Literature DB >> 10403421

Identification of clinically isolated vancomycin-resistant enterococci: comparison of API and BBL Crystal systems.

J M T Hamilton-Miller, S Shah.   

Abstract

Twenty-eight phenotypically separate strains of clinically isolated vancomycin-resistant enterococci have been investigated with two API identification kit systems (20 Strep and Rapid ID 32 Strep) and two BBL Crystal kits (Gram Positive and Rapid Gram Positive). All strains were identified as Enterococcus faecium by a reference laboratory. The Rapid ID 32 kit positively identified 15 of 28 strains (54%), but only two (7%) were identified correctly: 11 were identified as 'doubtful' or 'to genus level' and two gave 'unacceptable' profiles. The API 20 Strep kit identified 27 strains (96%), but only 16 (57%) were identified correctly as E. faecium. The Rapid ID 32 kit erred by either positively misidentifying vancomycin-resistant E. faecium as E. casseliflavus or E. gallinarum, or indicated that this was the most likely identification, while the API 20 Strep kit more commonly produced a misidentification as E. casseliflavus. The Crystal Gram Positive and Rapid Gram Positive kits correctly identified 26 (93%) and 27 (96%) of the strains, respectively.

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Year:  1999        PMID: 10403421     DOI: 10.1099/00222615-48-7-695

Source DB:  PubMed          Journal:  J Med Microbiol        ISSN: 0022-2615            Impact factor:   2.472


  7 in total

1.  Routine molecular identification of enterococci by gene-specific PCR and 16S ribosomal DNA sequencing.

Authors:  S Angeletti; G Lorino; G Gherardi; F Battistoni; M De Cesaris ; G Dicuonzo
Journal:  J Clin Microbiol       Date:  2001-02       Impact factor: 5.948

2.  Comparison of conventional and molecular methods for identification of aerobic catalase-negative gram-positive cocci in the clinical laboratory.

Authors:  P P Bosshard; S Abels; M Altwegg; E C Böttger; R Zbinden
Journal:  J Clin Microbiol       Date:  2004-05       Impact factor: 5.948

3.  Use of a genus- and species-specific multiplex PCR for identification of enterococci.

Authors:  Charlene R Jackson; Paula J Fedorka-Cray; John B Barrett
Journal:  J Clin Microbiol       Date:  2004-08       Impact factor: 5.948

4.  Rapid identification of clinically relevant Enterococcus species by fluorescence in situ hybridization.

Authors:  Nele Wellinghausen; Melanie Bartel; Andreas Essig; Sven Poppert
Journal:  J Clin Microbiol       Date:  2007-08-01       Impact factor: 5.948

5.  Detection of human intestinal catalase-negative, Gram-positive cocci by rRNA-targeted reverse transcription-PCR.

Authors:  Hiroyuki Kubota; Hirokazu Tsuji; Kazunori Matsuda; Takashi Kurakawa; Takashi Asahara; Koji Nomoto
Journal:  Appl Environ Microbiol       Date:  2010-06-25       Impact factor: 4.792

6.  Evaluation of D-xylose and 1% methyl-alpha-D-glucopyranoside fermentation tests for distinguishing Enterococcus gallinarum from Enterococcus faecium.

Authors:  D K Chen; L Pearce; A McGeer; D E Low; B M Willey
Journal:  J Clin Microbiol       Date:  2000-10       Impact factor: 5.948

7.  Evaluation of a PCR assay to detect enterococcusfaecalis in blood and determine glycopeptides resistance genes: van a and van B.

Authors:  Hamidreza Honarm; Mahsome Falah Ghavidel; Iraj Nikokar; Morteza Rahbar Taromsari
Journal:  Iran J Med Sci       Date:  2012-09
  7 in total

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