Literature DB >> 1624604

Rapid method for differentiating strains of Branhamella catarrhalis.

V Peiris1, J Heald.   

Abstract

The ability of Branhamella catarrhalis to cause nosocomial infections is a matter of some controversy. The API ZYM research kit for detecting 89 enzymes was used on 49 isolates of B catarrhalis to select enzymes of potential use in differentiating clinical isolates. Twenty nine enzymes were produced by all isolates (13 strongly positive) and many of these were esterases; 16 enzymes were not detected in any isolate (40 if a more stringent criterion was used). Twenty enzymes were selected to form a prototype biotyping panel which allowed 17 different patterns of reactivity to be recognised. Of the 49, 34 isolates were confined to the three commonest patterns. Only one isolate was untypable using this panel due to lack of reactivity. A kit with these 20 substrates may be sufficiently discriminatory to be useful in the rapid study of outbreaks of infection caused by B catarrhalis.

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Year:  1992        PMID: 1624604      PMCID: PMC495232          DOI: 10.1136/jcp.45.6.532

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  8 in total

1.  Serological typing of Branhamella catarrhalis strains on the basis of lipopolysaccharide antigens.

Authors:  M Vaneechoutte; G Verschraegen; G Claeys; A M Van Den Abeele
Journal:  J Clin Microbiol       Date:  1990-02       Impact factor: 5.948

2.  Restriction fragment mapping of Branhamella catarrhalis: a new tool for studying the epidemiology of this middle ear pathogen.

Authors:  D P Dickinson; B G Loos; D M Dryja; J M Bernstein
Journal:  J Infect Dis       Date:  1988-07       Impact factor: 5.226

3.  API ZYM: a simple rapid system for the detection of bacterial enzymes.

Authors:  M W Humble; A King; I Phillips
Journal:  J Clin Pathol       Date:  1977-03       Impact factor: 3.411

4.  Differentiation of neisseriaceae by isoenzyme electrophoresis.

Authors:  A I Braude; J A McCutchan; C Ison; P R Sargeaunt
Journal:  J Infect Dis       Date:  1983-02       Impact factor: 5.226

5.  Evaluation of restriction endonuclease analysis as an epidemiologic typing system for Branhamella catarrhalis.

Authors:  J E Patterson; T F Patterson; P Farrel; W J Hierholzer; M J Zervos
Journal:  J Clin Microbiol       Date:  1989-05       Impact factor: 5.948

6.  A note on susceptibility of Branhamella catarrhalis to heavy metals.

Authors:  T V Riley; M L Taylor
Journal:  J Appl Bacteriol       Date:  1989-08

Review 7.  Branhamella catarrhalis: an organism gaining respect as a pathogen.

Authors:  B W Catlin
Journal:  Clin Microbiol Rev       Date:  1990-10       Impact factor: 26.132

8.  Esterase electrophoresis: a molecular tool for studying the epidemiology of Branhamella catarrhalis nosocomial infection.

Authors:  B Picard; P Goullet; E Denamur; G Suermondt
Journal:  Epidemiol Infect       Date:  1989-12       Impact factor: 2.451

  8 in total
  3 in total

1.  Epidemiological typing of Moraxella catarrhalis by pulsed field gel electrophoresis.

Authors:  S M Davison; D E Low; R H Cruz; D Beaulieu; S R Scriver
Journal:  Can J Infect Dis       Date:  1995-05

2.  Use of API NH system for identification of Moraxella catarrhalis.

Authors:  V Peiris; C Bennett; S Norris
Journal:  J Clin Microbiol       Date:  1994-10       Impact factor: 5.948

Review 3.  Moraxella catarrhalis: from emerging to established pathogen.

Authors:  Cees M Verduin; Cees Hol; André Fleer; Hans van Dijk; Alex van Belkum
Journal:  Clin Microbiol Rev       Date:  2002-01       Impact factor: 26.132

  3 in total

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