Literature DB >> 7903973

A multicenter comparison of methods for typing strains of Pseudomonas aeruginosa predominantly from patients with cystic fibrosis. The International Pseudomonas aeruginosa Typing Study Group.

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Abstract

Typing methods in seven laboratories were compared for their ability to type reproducibly 200 strains of Pseudomonas aeruginosa, predominantly from patients with cystic fibrosis (CF). Methods included lipopolysaccharide (LPS) serotyping, phage susceptibility typing, bacteriocin production, pilin gene typing, and analysis by restriction fragment length polymorphism (RFLP) with a probe upstream from the exotoxin A gene. The methods differed substantially in their capacity to identify unique typing patterns and to type each strain reproducibly on three occasions. For strains from patients with CF, the RFLP typing method had the greatest discriminatory power (30 unique patterns, 105 [70%] of 150 typed reproducibly). LPS serotyping appeared to be equivalent to RFLP typing for discriminating among P. aeruginosa strains from the environment and from clinical sources other than CF patients. RFLP analysis appears to be the best method for typing P. aeruginosa strains with rough LPS (such as from patients with CF). LPS serotyping appears preferable for other indications as it is simpler to perform.

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Year:  1994        PMID: 7903973     DOI: 10.1093/infdis/169.1.134

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   7.759


  15 in total

1.  Evaluation of random amplified polymorphic DNA typing of Pseudomonas aeruginosa.

Authors:  M Campbell; E Mahenthiralingam; D P Speert
Journal:  J Clin Microbiol       Date:  2000-12       Impact factor: 5.948

2.  Use of pulsed-field gel electrophoresis as an epidemiologic tool during an outbreak of Pseudomonas aeruginosa lung infections in an intensive care unit.

Authors:  D Talon; G Capellier; A Boillot; Y Michel-Briand
Journal:  Intensive Care Med       Date:  1995-12       Impact factor: 17.440

3.  Comparison of ribotyping and genome fingerprinting of Pseudomonas aeruginosa isolates from cystic fibrosis patients.

Authors:  T Bennekov; H Colding; B Ojeniyi; M W Bentzon; N Høiby
Journal:  J Clin Microbiol       Date:  1996-01       Impact factor: 5.948

4.  Modification of dienes mutual inhibition test for epidemiological characterization of Pseudomonas aeruginosa isolates.

Authors:  Erik L Munson; Michael A Pfaller; Gary V Doern
Journal:  J Clin Microbiol       Date:  2002-11       Impact factor: 5.948

Review 5.  Epidemiology, Biology, and Impact of Clonal Pseudomonas aeruginosa Infections in Cystic Fibrosis.

Authors:  Michael D Parkins; Ranjani Somayaji; Valerie J Waters
Journal:  Clin Microbiol Rev       Date:  2018-08-29       Impact factor: 26.132

6.  Emergence of multidrug resistance in ubiquitous and dominant Pseudomonas aeruginosa serogroup O:11. The Greek Pseudomonas Aeruginosa Study Group.

Authors:  P T Tassios; V Gennimata; A N Maniatis; C Fock; N J Legakis
Journal:  J Clin Microbiol       Date:  1998-04       Impact factor: 5.948

7.  Comparison of three typing methods for Pseudomonas aeruginosa isolates from patients with cystic fibrosis.

Authors:  V Waters; J E A Zlosnik; Y C W Yau; D P Speert; S D Aaron; D S Guttman
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2012-07-29       Impact factor: 3.267

8.  Application of Whole-Genome Sequencing Data for O-Specific Antigen Analysis and In Silico Serotyping of Pseudomonas aeruginosa Isolates.

Authors:  Sandra Wingaard Thrane; Véronique L Taylor; Ole Lund; Joseph S Lam; Lars Jelsbak
Journal:  J Clin Microbiol       Date:  2016-04-20       Impact factor: 5.948

9.  Fluorescence-based DNA fingerprinting elucidates nosocomial transmission of phenotypically variable Pseudomonas aeruginosa in intensive care units.

Authors:  H Grundmann; C Schneider; F D Daschner
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1995-12       Impact factor: 3.267

10.  PCR-based detection of a cystic fibrosis epidemic strain of Pseudomonas Aeruginosa.

Authors:  Stavroula Panagea; Craig Winstanley; Yasmin N Parsons; Martin J Walshaw; Martin J Ledson; C Anthony Hart
Journal:  Mol Diagn       Date:  2003
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