4.3 Article

Analytical limits of four β-glucuronidase and β-galactosidase-based commercial culture methods used to detect Escherichia coli and total coliforms

期刊

JOURNAL OF MICROBIOLOGICAL METHODS
卷 75, 期 3, 页码 506-514

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.mimet.2008.08.001

关键词

E. coli; MI agar; Colilert; Chromocult Coliform agar ES; Readycult Coliforms 100; Total coliforms

资金

  1. CHUL (Centre Hospitalier Universitaire de Quebec)
  2. (Centre d'Expertise en Analyse Environnementale du Quebec)
  3. (Laboratoire de Sante Publique du Quebec)
  4. (Servei de Microbiologia, Centre de Diagnostic Biomedic, Universitat de Barcelona)
  5. (National Institute of Public Health)
  6. South African Institute for Medical Research

向作者/读者索取更多资源

Colilerte((R)) (Colilert), Readycult((R)) Coliforms 100 (Readycult), Chromocult((R)) Coliform agar ES (Chromocult), and MI agar (MI) are beta-galactosidase and p-glucuronidase-based commercial culture methods used to assess water quality. Their analytical performance, in terms of their respective ability to detect different strains of Escherichia coli and total coliforms, had never been systematically compared with pure cultures. Here, their ability to detect P-glucuronidase production from E. coli isolates was evaluated by using 74 E. coli strains of different geographic origins and serotypes encountered in fecal and environmental settings. Their ability to detect beta-galactosidase production was studied by testing the 74 E. coli strains as well as 33 reference and environmental non-E. coli total coliform strains. Chromocult. Ml, Readycult, and Colilert detected beta-glucuronidase production from respectively 79.9, 79.9, 81.1, and 51.4% of the 74 E. coli strains tested. These 4 methods detected beta-galactosidase production from respectively 85.1, 73.8, 84.1, and 84.1% of the total coliform strains tested. The results of the present study suggest that Colilert is the weakest method tested to detect beta-glucuronidase production and MI the weakest to detect P-galactosidase production. Furthermore, the high level of false-negative results for E. coli recognition obtained by all four methods suggests that they may not be appropriate for identification of presumptive E. coli strains. (C) 2008 Elsevier B.V. All rights reserved.

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