Literature DB >> 2347384

Comparison of clinical Acinetobacter strains using a carbon source growth assay.

L Dijkshoorn1, A Van Ooyen, W C Hop, M Theuns, M F Michel.   

Abstract

A quantitative carbon source growth assay, comprising ten carbon sources, was used to compare acinetobacter strains from three hospitals. The strains had been obtained during episodes of increased prevalence of isolations and were, for each hospital, assumed to be epidemiologically related. This assumption was supported by the electrophoretic protein profiles of the strains. Univariate analysis of growth data showed significant differences between strains from the three hospitals. Moreover, cluster analysis revealed that the major pattern in the data was related to the epidemiological origin of the strains. Exceptions to the epidemic-related pattern were observed. Thus, apart from epidemiological factors, other factors might contribute to carbon source growth profiles of the strains. It is concluded that the carbon growth assay may be useful to distinguish roughly between acinetobacter strains from different sites of origin. Further studies are required to analyse additional factors which influence carbon source growth of strains.

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Year:  1990        PMID: 2347384      PMCID: PMC2271785          DOI: 10.1017/s0950268800047452

Source DB:  PubMed          Journal:  Epidemiol Infect        ISSN: 0950-2688            Impact factor:   2.451


  13 in total

1.  The influence on numerical taxonomic similarities of errors in microbiological tests.

Authors:  P H Sneath; R Johnson
Journal:  J Gen Microbiol       Date:  1972-09

2.  Carbon source utilization tests as an aid to the classification of non-fermenting gram-negative bacteria.

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Journal:  J Gen Microbiol       Date:  1973-01

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Journal:  J Bacteriol       Date:  1968-05       Impact factor: 3.490

4.  Carbon assimilation by the Achromobacter-Moraxella group (Debord's tribe Mimease).

Authors:  G L Gilardi
Journal:  Am J Med Technol       Date:  1968-07

5.  Epidemic spread of Acinetobacter calcoaceticus in a neurosurgical department analyzed by electronic data processing.

Authors:  P Gerner-Smidt; L Hansen; A Knudsen; K Siboni; I Søgaard
Journal:  J Hosp Infect       Date:  1985-06       Impact factor: 3.926

6.  Control of an epidemic spread of a multi-resistant strain of Acinetobacter calcoaceticus in a hospital.

Authors:  W H Crombach; L Dijkshoorn; M van Noort-Klaassen; J Niessen; G van Knippenberg-Gordebeke
Journal:  Intensive Care Med       Date:  1989       Impact factor: 17.440

7.  The aerobic pseudomonads: a taxonomic study.

Authors:  R Y Stanier; N J Palleroni; M Doudoroff
Journal:  J Gen Microbiol       Date:  1966-05

8.  Hospital outbreak of multi-resistant Acinetobacter anitratus: an airborne mode of spread?

Authors:  K D Allen; H T Green
Journal:  J Hosp Infect       Date:  1987-03       Impact factor: 3.926

9.  Infections with Acinetobacter calcoaceticus (Herellea vaginicola): clinical and laboratory studies.

Authors:  R H Glew; R C Moellering; L J Kunz
Journal:  Medicine (Baltimore)       Date:  1977-03       Impact factor: 1.889

10.  Acinetobacter bacteriocin typing.

Authors:  H J Andrews
Journal:  J Hosp Infect       Date:  1986-03       Impact factor: 3.926

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  6 in total

1.  Comparison of outbreak and nonoutbreak Acinetobacter baumannii strains by genotypic and phenotypic methods.

Authors:  L Dijkshoorn; H Aucken; P Gerner-Smidt; P Janssen; M E Kaufmann; J Garaizar; J Ursing; T L Pitt
Journal:  J Clin Microbiol       Date:  1996-06       Impact factor: 5.948

Review 2.  Acinetobacter spp. as nosocomial pathogens: microbiological, clinical, and epidemiological features.

Authors:  E Bergogne-Bérézin; K J Towner
Journal:  Clin Microbiol Rev       Date:  1996-04       Impact factor: 26.132

3.  Endemic acinetobacter in intensive care units: epidemiology and clinical impact.

Authors:  L Dijkshoorn; R van Dalen; A van Ooyen; D Bijl; I Tjernberg; M F Michel; A M Horrevorts
Journal:  J Clin Pathol       Date:  1993-06       Impact factor: 3.411

4.  Comparison of amplified ribosomal DNA restriction analysis, random amplified polymorphic DNA analysis, and amplified fragment length polymorphism fingerprinting for identification of Acinetobacter genomic species and typing of Acinetobacter baumannii.

Authors:  J G Koeleman; J Stoof; D J Biesmans; P H Savelkoul; C M Vandenbroucke-Grauls
Journal:  J Clin Microbiol       Date:  1998-09       Impact factor: 5.948

5.  Genetic diversity and clonal relationships of Acinetobacter baumannii strains isolated in a neonatal ward: epidemiological investigations by allozyme, whole-cell protein and antibiotic resistance analysis.

Authors:  V Thurm; E Ritter
Journal:  Epidemiol Infect       Date:  1993-12       Impact factor: 2.451

6.  Clinical and epidemiological investigations of Acinetobacter genomospecies 3 in a neonatal intensive care unit.

Authors:  A Horrevorts; K Bergman; L Kollée; I Breuker; I Tjernberg; L Dijkshoorn
Journal:  J Clin Microbiol       Date:  1995-06       Impact factor: 5.948

  6 in total

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