Literature DB >> 8810502

High resolution DNA fingerprinting of Acinetobacter outbreak strains.

P Janssen1, L Dijkshoorn.   

Abstract

AFLP is a novel high resolution fingerprinting method that can be used to delineate intraspecific relationships among a large variety of organisms, including bacteria. In the present study, this method was tested for its usefulness in the epidemiological typing of Acinetobacter strains. A total of 25 Acinetobacter strains originating from five hospital outbreaks in three countries were used. Isolates from the same outbreak displayed identical banding patterns and each set of outbreak strains could be found in one particular AFLP cluster. These data are in good agreement with the results obtained by other typing methods previously used on the same set of strains, indicating that AFLP analysis may be a valuable alternative in epidemiological typing.

Mesh:

Year:  1996        PMID: 8810502     DOI: 10.1111/j.1574-6968.1996.tb08429.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  11 in total

Review 1.  Amplified-fragment length polymorphism analysis: the state of an art.

Authors:  P H Savelkoul; H J Aarts; J de Haas; L Dijkshoorn; B Duim; M Otsen; J L Rademaker; L Schouls; J A Lenstra
Journal:  J Clin Microbiol       Date:  1999-10       Impact factor: 5.948

2.  Comparison of Acinetobacter baumannii isolates from United Kingdom hospitals with predominant Northern European genotypes by amplified-fragment length polymorphism analysis.

Authors:  Richard P Spence; Tanny J K van der Reijden; Lenie Dijkshoorn; Kevin J Towner
Journal:  J Clin Microbiol       Date:  2004-02       Impact factor: 5.948

3.  Fluorescent amplified-fragment length polymorphism genotyping of Neisseria meningitidis identifies clones associated with invasive disease.

Authors:  J N Goulding; J V Hookey; J Stanley; W Olver; K R Neal; D A Ala'Aldeen; C Arnold
Journal:  J Clin Microbiol       Date:  2000-12       Impact factor: 5.948

4.  Genetic diversity of clinical and environmental isolates of Vibrio cholerae determined by amplified fragment length polymorphism fingerprinting.

Authors:  S C Jiang; M Matte; G Matte; A Huq; R R Colwell
Journal:  Appl Environ Microbiol       Date:  2000-01       Impact factor: 4.792

5.  Genetic diversity of Vibrio cholerae in Chesapeake Bay determined by amplified fragment length polymorphism fingerprinting.

Authors:  S C Jiang; V Louis; N Choopun; A Sharma; A Huq; R R Colwell
Journal:  Appl Environ Microbiol       Date:  2000-01       Impact factor: 4.792

6.  Specificity of rabbit antisera against lipopolysaccharide of Acinetobacter.

Authors:  R Pantophlet; L Brade; L Dijkshoorn; H Brade
Journal:  J Clin Microbiol       Date:  1998-05       Impact factor: 5.948

7.  Predictive fluorescent amplified-fragment length polymorphism analysis of Escherichia coli: high-resolution typing method with phylogenetic significance.

Authors:  C Arnold; L Metherell; G Willshaw; A Maggs; J Stanley
Journal:  J Clin Microbiol       Date:  1999-05       Impact factor: 5.948

8.  Pandemic spread of cholera: genetic diversity and relationships within the seventh pandemic clone of Vibrio cholerae determined by amplified fragment length polymorphism.

Authors:  Ruiting Lan; Peter R Reeves
Journal:  J Clin Microbiol       Date:  2002-01       Impact factor: 5.948

Review 9.  Acinetobacter baumannii: emergence of a successful pathogen.

Authors:  Anton Y Peleg; Harald Seifert; David L Paterson
Journal:  Clin Microbiol Rev       Date:  2008-07       Impact factor: 26.132

10.  Amplified-fragment length polymorphism analysis versus macro-restriction fragment analysis for molecular typing of Streptococcus pneumoniae isolates.

Authors:  J van Eldere; P Janssen; A Hoefnagels-Schuermans; S van Lierde; W E Peetermans
Journal:  J Clin Microbiol       Date:  1999-06       Impact factor: 5.948

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