Literature DB >> 12525923

Evaluation of the BactiCard Neisseria for identification of pathogenic Neisseria species and Moraxella catarrhalis.

W M Janda1, M C Montero, L M Wilcoski.   

Abstract

The BactiCard Neisseria (Remel, USA) is a chromogenic enzyme substrate system for identifying Neisseria gonorrhoeae, Neisseria meningitidis, Neisseria lactamica, and Moraxella catarrhalis. The identification system consists of a card with four test circles impregnated with chromogenic substrates for indoxyl butyrate esterase (IB), prolyl aminopeptidase (PRO), gamma-glutamyl aminopeptidase (GLUT), and ss-galactosidase (BGAL). These substrates permit the identification of Moraxella catarrhalis, Neisseria gonorrhoeae, Neisseria meningitidis, and Neisseria lactamica, respectively. After hydration of the circles with buffer, colonies from growth on selective media or a subculture are applied to the four circles. IB and BGAL reactions are read for a blue-green color after 2 and 15 min, respectively. PRO and GLUT reactions are read at 15 min for a red color after addition of a developer reagent. Identifications obtained with the BactiCard Neisseria were compared with those obtained using conventional procedures for 558 isolates in a blinded fashion. The BactiCard Neisseria identified 100% of 254 Neisseria gonorrhoeae, 100% of 125 Neisseria meningitidis, 53 (98.2%) of 54 Neisseria lactamica, and 123 (98.4%) of 125 Moraxella catarrhalis isolates. The BactiCard Neisseria is an accurate and rapid system for identification of these microorganisms in the clinical laboratory.

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Year:  2002        PMID: 12525923     DOI: 10.1007/s10096-002-0838-6

Source DB:  PubMed          Journal:  Eur J Clin Microbiol Infect Dis        ISSN: 0934-9723            Impact factor:   3.267


  18 in total

1.  Evaluation of five rapid systems for the identification of Neisseria gonorrhoeae.

Authors:  J Dolter; L Bryant; J M Janda
Journal:  Diagn Microbiol Infect Dis       Date:  1990 May-Jun       Impact factor: 2.803

2.  Rapid identification of Branhamella catarrhalis. A comparison of five rapid methods.

Authors:  M Louie; E G Ongsansoy; K R Forward
Journal:  Diagn Microbiol Infect Dis       Date:  1990 May-Jun       Impact factor: 2.803

3.  Characterization of Neisseria polysacchareae sp. nov. (Riou, 1983) in previously identified noncapsular strains of Neisseria meningitidis.

Authors:  M T Boquete; C Marcos; J A Sáez-Nieto
Journal:  J Clin Microbiol       Date:  1986-05       Impact factor: 5.948

4.  Effect of acidity and antimicrobial agent-like compounds on viability of Plesiomonas shigelloides.

Authors:  J M Janda
Journal:  J Clin Microbiol       Date:  1987-07       Impact factor: 5.948

5.  DNA probe confirmatory test for Neisseria gonorrhoeae.

Authors:  J S Lewis; D Kranig-Brown; D A Trainor
Journal:  J Clin Microbiol       Date:  1990-10       Impact factor: 5.948

6.  API QuadFERM+ with rapid DNase for identification of Neisseria spp. and Branhamella catarrhalis.

Authors:  W M Janda; K L Zigler; J J Bradna
Journal:  J Clin Microbiol       Date:  1987-02       Impact factor: 5.948

7.  Incidence of Neisseria gonorrhoeae isolates negative by Syva direct fluorescent-antibody test but positive by Gen-Probe accuprobe test in a sexually transmitted disease clinic population.

Authors:  J L Beebe; M P Rau; S Flageolle; B Calhoon; J S Knapp
Journal:  J Clin Microbiol       Date:  1993-09       Impact factor: 5.948

8.  Rapid identification of Branhamella catarrhalis with 4-methylumbelliferyl butyrate.

Authors:  M Vaneechoutte; G Verschraegen; G Claeys; P Flamen
Journal:  J Clin Microbiol       Date:  1988-06       Impact factor: 5.948

9.  Difficulties in differentiating Neisseria cinerea from Neisseria gonorrhoeae in rapid systems used for identifying pathogenic Neisseria species.

Authors:  J M Boyce; E B Mitchell
Journal:  J Clin Microbiol       Date:  1985-11       Impact factor: 5.948

10.  Evaluation of eight methods for identification of pathogenic Neisseria species: Neisseria-Kwik, RIM-N, Gonobio-Test, Minitek, Gonochek II, GonoGen, Phadebact Monoclonal GC OMNI Test, and Syva MicroTrak Test.

Authors:  J R Dillon; M Carballo; M Pauzé
Journal:  J Clin Microbiol       Date:  1988-03       Impact factor: 5.948

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