Literature DB >> 21975141

Genotyping of selected bacterial enteropathogens in Norway.

Bjørn-Arne Lindstedt1.   

Abstract

In Norway the Norwegian Institute of Public Health (NIPH) is the primary facility for nationwide surveillance of foodborne infections, and it is vital that we can perform rapid and high resolution identification of foodborne bacteria at the strain level. During the last decade a rapid introduction of DNA-based methods has been introduced, which show promise in enhancing the speed and discriminatory capability of the typing laboratory. The laboratory responsible for genotyping enteropathogens at NIPH is limited in staff, thus methods demanding reduced labour, high degree of automation and increased ease of interpretation is essential. We found that this could be achieved by focusing on MLVA for some of the most predominant enteropathogenic species. Bacterial genotyping is performed by several laboratories in Norway, however this review will address the use of routine genotyping by MLVA of common foodborne bacteria at NIPH. The emphasis will be on Escherichia coli, Salmonella typhimurium, Shigella spp. Yersinia enterocolitica and Listeria monocytogenes. This review is based on an oral presentation given at the 9th International Meeting on Microbial Epidemiological Markers in Wernigerode Germany on September 1st 2010. Copyright Â
© 2011 Elsevier GmbH. All rights reserved.

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Year:  2011        PMID: 21975141     DOI: 10.1016/j.ijmm.2011.09.005

Source DB:  PubMed          Journal:  Int J Med Microbiol        ISSN: 1438-4221            Impact factor:   3.473


  5 in total

1.  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

2.  Subtyping of a large collection of historical Listeria monocytogenes strains from Ontario, Canada, by an improved multilocus variable-number tandem-repeat analysis (MLVA).

Authors:  S Saleh-Lakha; V G Allen; J Li; F Pagotto; J Odumeru; E Taboada; M Lombos; K C Tabing; B Blais; D Ogunremi; G Downing; S Lee; A Gao; C Nadon; S Chen
Journal:  Appl Environ Microbiol       Date:  2013-08-16       Impact factor: 4.792

3.  Multiple-locus variable-number tandem-repeat analysis in genotyping Yersinia enterocolitica strains from human and porcine origins.

Authors:  S Virtanen; R Laukkanen-Ninios; P Ortiz Martínez; A Siitonen; M Fredriksson-Ahomaa; H Korkeala
Journal:  J Clin Microbiol       Date:  2013-05-01       Impact factor: 5.948

4.  Variable Number of Tandem Repeats (VNTR) analysis of Flavobacterium psychrophilum from salmonids in Chile and Norway.

Authors:  Patricia Apablaza; Øyvind J Brevik; Svein Mjøs; Samuel Valdebenito; Pedro Ilardi; Juan Battaglia; Inger Dalsgaard; Are Nylund
Journal:  BMC Vet Res       Date:  2015-07-14       Impact factor: 2.741

5.  Use of multiple-locus variable-number of tandem repeats analysis (MLVA) to investigate genetic diversity of Salmonella enterica subsp. enterica serovar Typhimurium isolates from human, food, and veterinary sources.

Authors:  Gergana Mateva; Karl Pedersen; Gitte Sørensen; Galina Asseva; Hristo Daskalov; Petar Petrov; Todor Kantardjiev; Irina Alexandar; Charlotta Löfström
Journal:  Microbiologyopen       Date:  2017-08-23       Impact factor: 3.139

  5 in total

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