isolates, including 21
isolates from five epidemiologically well-characterized outbreaks from
Pennsylvania and Minnesota, were analyzed by PFGE and MLVA. Strains in
PFGE clusters were defined as strains that differed by less than or
equal to one band by using XbaI and the confirmatory enzyme
SpeI. MLVA was performed by comparing the number of tandem
repeats at seven loci. From 6 to 30 alleles were found at the seven
loci, resulting in 64 MLVA types among the 80 isolates. MLVA correctly
identified the isolates from all five outbreaks if only a single-locus
variant was allowed. MLVA differentiated strains with unique PFGE
types. Additionally, MLVA discriminated strains within PFGE-defined
clusters that were not known to be part of an outbreak. In addition to
being a simple and validated method for E. coli O157:H7
outbreak detection, MLVA appears to have a sensitivity equal to that of
PFGE and a specificity superior to that of
PFGE.
* Corresponding
author. Mailing address: Infectious Diseases Epidemiology
Research Unit, University of Pittsburgh Graduate School of Public
Health and School of Medicine, 521 Parran Hall, 130 DeSoto St.,
Pittsburgh, PA 15261. Phone: (412) 624-3137. Fax: (412) 624-2256.
E-mail:
lharriso{at}edc.pitt.edu.
Journal of Clinical Microbiology, December 2003, p. 5389-5397, Vol. 41, No. 12
0095-1137/03/$08.00+0 DOI: 10.1128/JCM.41.12.5389-5397.2003
Copyright © 2003, American
Society for
Microbiology. All Rights Reserved.
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Copyright © 2003 by the American Society for Microbiology. All rights reserved.