Literature DB >> 17291612

Study of polymorphic variable-number of tandem repeats loci in the ECOR collection and in a set of pathogenic Escherichia coli and Shigella isolates for use in a genotyping assay.

Bjørn-Arne Lindstedt1, Lin Thorstensen Brandal, Lena Aas, Traute Vardund, Georg Kapperud.   

Abstract

The Escherichia coli (E. coli) reference collection, ECOR, consists of 72 strains that are representative of the genotypic diversity, as indexed by multilocus enzyme electrophoresis (MLEE), in the species as a whole. MLEE revealed 4 main phylogenetic groups designated A, B1, B2 and D. We present a study of the relationship between the ECOR strains as determined by polymorphisms in seven variable-number of tandem repeats (VNTR) loci. Seven tandem repeats that were present in more than one of the fully sequenced E. coli strains were selected, and primers were constructed in order to amplify the targets in all species where the loci were present. The combined result for all VNTR loci was adapted as a multiple-locus variable-number tandem repeats analysis (MLVA) and showed that the ECOR collection was divided into 63 distinct genotypes. The ECOR phylogenetic groups defined by MLEE were not well conserved by MLVA. A set of 61 pathogenic isolates of both E. coli and Shigella spp. was then tested with the same set of VNTR loci, and revealed 54 distinct genotypes. In addition, the MLVA method was used to genotype isolates from patients and suspected sources in a recent outbreak of E. coli O103 in Norway. The pathogenic E. coli isolates contained the diarrhea causing categories EIEC, EAEC, STEC, ETEC and EPEC. Shigella isolates were of species S. flexneri, S. boydii, S. sonnei and S. dysenteriae. The MLVA method rapidly genotyped all isolates in the study at a Simpson's index of diversity of D=0.98.

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Year:  2007        PMID: 17291612     DOI: 10.1016/j.mimet.2007.01.001

Source DB:  PubMed          Journal:  J Microbiol Methods        ISSN: 0167-7012            Impact factor:   2.363


  39 in total

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3.  Potentially human-pathogenic Escherichia coli O26 in Norwegian sheep flocks.

Authors:  C Sekse; M Sunde; B-A Lindstedt; P Hopp; T Bruheim; K S Cudjoe; B Kvitle; A M Urdahl
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4.  Evaluation of genetic diversity among aquatic and fecal isolates of Escherichia coli using multilocus variable number of tandem repeat analysis.

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Journal:  3 Biotech       Date:  2020-01-23       Impact factor: 2.406

5.  Occurrence and Spread of Quinolone-Resistant Escherichia coli on Dairy Farms.

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6.  PCR-based detection and molecular characterization of shiga toxin-producing Escherichia coli strains in a routine microbiology laboratory over 16 years.

Authors:  K Haugum; L T Brandal; B-A Lindstedt; A L Wester; K Bergh; J E Afset
Journal:  J Clin Microbiol       Date:  2014-06-11       Impact factor: 5.948

7.  Distribution of classical and nonclassical virulence genes in enterotoxigenic Escherichia coli isolates from Chilean children and tRNA gene screening for putative insertion sites for genomic islands.

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8.  Selection and validation of a multilocus variable-number tandem-repeat analysis panel for typing Shigella spp.

Authors:  Olivier Gorgé; Stéphanie Lopez; Valérie Hilaire; Olivier Lisanti; Vincent Ramisse; Gilles Vergnaud
Journal:  J Clin Microbiol       Date:  2008-01-23       Impact factor: 5.948

9.  Multiple-locus variable-number tandem-repeat analysis for clonal identification of Vibrio parahaemolyticus isolates by using capillary electrophoresis.

Authors:  Erika Harth-Chu; Romilio T Espejo; Richard Christen; Carlos A Guzmán; Manfred G Höfle
Journal:  Appl Environ Microbiol       Date:  2009-04-17       Impact factor: 4.792

10.  An abbreviated MLVA identifies Escherichia coli ST131 as the major extended-spectrum β-lactamase-producing lineage in the Copenhagen area.

Authors:  J B Nielsen; A Albayati; R L Jørgensen; K H Hansen; B Lundgren; K Schønning
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2012-11-06       Impact factor: 3.267

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