Development of glucosidase agar for the confirmation of water-borne Enterococcus

Analysis of 56 river water samples by the Enterolert (R) defined substrate technique, and standard m-Enterococcus agar isolation followed by confirmation, indicated that after 24 h incubation, Enterolert (R) significantly underestimated the true numbers of enterococci. Extending Enterolert (R) incubation to 36 h improved detection but also revealed false positives. These findings prompted the development of a novel confirmation medium we have termed glucosidase agar, which was prepared by dissolving Enterolert (R) substrate in 2% (w/v) bacteriological agar. Analysis of 1043 colonies arising on m-Enterococcus agar from 280 freshwater, marine and sewage effluent samples. demonstrated that a 2-4 It incubation oil glucosidase agar was a rapid and accurate means of confirming presumptive enterococci, when compared to standard confirmation procedures that take 48 h. The combination of primary isolation on ni-Enterococcus agar followed by confirmation on glucosidase agar permits maximum recovery of Enterococcus whilst effectively eliminating false positives/negatives and provides a reliable alternative use of the Enterolert defined substrate technology. (C) 2001 Elsevier Science Ltd. All rights reserved.